A method for the analysis of repeated binary outcomes in randomized clinical trials with non-compliance

Stat Med. 2001 Sep;20(17-18):2761-74. doi: 10.1002/sim.741.

Abstract

When analysing repeated binary data from randomized trials, the model-based approaches, such as generalized estimating equations, are frequently used. Such methods ignore compliance information and give the model-based intention-to-treat estimate of treatment effect. In this paper, the design-based (randomization-based) semi-parametric estimation procedure is given in the estimation of causal risk difference. The resulting risk difference estimator is interpreted as an extension of the instrumental variables estimator for a binary outcome which has the causal interpretation. Extension of the proposed method to stratified analysis is given for data from stratified randomization or meta-analysis. It yields a Mantel-Haenszel type risk difference estimator. As a special case of stratified analysis, the pattern mixture model which stratifies the data by pattern of missing data is performed. Application of the proposed method to a trial in which endpoints were the occurrences of fever over three courses is provided. The same ideas are applied to the causal risk ratio estimation.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Double-Blind Method
  • Fever / prevention & control
  • Humans
  • Leukemia, Myeloid / drug therapy
  • Macrophage Colony-Stimulating Factor / administration & dosage
  • Mathematical Computing
  • Multicenter Studies as Topic
  • Neutropenia / prevention & control
  • Randomized Controlled Trials as Topic / methods*
  • Statistics as Topic / methods*
  • Treatment Refusal*

Substances

  • Macrophage Colony-Stimulating Factor