导航希望与复杂性:土耳其父母与救世主兄弟姐妹的经历。

IF 1.5 4区 医学 Q3 HEMATOLOGY
Turkish Journal of Hematology Pub Date : 2025-02-28 Epub Date: 2025-01-23 DOI:10.4274/tjh.galenos.2025.2024.0419
İbrahim Eker, Hamide Nur Çevik Özdemir, Fırat Yılmaz, Akif Yeşilipek, Alphan Küpesiz, Vedat Uygun, Gülsün Karasu, Funda Tayfun Küpesiz, Orhan Gürsel, Barış Kuşkonmaz, Serap Aksoylar, Fatma Visal Okur, Gülcihan Özek, Musa Karakükcü, Başak Adaklı Aksoy, Özlem Tüfekçi, Zühre Kaya, Barış Malbora, Ahmet Emin Kürekçi, Ali Bülent Antmen
{"title":"导航希望与复杂性:土耳其父母与救世主兄弟姐妹的经历。","authors":"İbrahim Eker, Hamide Nur Çevik Özdemir, Fırat Yılmaz, Akif Yeşilipek, Alphan Küpesiz, Vedat Uygun, Gülsün Karasu, Funda Tayfun Küpesiz, Orhan Gürsel, Barış Kuşkonmaz, Serap Aksoylar, Fatma Visal Okur, Gülcihan Özek, Musa Karakükcü, Başak Adaklı Aksoy, Özlem Tüfekçi, Zühre Kaya, Barış Malbora, Ahmet Emin Kürekçi, Ali Bülent Antmen","doi":"10.4274/tjh.galenos.2025.2024.0419","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Preimplantation genetic diagnosis (PGD) with human leukocyte antigen (HLA) typing represents a significant advancement in treating inherited hematological disorders, particularly thalassemia major. This technology enables the birth of healthy children who can serve as compatible stem cell donors for their affected siblings. Türkiye is a world leader in both PGD+HLA typing technology and hematopoietic stem cell transplantation (HSCT) from savior siblings born through PGD+HLA typing. This study investigated the experiences of Turkish parents who underwent successful savior sibling procedures using PGD+HLA typing and then successful HSCT from the savior sibling for the treatment of the child with thalassemia major. We aimed to understand the medical, psychological, and sociocultural dimensions of this complex process within the Turkish healthcare context.</p><p><strong>Materials and methods: </strong>A qualitative study was undertaken using a descriptive phenomenological approach. In-depth interviews were conducted with parents from 16 families who had successfully completed PGD+HLA matching and subsequent stem cell transplantation processes from the savior sibling to the child with thalassemia. Data were analyzed using Colaizzi’s seven-step method and MAXQDA 20.0 software.</p><p><strong>Results: </strong>The analysis revealed six main themes: disease stage, treatment, recovery process, social/family, support systems, and recommendations. Parents reported significant emotional challenges but demonstrated unexpected resilience. Religious and cultural factors played nuanced roles, with most parents viewing the process as compatible with their beliefs. Economic burdens, prolonged hospitalizations, and geographical access to treatment centers emerged as key challenges. Extended family support and professional healthcare guidance were identified as crucial support mechanisms.</p><p><strong>Conclusion: </strong>This study highlights the complex interplay between advanced medical technologies and traditional values in Turkish society. The findings emphasize the need for comprehensive and culturally sensitive support systems and long-term follow-up for families. The results suggest the value of implementing multidisciplinary care teams and developing specialized support programs for families undergoing savior sibling procedures.</p>","PeriodicalId":23362,"journal":{"name":"Turkish Journal of Hematology","volume":" ","pages":"47-55"},"PeriodicalIF":1.5000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11869153/pdf/","citationCount":"0","resultStr":"{\"title\":\"Navigating Hope and Complexity: Turkish Parents’ Experiences with Savior Siblings\",\"authors\":\"İbrahim Eker, Hamide Nur Çevik Özdemir, Fırat Yılmaz, Akif Yeşilipek, Alphan Küpesiz, Vedat Uygun, Gülsün Karasu, Funda Tayfun Küpesiz, Orhan Gürsel, Barış Kuşkonmaz, Serap Aksoylar, Fatma Visal Okur, Gülcihan Özek, Musa Karakükcü, Başak Adaklı Aksoy, Özlem Tüfekçi, Zühre