Background: The ultimate custodians of Mental Health Care Users (MHCUs) when they get discharged from mental health institutions are their family members. Thus, the family members have a significant role in rendering comprehensive and multifaceted care to MHCUs.
Aim: The study investigated the family members' role in the care of mental health care users in South Africa.
Methods: An explorative, descriptive design was utilised. Family members who cared for their loved ones suffering from mental illness were selected using purposive sampling. Individual, in-depth, unstructured interviews were conducted. Data analysis was done using Colaizzi's method. The COREQ checklist was used to prepare this publication.
Results: (1) Mental health care users' family support to ensure treatment adherence. (2) Promotion of hygiene for MHCUs. (3) Knowledge deficit regarding mental illness and (4) Challenges encountered regarding care and support are the themes that emerged from the analysis.
Discussion: Family members play a significant role in the treatment of their loved ones suffering from mental disorders. Female next of kin are primarily involved in the treatment of MHCUs. Support from psychiatric mental health nurses and other health professionals is needed.
Implications For Practice: The involvement of more males would be more beneficial in the care of MHCUs in dealing with non-compliant users who may undermine females. Empowerment of family members by psychiatric mental health nurses requires priority. Further research on guidelines development to address the role issues among family members could enhance the care of MHCUs.
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http://dx.doi.org/10.1111/jpm.13161 | DOI Listing |
J Cell Mol Med
March 2025
Center for Reproductive Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, People's Republic of China.
Joubert syndrome (JS) is a rare neurodevelopmental disorder associated with mutations in genes involved in ciliary function. Germline variants in CPLANE1 have been implicated in JS. In this study, we investigated a family with three adverse pregnancies characterised by fetal malformations consistent with JS.
View Article and Find Full Text PDFAnn Med
December 2025
Department of Pulmonary and Critical Care Medicine, the Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Background: Chronic Obstructive Pulmonary Disease (COPD) is a heterogeneous condition with different risk factors, including family history. This study aimed to explore association between a family history of chronic airway disease and features and outcomes of COPD.
Methods: Participants were obtained from the RealDTC study between December 2016 and December 2022.
J Sci Med Sport
February 2025
School of Biological Sciences, Georgia Institute of Technology, United States of America.
Bull Cancer
March 2025
Pediatric Oncology, insitut Gustave-Roussy, Villejuif, France. Electronic address:
Amongst Ewing sarcoma family of tumours, (EFST), cutaneous/subcutaneous Ewing sarcoma are defined as tumours arising from cutaneous or subcutaneous tissue, not invading the underlying aponeurosis. They are rare tumours, with less than 200 patients published. They are typically small tumours (less than 5cm), and can arise at any anatomical location, with a particular tropism for distal, truncal and head/neck locations, compared to classical Ewing sarcoma.
View Article and Find Full Text PDFJ Am Coll Cardiol
March 2025
Faculty of Medicine, University of Montreal, Montreal, Quebec, Canada; Cardiovascular Genetics Centre, Montreal Heart Institute, Montreal, Quebec, Canada. Electronic address:
Background: The clinical impact of genetic testing in a contemporary real-life cohort of patients with heritable cardiomyopathies or arrhythmias is not well defined. Additionally, the genetic spectrum of these conditions in the French-Canadian population is unknown, and interpretation of genetic variants can be challenging because of a known founder effect.
Objectives: This study sought to evaluate the clinical utility of arrhythmia and cardiomyopathy genetic testing and assess the utility of allele frequency data from a local reference population.
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