Selective Serotonin Reuptake Inhibitor Use and Hip Fracture Risk Among Patients on Hemodialysis.
Aged
Aged, 80 and over
Depression
/ complications
Female
Follow-Up Studies
Hip Fractures
/ epidemiology
Humans
Incidence
Kidney Failure, Chronic
/ complications
Male
Middle Aged
Prognosis
Renal Dialysis
Retrospective Studies
Risk Assessment
/ methods
Risk Factors
Selective Serotonin Reuptake Inhibitors
/ adverse effects
United States
/ epidemiology
End-stage kidney disease (ESKD)
USRDS
antidepressants
anxiety
case-control
depression
drug safety
end-stage renal disease (ESRD)
hemodialysis
hip fracture
selective-serotonin reuptake inhibitor (SSRI)
Journal
American journal of kidney diseases : the official journal of the National Kidney Foundation
ISSN: 1523-6838
Titre abrégé: Am J Kidney Dis
Pays: United States
ID NLM: 8110075
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
29
12
2018
accepted:
16
07
2019
pubmed:
14
10
2019
medline:
1
5
2020
entrez:
14
10
2019
Statut:
ppublish
Résumé
Use of selective serotonin reuptake inhibitors (SSRIs) has been associated with hip fracture risk in the general population. This study examined this relationship among patients with kidney failure treated by hemodialysis, a unique high-risk subpopulation, within which the impact of SSRIs on hip fracture risk remains unexplored. Case-control study. Eligible cases of hip fracture among maintenance hemodialysis patients between January 1, 2009, and September 30, 2015, were identified using the US Renal Data System. Each case was matched on index date with 10 eligible controls. To be eligible, study participants needed to have more than 1 year of Medicare Parts A and B coverage and more than 3 years of Part D coverage. For a separate examination of new short-term SSRI exposure, we selected cases and controls with more than 18 months of Part D coverage and no prior antidepressant use for 1 year. During the 3-year Part D coverage period, use of SSRIs characterized as any (≥1 prescription filled), low, moderate, and high use (<20%, 20%-<80%, and≥80% of days covered by filled prescriptions, respectively). We selected cases using International Classification of Diseases, Ninth Revision codes 820.xx and 821.xx. In addition to 1 of these codes tied to a hospitalization, we required a corresponding surgical procedural code within 7 days of diagnosis. Conditional logistic regression to estimate unadjusted and multivariable-adjusted ORs and 95% CIs. We identified 4,912 cases and 49,120 controls. SSRI use was associated with increased hip fracture risk (adjusted OR, 1.25; 95% CI, 1.17-1.35). Risk for fracture was estimated for any, low, moderate, and high SSRI use: adjusted conditional ORs were 1.25 (95% CI, 1.17-1.35), 1.20 (95% CI, 1.08-1.32), 1.31 (95% CI, 1.18-1.43), and 1.26 (95% CI, 1.12-1.41), respectively. The association between hip fracture events and SSRI use was also seen in the examination of new short-term use (adjusted OR, 1.43; 95% CI, 1.23-1.67). Biomarkers of mineral bone disorder were not captured and accounted for in this analysis. We demonstrated an association between increased hip fracture risk and both long- and new short-term SSRI use. The stronger association with new short-term use may suggest an acute mechanism potentially related to falls.
Identifiants
pubmed: 31606233
pii: S0272-6386(19)30944-8
doi: 10.1053/j.ajkd.2019.07.015
pii:
doi:
Substances chimiques
Serotonin Uptake Inhibitors
0
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
351-360Informations de copyright
Published by Elsevier Inc.