Package 'MBNMAtime'

Description

Adds follow-up time (fups, fupcount) and arm (arms, narms) indices to a dataset.

Usage

add_index(data.ab, reference = 1)

Arguments

Value

A data frame similar to data.ab but with additional columns:

• arm Arm identifiers coded for each study

• fupcount Follow-up identifiers coded for each study

• fups The total number of follow-up measurements in each study

• narm The total number of arms in each study

If treatment or class are non-numeric or non-sequential (i.e. with missing numeric codes), treatments/classes in the returned data frame will be numbered and recoded to enforce sequential numbering (a warning will be shown stating this).

Examples

# Add indices to osteoarthritis pain dataset
data.ab <- add_index(osteopain)

# Add indices to dataset using different network reference treatment
data.ab <- add_index(osteopain, reference=3)

Description

A dataset from a systematic review of Randomised-Controlled Trials (RCTs) comparing different doses of alogliptin with placebo (Langford et al. 2016). The systematic review was simply performed and was intended to provide data to illustrate a statistical methodology rather than for clinical inference. Alogliptin is a treatment aimed at reducing blood glucose concentration in type II diabetes. The outcome is continuous, and aggregate data responses correspond to the mean change in HbA1c from baseline to follow-up. The dataset includes 14 Randomised-Controlled Trials (RCTs), comparing 5 different doses of alogliptin with placebo, leading to 6 different treatments (combination of dose and agent) within the network.

Usage

alog_pcfb

Format

A data frame in long format (one row per arm and study), with 46 rows and 9 variables:

• studyID Study identifiers

• clinicaltrialGov_ID The clinicaltrial.gov ID code

• agent Character data indicating the agent to which participants were randomised

• dose Numeric data indicating the standardised dose received

• treatment Character data indicating the treatment (combination of agent and dose) to which participants were randomised

• time Numeric data indicating the time at which the observation was measured (given in weeks)

• y Numeric data indicating the mean change from baseline in blood glucose concentration (mg/dL) in a study arm

• se Numeric data indicating the standard error for the mean change from baseline in blood glucose concentration (mg/dL) in a study arm

• n Numeric data indicating the number in each arm at each follow-up time

Details

alog_pcfb is a data frame in long format (one row per observation, arm and study), with the variables studyID, clinicaltrialGov_ID, agent, dose, treatment, time, y, se, and n.

References

Langford O, Aronson JK, van Valkenhoef G, Stevens RJ (2016). “Methods for meta-analysis of pharmacodynamic dose-response data with application to multi-arm studies of alogliptin.” Stat Methods Med Res. ISSN 1477-0334 (Electronic) 0962-2802 (Linking), doi:10.1177/0962280216637093, https://pubmed.ncbi.nlm.nih.gov/26994216/.

Description

Plot relative effects from NMAs performed at multiple time-bins

Usage

binplot(
  network,
  overlay.nma = c(0, stats::quantile(network$data.ab$time)),
  method = "common",
  link = "identity",
  lim = "cred",
  plot.bins = TRUE,
  legend = TRUE,
  ...
)

Arguments

Details

Performs several standard NMAs at different time "bins", time periods within which treatment effects are assumed to be constant over time. Separate NMAs are then performed within each time bin on data points from studies that fall within the time bin (only a single follow-up time is taken from each study to avoid double counting).

Note that the wider the time bin boundaries specified by the user, the larger the potential range of included follow-up times and this can introduce heterogeneity or inconsistency.

Results are plotted versus the network reference and are plotted on the specified link scale. Each time bin window is marked on the plot by vertical dashed lines. The NMA estimates within each time bin are plotted as a horizontal solid black line (the posterior median) with a shaded region indicating the 95% credible interval (prediction intervals can instead be plotted). The width of these shaded regions is equal to the range of study time-points included in the NMA performed within that timebin, which may therefore be more narrow than the time bin specified in the binplot() command due to the follow-up times at which data is available in included studies.

Value

Plots treatment effects from NMAs performed within discrete time bins. The object returned is a list containing the plot and a sublist of NMA results and predictions from each time bin specified in overlay.nma.

Overlaying NMA results

overlay.nma indicates regions of the data (defined as "time bins") over which it may be reasonable to "lump" different follow-up times from different studies together and assume a standard NMA model. For example:

• overlay.nma=c(5,10) indicates a single NMA of studies with follow-up times ⁠>5⁠ and ⁠<=10⁠

• overlay.nma=c(5,10,15) indicates two NMAs should be performed of studies with follow-up times ⁠>5⁠ and ⁠<=10⁠ of studies with follow-up times ⁠>10⁠ and ⁠<=15⁠

When used with MBNMA (via predict.mbnma()) this allows comparison to MBNMA results over a specific range of time within each time bin. It can be useful to assess which time-course function might be suitable when using binplot(), or to to assess if the MBNMA predictions are in agreement with predictions from an NMA model when using plot.mb.predict() for a specific range of time-points. This can be a general indicator of the fit of the time-course model.

However, it is important to note that the wider the range specified in overlay.nma, the more likely it is that different time-points are included, and therefore that there is greater heterogeneity/inconsistency in the NMA model. If overlay.nma includes several follow-up times for any study then only a single time-point will be taken (the one closest to mean(overlay.nma)). The NMA predictions are plotted over the range specified in overlay.nma as a horizontal line, with the 95%CrI shown by a grey rectangle. The NMA predictions represent those for any time-points within this range since they lump together data at all these time-points. Predictions for treatments that are disconnected from the network reference treatment at data points specified within overlay.nma cannot be estimated so are not included.

It is important to note that the NMA model is not necessarily the "correct" model, since it "lumps" different time-points together and ignores potential differences in treatment effects that may arise from this. The wider the range specified in overlay.nma, the greater the effect of "lumping" and the stronger the assumption of similarity between studies.

For an NMA model to be estimated and a corresponding prediction to be made from it, each time bin must include the network reference treatment (treatment=1) evaluated in at least 1 connected study in the time bin. If a given time bin does not meet this criteria then an NMA will not be calculated for it.

Examples

# Create an mb.network object from a dataset
alognet <- mb.network(alog_pcfb)

# Plot relative effects from NMAs calculated for a single time-bins
# Do not plot time-bin boundaries
binplot(alognet, overlay.nma=c(0,5), plot.bins=FALSE)

# Plot relative effects from NMAs at multiple time-bins
# With random treatment effects
binplot(alognet, overlay.nma=c(5,10,15,20),
  method="random")

Description

A dataset from a systematic review of Randomised-Controlled Trials (RCTs) for maintenance treatment of moderate to severe chronic obstructive pulmonary disease (COPD) (Karabis et al. 2013). Data are extracted from (Tallarita et al. 2019). SEs were imputed for three studies, and number of patients randomised were imputed for one study (LAS 39) in which they were missing, using the median standard deviation calculated from other studies in the dataset. The outcome is trough Forced Expiratory Volume in 1 second (FEV1), measured in litres and reported in each study arm as mean change from baseline to follow-up. The dataset includes 13 Randomised-Controlled Trials (RCTs), comparing 2 treatments (Tiotropium and Aclidinium) and placebo.

Usage

copd

Format

A data frame in long format (one row per arm and study), with 80 rows and 6 variables:

• studyID Study identifiers

• time Numeric data indicating the time at which the observation was measured (given in weeks)

• y Numeric data indicating the mean change from baseline in FEV1 (litres) in a study arm

• se Numeric data indicating the standard error for the mean change from baseline in FEV1 in a study arm

• treatment Factor data indicating the treatment to which participants were randomised

• n Numeric data indicating the number of participants randomised to each arm

Details

copd is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, y, se, treatment, and n.

References

Karabis A, Lindner L, Mocarski M, Huisman E, Greening A (2013). “Comparative efficacy of aclidinium versus glycopyrronium and tiotropium, as maintenance treatment of moderate to severe COPD patients: a systematic review and network meta-analysis.” Int J Chron Obstruct Pulmon Dis, 8, 405-423. doi:10.2147/COPD.S48967, https://pubmed.ncbi.nlm.nih.gov/24043936/.

Tallarita M, De lorio M, Baio G (2019). “A comparative review of network meta-analysis models in longitudinal randomized controlled trial.” Statistics in Medicine, 38(16), 3053-3072. doi:10.1002/sim.8169.

Description

Plot cumulative ranking curves from MBNMA models

Usage

cumrank(x, sucra = TRUE, ...)

Arguments

Value

Line plots showing the cumulative ranking probabilities for each agent/class for the ranked dose response paramtere in x. The object returned is a list which contains the plot (an object of ⁠class(c("gg", "ggplot")⁠) and a data frame of SUCRA values if sucra = TRUE.

Examples

# Using the alogliptin data
network <- mb.network(alog_pcfb)

# Estimate rankings  from an Emax dose-response MBNMA
emax <- mb.run(network, fun=temax())
ranks <- rank(emax, param=c("emax"))

# Plot cumulative rankings for both dose-response parameters simultaneously
# Note that SUCRA values are also returned
cumrank(ranks)

Description

This function creates JAGS code snippets for default MBNMA model priors.

Usage

default.priors(fun = tloglin())

Arguments

Value

A list, each element of which is a named JAGS snippet corresponding to a prior in the MBNMA JAGS code.

Examples

default.priors(fun=temax())

default.priors(fun=titp(p.expon=TRUE))

Description

Plot deviance contributions from an MBNMA model

Usage

devplot(
  mbnma,
  dev.type = "dev",
  plot.type = "box",
  xaxis = "time",
  facet = TRUE,
  n.iter = round(mbnma$BUGSoutput$n.iter/4),
  n.thin = mbnma$BUGSoutput$n.thin,
  ...
)

Arguments

Details

Deviances should only be plotted for models that have converged successfully. If deviance contributions have not been monitored in mbnma$parameters.to.save then additional iterations will have to be run to get results for these.

Deviance contributions cannot be calculated for models with a multivariate likelihood (i.e. those that account for correlation between observations) because the covariance matrix in these models is treated as unknown (if rho="estimate") and deviance contributions will be correlated.

