Literature DB >> 26390060

Health-related quality of life assessment in haemophilia patients on prophylaxis therapy: a systematic review of results from prospective clinical trials.

A O Oladapo1, J D Epstein2, E Williams3, D Ito1, A Gringeri4, L A Valentino5.   

Abstract

INTRODUCTION: Prophylaxis is effective in reducing the number of bleeding episodes in patients with severe or moderately severe haemophilia A and B, including those with inhibitors. However, data, predominantly from observational studies, suggest more equivocal effects on health-related quality of life (HRQoL). AIM: To examine the impact of prophylaxis on HRQoL from prospective clinical trials.
METHODS: We performed a systematic literature review of clinical trials evaluating the efficacy of prophylaxis with factor VIII, FIX or bypassing agents. Trials assessing HRQoL via validated instruments were selected and summarized.
RESULTS: Thirteen trials (haemophilia A [n = 8]; haemophilia B [n = 2]; inhibitors [n = 3]) met all inclusion criteria. HRQoL instruments included the EQ-5D, SF-36, Haem-QoL-A, Haem-A-QoL, Haemo-QoL and CHO-KLAT. Improvements in HRQoL following prophylaxis were observed with the EQ-VAS, SF-36 and haemophilia-specific instruments in adult patients and were associated with reduced pain, fewer restrictions in physical activities and better general health. Prophylaxis led to statistically significant or clinically meaningful HRQoL improvement in six trials and non-significant improvement in four trials; two trials found no improvement and one reported no data. Despite study differences, consistent trends suggested that patients previously treated solely on-demand and those who experienced marked reductions in the frequency of bleeding with prophylaxis had a greater improvement in HRQoL.
CONCLUSION: Contrary to findings of observational studies, the results from the majority of prospective trials using validated instruments showed positive trends for improved HRQoL with prophylaxis in adults.
© 2015 John Wiley & Sons Ltd.

Entities:  

Keywords:  FIX; FVIII; HRQoL; bypassing agents; haemophilia; prophylaxis

Mesh:

Year:  2015        PMID: 26390060     DOI: 10.1111/hae.12759

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


  16 in total

Review 1.  Factor VIII replacement is still the standard of care in haemophilia A.

Authors:  Louis Aledort; Pier Mannuccio Mannucci; Wolfgang Schramm; Michael Tarantino
Journal:  Blood Transfus       Date:  2019-12-11       Impact factor: 3.443

Review 2.  Coagulation Factor IX (Recombinant), Albumin Fusion Protein (Albutrepenonacog Alfa; Idelvion®): A Review of Its Use in Haemophilia B.

Authors:  Katherine A Lyseng-Williamson
Journal:  Drugs       Date:  2017-01       Impact factor: 9.546

3.  Total knee arthroplasty in patients with haemophilic arthropathy is effective and safe according to the outcomes at a mid-term follow-up.

Authors:  Rui Wang; Zhengming Wang; Yong Gu; Jingjing Zhang; Penghe Wang; Peijian Tong; Shuaijie Lv
Journal:  J Orthop Traumatol       Date:  2022-07-11

4.  Gene therapy in hemophilia A: a cost-effectiveness analysis.

Authors:  Nicoletta Machin; Margaret V Ragni; Kenneth J Smith
Journal:  Blood Adv       Date:  2018-07-24

5.  Patient preferences in the treatment of hemophilia A: impact of storage conditions on product choice.

Authors:  Bernd Tischer; Renato Marino; Mariasanta Napolitano
Journal:  Patient Prefer Adherence       Date:  2018-03-26       Impact factor: 2.711

Review 6.  An investigational RNAi therapeutic targeting antithrombin for the treatment of hemophilia A and B.

Authors:  Nicoletta Machin; Margaret V Ragni
Journal:  J Blood Med       Date:  2018-08-22

7.  Preferences and Health-Related Quality-of-Life Related to Disease and Treatment Features for Patients with Hemophilia A in a Canadian General Population Sample.

Authors:  Karissa Johnston; Jayson M Stoffman; Alexis T Mickle; Robert J Klaassen; Demitri Diles; Shade Olatunde; Lina Eliasson; Roxana Bahar
Journal:  Patient Prefer Adherence       Date:  2021-06-24       Impact factor: 2.711

Review 8.  New developments in the management of moderate-to-severe hemophilia B.

Authors:  Moniba Nazeef; John P Sheehan
Journal:  J Blood Med       Date:  2016-04-01

Review 9.  Potential role of a new PEGylated recombinant factor VIII for hemophilia A.

Authors:  Tung Thanh Wynn; Burak Gumuscu
Journal:  J Blood Med       Date:  2016-06-20

10.  Recombinant factor VIII Fc fusion protein for the treatment of severe haemophilia A: Final results from the ASPIRE extension study.

Authors:  Beatrice Nolan; Johnny Mahlangu; Ingrid Pabinger; Guy Young; Barbara A Konkle; Chris Barnes; Keiji Nogami; Elena Santagostino; K John Pasi; Liane Khoo; Bent Winding; Huixing Yuan; Joachim Fruebis; Dan Rudin; Johannes Oldenburg
Journal:  Haemophilia       Date:  2020-03-30       Impact factor: 4.287

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