Kaya, Barış Malbora, Ahmet Emin Kürekçi, Ali Bülent Antmen\",\"doi\":\"10.4274/tjh.galenos.2025.2024.0419\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Preimplantation genetic diagnosis (PGD) with human leukocyte antigen (HLA) typing represents a significant advancement in treating inherited hematological disorders, particularly thalassemia major. This technology enables the birth of healthy children who can serve as compatible stem cell donors for their affected siblings. Türkiye is a world leader in both PGD+HLA typing technology and hematopoietic stem cell transplantation (HSCT) from savior siblings born through PGD+HLA typing. This study investigated the experiences of Turkish parents who underwent successful savior sibling procedures using PGD+HLA typing and then successful HSCT from the savior sibling for the treatment of the child with thalassemia major. We aimed to understand the medical, psychological, and sociocultural dimensions of this complex process within the Turkish healthcare context.</p><p><strong>Materials and methods: </strong>A qualitative study was undertaken using a descriptive phenomenological approach. In-depth interviews were conducted with parents from 16 families who had successfully completed PGD+HLA matching and subsequent stem cell transplantation processes from the savior sibling to the child with thalassemia. Data were analyzed using Colaizzi’s seven-step method and MAXQDA 20.0 software.</p><p><strong>Results: </strong>The analysis revealed six main themes: disease stage, treatment, recovery process, social/family, support systems, and recommendations. Parents reported significant emotional challenges but demonstrated unexpected resilience. Religious and cultural factors played nuanced roles, with most parents viewing the process as compatible with their beliefs. Economic burdens, prolonged hospitalizations, and geographical access to treatment centers emerged as key challenges. Extended family support and professional healthcare guidance were identified as crucial support mechanisms.</p><p><strong>Conclusion: </strong>This study highlights the complex interplay between advanced medical technologies and traditional values in Turkish society. The findings emphasize the need for comprehensive and culturally sensitive support systems and long-term follow-up for families. The results suggest the value of implementing multidisciplinary care teams and developing specialized support programs for families undergoing savior sibling procedures.</p>\",\"PeriodicalId\":23362,\"journal\":{\"name\":\"Turkish Journal of Hematology\",\"volume\":\" \",\"pages\":\"47-55\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2025-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11869153/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Turkish Journal of Hematology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.4274/tjh.galenos.2025.2024.0419\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Hematology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.4274/tjh.galenos.2025.2024.0419","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景/目的:植入前遗传学诊断(PGD)与人类白细胞抗原(HLA)分型代表了遗传性血液病治疗的重大进展,特别是地中海贫血。这项技术使健康的孩子能够出生,这些孩子可以作为受影响的兄弟姐妹的相容干细胞供体。土耳其在PGD+HLA分型技术和通过PGD+HLA分型出生的救世主兄弟姐妹的造血干细胞移植方面处于世界领先地位。目的:本研究调查了土耳其父母的经验,他们使用植入前遗传学诊断(PGD)和人类白细胞抗原(HLA)分型成功地进行了救世主兄弟姐妹手术,然后成功地从救世主兄弟姐妹那里移植了造血干细胞,用于治疗他们的地中海贫血重型儿童。该研究旨在了解土耳其医疗保健背景下这一复杂过程的医学、心理和社会文化层面。材料与方法:采用描述现象学方法进行定性研究。我们对16位成功完成PGD+HLA配型的父母进行了深入访谈,这些父母随后成功地将这个救世主兄弟姐妹的干细胞移植到他们的地中海贫血孩子身上。数据分析采用Colaizzi七步法和MAXQDA 20.0软件。结果:分析揭示了六个主要主题:疾病阶段,治疗,康复过程,社会家庭,支持系统和建议。父母报告了重大的情感挑战,但表现出了意想不到的韧性。宗教和文化因素发挥了微妙的作用,大多数父母认为这个过程与他们的信仰是一致的。经济负担、住院时间延长和到达治疗中心的地理位置成为主要挑战。大家庭支持和保健专业指导被确定为关键的支持机制。结论:该研究突出了土耳其社会先进医疗技术与传统价值观之间复杂的相互作用。研究结果强调需要建立全面的、对文化敏感的支持系统,并对家庭进行长期随访。结果建议实施多学科的护理团队,并制定专门的支持方案,以家庭接受救主兄弟姐妹手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Navigating Hope and Complexity: Turkish Parents’ Experiences with Savior Siblings

