Introduction: Malignant haematological diseases (MHDs) are increasingly the focus of research interest due to their rising global disease burden and the continuous need for improved management strategies. The dynamic evolution of therapeutic protocols has significantly enhanced survival rates for patients with MHDs. However, many of these patients often experience deteriorated overall health, emphasizing the importance of addressing health-related quality of life (HrQoL).
Aim: This study aims to conduct a comparative analysis of the perspectives of MHD patients and hematologists regarding the nature and role of subjective assessment or HrQoL in routine clinical practice.
Materials and Methods: The study, designed as a pilot initiative, explores the need and feasibility of larger-scale research within patient and haematologist communities. The research protocol targeted two groups of participants: a maximum of 100 MHD patients treated at the Clinical Haematology Clinic of St. Marina University Hospital in Varna between March and April 2024, and all 12 haematologists in the clinic. Inclusion criteria for patients were a confirmed MHD diagnosis, signed informed consent, and age of at least 18 years.
The research was preceded by a literature review in PubMed and Google Scholar (as of April 2024) using key terms in Bulgarian and English: "health-related quality of life" and "malignant haematological diseases." Based on the literature, the team's experience, and the study’s objectives, two survey instruments were developed – one for MHD patients and one for medical professionals. A descriptive statistical approach was employed to analyse the collected data. Ethical approval for the protocol was obtained.
Results: The study found that medical professionals prioritize therapeutic outcomes over HrQoL, though they acknowledge the need for routine HrQoL assessments. Patients, however, value not only clinical improvement but also the preservation or enhancement of HRQoL. Both groups agreed on the need for psychological support to improve HrQoL, including in clinical settings.
Conclusion: Assessing HrQoL in MHD patients holds substantial social and personal importance, warranting its dedicated place in chronic disease management. Despite significant clinical and administrative workloads, medical professionals exhibit positive attitudes toward subjective health evaluations. Addressing these critical areas in routine care for MHD patients points to future research directions that could foster the development of effective practices and updated recommendations to support patients.
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