Literature DB >> 9795870

Cost-benefit analysis of a national thalassaemia prevention programme in Israel.

G Ginsberg1, T Tulchinsky, D Filon, A Goldfarb, L Abramov, E A Rachmilevitz.   

Abstract

OBJECTIVE: In Israel (population 5.7 million) there are around 200 known living subjects with thalassaemia major, of whom around 80% are from the northern district. This study aims at examining the costs and benefits of a national screening programme to prevent thalassaemia in Israel.
MEASUREMENTS AND MAIN RESULTS: The lifetime healthcare costs of caring for a person born with thalassaemia major are $284,154. The costs of the home infusion service (33.1%) actually exceed the costs of the chelating agent itself (22.1%). The remaining 44.8% of costs are due to stay in hospital, operations, outpatient visits, laboratory tests, therapists, etc. Lost earnings and premature mortality costs account for a further $51,843 and $141,944 respectively for each case. A national screening programme would cost $900,197 and prevent around 13.4 homozygotes being born, at a cost of $67,369 for each birth prevented. The benefit-cost ratio of the programme to the health services is 4.22:1, which increases to 6.01:1 when a societal perspective is taken. However, around 13.0 homozygote births are still expected to occur, the majority owing to lack of compliance of patients at various stages in the screening process. The addition of a national health education programme for the higher risk non-Jewish population either nationally or in selected regions will incur extra costs, which may be covered by increased benefits as a result of better compliance with the screening programme.
CONCLUSION: Israel should start to provide a nationwide thalassaemia screening programme as the monetary benefits to society (and even to the health services alone) will exceed the screening programmes costs.

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Year:  1998        PMID: 9795870     DOI: 10.1136/jms.5.3.120

Source DB:  PubMed          Journal:  J Med Screen        ISSN: 0969-1413            Impact factor:   2.136


  12 in total

1.  Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

Authors:  H Toledano-Alhadef; L Basel-Vanagaite; N Magal; B Davidov; S Ehrlich; V Drasinover; E Taub; G J Halpern; N Ginott; M Shohat
Journal:  Am J Hum Genet       Date:  2001-07-06       Impact factor: 11.025

2.  Economic burden of beta-thalassemia/Hb E and beta-thalassemia major in Thai children.

Authors:  Arthorn Riewpaiboon; Issarang Nuchprayoon; Kitti Torcharus; Kaemthong Indaratna; Montarat Thavorncharoensap; Bang-On Ubol
Journal:  BMC Res Notes       Date:  2010-01-30

3.  Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India.

Authors:  Nishi Madan; Satendra Sharma; S K Sood; Roshan Colah; Late H M Bhatia
Journal:  Indian J Hum Genet       Date:  2010-01

4.  Socio-demographic Profile and Economic Burden of Treatment of Transfusion Dependent Thalassemia.

Authors:  Amita Moirangthem; Shubha R Phadke
Journal:  Indian J Pediatr       Date:  2017-11-09       Impact factor: 1.967

Review 5.  Past, present & future scenario of thalassaemic care & control in India.

Authors:  Ishwar C Verma; Renu Saxena; Sudha Kohli
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

6.  Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh.

Authors:  Ajay F Christopher; Anita Kumari; Sunali Chaudhary; Sandhya Hora; Ziledar Ali; Satish C Agrawal
Journal:  Indian J Hum Genet       Date:  2013-04

7.  Prevention of β Thalassemia in Northern Israel - a Cost-Benefit Analysis.

Authors:  Ariel Koren; Lora Profeta; Luci Zalman; Haya Palmor; Carina Levin; Ronit Bril Zamir; Stavit Shalev; Orna Blondheim
Journal:  Mediterr J Hematol Infect Dis       Date:  2014-02-17       Impact factor: 2.576

8.  Rapid and Sensitive Assessment of Globin Chains for Gene and Cell Therapy of Hemoglobinopathies.

Authors:  Constantinos C Loucari; Petros Patsali; Thamar B van Dijk; Coralea Stephanou; Panayiota Papasavva; Maria Zanti; Ryo Kurita; Yukio Nakamura; Soteroulla Christou; Maria Sitarou; Sjaak Philipsen; Carsten W Lederer; Marina Kleanthous
Journal:  Hum Gene Ther Methods       Date:  2018-02       Impact factor: 2.396

9.  NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot study.

Authors:  Kanika Singh; Sunita Bijarnia-Mahay; V L Ramprasad; Ratna Dua Puri; Sandhya Nair; Sheetal Sharda; Renu Saxena; Sudha Kohli; Samarth Kulshreshtha; Indrani Ganguli; Kanwal Gujral; Ishwar C Verma
Journal:  BMC Med Genet       Date:  2020-11-02       Impact factor: 2.103

10.  A cost-of-illness analysis of β-Thalassaemia major in children in Sri Lanka - experience from a tertiary level teaching hospital.

Authors:  Hamish Reed-Embleton; Savinda Arambepola; Simon Dixon; Behrouz Nezafat Maldonado; Anuja Premawardhena; Mahinda Arambepola; Jahangir A M Khan; Stephen Allen
Journal:  BMC Pediatr       Date:  2020-05-27       Impact factor: 2.125

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