Value

Generates a plot of deviance contributions and returns a list containing the plot (as an object of class c("gg", "ggplot")), and a data.frame of posterior mean deviance/residual deviance contributions for each observation.

Examples

# Make network
alognet <- mb.network(alog_pcfb)

# Run MBNMA
mbnma <- mb.run(alognet, fun=tpoly(degree=2), intercept=FALSE)

# Plot residual deviance contributions in a scatterplot
devplot(mbnma)

# Plot deviance contributions in boxplots at each follow-up measurement
# Monitor for 500 additional iterations
devplot(mbnma, dev.type="dev", plot.type="box", xaxis="fup", n.iter=500)

Description

A dataset from of trials for reduction of haemoglobin A1c (HbA1c) in patients with type 2 diabetes(Ding and Fu 2013). Data are reported in each study arm as mean change from baseline to follow-up. The dataset includes 4 Randomised-Controlled Trials (RCTs), comparing 4 treatments.

Usage

diabetes

Format

A data frame in long format (one row per arm and study), with 28 rows and 7 variables:

• studyID Study identifiers

• treatment Numeric data indicating the treatment to which participants were randomised

• time Numeric data indicating the time at which the observation was measured (given in weeks)

• y Numeric data indicating the mean change from baseline in HbA1c in a study arm

• se Numeric data indicating the standard error for the mean change from baseline in HbA1c in a study arm

• sd Numeric data indicating the standard deviation for the mean change from baseline in HbA1c in a study arm

• n Numeric data indicating the number of participants in each arm at each time-point

Details

diabetes is a data frame in long format (one row per observation, arm and study), with the variables studyID, treatment, time, y, se, sd, and n.

References

Ding Y, Fu H (2013). “Bayesian indirect and mixed treatment comparisons across longitudinal time points.” Statistics in Medicine, 32, 2613-2628. doi:10.1002/sim.5688.

Description

Plot fitted values from MBNMA model

Usage

fitplot(
  mbnma,
  treat.labs = NULL,
  disp.obs = TRUE,
  n.iter = round(mbnma$BUGSoutput$n.iter/4),
  n.thin = mbnma$BUGSoutput$n.thin,
  ...
)

Arguments

Details

Fitted values should only be plotted for models that have converged successfully. If fitted values (theta) have not been monitored in mbnma$parameters.to.save then additional iterations will have to be run to get results for these.

Value

Generates a plot of fitted values from the MBNMA model and returns a list containing the plot (as an object of class c("gg", "ggplot")), and a data.frame of posterior mean fitted values for each observation.

Examples

# Make network
painnet <- mb.network(osteopain)

# Run MBNMA
mbnma <- mb.run(painnet,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="random"))

# Plot fitted values from the model
# Monitor fitted values for 500 additional iterations
fitplot(mbnma, n.iter=500)

Description

Automatically generate parameters to save for a time-course MBNMA model

Usage

gen.parameters.to.save(fun, model)

Arguments

Value

A character vector of parameter names that should be monitored in the model

Description

Get large vector of distinct colours using Rcolorbrewer

Usage

genmaxcols()

Description

Generates spline basis matrices for fitting to time-course function

Usage

genspline(
  x,
  spline = "bs",
  knots = 1,
  degree = 1,
  max.time = max(x),
  boundaries = NULL
)

Arguments

Value

A spline basis matrix with number of rows equal to length(x) and the number of columns equal to the number of coefficients in the spline.

Examples

x <- 0:100

genspline(x)

# Generate a quadratic B-spline with 1 equally spaced internal knot
genspline(x, spline="bs", knots=2, degree=2)

# Generate a natural spline with 2 knots at selected quantiles
genspline(x, spline="ns", knots=c(0.1, 0.5))

# Generate a piecewise linear spline with 3 equally spaced knots
genspline(x, spline="ls", knots=3)

Description

Takes the closest time point from each arm in each study to a specified time (t) within an mb.network object. Useful for network plots or exploring standard NMA.

Usage

get.closest.time(network, t = stats::median(network$data.ab$time))

Arguments

Value

A data frame in long format of responses at the closest time point to t in each arm of each study.

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Take a single follow-up time from each study...
# ...closest to 7
get.closest.time(network, t=7)

# ...closest to 20
get.closest.time(network, t=7)

# ...closest to the median follow-up across all studies
get.closest.time(network, t=26)

Description

Takes the earliest time point from each arm in each study within an mb.network object. Useful for network plots.

Usage

get.earliest.time(network)

Arguments

Value

A list containing:

• a data frame in long format of responses at the earliest time point in each arm of each study

• a vector of studyIDs

• a vector of treatment names

• a vector of class names (if included in network)

• a data frame of treatment -> class codings (if included in network)

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Generate a data set with only the earliest time point included in each study
get.earliest.time(network)

Description

Takes the latest time point from each arm in each study within an mb.network object. Useful for network plots.

Usage

get.latest.time(network)

Arguments

Value

A list containing:

• a data frame in long format of responses at the latest time point in each arm of each study

• a vector of studyIDs

• a vector of treatment names

• a vector of class names (if included in network)

• a data frame of treatment -> class codings (if included in network)

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Generate a data frame with only the latest time point included in each study
get.latest.time(network)

Description

Extracts specific information required for prediction from a time-course MBNMA model

Usage

get.model.vals(
  mbnma,
  E0 = 0,
  level = "treatments",
  lim = "cred",
  link = "identity"
)

Arguments

Value

A list containing named elements that correspond to different time-course parameters in mbnma. These elements contain MCMC results either taken directly from mbnma or (in the case of random time-course parameters specified as method="random") randomly generated using parameter values estimated in mbnma.

Additional elements contain the following values:

• timecourse A character object that specifies the time-course used in mbnma in terms of alpha, beta, mu, d and time. Consistency relative time-course parameters are specified in terms of mu and d.

• time.params A character vector that indicates the different time-course parameters that are required for the prediction

@noRd

Description

Identical to get.prior() in MBNMAdose. This function takes JAGS model presented as a string and identifies what prior values have been used for calculation.

Usage

get.prior(model)

Arguments

Details

Even if an MBNMA model that has not initialised successfully and results have not been calculated, the JAGS model for it is saved in MBNMA$model.arg$jagscode and therefore priors can still be obtained. This allows for priors to be changed even in failing models, which may help solve issues with initialisation.

Value

A character vector, each element of which is a line of JAGS code corresponding to a prior in the JAGS code.

Examples

# Create mb.network object using an MBNMAtime dataset
network <- mb.network(osteopain)

# Create mb.network object using an MBNMAdose dataset

# Run linear MBNMA
result <- mb.run(network, fun=tpoly(degree=1,
    pool.1="rel", method.1="random"))

# Obtain model prior values
get.prior(result$model.arg$jagscode)

# ...also equivalent to
print(result$model.arg$priors)

Description

Uses mbnma time-course parameter estimates to calculate treatment differences between treatments or classes at a particular time-point. Can be used to compare treatments evaluated in studies at different follow-up times, or even to compare treatments in different MBNMA models via a common comparator.

Usage

get.relative(
  mbnma,
  mbnma.add = NULL,
  time = max(mbnma$model.arg$jagsdata$time, na.rm = TRUE),
  treats = unique(c(mbnma$network$treatments, mbnma.add$network$treatments)),
  classes = NULL,
  lim = "cred"
)

Arguments

Details

get.relative() can also be used to perform a 2-stage MBNMA that allows synthesis of results from two different MBNMA models via a single common comparator. In an MBNMA model, all treatments must share the same time-course function. However, a 2-stage approach can enable fitting of different time-course functions to different sets ("subnetworks") of treatments. For example, some treatments may have rich time-course information, allowing for a more complex time-course function to be used, whereas others may be sparse, requiring a simpler time-course function.

Relative comparisons between treatments in the two datasets at specific follow-up times can then be estimated from MBNMA predicted effects versus a common comparator using the Bucher method and assuming consistency. See the MBNMAtime vignette for further details.

Value

An object of class "relative.array" list containing:

• The time-point for which results are estimated

• Matrices of posterior means, medians, SDs and upper and lower 95% credible intervals for the differences between each treatment

• An array containing MCMC results for the differences between all treatments specified in treats or all classes specified in classes.

Results are reported in tables as the row-defined treatment minus the column-defined treatment.

Examples

# Create an mb.network object from a dataset
alognet <- mb.network(alog_pcfb)

# Run a quadratic time-course MBNMA using the alogliptin dataset
mbnma <- mb.run(alognet,
  fun=tpoly(degree=2,
  pool.1="rel", method.1="random",
  pool.2="rel", method.2="common"
  )
)

# Calculate differences between all treatments at 20 weeks follow-up
allres <- get.relative(mbnma, time=20)

# Calculate difference between a subset of treatments at 10 weeks follow-up
subres <- get.relative(mbnma, time=10,
  treats=c("alog_50", "alog_25", "placebo"))



###########################
##### 2-stage MBNMA #####
###########################

# Using the osteoarthritis dataset
# With placebo (Pl_0) as common comparator between subnetworks

#### Sparse model ####

# Treatments on which time-course data is limited
sparse.trt <- c("Ce_100", "Ce_400", "Du_90", "Lu_200", "Lu_400",
  "Lu_NA", "Et_5", "Ox_44")

# Create a subnetwork of studies comparing these treatments
sparse.df <- osteopain %>% dplyr::group_by(studyID) %>%
  dplyr::filter(any(treatment %in% sparse.trt)) %>%
  dplyr::ungroup() %>%
  subset(treatment %in% c("Pl_0", sparse.trt))

sparse.net <- mb.network(sparse.df)

# Run a ITP MBNMA with a known rate
sparse.mbnma <- mb.run(sparse.net, fun=titp(method.rate=0.8, pool.rate="abs"))


#### Complex model ####

# Treatments on which time-course data is rich
rich.trt <- levels(osteopain$treatment)[!levels(osteopain$treatment) %in%
  c("Pl_0", "Ce_100", "Ce_400", "Du_90", "Lu_200",
    "Lu_400", "Lu_NA", "Et_5", "Ox_44")]

