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Risk of Potentially Inappropriate Medications in Adults With CKD: Findings From the Chronic Renal Insufficiency Cohort (CRIC) Study.
Hall, Rasheeda K; Blumenthal, Jacob B; Doerfler, Rebecca M; Chen, Jing; Diamantidis, Clarissa J; Jaar, Bernard G; Kusek, John W; Kallem, Krishna; Leonard, Mary B; Navaneethan, Sankar D; Sha, Daohang; Sondheimer, James H; Wagner, Lee-Ann; Yang, Wei; Zhan, Min; Fink, Jeffrey C.
Affiliation
  • Hall RK; Renal Section, Department of Medicine, School of Medicine, Duke University, and Durham Veterans Affairs Healthcare System, Durham, North Carolina. Electronic address: rasheeda.stephens@dm.duke.edu.
  • Blumenthal JB; Division of Gerontology & Geriatric Medicine School of Medicine, University of Maryland, Baltimore, Maryland; Baltimore Geriatrics Research, Department of Medicine, Education and Clinical Center (GRECC), Baltimore Veterans Affairs and Medical Center, Baltimore, Maryland.
  • Doerfler RM; Department of Medicine, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Chen J; Department of Medicine, School of Medicine, Tulane University, New Orleans, Louisiana.
  • Diamantidis CJ; Renal Section, Department of Medicine, School of Medicine, Duke University, and Durham Veterans Affairs Healthcare System, Durham, North Carolina.
  • Jaar BG; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland.
  • Kusek JW; Center for Clinical Epidemiology and Biostatistics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kallem K; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Leonard MB; Department of Pediatrics, Stanford University School of Medicine, Palo Alto, California.
  • Navaneethan SD; Section of Nephrology, Department of Medicine, Baylor College of Medicine, Houston, Texas.
  • Sha D; Center for Clinical Epidemiology and Biostatistics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Sondheimer JH; Department of Medicine, School of Medicine, Wayne State University, Detroit, Michigan.
  • Wagner LA; Department of Medicine, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Yang W; Center for Clinical Epidemiology and Biostatistics, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Zhan M; Department of Epidemiology and Public Health, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Fink JC; Department of Medicine, School of Medicine, University of Maryland, Baltimore, Maryland.
Am J Kidney Dis ; 78(6): 837-845.e1, 2021 12.
Article in En | MEDLINE | ID: mdl-34029681
ABSTRACT
RATIONALE &

OBJECTIVE:

Adults with chronic kidney disease (CKD) may be at increased risk of adverse effects from use of potentially inappropriate medications (PIMs). Our objective was to assess whether PIM exposure has an independent association with CKD progression, hospitalizations, mortality, or falls. STUDY

DESIGN:

Retrospective observational study. SETTING &

PARTICIPANTS:

Chronic Renal Insufficiency Cohort (CRIC) study; 3,929 adults with CKD enrolled 2003-2008 and followed prospectively until December 2011. EXPOSURE PIM exposure was defined as prescriptions for any medications to be avoided in older adults as defined by the 2015 American Geriatrics Society Beers Criteria.

OUTCOME:

Hospitalization count, death, a composite kidney disease end point of CKD progression or initiation of kidney replacement therapy (KRT), KRT, and fall events assessed 1 year after PIM exposure. ANALYTICAL

APPROACH:

Logistic regression and Poisson regression to estimate the associations of PIM exposure with each outcome.

RESULTS:

The most commonly prescribed PIMs were proton pump inhibitors and α-blockers. In unadjusted models, any PIM exposure (compared to none) was associated with hospitalizations, death, and fall events. After adjustment, exposure to 1, 2, or≥3 PIMs had a graded association with a higher hospitalization rate (rate ratios of 1.09 [95% CI, 1.01-1.17], 1.18 [95% CI, 1.07-1.30], and 1.35 [95% CI, 1.19-1.53], respectively) and higher odds of mortality (odds ratios of 1.19 [95% CI, 0.91-1.54], 1.62 [95% CI, 1.21-2.17], and 1.65 [95% CI, 1.14-2.41], respectively). In a cohort subset reporting falls (n=1,109), prescriptions for≥3 PIMs were associated with an increased risk of falls (adjusted OR, 2.85 [95% CI, 1.54-5.26]). PIMs were not associated with CKD progression or KRT. Age did not modify the association between PIM count and outcomes.

LIMITATIONS:

Measurement bias; confounding by indication.

CONCLUSIONS:

Adults of any age with CKD who are prescribed PIMs have an increased risk of hospitalization, mortality, and falls with the greatest risk occurring after more than 1 PIM prescription.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Renal Insufficiency, Chronic / Potentially Inappropriate Medication List Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans Language: En Journal: Am J Kidney Dis Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Renal Insufficiency, Chronic / Potentially Inappropriate Medication List Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans Language: En Journal: Am J Kidney Dis Year: 2021 Type: Article