One day at a time: Life with Glanzmann thrombasthenia - Qualitative results from the GT 360 study.

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-11-15 DOI:10.1111/hae.15126
Kate Khair, Simon Fletcher, Kathryn Jenner, Michael Holland
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引用次数: 0

Abstract

Introduction: Glanzmann thrombasthenia (GT) is a platelet function disorder. Symptoms include bruising and bleeding, which may be severe and life-threatening. The day-to-day experiences of those affected remain poorly documented.

Aims: The Glanzmann's 360 study aimed to better understand the daily realities of living with GT, exploring psychological, social and medical challenges to identify unmet need.

Methods: People with GT over 18 and caregivers of children with GT participated. Mixed methods research was used, including a survey and in-depth interviews. The interviews, reported here, were audio-recorded, transcribed and thematically analysed.

Results: Nineteen interviews were conducted; 14 with people with GT and five caregivers. Mean age of those with GT was 32.9 years (range 2-78 years). Eight themes emerged: Diagnosis, Bleeding and Treatment, Menstruation, Fatigue, Identity, Abuse, Pregnancy, and The Future. Three participants described misdiagnosis. Caregivers reported early recognition and prompt diagnosis of their children. Bruising, the most commonly reported symptom, led to assumption of abuse. Six (32%) participants reported joint bleeds. External bleeding was normalised. Access to home treatment and local care were limited. Fatigue caused by anaemia was described. All women reported heavy menstrual bleeding. Choices around pregnancy were limited by 'medical pessimism'. Nevertheless, participants remained hopeful for the development of improved treatment options.

Conclusion: People with GT face significant and often overlooked challenges. There is need for improved medical and psychological treatment and support, increased awareness of these needs amongst healthcare professionals, and research into developing comprehensive care models that address medical and psychosocial needs of people with GT.

一天一天过:格兰兹曼血栓形成症患者的生活--GT 360 研究的定性结果。
导言格兰兹曼血栓形成症(GT)是一种血小板功能失调症。症状包括瘀伤和出血,严重时可危及生命。格兰兹曼 360 研究旨在更好地了解 GT 患者的日常生活现状,探讨心理、社会和医疗方面的挑战,以确定尚未满足的需求:方法:18 岁以上的 GT 患者和 GT 儿童的照顾者参与了这项研究。研究采用了混合方法,包括调查和深入访谈。本文报告的访谈均经过录音、转录和主题分析:共进行了 19 次访谈,其中 14 次针对 GT 患者,5 次针对照顾者。GT 患者的平均年龄为 32.9 岁(2-78 岁不等)。出现了八个主题:诊断、出血和治疗、月经、疲劳、身份、虐待、怀孕和未来。三名参与者描述了误诊情况。照顾者报告说,他们的孩子得到了早期识别和及时诊断。瘀伤是最常报告的症状,这导致了对虐待的假设。六名参与者(32%)报告了关节出血。外伤出血已恢复正常。获得家庭治疗和当地护理的机会有限。贫血导致的疲劳也有所描述。所有妇女都报告有大量月经出血。医疗悲观主义 "限制了她们对怀孕的选择。尽管如此,参与者仍对改进治疗方案充满希望:结论:GT 患者面临着巨大的、往往被忽视的挑战。有必要改善医疗和心理治疗及支持,提高医护人员对这些需求的认识,并研究开发综合护理模式,以满足 GT 患者的医疗和心理需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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