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Pengalaman Hidup Pasien Chronic Kidney Disease yang Menjalani Hemodialisis: Scoping Review Rahmah, Tira Nur; Pujikurniawati, Citra Reza; Hendriyani, Desy; Handayani, Meyla Sari; Wahyuni, Hera; Sridiawati, Essy; Trisyani, Yanny
MAHESA : Malahayati Health Student Journal Vol 5, No 8 (2025): Volume 5 Nomor 8 (2025)
Publisher : Universitas Malahayati

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.33024/mahesa.v5i8.18937

Abstract

ABSTRACT Chronic Kidney Disease is a global health problem that occurs every year. Patients can survive by undergoing hemodialysis therapy, but it still leaves a number of important issues as a result of hemodialysis therapy. The purpose of this study was to identify the life experiences of chronic kidney disease patients undergoing hemodialysis. This study used a literature review method with a scoping review approach to explore the experiences of chronic kidney failure patients undergoing hemodialysis. Searches of three databases includes EBSCOhost, PubMed, and Scopus. The keywords used in English were “chronic kidney disease” OR “chronic renal failure” OR “CKD” OR “ESRD” AND “life experiences” OR “lived experiences” AND “during hemodialysis” OR “undergoing hemodialysis”. There were several interrelated themes in exploring the experiences of chronic kidney failure patients undergoing hemodialysis, including emotional and social support, physical and life limitations, psychological impact, economic difficulties, changes in health and knowledge about treatment, and dependence. These findings suggest that the experiences felt by patients with chronic renal failure undergoing hemodialysis are interconnected and have a significant influence on patients' overall quality of life. The implications of these findings suggest that a holistic approach in the care of hemodialysis patients is necessary so that medical interventions cover the physical, emotional, social, and economic aspects of patients. This study provides important insights for healthcare professionals to design more comprehensive and patient-centered interventions. Keywords: Chronic Kidney Disease, Hemodialysis, Life experience  ABSTRAK Chronic Kidney Disease adalah masalah kesehatan global yang sering terjadi di setiap tahunnya. Pasien bisa bertahan hidup dengan menjalani terapi hemodialisis, namun masih menyisakan sejumlah persoalan penting sebagai dampak dari terapi hemodialisis. Tujuan penelitian ini adalah untuk mengidentifikasi pengalaman hidup pasien chronic kidney disease yang menjalani hemodialisis. Penelitian ini menggunakan metode literature review dengan pendekatan scoping review untuk mengeksplorasi pengalaman pasien gagal ginjal kronis yang menjalani hemodialisis. Pencarian menggunakan tiga database terdiri dari EBSCOhost, PubMed, dan Scopus. Kata kunci yang digunakan dalam bahasa Inggris yaitu “chronic kidney disease” OR “chronic renal failure” OR “CKD” OR “ESRD” AND “life experiences” OR “lived experience” AND “during hemodialysis” OR “undergoing hemodialysis”. Terdapat beberapa tema yang saling berkaitan satu sama lain dalam mengeksplorasi pengalaman pasien gagal ginjal kronis yang menjalani hemodialisis, diantaranya dukungan emosional dan sosial, keterbatasan fisik dan hidup, dampak psikologis, kesulitan ekonomi, perubahan kesehatan dan pengetahuan tentang perawatan, serta ketergantungan. Temuan ini menunjukkan bahwa pengalaman yang dirasakan oleh pasien dengan gagal ginjal kronis yang menjalani hemodialisis saling berhubungan dan memiliki pengaruh signifikan terhadap kualitas hidup pasien secara keseluruhan. Implikasi dari temuan ini menunjukkan bahwa pendekatan holistik dalam perawatan pasien hemodialisis sangat diperlukan agar intervensi medis mencakup aspek fisik, emosional, sosial, dan ekonomi pasien. Penelitian ini memberikan wawasan penting bagi tenaga kesehatan untuk merancang intervensi yang lebih komprehenif dan berpusat pada pasien.  Kata Kunci: Chronic Kidney Disease, Hemodialisis, Pengalaman Hidup
Mapping Telehealth Interventions Supporting Self-Management in Coronary Artery Disease: Characteristics, Outcomes, and Evidence Gaps—A Scoping Review Hendriyani, Desy; Pahria, Tuti; Purba, Chandra Isabella Hostanida; Fauzan, Naufal Hafizh
Journal of Applied Nursing and Health Vol. 8 No. 2 (2026): Journal of Applied Nursing and Health
Publisher : Chakra Brahmanda Lentera Institute

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.55018/janh.v8i2.678

Abstract

Background: Coronary artery disease (CAD) remains a major cause of morbidity and mortality worldwide, requiring long-term self-management to prevent recurrent cardiovascular events. Telehealth has emerged as a promising approach to support self-management through remote monitoring, education, lifestyle modification, and patient–provider communication. This scoping review aimed to map and synthesise the available evidence on telehealth-supported self-management interventions and their outcomes among adults with CAD. Methods: This scoping review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews (PRISMA-ScR) guidelines and the Arksey and O’Malley framework refined by the Joanna Briggs Institute (JBI). Guided by the Population–Concept–Context (PCC) framework, literature searches were conducted in PubMed, ScienceDirect, Scopus, and EBSCOhost for studies published between 2016 and 2026. Four reviewers independently screened titles, abstracts, and full texts against predefined eligibility criteria. Data were charted using a structured extraction form, and methodological quality was appraised using JBI critical appraisal tools. Findings were synthesised using descriptive evidence mapping and narrative descriptive analysis. Results: Following the screening and eligibility assessment, 17 studies met the inclusion criteria and were included in the final synthesis. The included studies described a wide range of telehealth-supported self-management interventions, including mobile health applications, web-based platforms, telemonitoring systems, wearable devices, text messaging programs, cardiac telerehabilitation, and artificial intelligence-assisted technologies. Narrative descriptive synthesis showed that interventions commonly incorporated self-management components, including physical activity promotion, medication adherence support, dietary modification, smoking cessation, symptom monitoring, and psychosocial support. Across studies, reported outcomes included improvements in self-efficacy, health literacy, physical activity, medication adherence, quality of life, cardiovascular risk-factor management, and selected clinical indicators. Common intervention characteristics included personalized feedback, remote monitoring, nurse-led support, and multidisciplinary collaboration. The evidence also highlighted gaps related to long-term sustainability, implementation in resource-limited settings, digital equity, and adaptation across diverse healthcare contexts. Conclusion: This scoping review mapped the current evidence on telehealth-supported self-management for adults with CAD and demonstrated substantial diversity in intervention modalities, self-management strategies, and reported outcomes. The findings highlight important knowledge gaps related to implementation, sustainability, and equity, particularly in low-resource settings. Future research should prioritize implementation-focused studies, culturally adaptable telehealth models, and long-term evaluations to support the integration of telehealth into secondary prevention and CAD management