Abstract
Background
The objective of the study was to determine whether chronic osteomyelitis (COM) is
associated with increased risk of new-onset atrial fibrillation (AF).
Methods
A national insurance claim data set of 23 million enrollees was used to identify 19,002
patients with newly-diagnosed COM and 76,008 randomly selected age- and sex-matched
control subjects between January 1, 2000 and December 31, 2009 for comparing the risk
and incidence of AF. The study end point was defined as the first diagnosis of AF,
death, withdrawal from the insurance program, or the end of 2010.
Results
During a follow-up period of 91,927 person-years, the incidence of new-onset AF in
COM cohort was 1.42-fold higher than for the non-COM cohort (4.54 vs 3.19 per 1000
person-years). After adjusting for age, sex, and classical AF risk factors such as
hypertension, diabetes, heart failure, coronary artery disease, and valvular heart
disease, the risk of new-onset AF remained significantly higher in the COM cohort
(hazard ratio [HR], 1.33; 95% confidence interval [CI], 1.18-1.49; P < 0.0001). In age-stratified analysis, the younger population carried a higher risk
for incident AF than the elderly population (from HR 2.05; 95% CI, 1.12-3.74 in age
younger than 50 years to HR 1.19; 95% CI, 0.95-1.49 in age 80 years and older). The
adjusted Kaplan-Meier analysis showed a lower AF-free survival rate in the COM group
compared with the control group (log-rank P < 0.0001) during the follow-up period.
Conclusions
This study showed that patients with COM carry an increased risk for developing new-onset
AF, particularly in the younger population. Further studies are required to explore
the underlying mechanisms that link COM and AF.
Résumé
Introduction
L’étude avait pour but de déterminer si l’ostéomyélite chronique (OC) est associée
à un risque accru d’apparition de la fibrillation auriculaire (FA).
Méthodes
Un ensemble national de données portant sur les demandes d’indemnisation de 23 millions
de participants a servi à repérer 19 002 patients ayant récemment reçu un diagnostic
d’OC et 76 008 sujets témoins appariés selon l’âge et le sexe et sélectionnés au hasard
du 1er janvier 2000 au 31 décembre 2009. L’objectif était de comparer le risque de survenue
de la FA et son incidence. La fin de l’étude coïncidait avec un premier diagnostic
de FA, la mort, le retrait du régime d’assurance ou la fin de l’année 2010.
Résultats
Au cours d’une période de suivi équivalant à 91 927 années-personnes, l’incidence
de la FA au sein de la cohorte OC était 1,42 fois plus élevée que dans la cohorte
témoin (4,54 vs 3,19 pour 1000 années-personnes). Après ajustement en fonction de
l’âge, du sexe et des facteurs de risque habituels de la FA tels que l’hypertension,
le diabète, l’insuffisance cardiaque, la coronaropathie et la valvulopathie, le risque
d’apparition de la FA demeurait significativement plus élevé dans la cohorte OC (rapport
de risques instantanés [RRI] : 1,33; intervalle de confiance [IC] à 95 % : 1,18-1,49;
p < 0,0001). Selon une analyse stratifiée en fonction de l’âge, les sujets plus jeunes
présentaient un risque d’apparition de la FA supérieur, comparativement aux sujets
âgés (RRI : 2,05; IC à 95 % : 1,12-3,74 pour les sujets de moins de 50 ans; RRI :
1,19; IC à 95 % : 0,95-1,49 pour les sujets de 80 ans et plus). L’analyse ajustée
de Kaplan-Meier a révélé que le taux de survie sans FA était plus faible dans le groupe
OC que dans le groupe témoin (p [test de Mantel-Haenszel] < 0,0001) durant la période de suivi.
Conclusions
Cette étude a montré que le risque d’apparition de la FA est plus grand chez les patients
atteints d’OC, en particulier chez les plus jeunes. D’autres études devront être menées
pour expliciter les mécanismes sous-jacents liant l’OC et la FA.
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Article info
Publication history
Published online: April 21, 2016
Accepted:
April 18,
2016
Received:
October 9,
2015
Footnotes
See editorial by Shahid et al., pages 1366–1368 of this issue.
See page 1394 for disclosure information.
Identification
Copyright
© 2016 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.