Objectives: To evaluate the effectiveness of naloxone in human shock;
and to estimate the methodologic quality of the clinical trials. Data
Sources: Computerized bibliographic search on MEDLINE covering the per
iod from January 1979 to July 1996, review of references of all papers
found on the subject, and contact with primary investigators of eligi
ble studies. Study Selection: To be included in this study, a paper sh
ould be a randomized, clinical trial published in a peer-reviewed jour
nal evaluating naloxone in human shock, regardless of the patient's ag
e (adult, child, neonate). Three independent readers reviewed 61 human
publications and selected five clinical trials. Overall agreement on
study selection was perfect (concordance: 100%), We excluded a posteri
ori two studies whose authors were unable to provide us with the raw d
ata to complete contingency tables. This meta analysis deals with thre
e studies including 61 patients with septic shock. Data Extraction: Th
ree independent reviewers extracted data on study design, intervention
, outcome, and methodologic quality. The intraclass correlation coeffi
cient was 0.7, The quality score of each study was 48, 60, and 61, on
a scale of 104. Data Synthesis: Naloxone therapy was associated with s
tatistically significant hemodynamic improvement (typical odds ratio:
0.241; 95% confidence interval: 0.08 to 0.68), The overall effect size
was 0.89. However, a publication bias was possible. The case fatality
rate was not decreased by naloxone (typical odds ratio: 0.60; 95% con
fidence interval: 0.21 to 1.67); a chi-square analysis detected signif
icant heterogeneity for the latter outcome (p < .05). Conclusions: Nal
oxone improves blood pressure. However, the clinical usefulness of nal
oxone to treat shock remains to be determined and additional randomize
d clinical trials are needed to assess its usefulness.