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Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort

Observational studies have demonstrated that de-escalation of antimicrobial therapy is independently associated with lower mortality. This most probably results from confounding by indication. Reaching clinical stability is associated with the decision to de-escalate and with survival. However, stud...

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Autores principales: van Heijl, Inger, Schweitzer, Valentijn A., Boel, C. H. Edwin, Oosterheert, Jan Jelrik, Huijts, Susanne M., Dorigo-Zetsma, Wendelien, van der Linden, Paul D., Bonten, Marc J. M., van Werkhoven, Cornelis H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764693/
https://www.ncbi.nlm.nih.gov/pubmed/31560686
http://dx.doi.org/10.1371/journal.pone.0218062
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author van Heijl, Inger
Schweitzer, Valentijn A.
Boel, C. H. Edwin
Oosterheert, Jan Jelrik
Huijts, Susanne M.
Dorigo-Zetsma, Wendelien
van der Linden, Paul D.
Bonten, Marc J. M.
van Werkhoven, Cornelis H.
author_facet van Heijl, Inger
Schweitzer, Valentijn A.
Boel, C. H. Edwin
Oosterheert, Jan Jelrik
Huijts, Susanne M.
Dorigo-Zetsma, Wendelien
van der Linden, Paul D.
Bonten, Marc J. M.
van Werkhoven, Cornelis H.
author_sort van Heijl, Inger
collection PubMed
description Observational studies have demonstrated that de-escalation of antimicrobial therapy is independently associated with lower mortality. This most probably results from confounding by indication. Reaching clinical stability is associated with the decision to de-escalate and with survival. However, studies rarely adjust for this confounder. We quantified the potential confounding effect of clinical stability on the estimated impact of de-escalation on mortality in patients with community-acquired pneumonia. Data were used from the Community-Acquired Pneumonia immunization Trial in Adults (CAPiTA). The primary outcome was 30-day mortality. We performed Cox proportional-hazards regression with de-escalation as time-dependent variable and adjusted for baseline characteristics using propensity scores. The potential impact of unmeasured confounding was quantified through simulating a variable representing clinical stability on day three, using data on prevalence and associations with mortality from the literature. Of 1,536 included patients, 257 (16.7%) were de-escalated, 123 (8.0%) were escalated and in 1156 (75.3%) the antibiotic spectrum remained unchanged. Crude 30-day mortality was 3.5% (9/257) and 10.9% (107/986) in the de-escalation and continuation groups, respectively. The adjusted hazard ratio of de-escalation for 30-day mortality (compared to patients with unchanged coverage), without adjustment for clinical stability, was 0.39 (95%CI: 0.19–0.79). If 90% to 100% of de-escalated patients were clinically stable on day three, the fully adjusted hazard ratio would be 0.56 (95%CI: 0.27–1.12) to 1.04 (95%CI: 0.49–2.23), respectively. The simulated confounder was substantially stronger than any of the baseline confounders in our dataset. Quantification of effects of de-escalation on patient outcomes without proper adjustment for clinical stability results in strong negative bias. This study suggests the effect of de-escalation on mortality needs further well-designed prospective research to determine effect size more accurately.
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spelling pubmed-67646932019-10-12 Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort van Heijl, Inger Schweitzer, Valentijn A. Boel, C. H. Edwin Oosterheert, Jan Jelrik Huijts, Susanne M. Dorigo-Zetsma, Wendelien van der Linden, Paul D. Bonten, Marc J. M. van Werkhoven, Cornelis H. PLoS One Research Article Observational studies have demonstrated that de-escalation of antimicrobial therapy is independently associated with lower mortality. This most probably results from confounding by indication. Reaching clinical stability is associated with the decision to de-escalate and with survival. However, studies rarely adjust for this confounder. We quantified the potential confounding effect of clinical stability on the estimated impact of de-escalation on mortality in patients with community-acquired pneumonia. Data were used from the Community-Acquired Pneumonia immunization Trial in Adults (CAPiTA). The primary outcome was 30-day mortality. We performed Cox proportional-hazards regression with de-escalation as time-dependent variable and adjusted for baseline characteristics using propensity scores. The potential impact of unmeasured confounding was quantified through simulating a variable representing clinical stability on day three, using data on prevalence and associations with mortality from the literature. Of 1,536 included patients, 257 (16.7%) were de-escalated, 123 (8.0%) were escalated and in 1156 (75.3%) the antibiotic spectrum remained unchanged. Crude 30-day mortality was 3.5% (9/257) and 10.9% (107/986) in the de-escalation and continuation groups, respectively. The adjusted hazard ratio of de-escalation for 30-day mortality (compared to patients with unchanged coverage), without adjustment for clinical stability, was 0.39 (95%CI: 0.19–0.79). If 90% to 100% of de-escalated patients were clinically stable on day three, the fully adjusted hazard ratio would be 0.56 (95%CI: 0.27–1.12) to 1.04 (95%CI: 0.49–2.23), respectively. The simulated confounder was substantially stronger than any of the baseline confounders in our dataset. Quantification of effects of de-escalation on patient outcomes without proper adjustment for clinical stability results in strong negative bias. This study suggests the effect of de-escalation on mortality needs further well-designed prospective research to determine effect size more accurately. Public Library of Science 2019-09-27 /pmc/articles/PMC6764693/ /pubmed/31560686 http://dx.doi.org/10.1371/journal.pone.0218062 Text en © 2019 van Heijl et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
van Heijl, Inger
Schweitzer, Valentijn A.
Boel, C. H. Edwin
Oosterheert, Jan Jelrik
Huijts, Susanne M.
Dorigo-Zetsma, Wendelien
van der Linden, Paul D.
Bonten, Marc J. M.
van Werkhoven, Cornelis H.
Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title_full Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title_fullStr Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title_full_unstemmed Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title_short Confounding by indication of the safety of de-escalation in community-acquired pneumonia: A simulation study embedded in a prospective cohort
title_sort confounding by indication of the safety of de-escalation in community-acquired pneumonia: a simulation study embedded in a prospective cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764693/
https://www.ncbi.nlm.nih.gov/pubmed/31560686
http://dx.doi.org/10.1371/journal.pone.0218062
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