How should randomised trials including multiple pregnancies be analysed?

BJOG. 2004 Mar;111(3):213-9. doi: 10.1111/j.1471-0528.2004.00059.x.

Abstract

Objective: To compare the effects of four methods of analysis on the results of randomised controlled trials that recruit women with multiple pregnancies and measure outcomes on their babies.

Design: Analysis of one real and two simulated data sets.

Setting: Secondary analysis of perinatal randomised controlled trials.

Population: Randomised controlled trials including women with multiple pregnancies.

Methods: The analytical methods compared were (a) assuming independence among babies, (b) analysing outcomes per women, counting a woman as having an outcome if any of her babies had it (equivalent to selecting the worst outcome among any of a woman's babies), (c) randomly selecting one baby from each set of multiples for inclusion in the analysis, (d) adjustment of the analysis to take account of non-independence of babies from multiple pregnancies, using methods developed for analysis of cluster randomised trials.

Main outcome measures: Odds ratios for trials' main outcomes.

Results: Results from application of cluster trial methods were similar to those from assuming independence among babies, but with slightly wider confidence intervals, reflecting the reduced effective sample size caused by non-independence between babies from the same pregnancy. Results were more variable using the other two methods, and in some cases, departed markedly from the results of the cluster trial methods.

Conclusions: Cluster trial methods provide a simple way of adjusting the analysis to take account of non-independence between babies from the same pregnancy. Random selection and analysis by pregnancy (methods (b) and (c)) have disadvantages and do not report outcomes for all of the babies in the trial. This may cause problems with incorporating trials analysed using these methods into systematic reviews.

Publication types

  • Comparative Study

MeSH terms

  • Cluster Analysis
  • Data Interpretation, Statistical
  • Embryonic and Fetal Development / drug effects
  • Female
  • Humans
  • Odds Ratio
  • Pregnancy
  • Pregnancy Outcome
  • Pregnancy, Multiple / statistics & numerical data*
  • Prenatal Care / methods
  • Randomized Controlled Trials as Topic / statistics & numerical data*
  • Thyrotropin-Releasing Hormone / administration & dosage

Substances

  • Thyrotropin-Releasing Hormone