Literature DB >> 28806858

The haemtrack home therapy reporting system: Design, implementation, strengths and weaknesses: A report from UK Haemophilia Centre Doctors Organisation.

C R M Hay1,2, H Xiang2, M Scott2,3, P W Collins4, R Liesner5, G Dolan6, R Hollingsworth7.   

Abstract

INTRODUCTION: Haemtrack is an electronic home treatment diary for patients with inherited bleeding disorders, introduced in 2008. It aimed to improve the timeliness and completeness of patient-reported treatment records, to facilitate analysis of treatment and outcome trends. The system is easy to use, responsive and accessible.
METHODS: The software uses Microsoft technologies with a SQL Server database and an ASP.net website front-end, running on personal computers, android and I-phones. Haemtrack interfaces with the UK Haemophilia Centre Information System and the National Haemophilia Database (NHD). Data are validated locally by Haemophilia Centres and centrally by NHD. Data collected include as follows: treatment brand, dose and batch number, time/date of bleed onset and drug administration, reasons for treatment (prophylaxis, bleed, follow-up), bleed site, severity, pain-score and outcome.
RESULTS: Haemtrack was used by 90% of haemophilia treatment centres (HTCs) in 2015, registering 2683 patients using home therapy of whom 1923 used Haemtrack, entering >17 000 treatments per month. This included 68% of all UK patients with severe haemophilia A. Reporting compliance varied and 55% of patients reported ≥75% of potential usage. Centres had a median 78% compliance overall. A strategy for progressively improving compliance is in place. Age distribution and treatment intensity were similar in Haemtrack users/non-users with severe haemophilia treated prophylactically.
CONCLUSION: The Haemtrack system is a valuable tool that may improve treatment compliance and optimize treatment regimen. Analysis of national treatment trends and large-scale longitudinal, within-patient analysis of changes in regimen and/or product will provide valuable insights that will guide future clinical practice.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  haemophilia; haemtrack; home therapy; patient-reported outcomes

Mesh:

Year:  2017        PMID: 28806858     DOI: 10.1111/hae.13287

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  7 in total

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Authors:  Elena A Boccalandro; Giuseppe Dallari; Pier Mannuccio Mannucci
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2.  Expert opinion on current and future prophylaxis therapies aimed at improving protection for people with hemophilia A.

Authors:  Angelika Batorova; Ana Boban; Melen Brinza; Toshiko Lissitchkov; Laszlo Nemes; Irena Zupan Preložnik; Petr Smejkal; Nadezhda Zozulya; Jerzy Windyga
Journal:  J Med Life       Date:  2022-04

Review 3.  Therapies for rare diseases: therapeutic modalities, progress and challenges ahead.

Authors:  Erik Tambuyzer; Benjamin Vandendriessche; Christopher P Austin; Philip J Brooks; Kristina Larsson; Katherine I Miller Needleman; James Valentine; Kay Davies; Stephen C Groft; Robert Preti; Tudor I Oprea; Marco Prunotto
Journal:  Nat Rev Drug Discov       Date:  2019-12-13       Impact factor: 84.694

Review 4.  Telehealth Interventions for Improving Self-Management in Patients With Hemophilia: Scoping Review of Clinical Studies.

Authors:  Wenji Qian; Teddy Tai-Ning Lam; Henry Hon Wai Lam; Chi-Kong Li; Yin Ting Cheung
Journal:  J Med Internet Res       Date:  2019-07-10       Impact factor: 5.428

5.  Twelve-month prevalence of haemarthrosis and joint disease using the Haemophilia Joint Health score: evaluation of the UK National Haemophilia Database and Haemtrack patient reported data: an observational study.

Authors:  Richard A Wilkins; David Stephensen; Heidi Siddle; Martin J Scott; Hua Xiang; Elizabeth Horn; Ben Palmer; Graham J Chapman; Michael Richards; Rebecca Walwyn; Anthony Redmond
Journal:  BMJ Open       Date:  2022-01-12       Impact factor: 2.692

6.  First experience of a hemophilia monitoring platform: florio HAEMO.

Authors:  Ester Zapotocka; Angelika Batorova; Ernest Bilic; Ana Boban; Carmen Escuriola Ettingshausen; Barbara Faganel Kotnik; Radomira Hrdlickova; Pawel Laguna; Jan Machal; Laszlo Nemes; Irena Preloznik Zupan; Gediminas Puras; Marianna Zombori
Journal:  Res Pract Thromb Haemost       Date:  2022-03-13

7.  An Electronic Patient-Reported Outcome Mobile App for Data Collection in Type A Hemophilia: Design and Usability Study.

Authors:  Francesco Petracca; Rosaria Tempre; Maria Cucciniello; Oriana Ciani; Elena Pompeo; Luigi Sannino; Valeria Lovato; Giancarlo Castaman; Alessandra Ghirardini; Rosanna Tarricone
Journal:  JMIR Form Res       Date:  2021-12-01
  7 in total

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