# Create a subnetwork of studies comparing these treatments
rich.df <- osteopain %>% dplyr::group_by(studyID) %>%
  dplyr::filter(any(treatment %in% rich.trt)) %>%
  dplyr::ungroup() %>%
  subset(treatment %in% c("Pl_0", rich.trt))

rich.net <- mb.network(rich.df)

# Run a Emax MBNMA
rich.mbnma <- mb.run(rich.net, temax(p.expon = FALSE))


#### Calculate relative effects between models ####

# At 10 weeks follow-up
rels.sparse <- get.relative(sparse.mbnma, time=10)
rels.rich <- get.relative(rich.mbnma, time=10)

rels.all <- get.relative(mbnma=rich.mbnma,
  mbnma.add=sparse.mbnma, time=10)

print(rels.all$median)

Description

Converts MBNMA data frame to a list for use in JAGS model

Usage

getjagsdata(
  data.ab,
  fun = NULL,
  class = FALSE,
  rho = NULL,
  covstruct = "CS",
  link = "identity",
  sdscale = FALSE,
  cfb = NULL
)

Arguments

Value

A named list of numbers, vector, matrices and arrays to be sent to JAGS. List elements are:

• y An array of mean responses for each observation in each arm within each study

• se An array of standard errors for each observation in each arm within each study

• time A matrix of follow-up times within each study

• fups A numeric vector with the number of follow-up measurements per study

• narm A numeric vector with the number of arms per study

• NS The total number of studies in the dataset

• NT The total number of treatments in the dataset

• treat A matrix of treatment codes within each study

• Nclass Optional. The total number of classes in the dataset

• class Optional. A matrix of class codes within each study

• classkey Optional. A vector of class codes that correspond to treatment codes. Same length as the number of treatment codes.

• mat.triangle Optional. A matrix with number indicating how to fill covariance matrices within the JAGS code.

• mat.order Optional. A matrix with number indicating what order to fill covariance matrices within the JAGS code.

• timedif.0 Optional. A vector of the difference in times between the first and second follow-up time in each study.

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)
jagsdat <- getjagsdata(network$data.ab)


# Get JAGS data with class
netclass <- mb.network(goutSUA_CFBcomb)
jagsdat <- getjagsdata(netclass$data.ab, class=TRUE)


# Get JAGS data that allows for modelling correlation between time points
painnet <- mb.network(osteopain)
jagsdat <- getjagsdata(painnet$data.ab, rho="dunif(0,1)", covstruct="AR1")

Description

Converts data frame to a list for use in JAGS NMA model

Usage

getnmadata(data.ab, link = "identity", sdscale = FALSE)

Arguments

Value

A named list of numbers, vector, matrices and arrays to be sent to JAGS. List elements are:

• y An array of mean responses for each observation in each arm within each study

• se An array of standard errors for each observation in each arm within each study

• narm A numeric vector with the number of arms per study

• NS The total number of studies in the dataset

• NT The total number of treatments in the dataset

• treat A matrix of treatment codes within each study

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Construct a dataset with the latest time point in each study
data.ab <- get.latest.time(network)$data.ab
getnmadata(data.ab)

Description

A dataset from a systematic review of interventions for lowering Serum Uric Acid (SUA) concentration in patients with gout (not published previously). The outcome is continuous, and aggregate data responses correspond to the mean change from baseline in SUA in mg/dL. Overall there are 41 treatments of 8 agents in the network. Standard deviations have been imputed for 181 observations.

Usage

goutSUA_CFB

Format

A data frame with 224 rows and 7 variables:

• studyID Study identifiers

• time Numeric data indicating follow-up times

• y Numeric data indicating the mean response for a given observation

• se Numeric data indicating the standard error for a given observation

• treatment Treatment identifiers as factors. Labels are shortened treatment names.

• treatname Character data giving the full names of each treatment in the format agent_dose

• class Shortened agent names stored as factors.

Details

goutSUA_CFB is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, y, se, treatment, treatname and class.

Source

Pfizer Ltd.

Description

A dataset from a systematic review of interventions for lowering Serum Uric Acid (SUA) concentration in patients with gout (not published previously). The outcome is continuous, and aggregate data responses correspond to the mean change from baseline in SUA in mg/dL. Treatments with similar doses have been pooled together to improve network connectivity and facilitate evidence synthesis, resulting in 19 treatments of 7 agents included in the network. Standard deviations have been imputed for 181 observations.

Usage

goutSUA_CFBcomb

Format

A data frame with 224 rows and 7 variables:

• studyID Study identifiers

• time Numeric data indicating follow-up times

• y Numeric data indicating the mean response for a given observation

• se Numeric data indicating the standard error for a given observation

• treatment Treatment identifiers as factors. Labels are shortened treatment names.

• treatname Character data giving the full names of each treatment in the format agent_dose

• class Shortened agent names stored as factors.

Details

goutSUA_CFBcomb is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, y, se, treatment, treatname and class.

Source

Pfizer Ltd.

Description

A dataset from of trials for pain reduction for patients with osteoarthritis treated with HA-based viscosupplements(Jansen et al. 2015). Data are reported in each study arm as mean change from baseline to follow-up on a visual analogue scale (0-100). The dataset includes 16 Randomised-Controlled Trials (RCTs), comparing 6 treatments and placebo.

Usage

hyalarthritis

Format

A data frame in long format (one row per arm and study), with 150 rows and 6 variables:

• studyID Study identifiers

• time Numeric data indicating the time at which the observation was measured (given in weeks)

• treatment Factor data indicating the treatment to which participants were randomised

• n Numeric data indicating the number of participants randomised to each arm

• y Numeric data indicating the mean change from baseline in HbA1c in a study arm

• se Numeric data indicating the standard error for the mean change from baseline in HbA1c in a study arm

Details

hyalarthritis is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, treatment, n, y, and se.

References

Jansen JP, Vieira MC, Cope S (2015). “Network meta-analysis of longitudinal data using fractional polynomials.” Stat Med, 34(15), 2294-311. ISSN 1097-0258 (Electronic) 0277-6715 (Linking), doi:10.1002/sim.6492, https://pubmed.ncbi.nlm.nih.gov/25877808/.

Description

Identify comparisons informed by both direct and indirect evidence from independent sources, which therefore fulfil the criteria for testing for inconsistency via node-splitting. Follows the method of van Valkenhoef van Valkenhoef et al. (2016).

Usage

inconsistency.loops(data)

Arguments

Details

Similar to gemtc::mtc.nodesplit() but uses a fixed reference treatment and therefore suggests fewer loops in which to test for inconsistency. Heterogeneity can also be parameterised as inconsistency and so testing for inconsistency in additional loops whilst changing the reference treatment would also be identifying heterogeneity. Depends on igraph.

Value

A data frame of comparisons that are informed by direct and indirect evidence from independent sources. Each row of the data frame is a different treatment comparison. Numerical codes in t1 and t2 correspond to treatment codes.

References

van Valkenhoef G, Dias S, Ades AE, Welton NJ (2016). “Automated generation of node-splitting models for assessment of inconsistency in network meta-analysis.” Res Synth Methods, 7(1), 80-93. ISSN 1759-2887 (Electronic) 1759-2879 (Linking), doi:10.1002/jrsm.1167, https://pubmed.ncbi.nlm.nih.gov/26461181/.

Examples

data <- data.frame(studyID=c(1,1,2,2,3,3,4,4,5,5,5),
  treatment=c(1,2,1,3,2,3,3,4,1,2,4)
  )

# Identify comparisons informed by direct and indirect evidence
inconsistency.loops(data)

Description

Identify unique contrasts within a network that make up all the head-to-head comparisons. Repetitions of the same treatment comparison are grouped together.

Usage

mb.comparisons(data)

Arguments

Value

A data frame of unique comparisons in which each row represents a different comparison. t1 and t2 indicate the treatment codes that make up the comparison. nr indicates the number of times the given comparison is made within the network.

If there is only a single observation for each study within the dataset (i.e. as for standard network meta-analysis) nr will represent the number of studies that compare treatments t1 and t2.

If there are multiple observations for each study within the dataset (as in time-course MBNMA) nr will represent the number of time points in the dataset in which treatments t1 and t2 are compared.

Examples

data <- data.frame(studyID=c(1,1,2,2,3,3,4,4,5,5,5),
  treatment=c(1,2,1,3,2,3,3,4,1,2,4)
  )

# Identify comparisons informed by direct and indirect evidence
mb.comparisons(data)

Description

Converts an object of class mb.network from arm-based long MBNMA data to a data frame with contrast data (a separate contrast for each treatment comparison at each time point within each study). Data can be either long or wide.

Usage

mb.make.contrast(network, datatype = NULL, format = "wide")

Arguments

Value

A data frame with the following columns. In wide format, some columns are given the indices 1 and 2 to indicate each arm in a given treatment comparison.:

• t The treatment in each arm

• TE The treatment effect (mean difference, log-odds) for the treatment in arm 1 versus the treatment in arm 2

• seTE The standard error for the treatment effect (mean difference, log-odds) for the treatment in arm 1 versus the treatment in arm 2

• y The mean response in each arm

• se The standard error of the mean in each arm

• r The number of responders in each arm

• n The total number of participants in each arm

• fupcount Follow-up identifier

• time The time the data are reported

• studyID Study identifier

Examples

# Create mb.network
network <- mb.network(osteopain)

# Convert to wide contrast data
mb.make.contrast(network, format="wide")

# Convert to long contrast data
mb.make.contrast(network, format="long")

Description

Identify comparisons informed by both direct and indirect evidence from independent sources in MBNMA datasets with repeated measurements in each study. These comparisons are therefore those which fulfil the criteria for testing for inconsistency via node-splitting, following the method of van Valkenhoef van Valkenhoef et al. (2016).