Objective: Preimplantation genetic diagnosis (PGD) with human leukocyte antigen (HLA) typing represents a significant advancement in treating inherited hematological disorders, particularly thalassemia major. This technology enables the birth of healthy children who can serve as compatible stem cell donors for their affected siblings. Türkiye is a world leader in both PGD+HLA typing technology and hematopoietic stem cell transplantation (HSCT) from savior siblings born through PGD+HLA typing. This study investigated the experiences of Turkish parents who underwent successful savior sibling procedures using PGD+HLA typing and then successful HSCT from the savior sibling for the treatment of the child with thalassemia major. We aimed to understand the medical, psychological, and sociocultural dimensions of this complex process within the Turkish healthcare context.

Materials and methods: A qualitative study was undertaken using a descriptive phenomenological approach. In-depth interviews were conducted with parents from 16 families who had successfully completed PGD+HLA matching and subsequent stem cell transplantation processes from the savior sibling to the child with thalassemia. Data were analyzed using Colaizzi’s seven-step method and MAXQDA 20.0 software.

Results: The analysis revealed six main themes: disease stage, treatment, recovery process, social/family, support systems, and recommendations. Parents reported significant emotional challenges but demonstrated unexpected resilience. Religious and cultural factors played nuanced roles, with most parents viewing the process as compatible with their beliefs. Economic burdens, prolonged hospitalizations, and geographical access to treatment centers emerged as key challenges. Extended family support and professional healthcare guidance were identified as crucial support mechanisms.

Conclusion: This study highlights the complex interplay between advanced medical technologies and traditional values in Turkish society. The findings emphasize the need for comprehensive and culturally sensitive support systems and long-term follow-up for families. The results suggest the value of implementing multidisciplinary care teams and developing specialized support programs for families undergoing savior sibling procedures.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
2.90
自引率
3.80%
发文量
45
审稿时长
1 months
期刊介绍: The Turkish Journal of Hematology is published quarterly (March, June, September, and December) by the Turkish Society of Hematology. It is an independent, non-profit peer-reviewed international English-language periodical encompassing subjects relevant to hematology. The Editorial Board of The Turkish Journal of Hematology adheres to the principles of the World Association of Medical Editors (WAME), International Council of Medical Journal Editors (ICMJE), Committee on Publication Ethics (COPE), Consolidated Standards of Reporting Trials (CONSORT) and Strengthening the Reporting of Observational Studies in Epidemiology (STROBE). The aim of The Turkish Journal of Hematology is to publish original hematological research of the highest scientific quality and clinical relevance. Additionally, educational material, reviews on basic developments, editorial short notes, images in hematology, and letters from hematology specialists and clinicians covering their experience and comments on hematology and related medical fields as well as social subjects are published. As of December 2015, The Turkish Journal of Hematology does not accept case reports. Important new findings or data about interesting hematological cases may be submitted as a brief report.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信