Evidence map›Paper›PMID 37346462›Full record

ArticleResearch and practice in thrombosis and haemostasis2023

Patients' and health care providers' perspectives on quality of hemophilia care in the Netherlands: a questionnaire and interview study.

Martijn R Brands, Lotte Haverman, Jelmer J Muis, Mariëtte H E Driessens, Felix J M van der Meer, Geertje Goedhart, Stephan Meijer, Marianne de Jong, Johanna G van der Bom, Marjon H Cnossen and 5 more

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Article in Research and practice in thrombosis and haemostasis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Martijn R BrandsDepartment of Pediatric Hematology, Emma Children's Hospital, Amsterdam University Medical Centers location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Lotte HavermanAmsterdam Reproduction & Development, Public Health, Amsterdam, the Netherlands.
Jelmer J MuisAmsterdam Reproduction & Development, Public Health, Amsterdam, the Netherlands.
Mariëtte H E DriessensNetherlands Hemophilia Patient Society, Nijkerk, the Netherlands.
Felix J M van der MeerHemoNED Foundation, Leiden, the Netherlands.
Geertje GoedhartHemoNED Foundation, Leiden, the Netherlands.
Stephan MeijerNetherlands Hemophilia Patient Society, Nijkerk, the Netherlands.
Marianne de JongBuroMD, Utrecht, the Netherlands.
Johanna G van der BomDepartment of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.
Marjon H CnossenDepartment of Pediatric Hematology, Sophia Children's Hospital, Erasmus University Medical Center, Erasmus University Rotterdam, Rotterdam, the Netherlands.
Karin FijnvandraatDepartment of Pediatric Hematology, Emma Children's Hospital, Amsterdam University Medical Centers location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
Samantha C GouwDepartment of Pediatric Hematology, Emma Children's Hospital, Amsterdam University Medical Centers location University of Amsterdam, Meibergdreef 9, Amsterdam, the Netherlands.
HiN6 Steering Group
SYMPHONY consortium@SYMPHONY_NL
SYMPHONY consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hemophilia care has improved greatly because of advances in treatment options and comprehensive care. In-depth insight into the perspectives of persons with hemophilia and health care providers on their care may provide targets for further improvements. Objectives: To assess satisfaction of the hemophilia population with their care, to explore factors determining care satisfaction, and to identify areas for potential health care improvements, including digital health tools. Methods: First, to assess care satisfaction and factors determining satisfaction and health care improvements, data from a nationwide, cross-sectional questionnaire among 867 adult and pediatric Dutch persons with hemophilia A or B were analyzed. This included the Hemophilia Patient Satisfaction Scale questionnaire, Canadian Hemophilia Outcomes Kids' Life Assessment Tool satisfaction questions, a visual analog scale satisfaction score, and open questions. Second, to further explore factors determining satisfaction and health care improvements, semistructured interviews were conducted with 19 persons with hemophilia or their parents and 18 health care providers. Results: High care satisfaction was found, with an overall median Hemophilia Patient Satisfaction Scale score of 12 (IQR, 6-21). Participants in the interviews reported that patient-professional interactions, availability of care, and coordination of care were major factors determining satisfaction. Suggested health care improvements included improved information provision and coordination of care, especially shared care with professionals not working within comprehensive care centers. Participants suggested that digital health tools could aid in this. Conclusion: Satisfaction with hemophilia care is high among persons with hemophilia in the Netherlands, although several potential improvements have been identified. Accentuating these is especially relevant in the current era of treatment innovations, in which we might focus less on other aspects of care.

Indexed as

health policyhemophilia Ahemophilia Bpatient satisfactionquality of health caretelemedicine

Identifiers

PMID37346462
PMCPMC10279896

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.