Usage

mb.nodesplit.comparisons(network)

Arguments

Details

Similar to gemtc::mtc.nodesplit() but uses a fixed reference treatment and therefore suggests fewer loops in which to test for inconsistency. Heterogeneity can also be parameterised as inconsistency and so testing for inconsistency in additional loops whilst changing the reference treatment would also be identifying heterogeneity. Depends on igraph.

Value

A data frame of comparisons that are informed by direct and indirect evidence from independent sources. Each row of the data frame is a different treatment comparison. Numerical codes in t1 and t2 correspond to treatment codes.

References

van Valkenhoef G, Dias S, Ades AE, Welton NJ (2016). “Automated generation of node-splitting models for assessment of inconsistency in network meta-analysis.” Res Synth Methods, 7(1), 80-93. ISSN 1759-2887 (Electronic) 1759-2879 (Linking), doi:10.1002/jrsm.1167, https://pubmed.ncbi.nlm.nih.gov/26461181/.

Examples

# Create mb.network object
network <- mb.network(osteopain)

# Identify comparisons informed by direct and indirect evidence
mb.nodesplit.comparisons(network)

Description

Fits a Bayesian time-course model for model-based network meta-analysis (MBNMA) that can account for repeated measures over time within studies by applying a desired time-course function. Follows the methods of Pedder et al. (2019).

Usage

mb.run(
  network,
  fun = tpoly(degree = 1),
  positive.scale = FALSE,
  intercept = NULL,
  link = "identity",
  sdscale = FALSE,
  parameters.to.save = NULL,
  rho = 0,
  covar = "varadj",
  omega = NULL,
  corparam = FALSE,
  class.effect = list(),
  UME = FALSE,
  pd = "pv",
  parallel = FALSE,
  priors = NULL,
  n.iter = 20000,
  n.chains = 3,
  n.burnin = floor(n.iter/2),
  n.thin = max(1, floor((n.iter - n.burnin)/1000)),
  model.file = NULL,
  jagsdata = NULL,
  ...
)

Arguments

Value

An object of S3 class ⁠c("mbnma", "rjags")`` containing parameter results from the model. Can be summarized by ⁠print()⁠and can check traceplots using⁠R2jags::traceplot()⁠or various functions from the package⁠mcmcplots‘.#’

If there are errors in the JAGS model code then the object will be a list consisting of two elements - an error message from JAGS that can help with debugging and model.arg, a list of arguments provided to mb.run() which includes jagscode, the JAGS code for the model that can help users identify the source of the error.

Time-course parameters

Nodes that are automatically monitored (if present in the model) have the same name as in the time-course function for named time-course parameters (e.g. emax). However, for named only as beta.1, beta.2, beta.3 or beta.4 parameters may have an alternative interpretation.

Details of the interpretation and model specification of different parameters can be shown by using the summary() method on an "mbnma" object generated by mb.run().

Parameters modelled using relative effects

• If pooling is relative (e.g. pool.1="rel") for a given parameter then the named parameter (e.g. emax) or a numbered d parameter (e.g. d.1) corresponds to the pooled relative effect for a given treatment compared to the network reference treatment for this time-course parameter.

• sd. followed by a named (e.g. emax, beta.1) is the between-study SD (heterogeneity) for relative effects, reported if pooling for a time-course parameter is relative (e.g. pool.1="rel") and the method for synthesis is random (e.g. ⁠method.1="random⁠).

• If class effects are modelled, parameters for classes are represented by the upper case name of the time-course parameter they correspond to. For example if class.effect=list(emax="random"), relative class effects will be represented by EMAX. The SD of the class effect (e.g. sd.EMAX, sd.BETA.1) is the SD of treatments within a class for the time-course parameter they correspond to.

Parameters modelled using absolute effects

• If pooling is absolute (e.g. pool.1="abs") for a given parameter then the named parameter (e.g. emax) or a numbered beta parameter (e.g. beta.1) corresponds to the estimated absolute effect for this time-course parameter.

• For an absolute time-course parameter if the corresponding method is common (e.g. method.1="common") the parameter corresponds to a single common parameter estimated across all studies and treatments. If the corresponding method is random (e.g. method.1="random") then parameter is a mean effect around which the study-level absolute effects vary with SD corresponding to sd. followed by the named parameter (e.g. sd.emax, sd.beta.1) .

Other model parameters

• rho The correlation coefficient for correlation between time-points. Its interpretation will differ depending on the covariance structure specified in covar

• totresdev The residual deviance of the model

• deviance The deviance of the model

Time-course function

Several general time-course functions with up to 4 time-course parameters are provided, but a user-defined time-course relationship can instead be used. Details can be found in the respective help files for each function.

Available time-course functions are:

• Log-linear: tloglin()

• Polynomial: tpoly()

• Integrated Two-Component Prediction (ITP): titp()

• Emax: temax()

• Fractional polynomial: tfpoly()

• Splines (various spline types can be used): tspline()

• User-defined: tuser()

Correlation between observations

When modelling correlation between observations using rho, values for rho must imply a positive semidefinite covariance matrix.

Advanced options

model.file and jagsdata can be used to run an edited JAGS model and dataset. This allows users considerably more modelling flexibility than is possible using the basic MBNMAtime syntax, though requires strong understanding of JAGS and the MBNMA modelling framework. Treatment-specific priors, meta-regression and bias-adjustment are all possible in this way, and it allows users to make use of the subsequent functions in MBNMAtime (plotting, prediction, ranking) whilst fitting these more complex models.

References

Friedrich JO, Adhikari NKJ, Beyene J (2011). “Ratio of means for analyzing continuous outcomes in meta-analysis performed as well as mean difference methods.” Journal of Clinical Epidemiology, 64(5), 556-564. doi:10.1016/j.jclinepi.2010.09.016.

Jansen JP, Vieira MC, Cope S (2015). “Network meta-analysis of longitudinal data using fractional polynomials.” Stat Med, 34(15), 2294-311. ISSN 1097-0258 (Electronic) 0277-6715 (Linking), doi:10.1002/sim.6492, https://pubmed.ncbi.nlm.nih.gov/25877808/.

Pedder H, Dias S, Bennetts M, Boucher M, Welton NJ (2019). “Modelling time-course relationships with multiple treatments: Model-Based Network Meta-Analysis for continuous summary outcomes.” Res Synth Methods, 10(2), 267-286.

Plummer M (2008). “Penalized loss functions for Bayesian model comparison.” Biostatistics, 9(3), 523-39. ISSN 1468-4357 (Electronic) 1465-4644 (Linking), https://pubmed.ncbi.nlm.nih.gov/18209015/.

Plummer M (2017). JAGS user manual. https://people.stat.sc.edu/hansont/stat740/jags_user_manual.pdf.

Spiegelhalter DJ, Best NG, Carlin BP, van der Linde A (2002). “Bayesian measures of model complexity and fit.” J R Statistic Soc B, 64(4), 583-639.

Examples

# Create mb.network object
network <- mb.network(osteopain)

# Fit a linear time-course MBNMA with:
# random relative treatment effects on the slope
mb.run(network, fun=tpoly(degree=1, pool.1="rel", method.1="random"))

# Fit an emax time-course MBNMA with:
# fixed relative treatment effects on emax
# a common parameter estimated independently of treatment
# a common Hill parameter estimated independently of treatment
# a prior for the Hill parameter (normal with mean 0 and precision 0.1)
# data reported as change from baseline
result <- mb.run(network, fun=temax(pool.emax="rel", method.emax="common",
                                    pool.et50="abs", method.et50="common",
                                    pool.hill="abs", method.hill="common"),
                 priors=list(hill="dunif(0.5, 2)"),
                 intercept=TRUE)


#### commented out to prevent errors from JAGS version in github actions build ####
# Fit a log-linear MBNMA with:
# random relative treatment effects on the rate
# an autoregressive AR1 covariance structure
# modelled as standardised mean differences
# copdnet <- mb.network(copd)
# result <- mb.run(copdnet, fun=tloglin(pool.rate="rel", method.rate="random"),
#                covar="AR1", rho="dunif(0,1)", link="smd")



####### Examine MCMC diagnostics (using mcmcplots package) #######

# Traceplots
# mcmcplots::traplot(result)

# Plots for assessing convergence
# mcmcplots::mcmcplot(result, c("rate", "sd.rate", "rho"))

########## Output ###########

# Print R2jags output and summary
print(result)
summary(result)

# Plot forest plot of results
plot(result)


###### Additional model arguments ######

# Use gout dataset
goutnet <- mb.network(goutSUA_CFBcomb)

# Define a user-defined time-course relationship for use in mb.run
timecourse <- ~ exp(beta.1 * time) + (time^beta.2)

# Run model with:
# user-defined time-course function
# random relative effects on beta.1
# default common effects on beta.2
# default relative pooling on beta.1 and beta.2
# common class effect on beta.2
mb.run(goutnet, fun=tuser(fun=timecourse, method.1="random"),
       class.effect=list(beta.1="common"))

# Fit a log-linear MBNMA
# with variance adjustment for correlation between time-points
result <- mb.run(network, fun=tloglin(),
                 rho="dunif(0,1)", covar="varadj")

Description

Update MBNMA to obtain deviance contributions or fitted values

Usage

mb.update(
  mbnma,
  param = "theta",
  n.iter = mbnma$BUGSoutput$n.iter,
  n.thin = mbnma$BUGSoutput$n.thin
)

Arguments

Value

A data frame containing posterior means for the specified param at each observation, arm and study.

