Literature DB >> 11317481

Pharmacosurveillance and quality of care of thalassaemic patients. A large scale epidemiological survey.

R Arboretti1, G Tognoni, D Alberti.   

Abstract

OBJECTIVE: For adolescent thalassaemic patients, parenteral iron-chelation therapy is still a burden and a major reason for unsatisfactory compliance. The introduction of a new pharmaceutical preparation of deferoxamine (Desferal) claimed to be better tolerated was accompanied by an epidemiological study on the quality of care and life of the Italian thalassaemic population and on the acceptability and safety profile of the new preparation compared with the old one.
METHODS: This was a two-period prospective survey of 867 patients (12% of the registered thalassaemic patient population) in a sample of centres representative of the different contexts of care.
RESULTS: The majority of patients (81%) reported an overall positive opinion about the quality of care (median satisfaction score 7.4). Judgement was more critical among patients over 15 years, unemployed, less compliant with chelation treatment and with higher mean serum ferritin levels. The co-morbidity profile did not appear to influence patients' satisfaction scores, but 21% of respondents associated great discomfort with the use of Desferal, which appeared in a multivariate analysis to be a strong predictor [odds ratio (OR) 2.15, 95% confidence interval (CI) 1.20-3.83] of negative perception. Quality of life was reported as fair or poor (score below 6) by 21% of patients. Over a total of 29,066 infusions included in the comparison of the safety of the new versus the old preparation, the reported incidences of any adverse event (AE) were 51% versus 57%, respectively, and 8.2% versus 9.3% for severe AEs. Comparing the new with the old preparation, the adjusted relative risk of severe AEs was 0.79 (95% CI 0.65-0.96).
CONCLUSION: While oral chelation therapies are still under evaluation, the overall quality of care and perceived quality of life of a representative sample of the Italian population of thalassaemic patients show that room for improvement depends more on the contexts of life and care than on strictly medical conditions. Comprehensive epidemiological surveillance is needed as a routine component of the care of this highly morbidity-burdened population to ensure timely appreciation of unmet needs and to assess the yield of innovative treatment schedules.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11317481     DOI: 10.1007/s002280000251

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  10 in total

1.  Cost effectiveness of once-daily oral chelation therapy with deferasirox versus infusional deferoxamine in transfusion-dependent thalassaemia patients: US healthcare system perspective.

Authors:  Thomas E Delea; Oleg Sofrygin; Simu K Thomas; Jean-Francois Baladi; Pradyumna D Phatak; Thomas D Coates
Journal:  Pharmacoeconomics       Date:  2007       Impact factor: 4.981

2.  Psychometric properties of the Specific Thalassemia Quality of Life Instrument for adults.

Authors:  Georgios N Lyrakos; Demetra Vini; Helen Aslani; Marouso Drosou-Servou
Journal:  Patient Prefer Adherence       Date:  2012-07-02       Impact factor: 2.711

Review 3.  Deferasirox : a review of its use in the management of transfusional chronic iron overload.

Authors:  Lily P H Yang; Susan J Keam; Gillian M Keating
Journal:  Drugs       Date:  2007       Impact factor: 9.546

4.  Efficacy and safety of Iranian made Deferasirox (Osveral®) in Iranian major thalassemic patients with transfusional iron overload: A one year prospective multicentric open-label non-comparative study.

Authors:  P Eshghi; Z Farahmandinia; M Molavi; M Naderi; M Jafroodi; H Hoorfar; K Davari; A Azarkeivan; B Keikhaie; S Ansari; M Arasteh
Journal:  Daru       Date:  2011       Impact factor: 3.117

Review 5.  The impact of iron overload and its treatment on quality of life: results from a literature review.

Authors:  Linda Abetz; Jean-Francois Baladi; Paula Jones; Diana Rofail
Journal:  Health Qual Life Outcomes       Date:  2006-09-28       Impact factor: 3.186

6.  Quality of life, clinical effectiveness, and satisfaction in patients with beta thalassemia major and sickle cell anemia receiving deferasirox chelation therapy.

Authors:  Sefika Pinar Senol; Eyup Naci Tiftik; Selma Unal; Aydan Akdeniz; Bahar Tasdelen; Bahar Tunctan
Journal:  J Basic Clin Pharm       Date:  2016-03

7.  Transfusion-dependent low-risk myelodysplastic patients receiving deferasirox: Long-term follow-up.

Authors:  Salvatore Improta; Maria Rosaria Villa; Antonio Volpe; Angela Lombardi; Paola Stiuso; Nicola Cantore; Lucia Mastrullo
Journal:  Oncol Lett       Date:  2013-10-10       Impact factor: 2.967

8.  Quality of life in patients with thalassemia major.

Authors:  Sh Ansari; A Baghersalimi; A Azarkeivan; M Nojomi; A Hassanzadeh Rad
Journal:  Iran J Ped Hematol Oncol       Date:  2014-04-20

9.  Effectiveness of Deferasirox in Pediatric Thalassemia Patients: Experience from a Tertiary Care Hospital of Odisha.

Authors:  Mousumee Panigrahi; Trupti Rekha Swain; Rabindra Kumar Jena; Ashutosh Panigrahi; Nishant Debta
Journal:  Indian J Pharmacol       Date:  2020-08-04       Impact factor: 1.200

10.  A systematic review of adherence to iron chelation therapy among children and adolescents with thalassemia.

Authors:  Paavani S Reddy; Margaret Locke; Sherif M Badawy
Journal:  Ann Med       Date:  2022-12       Impact factor: 4.709

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.