Evidence map›Paper›PMID 32671950›Full record

ArticleHIV medicine2020

Polypharmacy and potential drug-drug interactions for people with HIV in the UK from the Climate-HIV database.

C Okoli, A Schwenk, M Radford, M Myland, S Taylor, A Darley, J Barnes, A Fox, F Grimson, I Reeves and 7 more

Open access · hybridAbstract read
In one paragraph

Article in HIV medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  5. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 1 country.

C OkoliViiV Healthcare, Brentford, UK.ORCID 0000-0002-9424-2873
A SchwenkNorth Middlesex University Hospital NHS Trust, London, UK.
M RadfordViiV Healthcare, Brentford, UK.
M MylandIQVIA Real World Insights, UK & Ireland, London, UK.
S TaylorBirmingham Heartlands HIV Service, Department of Infection and Immunology, Birmingham Heartlands Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
A DarleyNottingham University Hospitals NHS Trust, Nottingham, UK.
J BarnesBirmingham Heartlands HIV Service, Department of Infection and Immunology, Birmingham Heartlands Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
A FoxNottingham University Hospitals NHS Trust, Nottingham, UK.
F GrimsonIQVIA Real World Insights, UK & Ireland, London, UK.
I ReevesHomerton University Hospital NHS Foundation Trust, London, UK.
S MunshiHomerton University Hospital NHS Foundation Trust, London, UK.
A CroucherHomerton University Hospital NHS Foundation Trust, London, UK.
N BoxallIQVIA Real World Insights, UK & Ireland, London, UK.
P BennViiV Healthcare, Brentford, UK.
A PaiceViiV Healthcare, Brentford, UK.
J van WykViiV Healthcare, Brentford, UK.
S KhooUniversity of Liverpool, Liverpool, UK.
ViiV Healthcare (United Kingdom) · GBHomerton University Hospital NHS Foundation Trust · GBIQVIA (United Kingdom) · GBNottingham University Hospitals NHS Trust · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBNorth Middlesex University Hospital NHS Trust · GBUniversity of Liverpool · GB

Funding

Medical Research Council MR/V020498/1ViiV Healthcare
6 · The paper itself

Abstract

objectivesPeople with HIV (PWHIV) are likely to need therapies for comorbidities as they age. We assessed risk of drug-drug interactions (DDIs) in PWHIV.

methodsThe Climate-HIV electronic recording system was used to cross-sectionally analyse records from PWHIV aged ≥ 18 years attending four UK HIV units with a current antiretroviral (ARV) prescription in February 2018. Antiretroviral and non-ARV medications were categorized by clinical significance of DDIs (University of Liverpool DDI tool). Potential DDIs were predicted using treatment guidelines for commonly recorded comorbidities.

resultsAmong 4630 PWHIV (44% female), 41% were ≥ 50 years old. The average number of non-ARV comedications increased from < 1 for patients aged ≤ 24 years to > 5 for patients aged ≥ 75 years; 65% were taking one or more non-ARV comedications. The median (interquartile range) number of non-ARVs was 1 (0-2) and 2 (1-5) for those aged < 50 and ≥ 50 years, respectively. Common comorbidities/concurrent health conditions occurred more frequently in patients aged ≥ 50 years vs. < 50 (53% vs. 34%). Boosted protease inhibitors were associated with the highest proportion of contraindicated comedications; dolutegravir and raltegravir had the fewest. For non-ARVs, sildenafil and quetiapine were most likely to result in DDIs. Guideline-recommended treatments for hepatitis C, hepatitis B, and tuberculosis had the highest proportions of contraindications when combined with ARV regimens, while treatments for hepatitis C, malignancy, and mental health conditions had the highest proportion of combinations potentially causing DDIs requiring dose monitoring or adjustment.

conclusionsNon-ARV use by PWHIV is high and increases with age. Treatment decisions for ageing PWHIV should consider guideline recommendations for comorbidities.

Indexed as

AdultAgedAge FactorsAnti-HIV AgentsClinical Decision-MakingComorbidityContraindications, DrugCross-Sectional StudiesDrug InteractionsFemaleHIV InfectionsHumansMaleMiddle AgedPolypharmacyPractice Guidelines as TopicAnti-HIV Agentscomorbidityconcomitant medicationdrug-drug interactionsHIVpolypharmacy

Identifiers

PMID32671950
PMCPMC7497154
OpenAlexW3043029748

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.