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Run Emax model
emax <- mb.run(network, fun=temax())

# Update model for 500 iterations to monitor fitted values
mb.update(emax, param="theta", n.iter=500)

# Update model for 500 iterations to monitor residual deviance contributions
mb.update(emax, param="resdev", n.iter=500)

# Update model for 500 iterations to monitor deviance contributions
mb.update(emax, param="dev", n.iter=500)

Description

Validates that a dataset fulfils requirements for MBNMA

Usage

mb.validate.data(data.ab, single.arm = FALSE, CFB = TRUE)

Arguments

Details

Checks done within the validation:

• Checks data.ab has required column names

• Checks there are no NAs

• Checks that all SEs are positive

• Checks that studies have baseline measurement (unless change from baseline data is being used)

• Checks that arms are balanced at each time point

• Checks that class codes are consistent within each treatment

• Checks that treatment codes are consistent across different time points within a study

• Checks that studies have at least two arms (if single.arm = FALSE)

• Checks that standsd values are consistent within a study

Value

An error or warnings if checks are not passed. Runs silently if checks are passed

Description

Writes JAGS code for a Bayesian time-course model for model-based network meta-analysis (MBNMA).

Usage

mb.write(
  fun = tpoly(degree = 1),
  link = "identity",
  positive.scale = TRUE,
  intercept = NULL,
  rho = 0,
  covar = "varadj",
  omega = NULL,
  corparam = TRUE,
  sdscale = FALSE,
  class.effect = list(),
  UME = FALSE
)

Arguments

Value

A single long character string containing the JAGS model generated based on the arguments passed to the function.

Examples

# Write a linear time-course MBNMA:
# random treatment effects on beta.1
# equal baselines in study arms
model <- mb.write(fun=tpoly(degree=1, pool.1="rel", method.1="random"))

# Write an emax time-course MBNMA with:
# a Hill parameter
# no intercept
model <- mb.write(fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="common", pool.hill="abs", method.hill="common"),
  intercept=TRUE)

# Write a log-linear time-course MBNMA with:
# AR1 correlation between time points
model <- mb.write(fun=tloglin(),
  rho="dunif(0,1)", covar="AR1")

# Define a user-defined time-course relationship for the MBNMA JAGS model
userfun <- ~ (exp(beta.1 * time) / (beta.2 * time))
model <- mb.write(fun=tuser(fun=userfun,
    pool.1="rel", method.1="random",
    pool.2="rel", method.2="common"))

Description

Run an NMA model

Usage

nma.run(
  data.ab,
  treatments = NULL,
  method = "common",
  link = "identity",
  sdscale = FALSE,
  ...
)

Arguments

Value

Returns an object of class("nma", "rjags")

Examples

network <- mb.network(osteopain)

# Get the latest time point
late.time <- get.latest.time(network)

# Get the closest time point to a given value (t)
early.time <- get.closest.time(network, t=7)

# Run NMA on the data
nma.run(late.time$data.ab, treatments=late.time$treatments,
  method="random")

Description

A dataset from a systematic review of pharmacological treatments for reducing body weight in patients with obesity. The outcome is continuous, and aggregate data responses are given as mean change from baseline in body weight (KG). Overall there are 35 RCTs investigating 26 treatments of 16 agents (/combinations of agents) in the network. Standard deviations have been imputed for 421 observations.

Usage

obesityBW_CFB

Format

A data frame with 710 rows and 7 variables:

• studyID Study identifiers

• time Numeric data indicating follow-up times

• y Numeric data indicating the mean response for a given observation

• se Numeric data indicating the standard error for a given observation

• n Numeric data indicating the number of participants used to calculate means for each observation

• treatment Treatment identifiers as factors. Labels are shortened treatment names.

• treatname Character data giving the full names of each treatment in the format agent_dose

• agent Agent (drug) names stored as characters

• class The drug class of the agent (a broader category than agent) stored as characters

Details

obesityBW_CFB is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, y, se, n, treatment, treatname, agent and class.

Source

Pfizer Ltd.

Description

A dataset containing results on the WOMAC pain scale (0-10) over time for studies investigating 29 treatments for pain relief in patients with osteoarthritis. Standard deviations have been imputed for 269 observations.

Usage

osteopain

Format

A data frame with 417 rows and 7 variables:

• studyID Study identifiers

• time Numeric data indicating follow-up times

• y Numeric data indicating the mean response for a given observation

• se Numeric data indicating the standard error for a given observation

• treatment Treatment identifiers as factors. Labels are shortened treatment names.

• arm Arm identifiers coded for each study

• treatname Character data giving the full names of each treatment

Details

osteopain is a data frame in long format (one row per observation, arm and study), with the variables studyID, time, y, se, treatment, arm and treatname.

Source

Pfizer Ltd.

Description

Uses results from MBNMA JAGS models to calculate pD via the plugin method (Spiegelhalter et al. 2002). Can only be used for models with known standard errors or covariance matrices (typically univariate).

Usage

pDcalc(
  obs1,
  obs2,
  fups = NULL,
  narm,
  NS,
  theta.result,
  resdev.result,
  likelihood = "normal",
  type = "time"
)

Arguments

Details

Method for calculating pD via the plugin method proposed by (Spiegelhalter et al. 2002). Standard errors / covariance matrices must be assumed to be known. To obtain values for theta.result and resdev.result these parameters must be monitored when running the JAGS model.

For non-linear time-course MBNMA models residual deviance contributions may be skewed, which can lead to non-sensical results when calculating pD via the plugin method. Alternative approaches are to use pV (pv) as an approximation (Plummer 2008) or pD calculated by Kullback–Leibler divergence (pd.kl) or using an optimism adjustment (popt) (Plummer 2008).

Value

A numeric value for the effective number of parameters, pD, calculated via the plugin method

References

TO ADD pV REF

Examples

# Using the alogliptin dataset
network <- mb.network(alog_pcfb)

# Run Emax model saving predicted means and residual deviance contributions
emax <- mb.run(network, fun=temax(),
  parameters.to.save=c("theta", "resdev"), intercept=FALSE)

# Get matrices of observed data
jagsdat <- getjagsdata(network$data.ab)

# Plugin estimation of pD is problematic with non-linear models as it often leads to
#negative values, hence use of pV, pd.kl and popt as other measures for the effective
#number of parameters
pDcalc(obs1=jagsdat$y, obs2=jagsdat$se,
  fups=jagsdat$fups, narm=jagsdat$narm, NS=jagsdat$NS,
  theta.result = emax$BUGSoutput$mean$theta,
  resdev.result = emax$BUGSoutput$mean$resdev
  )

Description

Creates an object of class("mb.network"). Various MBNMA functions can subsequently be applied to this object.

Usage

## S3 method for class 'mb.network'
plot(
  x,
  edge.scale = 1,
  label.distance = 0,
  level = "treatment",
  remove.loops = FALSE,
  v.color = "connect",
  v.scale = NULL,
  layout = igraph::in_circle(),
  legend = TRUE,
  legend.x = "bottomleft",
  legend.y = NULL,
  ...
)

mb.network(data.ab, reference = 1, cfb = NULL, description = "Network")

Arguments

Details

The S3 method plot() on an mb.network object generates a network plot that shows how different treatments are connected within the network via study comparisons. This can be used to identify how direct and indirect evidence are informing different treatment comparisons. Depends on igraph.

Missing values (NA) cannot be included in the dataset. Studies must have a baseline measurement and more than a single follow-up time (unless change from baseline data are being used). Data must be present for all arms within a study at each follow-up time.

Value

Returns an object of class "igraph", which can be modified by other functions within the igraph package.

An object of class("mb.network") which is a list containing:

• description A short description of the network

• data.ab A data frame containing the arm-level network data (treatment identifiers will have been recoded to a sequential numeric code)

• studyID A character vector with the IDs of included studies.

• cfb A logical vector indicating which studies report change from baseline data

• treatments A character vector indicating the treatment identifiers that correspond to the new treatment codes.

• classes A character vector indicating the class identifiers (if included in the original data) that correspond to the new class codes.

Methods (by generic)

• plot(mb.network): Generate a network plot

Examples

# Create an mb.network object from the data
network <- mb.network(osteopain)

# Arrange network plot in a star with the reference treatment in the centre
plot(network, layout=igraph::as_star())

# Generate a network plot at the class level that removes loops indicating comparisons
#within a node
goutnet <- mb.network(goutSUA_CFB)
plot(goutnet, level="class", remove.loops=TRUE)

# Generate a network plot at the treatment level that colours nodes by class
plot(goutnet, v.color="class", remove.loops=TRUE)

# Plot network in which node size is proportional to number of participants
alognet <- mb.network(alog_pcfb)
plot(alognet, v.scale=2)



# Using the osteoarthritis dataset
print(osteopain)

# Define network
network <- mb.network(osteopain, description="Osteoarthritis Dataset")

# Define network with different network reference treatment
network <- mb.network(osteopain, reference="Ce_200")


# Using the alogliptin dataset
network <- mb.network(alog_pcfb, description="Alogliptin Dataset")

# Examine networks
print(network)
plot(network)

Description

Plots predicted responses from a time-course MBNMA model

Usage

## S3 method for class 'mb.predict'
plot(
  x,
  disp.obs = FALSE,
  overlay.ref = TRUE,
  overlay.nma = NULL,
  method = "random",
  col = "blue",
  max.col.scale = NULL,
  treat.labs = NULL,
  plot.bins = TRUE,
  ...
)

Arguments

Details

For the S3 method plot(), if disp.obs is set to TRUE it is advisable to ensure predictions in predict are estimated using an even sequence of time points to avoid misrepresentation of shaded densities. Shaded counts of observations will be relative to the treatment plotted in each panel rather than to the network reference treatment if disp.obs is set to TRUE.

Overlaying NMA results

overlay.nma indicates regions of the data (defined as "time bins") over which it may be reasonable to "lump" different follow-up times from different studies together and assume a standard NMA model. For example:

• overlay.nma=c(5,10) indicates a single NMA of studies with follow-up times ⁠>5⁠ and ⁠<=10⁠

• overlay.nma=c(5,10,15) indicates two NMAs should be performed of studies with follow-up times ⁠>5⁠ and ⁠<=10⁠ of studies with follow-up times ⁠>10⁠ and ⁠<=15⁠

When used with MBNMA (via predict.mbnma()) this allows comparison to MBNMA results over a specific range of time within each time bin. It can be useful to assess which time-course function might be suitable when using binplot(), or to to assess if the MBNMA predictions are in agreement with predictions from an NMA model when using plot.mb.predict() for a specific range of time-points. This can be a general indicator of the fit of the time-course model.

