Erschienen in:
28.06.2018 | Original
Increasing evidence-based interventions in patients with acute infections in a resource-limited setting: a before-and-after feasibility trial in Gitwe, Rwanda
verfasst von:
Olivier Urayeneza, Pierre Mujyarugamba, Zacharie Rukemba, Vincent Nyiringabo, Polyphile Ntihinyurwa, John I. Baelani, Arthur Kwizera, Danstan Bagenda, Mervyn Mer, Ndidiamaka Musa, Julia T. Hoffman, Ashok Mudgapalli, Austin M. Porter, Niranjan Kissoon, Hanno Ulmer, Lori A. Harmon, Joseph C. Farmer, Martin W. Dünser, Andrew J. Patterson, for the Sepsis in Resource-Limited Nations Workgroup of the Surviving Sepsis Campaign
Erschienen in:
Intensive Care Medicine
|
Ausgabe 9/2018
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Abstract
Objective
To evaluate whether a focused education program and implementation of a treatment bundle
increases the rate of early evidence-based interventions in patients with acute infections.
Design
Single-center, prospective, before-and-after feasibility trial.
Setting
Emergency department of a sub-Saharan African district hospital.
Patients
Patients > 28 days of life admitted to the study hospital for an acute infection.
Interventions
The trial had three phases (each of 4 months). Interventions took place during the second (educational program followed by implementation of the treatment bundle) and third (provision of resources to implement treatment bundle) phases.
Measurements and main results
Demographic, clinical, and laboratory data were collected at study enrollment; 24, 48, and 72 h after hospital admission; and at discharge. A total of 1594 patients were enrolled (pre-intervention, n = 661; intervention I, n = 531; intervention II, n = 402). The rate of early evidence-based interventions per patient during Intervention Phase I was greater than during the pre-intervention phase (74 ± 17 vs. 79 ± 15%, p < 0.001). No difference was detected when data were compared between Intervention Phases I and II (79 ± 15 vs. 80 ± 15%, p = 0.58). No differences in the incidence of blood transfusion (pre-intervention, 6%; intervention I, 7%; intervention II, 7%) or severe adverse events in the first 24 h (allergic reactions: pre-intervention, 0.2%; intervention I, 0%; intervention II, 0%; respiratory failure: pre-intervention, 2%; intervention I, 2%; intervention II, 2%; acute renal failure: pre-intervention, 2%; intervention I, 2%; intervention II, 1%) were observed.
Conclusions
Our results indicate that a focused education program and implementation of an infection treatment bundle in clinical practice increased the rate of early evidence-based interventions in patients with acute infections (mostly malaria) admitted to a sub-Saharan African district hospital. Provision of material resources did not further increase this rate. While no safety issues were detected, this could be related to the very low disease severity of the enrolled patient population (
http://www.clinicaltrials.gov: NCT02697513).