Quality of life and associated factors among HIV positive patients after completion of treatment for Cryptococcal meningitis.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
03 2021
Historique:
received: 16 06 2020
accepted: 13 11 2020
revised: 15 03 2021
pubmed: 4 3 2021
medline: 25 6 2021
entrez: 3 3 2021
Statut: epublish

Résumé

Cryptococcal meningitis (CCM) remains one of the leading causes of mortality among HIV infected patients. Due to factors such as the severity of CCM pathology, the quality of life (QOL) of patients post-treatment is likely to be poor. Few studies have reported on QOL of CCM patients post treatment completion. We used data collected among patients in the CryptoDex trial (ISRCTN59144167) to determine QOL and associated factors at week 10 and six months from treatment initiation. CryptoDex was a double-blind placebo-controlled trial of adjunctive dexamethasone in HIV infected adults with CCM, conducted between 2013 and 2015 in six countries in Asia and Africa. QOL was determined using the descriptive and Visual Analog Scales (VAS) of the EuroQol Five-Dimension-Three-Level (EQ-5D-3L) tool. We derived index scores, and described these and the VAS scores at 10 weeks and 6 months; and used linear regression to determine the relationship between various characteristics and VAS scores at both time points. VAS scores were interpreted as very good (81-100), good (51-80), normal (31-50) and bad/very bad (0-30). Of 451 patients enrolled in the trial, 238 had QOL evaluations at week 10. At baseline, their mean age (SD) was 35.2(8.5) years. The mean index scores (SD) were 0.785(0.2) and 0.619(0.4) among African and Asian patients respectively at week 10, and 0.879(0.2) and 0.731(0.4) among African and Asian patients respectively at month six. The overall mean VAS score (SD) at 10 weeks was 57.2 (29.7), increasing significantly to 72(27.4) at month six (p<0.001). At week 10, higher VAS score was associated with greater weight (p = 0.007) and being African (p<0.001), while lower VAS score was associated with positive yeast culture at day 14 (p = 0.026). At month six, higher VAS score remained associated with African origin (p = 0.006) while lower VAS score was associated with positive yeast culture (p = 0.006). Lower VAS scores were associated with higher number of inpatient days at 10 weeks and 6 months (p = 0.003 and 0.002 respectively). QOL was good among patients that had completed therapy for CCM, but below perfect. Strategies to improve QOL among CCM survivors are required.

Sections du résumé

BACKGROUND
Cryptococcal meningitis (CCM) remains one of the leading causes of mortality among HIV infected patients. Due to factors such as the severity of CCM pathology, the quality of life (QOL) of patients post-treatment is likely to be poor. Few studies have reported on QOL of CCM patients post treatment completion. We used data collected among patients in the CryptoDex trial (ISRCTN59144167) to determine QOL and associated factors at week 10 and six months from treatment initiation.
METHODOLOGY
CryptoDex was a double-blind placebo-controlled trial of adjunctive dexamethasone in HIV infected adults with CCM, conducted between 2013 and 2015 in six countries in Asia and Africa. QOL was determined using the descriptive and Visual Analog Scales (VAS) of the EuroQol Five-Dimension-Three-Level (EQ-5D-3L) tool. We derived index scores, and described these and the VAS scores at 10 weeks and 6 months; and used linear regression to determine the relationship between various characteristics and VAS scores at both time points. VAS scores were interpreted as very good (81-100), good (51-80), normal (31-50) and bad/very bad (0-30).
RESULTS
Of 451 patients enrolled in the trial, 238 had QOL evaluations at week 10. At baseline, their mean age (SD) was 35.2(8.5) years. The mean index scores (SD) were 0.785(0.2) and 0.619(0.4) among African and Asian patients respectively at week 10, and 0.879(0.2) and 0.731(0.4) among African and Asian patients respectively at month six. The overall mean VAS score (SD) at 10 weeks was 57.2 (29.7), increasing significantly to 72(27.4) at month six (p<0.001). At week 10, higher VAS score was associated with greater weight (p = 0.007) and being African (p<0.001), while lower VAS score was associated with positive yeast culture at day 14 (p = 0.026). At month six, higher VAS score remained associated with African origin (p = 0.006) while lower VAS score was associated with positive yeast culture (p = 0.006). Lower VAS scores were associated with higher number of inpatient days at 10 weeks and 6 months (p = 0.003 and 0.002 respectively).
CONCLUSION
QOL was good among patients that had completed therapy for CCM, but below perfect. Strategies to improve QOL among CCM survivors are required.