However, it is important to note that the wider the range specified in overlay.nma, the more likely it is that different time-points are included, and therefore that there is greater heterogeneity/inconsistency in the NMA model. If overlay.nma includes several follow-up times for any study then only a single time-point will be taken (the one closest to mean(overlay.nma)). The NMA predictions are plotted over the range specified in overlay.nma as a horizontal line, with the 95%CrI shown by a grey rectangle. The NMA predictions represent those for any time-points within this range since they lump together data at all these time-points. Predictions for treatments that are disconnected from the network reference treatment at data points specified within overlay.nma cannot be estimated so are not included.

It is important to note that the NMA model is not necessarily the "correct" model, since it "lumps" different time-points together and ignores potential differences in treatment effects that may arise from this. The wider the range specified in overlay.nma, the greater the effect of "lumping" and the stronger the assumption of similarity between studies.

For an NMA model to be estimated and a corresponding prediction to be made from it, each time bin must include the network reference treatment (treatment=1) evaluated in at least 1 connected study in the time bin. If a given time bin does not meet this criteria then an NMA will not be calculated for it.

Examples

# Create an mb.network object from a dataset
copdnet <- mb.network(copd)

# Run an MBNMA model with a log-linear time-course
loglin <- mb.run(copdnet,
  fun=tloglin(pool.rate="rel", method.rate="common"),
  rho="dunif(0,1)", covar="varadj")

# Predict responses using the original dataset to estimate the network reference
#treatment response
df.ref <- copd[copd$treatment=="Placebo",]
predict <- predict(loglin, times=c(0:20), E0=0, ref.resp=df.ref)

# Plot the predicted responses with observations displayed on plot as green shading
plot(predict, disp.obs=TRUE, overlay.ref=FALSE, col="green")

# Plot the predicted responses with the median network reference treatment response overlayed
#on the plot
plot(predict, disp.obs=FALSE, overlay.ref=TRUE)

# Plot predictions from NMAs calculated between different time-points
plot(predict, overlay.nma=c(5,10), n.iter=20000)
plot(predict, overlay.nma=c(5,10,15,20), n.iter=20000)
# Time-course fit may be less well at 15-20 weeks follow-up

Description

Plot histograms of rankings from MBNMA models

Usage

## S3 method for class 'mb.rank'
plot(x, treat.labs = NULL, ...)

Arguments

Value

A histogram that shows rankings for each treatment/agent/prediction. The object returned is an object of class c("gg", "ggplot").

Examples

# Create an mb.network object from a dataset
painnet <- mb.network(osteopain)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(painnet,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="random"),
  positive.scale=TRUE)

# Calculate treatment rankings for AUC and emax
ranks <- rank(emax,
  param=c("auc"),
  int.range=c(0,15), n.iter=500)

# Plot histograms for ranking by AUC
plot(ranks)

Description

Generates a forest plot for time-course parameters of interest from results from time-course MBNMA models. Posterior densities are plotted above each result using ggdist:stat_:halfeye()

Usage

## S3 method for class 'mbnma'
plot(x, params = NULL, treat.labs = NULL, class.labs = NULL, ...)

Arguments

Value

A forest plot of class c("gg", "ggplot") that has separate panels for different time-course parameters

Examples

# Create an mb.network object from a dataset
alognet <- mb.network(alog_pcfb)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(alognet,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="rel", method.et50="common"),
  intercept=FALSE)

# Generate forest plot
plot(emax)

# Plot results for only one time-course parameter
plot(emax, params="emax")

Description

Within a MBNMA time-course network, split contributions into direct and indirect evidence and test for consistency between them. Closed loops of treatments in which it is possible to test for consistency are those in which direct and indirect evidence are available from independent sources van Valkenhoef van Valkenhoef et al. (2016).

Usage

## S3 method for class 'nodesplit'
plot(x, plot.type = NULL, params = NULL, ...)

mb.nodesplit(
  network,
  comparisons = mb.nodesplit.comparisons(network),
  nodesplit.parameters = "all",
  fun = tpoly(degree = 1),
  times = NULL,
  lim = "cred",
  ...
)

Arguments

Details

The S3 method plot() on an mb.nodesplit object generates either forest plots of posterior medians and 95\% credible intervals, or density plots of posterior densities for direct and indirect evidence.

Note that by specifying the times argument a user can perform a node-split of treatment effects at a specific time-point. This will give the treatment effect for both direct, indirect, and MBNMA estimates at this time point.

Value

Plots the desired graph(s) and returns an object (or list of objects if plot.type=NULL) of class(c("gg", "ggplot")), which can be edited using ggplot commands.

A an object of class("mb.nodesplit") that is a list containing elements d.X.Y (treatment 1 = X, treatment 2 = Y). Each element (corresponding to each comparison) contains additional numbered elements corresponding to each parameter in the time-course function on which node splitting was performed. These elements then contain:

• ⁠overlap matrix⁠ MCMC results for the difference between direct and indirect evidence

• p.values Bayesian p-value for the test of consistency between direct and indirect evidence

• quantiles

• forest.plot

• density.plot

• direct MCMC results for the direct evidence

• indirect MCMC results for the indirect evidence

Functions

• plot(nodesplit): Plot outputs from nodesplit models

References

van Valkenhoef G, Dias S, Ades AE, Welton NJ (2016). “Automated generation of node-splitting models for assessment of inconsistency in network meta-analysis.” Res Synth Methods, 7(1), 80-93. ISSN 1759-2887 (Electronic) 1759-2879 (Linking), doi:10.1002/jrsm.1167, https://pubmed.ncbi.nlm.nih.gov/26461181/.

Examples

# Create mb.network object
painnet <- mb.network(osteopain)

# Identify comparisons informed by direct and indirect evidence
splits <- mb.nodesplit.comparisons(painnet)

# Fit a log-linear time-course MBNMA (takes a while to run)
result <- mb.nodesplit(painnet, comparisons=splits, nodesplit.parameters="all",
  fun=tloglin(pool.rate="rel", method.rate="common"),
  rho="dunif(0,1)", covar="varadj"
  )

# Fit an emax time-course MBNMA with a node-split on emax parameters only
result <- mb.nodesplit(painnet, comparisons=splits, nodesplit.parameters="emax",
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="rel", method.et50="common"))

# Inspect results
print(result)
summary(result)

# Plot results
plot(result)

Description

Used to predict effects over time for different treatments or to predict the results of a new study. For MBNMA models that include consistency relative effects on time-course parameters, this is calculated by combining relative treatment effects with a given reference treatment response (specific to the population of interest).

Usage

## S3 method for class 'mbnma'
predict(
  object,
  times = seq(0, max(object$model.arg$jagsdata$time, na.rm = TRUE), length.out = 30),
  E0 = 0,
  treats = NULL,
  level = "treatment",
  ref.resp = NULL,
  synth = "common",
  lim = "cred",
  ...
)

Arguments

Details

By default the network reference treatment baseline (E0) and time-course parameter values are set to zero so that predict() estimates mean differences (/relative treatment effects) over time versus the network reference treatment.

ref.resp only needs to be specified if mbnma has been estimated using consistency relative effects (pool="rel") for any time-course parameters, as these inform the absolute values of the network reference treatment parameters which can then be added to the relative effects to calculate specific predictions.

Value

An S3 object of class mb.predict that contains the following elements:

• summary A named list of data frames. Each data frame contains a summary of predicted responses at follow-up times specified in times for each treatment specified in treats

• pred.mat A named list of matrices. Each matrix contains the MCMC results of predicted responses at follow-up times specified in times for each treatment specified in treats

Examples

# Create an mb.network object from a dataset
network <- mb.network(osteopain)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(network,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="common"))

# Predict responses using a stochastic baseline (E0) and a distribution for the
#network reference treatment
preds <- predict(emax, times=c(0:10),
  E0=~rnorm(n, 7, 0.5),
  ref.resp=list(emax=~rnorm(n, -0.5, 0.05)))
summary(preds)

# Predict responses using the original dataset to estimate the network reference
#treatment response
paindata.ref <- osteopain[osteopain$treatname=="Placebo_0",]
preds <- predict(emax, times=c(5:15),
  E0=10,
  ref.resp=paindata.ref)
summary(preds)

# Repeat the above prediction but using a random effects meta-analysis of the
#network reference treatment response
preds <- predict(emax, times=c(5:15),
  E0=10,
  ref.resp=paindata.ref,
  synth="random")
summary(preds)

Description

Print mb.network information to the console

Usage

## S3 method for class 'mb.network'
print(x, ...)

Arguments

Value

Prints the contents of x to the console.

Description

Print summary information from an mb.predict object

Usage

## S3 method for class 'mb.predict'
print(x, ...)

Arguments

Description

Prints a summary of rankings for each parameter

Usage

## S3 method for class 'mb.rank'
print(x, ...)

Arguments

Value

Prints summary details of treatment rankings to the console

Description

Prints basic results from a node-split to the console

Usage

## S3 method for class 'nodesplit'
print(x, groupby = "time.param", ...)

Arguments

Value

Prints summary details of nodesplit results to the console

Description

Print posterior medians (95% credible intervals) for table of relative effects/mean differences between treatments/classes

Usage

## S3 method for class 'relative.array'
print(x, digits = 2, ...)

Arguments

Value

Prints a league table of treatment effects to the console

Description

Useful for graphs drawn using igraph to reposition labels relative to vertices when vertices are laid out in a circle (as is common in network plots). igraph interprets position within vertex.label.degree as radians, so it is necessary to convert locations into radian values. This is the main role of this function.

Usage

radian.rescale(x, start = 0, direction = 1)

Arguments

Value

A numeric vector of rescaled values

References

https://gist.github.com/kjhealy/834774/a4e677401fd6e4c319135dabeaf9894393f9392c

Description

Set rank as a method

Usage

rank(x, ...)

