Use of different anticholinergic scales and their correlation with anticholinergic symptom burden in a cohort of people living with HIV.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
15 Nov 2023
Historique:
received: 23 06 2023
accepted: 24 10 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: aheadofprint

Résumé

How to detect the clinical impact of anticholinergic (AC) burden in people with HIV (PWH) remains poorly investigated. We cross-sectionally described the prevalence and type of AC signs/symptoms and the screening accuracy of three AC scales in detecting their presence in a modern cohort of PWH. We calculated AC Burden Scale (ABS), AC Risk Score (ARS) and AC Drug Score (ADS) in 721 adult PWH and recorded the presence of AC signs/symptoms over the previous 3 months. High AC risk was defined by ABS score  ≥2, and ARS or ADS score  ≥3. Comparisons among the scale were based on Cohen's inter-rater agreement, and their screening accuracy was assessed by receiver operating characteristics (ROC) curves and performance measures. We enrolled 721 PWH, of whom 72.0% of participants were male; the median age was 53 years, and 164 participants (22.7%) were on at least one AC drug. Among these, 28.6% experienced at least one AC sign/symptom. Agreement in AC risk classification was substantial only between ARS and ADS (k = 0.6). Lower and higher risk of AC signs/symptoms was associated with dual regimens [adjusted OR (aOR) = 0.12 versus three-drug regimens, P = 0.002] and increasing number of AC drugs (aOR = 12.91, P < 0.001). Depression and COPD were also associated with higher risk of AC signs/symptoms in analysis unadjusted for number of AC drugs. ABS and ADS showed the best area under the ROC curve (AUROC) of 0.85 (0.78-0.92) and 0.84 (0.75-0.92; P < 0.001 for both). However, at the cut-off used for the general population, the sensitivity of all three scales was very low (34.0%, 46.8% and 46.8%). Up to one-fourth of participants in our cohort were exposed to at least one AC drug, and among them AC signs/symptoms affected more than one-fourth. Both polypharmacy (as number of antiretrovirals and of co-medications with AC properties) and to a lesser extent specific comorbidities shaped the risk of developing AC signs/symptoms. Sensitive screenings for AC risk in PWH should prefer ABS or ADS based on lower cut-offs than those suggested for the general population.

Identifiants

pubmed: 37965917
pii: 7420641
doi: 10.1093/jac/dkad348
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Maria Mazzitelli (M)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Mattia Trunfio (M)

Infectious Diseases Unit, Department of Medical Sciences, University of Turin at Amedeo di Savoia Hospital, 10149 Turin, Italy.
HIV Neurobehavioral Research Program and Departments of Neurosciences and Psychiatry, School of Medicine, University of California, San Diego, CA, USA.

Alessandra Coin (A)

Geriatric Unit, Padua University Hospital, 35128 Padua, Italy.

Lolita Sasset (L)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Jacopo Farina (J)

Geriatric Unit, Padua University Hospital, 35128 Padua, Italy.

Monica Brundu (M)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Vincenzo Scaglione (V)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.

Maria Devita (M)

General Psychology Department, Padua University, 35131 Padua, Italy.

Giuseppe Sergi (G)

Geriatric Unit, Padua University Hospital, 35128 Padua, Italy.

Anna M Cattelan (AM)

Infectious and Tropical Diseases Unit, Padua University Hospital, 35128 Padua, Italy.
Department of Molecular Medicine, Padua University, 35128 Padua, Italy.

Classifications MeSH