Statistical analysis plan for the HEAT trial: a multicentre randomised placebo-controlled trial of intravenous paracetamol in intensive care unit patients with fever and infection

Crit Care Resusc. 2013 Dec;15(4):279-86.

Abstract

Background and objective: We describe the statistical analysis plan (SAP) for the Permissive Hyperthermia through Avoidance of Paracetamol in Known or Suspected Infection in the Intensive Care Unit (HEAT) trial, a 700-patient, prospective, randomised, Phase 2b, multicentre, double-blind, parallel-groups, placebo-controlled trial of paracetamol administration for the treatment of fever in critically ill patients with known or suspected infection.

Methods: The data fields described are those outlined in the study protocol published previously. We describe the plan for the presentation and comparison of baseline characteristics, process measures and outcomes. We describe baseline characteristics, and define and categorise trial outcomes according to their assigned importance.

Results and conclusions: We developed an SAP for the HEAT trial, and produced a mock Consolidated Standards of Reporting Trials diagram and tables. Our prespecified SAP accords with high-quality standards of internal validity and should minimise future analysis bias.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Acetaminophen / administration & dosage
  • Acetaminophen / therapeutic use*
  • Administration, Intravenous
  • Antipyretics / administration & dosage
  • Antipyretics / therapeutic use*
  • Clinical Trials, Phase II as Topic*
  • Critical Care / methods*
  • Data Interpretation, Statistical
  • Fever / drug therapy*
  • Humans
  • Infections / drug therapy*
  • Intensive Care Units
  • Intention to Treat Analysis
  • New Zealand
  • Outcome Assessment, Health Care
  • Research Design

Substances

  • Antipyretics
  • Acetaminophen