Arguments

Value

Uses the rank method

Description

Rank predictions at a specific time point

Usage

## S3 method for class 'mb.predict'
rank(
  x,
  time = max(x$summary[[1]]$time),
  lower_better = FALSE,
  treats = names(x$summary),
  ...
)

Arguments

Value

Returns an object of class("mb.rank") containing ranked predictions

Examples

# Create an mb.network object from a dataset
network <- mb.network(osteopain)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(network,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="common"))

# Predict responses using a stochastic baseline (E0) and a distribution for the
#network reference treatment
preds <- predict(emax, E0=7,
  ref.resp=list(emax=~rnorm(n, -0.5, 0.05)))

# Rank predictions at latest predicted time-point
rank(preds, lower_better=TRUE)


#### Rank predictions at 5 weeks follow-up ####

# First ensure responses are predicted at 5 weeks
preds <- predict(emax, E0=7,
  ref.resp=list(emax=~rnorm(n, -0.5, 0.05)),
  times=c(0,5,10))

# Rank predictions at 5 weeks follow-up
ranks <- rank(preds, lower_better=TRUE, time=5)

# Plot ranks
plot(ranks)

Description

Ranks desired parameters saved from a time-course MBNMA model from "best" to "worst".

Usage

## S3 method for class 'mbnma'
rank(
  x,
  param = "auc",
  lower_better = FALSE,
  treats = NULL,
  int.range = NULL,
  n.iter = x$BUGSoutput$n.sims,
  ...
)

Arguments

Details

"auc" can be specified in param to rank treatments based on Area Under the Curve (AUC). This accounts for the effect of multiple time-course parameters simultaneously on the treatment response, but will be impacted by the range of time over which AUC is calculated (int.range). This requires integration over int.range and can take some time to run (particularly) for spline functions as this uses the trapezoid method rather than adaptive quadrature). Note that "auc" can only be calculated at the treatment-level in class effect models.

As with other post-estimation functions, rank() should only be performed on models which have successfully converged. Note that rankings can be very sensitive to even small changes in treatment effects and therefore failure to converge in only one parameter may have substantial impact on rankings.

Value

A named list whose elements include:

• summary.rank A data frame containing mean, sd, and quantiles for the ranks of each treatment given in treats

• prob.matrix A matrix of the proportions of MCMC results for which each treatment/class in treats ranked in which position for the given parameter

• rank.matrix A matrix of the ranks of MCMC results for each treatment/class in treats for the given parameter.

Examples

# Create an mb.network object from a dataset
network <- mb.network(alog_pcfb)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(network,
  fun=temax(pool.emax="rel", method.emax="common",
            pool.et50="rel", method.et50="random"),
  intercept=FALSE)

# Rank treatments by time-course parameter from the model with lower scores being better
rank(emax, param=c("emax"), lower_better=TRUE)

# Rank treatments 1-3 by AUC
rank(emax, param="auc", treats=c(1:3), lower_better=TRUE,
  int.range=c(0,20))

Description

Calculates ranking probabilities for AUC from a time-course MBNMA

Usage

rankauc(
  mbnma,
  lower_better = FALSE,
  treats = NULL,
  level = "treatments",
  int.range = c(0, max(mbnma$network$data.ab$time)),
  n.iter = mbnma$BUGSoutput$n.sims,
  subdivisions = 100,
  ...
)

Arguments

Details

"auc" can be specified in param to rank treatments based on Area Under the Curve (AUC). This accounts for the effect of multiple time-course parameters simultaneously on the treatment response, but will be impacted by the range of time over which AUC is calculated (int.range). This requires integration over int.range and can take some time to run (particularly) for spline functions as this uses the trapezoid method rather than adaptive quadrature). Note that "auc" can only be calculated at the treatment-level in class effect models.

As with other post-estimation functions, rank() should only be performed on models which have successfully converged. Note that rankings can be very sensitive to even small changes in treatment effects and therefore failure to converge in only one parameter may have substantial impact on rankings.

Value

A named list whose elements include:

• summary.rank A data frame containing mean, sd, and quantiles for the ranks of each treatment given in treats

• prob.matrix A matrix of the proportions of MCMC results for which each treatment/class in treats ranked in which position for the given parameter

• rank.matrix A matrix of the ranks of MCMC results for each treatment/class in treats for the given parameter.

Description

Identify unique contrasts relative to each study reference within a network. Repetitions of the same treatment comparison are grouped together.

Usage

ref.comparisons(data)

Arguments

Value

A data frame of unique comparisons in which each row represents a different comparison. t1 and t2 indicate the treatment codes that make up the comparison. nr indicates the number of times the given comparison is made within the network.

If there is only a single observation for each study within the dataset (i.e. as for standard network meta-analysis) nr will represent the number of studies that compare treatments t1 and t2.

If there are multiple observations for each study within the dataset (as in MBNMAtime) nr will represent the number of time points in the dataset in which treatments t1 and t2 are compared.

Description

Synthesises single arm studies with repeated measures by applying a particular time-course function. Used in predicting mean responses from a time-course MBNMA. The same parameterisation of the time course must be used as in the MBNMA.

Usage

ref.synth(
  data.ab,
  mbnma,
  synth = "random",
  link = mbnma$model.arg$link,
  n.iter = mbnma$BUGSoutput$n.iter,
  n.burnin = mbnma$BUGSoutput$n.burnin,
  n.thin = mbnma$BUGSoutput$n.thin,
  n.chains = mbnma$BUGSoutput$n.chains,
  ...
)

Arguments

Details

data.ab can be a collection of studies that closely resemble the population of interest intended for the prediction, which could be different to those used to estimate the MBNMA model, and could be include single arms of RCTs or observational studies. If other data is not available, the data used to estimate the MBNMA model can be used by selecting only the studies and arms that specify the network reference treatment responses.

Value

A list of named elements corresponding to each time-course parameter within an MBNMA model that contain the median posterior value for the network reference treatment response.

Examples

# Create an mb.network object from a dataset
network <- mb.network(osteopain)

# Run an MBNMA model with an Emax time-course
emax <- mb.run(network,
  fun=temax(pool.emax="rel", method.emax="common",
    pool.et50="abs", method.et50="random"))

# Generate a set of studies with which to estimate the network reference treatment response
paindata.ref <- osteopain[osteopain$treatname=="Placebo_0",]

# Estimate the network reference treatment effect using common effects meta-analysis
ref.synth(data.ab=paindata.ref, mbnma=emax, synth="common")

# Estimate the network reference treatment effect using random effects meta-analysis
ref.synth(data.ab=paindata.ref, mbnma=emax, synth="random")

Description

Ensures ref.resp takes the correct form to allow for synthesis of network reference treatment effect if data is provided for meta-analysis

Usage

ref.validate(data.ab)

Arguments

Value

Returns data.ab, the data frame used to estimate the network reference treatment time-course function, with additional required indices added.

Description

Removes any loops from MBNMA model JAGS code that do not contain any expressions

Usage

remove.loops(model)

Arguments

Value

A character vector of JAGS MBNMA model code that has had empty loops removed from it

Description

Identical to replace.prior() in MBNMAdose.

Usage

replace.prior(priors, model = NULL, mbnma = NULL)

Arguments

Details

This function takes new priors, as specified by the user, and adds them to the JAGS code from an MBNMA model. New priors replace old priors in the JAGS model.

Values in priors can include any JAGS functions/distributions (e.g. censoring/truncation).

Value

A character object of JAGS MBNMA model code that includes the new priors in place of original priors

Description

Print summary mb.network information to the console

Usage

## S3 method for class 'mb.network'
summary(object, ...)

Arguments

Value

Prints summary details of x to the console.

Description

Prints a summary table of the mean of MCMC iterations at each time point for each treatment

Usage

## S3 method for class 'mb.predict'
summary(object, ...)

Arguments

Value

A matrix containing times at which responses have been predicted (time) and an additional column for each treatment for which responses have been predicted. Each row represents mean MCMC predicted responses for each treatment at a particular time.

Examples

# Define network
network <- mb.network(obesityBW_CFB, reference="plac")

# Run an MBNMA with a quadratic time-course function
quad <- mb.run(network,
  fun=tpoly(degree=2, pool.1="rel", method.1="common",
    pool.2="rel", method.2="common"),
  intercept=TRUE)

# Predict responses
pred <- predict(quad, times=c(0:50), treats=c(1:5),
  ref.resp = network$data.ab[network$data.ab$treatment==1,],
  E0=10)

# Generate summary of predictions
summary(pred)

Description

Print summary MBNMA results to the console

Usage

## S3 method for class 'mbnma'
summary(object, ...)

Arguments

Value

Prints summary details of the model results to the console

Description

Takes node-split results and produces summary data frame

Usage

## S3 method for class 'nodesplit'
summary(object, ...)

Arguments

Value

A data frame of summary node-split results with the following variables:

• Comparison The treatment comparison on which a node-split has been performed

• Time.Param The time-course parameter on which a node-split has been performed

• Evidence The evidence contribution for the given comparison (either "Direct" or "Indirect")

• Median The posterior median

• ⁠2.5%⁠ The lower 95% credible interval limit

• ⁠97.5%⁠ The upper 95% credible interval limit

• p.value The Bayesian p-value for the overlap between direct and indirect evidence for the given comparison (it will therefore have an identical value for direct and indirect evidence within a particular comparison and time-course parameter)

Description

** For version 0.2.3: to ensure positive posterior values, et50 and hill parameters are now modeled on the natural scale using a half-normal prior rather than a symmetrical prior on the exponential scale to improve model stability **

Usage

temax(
  pool.emax = "rel",
  method.emax = "common",
  pool.et50 = "rel",
  method.et50 = "common",
  pool.hill = NULL,
  method.hill = NULL,
  p.expon = FALSE
)

Arguments

Details

• Emax represents the maximum response.

