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Moving beyond symptom reduction: A meta-analysis on the effect of exposure therapy for PTSD on quality of life.
Kaur, Kiran; Asnaani, Anu; Levy, Hannah C; Miller, Madeleine L; Tolin, David F; McLean, Carmen P.
Afiliação
  • Kaur K; Department of Psychology, University of Utah, Salt Lake City, Utah, USA.
  • Asnaani A; Department of Psychology, University of Utah, Salt Lake City, Utah, USA.
  • Levy HC; Anxiety Disorders Center, The Institute of Living/Hartford Hospital, Hartford, Connecticut, USA.
  • Miller ML; National Center for PTSD, Dissemination and Training Division, VA Palo Alto Health Care System, Menlo Park, California, USA.
  • Tolin DF; Anxiety Disorders Center, The Institute of Living/Hartford Hospital, Hartford, Connecticut, USA.
  • McLean CP; Yale University School of Medicine, New Haven, Connecticut, USA.
J Clin Psychol ; 2024 Jun 14.
Article em En | MEDLINE | ID: mdl-38875442
ABSTRACT

OBJECTIVES:

Quality of life (QOL) is a multidimensional construct including emotional well-being, life satisfaction, and physical health. Individuals with posttraumatic stress disorder (PTSD) consistently report low QOL, highlighting the importance of assessing the effectiveness of first-line PTSD treatments (e.g., exposure-based therapies) on QOL. This meta-analysis examined the efficacy of exposure therapy for PTSD on QOL compared to control conditions (e.g., waitlist, medication, treatment-as-usual) at posttreatment and follow-up (ranging from 1 month to 2 years).

METHODS:

Building on a previous meta-analysis of exposure-based therapy for PTSD, we searched PsycINFO and Medline in December 2021, July 2022, and March 2023 to include randomized controlled trials of exposure-based treatments for adult PTSD assessing QOL. We screened 295 abstracts for initial eligibility; 20 articles met inclusion criteria and were included (N = 2729 participants). Risk of bias was evaluated using the Cochrane Risk of Bias tool 2.0.

RESULTS:

At posttreatment, exposure-based therapies showed a medium effect on QOL relative to control conditions (k = 25, g = 0.67). This effect was not observed at follow-up for the small subset of studies with follow-up data (k = 8, g = 0.16). At posttreatment, effect size varied significantly as a function of the control condition (p < .0001). There were no differences in QOL effects across exposure therapies at posttreatment or follow-up (p = .09).

CONCLUSION:

Exposure therapy was associated with greater improvement in QOL compared to control conditions at posttreatment. Exposure was not superior to control conditions at follow-up, and the longer-term impact of exposure on QOL is unclear. The implications of these findings are discussed, along with the need for more PTSD treatment studies to examine QOL outcomes at posttreatment and follow-up.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article