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Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study

Background: The World Health Organization(WHO) International Classification of Diseases, 11th version (ICD-11), has proposed a new trauma-related diagnosis of complex posttraumatic stress disorder (CPTSD), separate and distinct from posttraumatic stress disorder (PTSD). However, to date, no study ha...

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Autores principales: Zerach, Gadi, Shevlin, Mark, Cloitre, Marylene, Solomon, Zahava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541897/
https://www.ncbi.nlm.nih.gov/pubmed/31191830
http://dx.doi.org/10.1080/20008198.2019.1616488
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author Zerach, Gadi
Shevlin, Mark
Cloitre, Marylene
Solomon, Zahava
author_facet Zerach, Gadi
Shevlin, Mark
Cloitre, Marylene
Solomon, Zahava
author_sort Zerach, Gadi
collection PubMed
description Background: The World Health Organization(WHO) International Classification of Diseases, 11th version (ICD-11), has proposed a new trauma-related diagnosis of complex posttraumatic stress disorder (CPTSD), separate and distinct from posttraumatic stress disorder (PTSD). However, to date, no study has examined CPTSD over time. Objectives: This prospective study aimed to examine predictors and outcomes of latent classes of PTSD and CPTSD following war captivity. Method: A sample of 183 Israeli former prisoners of the 1973 Yom Kippur War (ex-POWs) participated in a 24-year longitudinal study with three waves of measurements (T1: 1991, T2: 2008, and T3: 2015). Participants completed validated self-report measures, and their cognitive performance was assessed using the Montreal Cognitive Assessment (MoCA). Results: A Latent Class Analysis (LCA) identified three main classes at T2: (1) a small class with low probability to meet PTSD and CPTSD clusters criteria (15.26%); (2) a class high only in PTSD symptoms (42.37%) and (3) a class high only in CPTSD symptoms (42.37%). Importantly, higher levels of psychological suffering in captivity at T1 were associated with higher odds of being in the CPTSD class at T2. In addition, CPTSD at T2 was more strongly associated with low self-rated health, functional impairment, and cognitive performance at T3, compared to the PTSD only class. Conclusions: Adulthood prolonged trauma of severe interpersonal intensity such as war captivity is related to CPTSD, years after the end of the war. Exposure to psychological suffering in captivity is a risk factor for future endorsement of CPTSD symptoms. CPTSD among ex-POWs is a marker for future dire mental health and functional consequences.
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spelling pubmed-65418972019-06-12 Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study Zerach, Gadi Shevlin, Mark Cloitre, Marylene Solomon, Zahava Eur J Psychotraumatol Basic Research Article Background: The World Health Organization(WHO) International Classification of Diseases, 11th version (ICD-11), has proposed a new trauma-related diagnosis of complex posttraumatic stress disorder (CPTSD), separate and distinct from posttraumatic stress disorder (PTSD). However, to date, no study has examined CPTSD over time. Objectives: This prospective study aimed to examine predictors and outcomes of latent classes of PTSD and CPTSD following war captivity. Method: A sample of 183 Israeli former prisoners of the 1973 Yom Kippur War (ex-POWs) participated in a 24-year longitudinal study with three waves of measurements (T1: 1991, T2: 2008, and T3: 2015). Participants completed validated self-report measures, and their cognitive performance was assessed using the Montreal Cognitive Assessment (MoCA). Results: A Latent Class Analysis (LCA) identified three main classes at T2: (1) a small class with low probability to meet PTSD and CPTSD clusters criteria (15.26%); (2) a class high only in PTSD symptoms (42.37%) and (3) a class high only in CPTSD symptoms (42.37%). Importantly, higher levels of psychological suffering in captivity at T1 were associated with higher odds of being in the CPTSD class at T2. In addition, CPTSD at T2 was more strongly associated with low self-rated health, functional impairment, and cognitive performance at T3, compared to the PTSD only class. Conclusions: Adulthood prolonged trauma of severe interpersonal intensity such as war captivity is related to CPTSD, years after the end of the war. Exposure to psychological suffering in captivity is a risk factor for future endorsement of CPTSD symptoms. CPTSD among ex-POWs is a marker for future dire mental health and functional consequences. Taylor & Francis 2019-05-28 /pmc/articles/PMC6541897/ /pubmed/31191830 http://dx.doi.org/10.1080/20008198.2019.1616488 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research Article
Zerach, Gadi
Shevlin, Mark
Cloitre, Marylene
Solomon, Zahava
Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title_full Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title_fullStr Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title_full_unstemmed Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title_short Complex posttraumatic stress disorder (CPTSD) following captivity: a 24-year longitudinal study
title_sort complex posttraumatic stress disorder (cptsd) following captivity: a 24-year longitudinal study
topic Basic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541897/
https://www.ncbi.nlm.nih.gov/pubmed/31191830
http://dx.doi.org/10.1080/20008198.2019.1616488
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