Development of a clinical prediction rule to diagnose Pneumocystis jirovecii pneumonia in the World Health Organization’s algorithm for seriously ill HIV-infected patients

Southern African Journal of HIV Medicine

 
 
Field Value
 
Title Development of a clinical prediction rule to diagnose Pneumocystis jirovecii pneumonia in the World Health Organization’s algorithm for seriously ill HIV-infected patients
 
Creator Maartens, Gary Stewart, Annemie Griesel, Rulan Kengne, Andre P. Dube, Felix Nicol, Mark Rangaka, Molebogeng X. Mendelson, Marc
 
Subject HIV; pneumocystis jirovecii pneumonia; clinical prediction rule; quantitative real time PCR; beta-D-glucan; tuberculosis HIV; pneumocystis jirovecii pneumonia; clinical prediction rule; quantitative real time PCR; beta-D-glucan; tuberculosis
Description Background: The World Health Organization (WHO) algorithm for the diagnosis of tuberculosis in seriously ill HIV-infected patients recommends that treatment for Pneumocystis jiroveciipneumonia (PJP) should be considered without giving clear guidance on selecting patients for empiric PJP therapy. PJP is a common cause of hospitalisation in HIV-infected patients in resource-poor settings where diagnostic facilities are limited.Methods: We developed clinical prediction rules for PJP in a prospective cohort of HIV-infected inpatients with WHO danger signs and cough of any duration. The reference standard for PJP was 1000 copies/mL of P. jirovecii DNA on real-time sputum polymerase chain reaction (PCR). Four potentially predictive variables were selected for regression models: dyspnoea, chest X-ray, haemoglobin and oxygen saturation. Respiratory rate was explored as a replacement for oxygen saturation as pulse oximetry is not always available in resource-poor settings.Results: We enrolled 500 participants. After imputation for missing values, there were 56 PJP outcome events. Dyspnoea was not independently associated with PJP. Oxygen saturation and respiratory rate were inversely correlated. Two clinical prediction rules were developed: chest X-ray possible/likely PJP, haemoglobin ≥ 9 g/dL and either oxygen saturation 94% or respiratory rate. The area under the receiver operating characteristic curve of the clinical prediction rule models was 0.761 (95% CI 0.683–0.840) for the respiratory rate model and 0.797 (95% CI 0.725–0.868) for the oxygen saturation model. Both models had zero probability for PJP for scores of zero, and positive likelihood ratios exceeded 10 for high scores.Conclusion: We developed simple clinical prediction rules for PJP, which, if externally validated, could assist decision-making in the WHO seriously ill algorithm.
 
Publisher AOSIS
 
Contributor National Institutes of Health grant number R01 AI 96735-01
Date 2018-07-23
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — Prospective cohort study
Format text/html application/epub+zip application/xml application/pdf
Identifier 10.4102/sajhivmed.v19i1.851
 
Source Southern African Journal of HIV Medicine; Vol 19, No 1 (2018); 6 pages 2078-6751 1608-9693
 
Language eng
 
Relation
The following web links (URLs) may trigger a file download or direct you to an alternative webpage to gain access to a publication file format of the published article:

https://sajhivmed.org.za/index.php/hivmed/article/view/851/1228 https://sajhivmed.org.za/index.php/hivmed/article/view/851/1227 https://sajhivmed.org.za/index.php/hivmed/article/view/851/1230 https://sajhivmed.org.za/index.php/hivmed/article/view/851/1225
 
Coverage South Africa — Age 18 years or older; HIV inpatients
Rights Copyright (c) 2018 Gary Maartens https://creativecommons.org/licenses/by/4.0
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