Trauma & major bleeding

Use of Bayesian Statistics to Reanalyze Data From the Pragmatic Randomized Optimal Platelet and Plasma Ratios Trial

JAMA Netw OpenPublished Post hoc bayesian reanalysis of the Pragmatic Randomized Optimal Platelet and Plasma Ratios (PROPPR) randomised trial

Authors' conclusion

In this quality improvement study, a post hoc bayesian analysis of the PROPPR Trial found evidence in support of mortality reduction with a balanced resuscitation strategy for patients in hemorrhagic shock.

Study context

Population
Severely injured trauma patients anticipated to require large volume transfusions, 12 US level I trauma centers, 2012–201312 US level I trauma centers
Participants
680 participants
Comparison
Balanced transfusion vs RBC-heavy strategy
Primary endpoint
24-hour and 30-day all-cause mortality (posterior probabilities of superiority)
Follow-up
24 hours and 30 days
Methodological detailsquality improvement study, multiple hierarchical models, multicentre
  • Quality improvement study
  • Multiple hierarchical models
  • Multicentre

Primary result

As reported in the abstract

Mortality, bayesian analysis
1:1:1 vs 1:1:2Relative risk (95% CrI)
24-hour mortality; 95% CrI; Bayes factor 13.7; 93% probability of superiority
0.75(0.45–1.11)
30-day mortality; 95% CrI; Bayes factor 6.56; 87% probability of superiority
0.82(0.57–1.16)

Further findings

24-h mortality, original frequentist analysis

Adjusted RR
0.75 (95% CI, 0.52-1.08); P = .12
No significant difference in mortality between the groups (12.7% vs 17.0%)

30-day mortality, original frequentist analysis

Adjusted RR
0.86 (95% CI, 0.65-1.12); P = .26
No significant difference in mortality between the groups (22.4% vs 26.1%)

Original publication

Use of Bayesian Statistics to Reanalyze Data From the Pragmatic Randomized Optimal Platelet and Plasma Ratios Trial. JAMA Netw Open. Published 1 February 2023. doi:10.1001/jamanetworkopen.2023.0421

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