• ET50 represents the time at which 50% of the maximum response is achieved. This can only take positive values and so is modeled on the exponential scale and assigned a symmetrical normal prior Alternatively it can be assigned a normal prior truncated at zero (half-normal) (this will be the default in MBNMAtime version >=0.2.3).

• Hill is the Hill parameter, which allows for a sigmoidal function. This can only take positive values and so is modeled on the exponential scale and assigned a symmetrical normal prior Alternatively it can be assigned a normal prior truncated at zero (half-normal) (this will be the default in MBNMAtime version >=0.2.3).

Without Hill parameter:

$\frac{E_{max}\times{x}}{ET_{50}+x}$

With Hill parameter:

$\frac{E_{max}\times{x^{hill}}}{ET_{50}\times{hill}+x^{hill}}$

Value

An object of class("timefun")

Time-course parameters

Time-course parameters in the model must be specified using a pool and a method prefix.

pool is used to define the approach used for pooling of a given time-course parameter and can take any of:

method is used to define the model used for meta-analysis for a given time-course parameter and can take any of the following values:

When relative effects are modelled on more than one time-course parameter, correlation between them is automatically estimated using a vague inverse-Wishart prior. This prior can be made slightly more informative by specifying the scale matrix omega and by changing the degrees of freedom of the inverse-Wishart prior using the priors argument in mb.run().

References

Lu G, Ades AE (2004). “Combination of direct and indirect evidence in mixed treatment comparisons.” Stat Med, 23(20), 3105-24. ISSN 0277-6715 (Print) 0277-6715 (Linking), doi:10.1002/sim.1875, https://pubmed.ncbi.nlm.nih.gov/15449338/.

Examples

# Model without a Hill parameter
temax(pool.emax="rel", method.emax="random", pool.et50="abs", method.et50="common")

# Model including a Hill parameter and defaults for Emax and ET50 parameters
temax(pool.hill="abs", method.hill="common")

Description

As first described for use in Network Meta-Analysis by Jansen et al. (2015).

Usage

tfpoly(
  degree = 1,
  pool.1 = "rel",
  method.1 = "common",
  pool.2 = "rel",
  method.2 = "common",
  method.power1 = 0,
  method.power2 = 0
)

Arguments

Details

• $\beta_1$ represents the 1st coefficient.

• $\beta_2$ represents the 2nd coefficient.

• $p_1$ represents the 1st power

• $p_2$ represents the 2nd power

For a polynomial of degree=1:

${\beta_1}x^{p_1}$

For a polynomial of degree=2:

${\beta_1}x^{p_1}+{\beta_2}x^{p_2}$

$x^{(p)}$ is a regular power except where $p=0$, where $x^{(0)}=ln(x)$. If a fractional polynomial power $p_m$ repeats within the function it is multiplied by another $ln(x)$.

Value

An object of class("timefun")

Time-course parameters

Time-course parameters in the model must be specified using a pool and a method prefix.

pool is used to define the approach used for pooling of a given time-course parameter and can take any of:

method is used to define the model used for meta-analysis for a given time-course parameter and can take any of the following values:

When relative effects are modelled on more than one time-course parameter, correlation between them is automatically estimated using a vague inverse-Wishart prior. This prior can be made slightly more informative by specifying the scale matrix omega and by changing the degrees of freedom of the inverse-Wishart prior using the priors argument in mb.run().

References

Jansen JP, Vieira MC, Cope S (2015). “Network meta-analysis of longitudinal data using fractional polynomials.” Stat Med, 34(15), 2294-311. ISSN 1097-0258 (Electronic) 0277-6715 (Linking), doi:10.1002/sim.6492, https://pubmed.ncbi.nlm.nih.gov/25877808/.

Lu G, Ades AE (2004). “Combination of direct and indirect evidence in mixed treatment comparisons.” Stat Med, 23(20), 3105-24. ISSN 0277-6715 (Print) 0277-6715 (Linking), doi:10.1002/sim.1875, https://pubmed.ncbi.nlm.nih.gov/15449338/.

Royston P, Altman D (1994). “Regression Using Fractional Polynomials of Continuous Covariates: Parsimonious Parametric Modelling.” Journal of the Royal Statistical Society: Series C, 43(3), 429-467.

Examples

# 1st order fractional polynomial with random effects
tfpoly(pool.1="rel", method.1="random")

# 2nd order fractional polynomial
# with a single absolute parameter estimated for the 2nd coefficient
# 1st power equal to zero
tfpoly(degree=2, pool.1="rel", method.1="common",
  pool.2="abs", method.2="random",
  method.power1=0)

Description

Plot raw responses over time by treatment or class

Usage

timeplot(network, level = "treatment", plotby = "arm", link = "identity", ...)

Arguments

Details

Plots can be faceted by either treatment (level="treatment") or class (level="class") to investigate similarity of treatment responses within classes/agents. Points represent observed responses and lines connect between observations within the same study and arm.

Value

The function returns an object of ⁠class(c("gg", "ggplot")⁠. Characteristics of the object can therefore be amended as with other plots generated by ggplot().

Examples

# Make network
goutnet <- mb.network(goutSUA_CFB)

# Use timeplot to plot responses grouped by treatment
timeplot(goutnet)

# Use timeplot ot plot resposes grouped by class
timeplot(goutnet, level="class")

# Plot matrix of relative effects
timeplot(goutnet, level="class", plotby="rel")

# Plot using Standardised Mean Differences
copdnet <- mb.network(copd)
timeplot(copdnet, plotby="rel", link="smd")

Description

Similar parameterisation to the Emax model but with non-asymptotic maximal effect (Emax). Proposed by proposed by Fu and Manner (2010)

Usage

titp(
  pool.emax = "rel",
  method.emax = "common",
  pool.rate = "rel",
  method.rate = "common",
  p.expon = FALSE
)

Arguments

Details

${E_{max}}\times\frac{(1-exp(-{rate}\times{x}))}{(1-exp(-{rate}\times{max(x)}))}$

Value

An object of class("timefun")

Time-course parameters

Time-course parameters in the model must be specified using a pool and a method prefix.

pool is used to define the approach used for pooling of a given time-course parameter and can take any of:

method is used to define the model used for meta-analysis for a given time-course parameter and can take any of the following values:

References

Fu H, Manner D (2010). “Bayesian adaptive dose-finding studies with delayed responses.” J Biopharm Stat, 20(5), 1055-1070. doi:10.1080/10543400903315740.

Lu G, Ades AE (2004). “Combination of direct and indirect evidence in mixed treatment comparisons.” Stat Med, 23(20), 3105-24. ISSN 0277-6715 (Print) 0277-6715 (Linking), doi:10.1002/sim.1875, https://pubmed.ncbi.nlm.nih.gov/15449338/.

Examples

titp(pool.emax="rel", method.emax="random")
titp(pool.emax="abs")

Description

$rate\times{log(x + 1)}$

Usage

tloglin(pool.rate = "rel", method.rate = "common")

Arguments

Value

An object of class("timefun")

Time-course parameters

Time-course parameters in the model must be specified using a pool and a method prefix.

pool is used to define the approach used for pooling of a given time-course parameter and can take any of:

method is used to define the model used for meta-analysis for a given time-course parameter and can take any of the following values:

References

Lu G, Ades AE (2004). “Combination of direct and indirect evidence in mixed treatment comparisons.” Stat Med, 23(20), 3105-24. ISSN 0277-6715 (Print) 0277-6715 (Linking), doi:10.1002/sim.1875, https://pubmed.ncbi.nlm.nih.gov/15449338/.

Examples

tloglin(pool.rate="rel", method.rate="random")
tloglin(pool.rate="abs")

Description

Polynomial time-course function

Usage

tpoly(
  degree = 1,
  pool.1 = "rel",
  method.1 = "common",
  pool.2 = "rel",
  method.2 = "common",
  pool.3 = "rel",
  method.3 = "common",
  pool.4 = "rel",
  method.4 = "common"
)

Arguments

Details

• $\beta_1$ represents the 1st coefficient.

• $\beta_2$ represents the 2nd coefficient.

• $\beta_3$ represents the 3rd coefficient.

• $\beta_4$ represents the 4th coefficient.

Linear model:

$\beta_1{x}$

Quadratic model:

$\beta_1{x} + \beta_2{x^2}$

Cubic model:

$\beta_1{x} + \beta_2{x^2} + \beta_3{x^3}$

Quartic model:

$\beta_1{x} + \beta_2{x^2} + \beta_3{x^3} + \beta_4{x^4}$

Value

An object of class("timefun")

Time-course parameters

Time-course parameters in the model must be specified using a pool and a method prefix.

pool is used to define the approach used for pooling of a given time-course parameter and can take any of:

method is used to define the model used for meta-analysis for a given time-course parameter and can take any of the following values:

When relative effects are modelled on more than one time-course parameter, correlation between them is automatically estimated using a vague inverse-Wishart prior. This prior can be made slightly more informative by specifying the scale matrix omega and by changing the degrees of freedom of the inverse-Wishart prior using the priors argument in mb.run().

References

Lu G, Ades AE (2004). “Combination of direct and indirect evidence in mixed treatment comparisons.” Stat Med, 23(20), 3105-24. ISSN 0277-6715 (Print) 0277-6715 (Linking), doi:10.1002/sim.1875, https://pubmed.ncbi.nlm.nih.gov/15449338/.

Examples

# Linear model with random effects
tpoly(pool.1="rel", method.1="random")

# Quadratic model with a single absolute parameter estimated for the 2nd coefficient
tpoly(pool.1="rel", method.1="common", pool.2="abs", method.2="random")

Description

Used to fit B-splines, natural cubic splines, and piecewise linear splines(Perperoglu et al. 2019).

Usage

tspline(
  type = "bs",
  knots = 1,
  degree = 1,
  pool.1 = "rel",
  method.1 = "common",
  pool.2 = "rel",
  method.2 = "common",
  pool.3 = "rel",
  method.3 = "common",
  pool.4 = "rel",
  method.4 = "common"
)

Arguments