Identifiants

pubmed: 33657099
doi: 10.1371/journal.pntd.0008983
pii: PNTD-D-20-01073
pmc: PMC7959361
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Antifungal Agents 0
Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0008983

Subventions

Organisme : Medical Research Council
ID : MC_UU_00027/1
Pays : United Kingdom

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

PLoS One. 2015 Jun 03;10(6):e0126810
pubmed: 26039733
N Engl J Med. 2016 Feb 11;374(6):542-54
pubmed: 26863355
Value Health. 2011 Dec;14(8):1142-5
pubmed: 22152185
Clin Epidemiol. 2014 May 13;6:169-82
pubmed: 24872723
J Gen Intern Med. 2005 Jan;20(1):21-7
pubmed: 15693923
Ann Intern Med. 2011 Aug 16;155(4):209-16
pubmed: 21768555
N Engl J Med. 2018 Mar 15;378(11):1004-1017
pubmed: 29539274
Lancet Infect Dis. 2017 Aug;17(8):873-881
pubmed: 28483415
J Infect. 2001 Nov;43(4):226-33
pubmed: 11869059
Health Qual Life Outcomes. 2018 Sep 24;16(1):194
pubmed: 30249245
N Engl J Med. 2013 Apr 4;368(14):1291-1302
pubmed: 23550668
Arch Public Health. 2014 Nov 17;72(1):40
pubmed: 25671112
Curr Clin Microbiol Rep. 2016;3:92-102
pubmed: 27257597
Clin Infect Dis. 2014 Mar;58(5):736-45
pubmed: 24319084
Lancet Infect Dis. 2014 Apr;14(4):281-90
pubmed: 24602844
JAMA. 2002 Dec 18;288(23):3027-34
pubmed: 12479768
PLoS One. 2019 Jan 30;14(1):e0210287
pubmed: 30699151
Popul Health Metr. 2003 Dec 16;1(1):11
pubmed: 14678566
Trials. 2014 Nov 12;15:441
pubmed: 25391338
Clin Infect Dis. 2008 Jun 1;46(11):1694-701
pubmed: 18433339
Clin Infect Dis. 1999 Jan;28(1):82-92
pubmed: 10028076
Open Forum Infect Dis. 2015 Dec 28;2(4):ofv157
pubmed: 26716103
F1000Res. 2019 May 28;8:
pubmed: 31275560
AIDS. 2009 Feb 20;23(4):525-30
pubmed: 19182676

Auteurs

Jonathan Kitonsa (J)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Julius Kiwanuka (J)

Department of Epidemiology and Biostatistics, School of Public Health, Makerere University Kampala, Uganda.

Zacchaeus Anywaine (Z)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Sheila Kansiime (S)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Kenneth Katumba (K)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Namirembe Aeron (N)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Justin Beardsley (J)

Oxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme Vietnam, Ho Chi Minh City, Vietnam.
Marie Bashir Institute, Westmead Clinical School, University of Sydney, Sydney, Australia.

Freddie Kibengo (F)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Alastair Gray (A)

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.

Pontiano Kaleebu (P)

Medical Research Council / Uganda Virus Research institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.

Jeremy Day (J)

Oxford University Clinical Research Unit, Wellcome Trust Major Overseas Programme Vietnam, Ho Chi Minh City, Vietnam.
Nuffield Department of Clinical Medicine, University of Oxford, Old Road Campus, Headington, Oxford,United Kingdom.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH