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Article

Transplantation in Low Resource Countries

1
Cure2Children Foundation, Via Marconi 30, 50131 Florence, Italy
2
Pakistan Institute of Medical Sciences Children’s Hospital, Islamabad
3
National Institute of Blood Diseases, Karachi, Pakistan
*
Author to whom correspondence should be addressed.
Thalass. Rep. 2011, 1(s2), e9; https://doi.org/10.4081/thal.2011.s2.e9
Submission received: 1 December 2011 / Revised: 15 December 2011 / Accepted: 28 December 2011 / Published: 30 December 2011

Abstract

Thalassemia major (TM) is the most common deadly genetic disorder, a major cause of chronic non-infectious morbidity and financial burden in many low and middle-income regions. In these settings few children reach adulthood because proper long-term supportive care is seldom available. Bone marrow transplantation (BMT) is the only available curative modality and it can be very successful and cost-effective for young children with low-risk features and a compatible related donor. However, in countries where TM is most prevalent, there is a dire shortage of BMT centers. The Cure2Children Foundation has supported a feasibility study evaluating safety, efficacy and costs of developing a new BMT center in an underserved lower-middle-income country with relatively untrained professionals within a structured collaboration and knowledge-transfer program. A total of 24 consecutive patients who underwent BMT in Pakistan between September 2008 and August 2010 are included in this prospective analysis, 17 from an established bone marrow transplant center, the National Institute for Blood Diseases in Karachi, Pakistan and the initial 7 BMTs from a start up unit in a government civil hospital, the Pakistan Institute of Medical Sciences Children’s Hospital in Islamabad. Patients were matched for age, nutritional status, growth, disease, disease status and post-BMT follow-up time. All patients had a matched-related sibling donor, were younger than 10 years of age at the time of transplantation, received the same conditioning regimen. All needy families could rely on a support program throughout the 8-month post-transplant period. The Cure2Children Foundation provided professional and financial support as well as a structured web-based data management and cooperation platform. At a median follow up of 19.6 months (range 8.7 to 31.5) actuarial thalassemia-free survival is 85.6% and 85.7% and overall survival 94.1% and 85.7% in the established and start-up center respectively with no statistically significant differences. Other outcome indices like infectious complications, engraftment parameters, transplant-related complications, and post-BMT performance scores also did not differ. The median cost of matched-related transplants in the start-up center, including pre-BMT evaluation, was 11,513 USD (range 7518 to 21,176). Within structured cooperation strategies bone marrow transplantation for thalassemia major can be performed safely, effectively, and affordably even in start-up centers in lower-middleincome countries, like Pakistan, were most thalassemia patients live. This observation may have important implications to increase access to cure for thalassemia worldwide.

Keywords: transplantation developing countries transplantation developing countries

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MDPI and ACS Style

Faulkner, L.; Yaqub, N.; Khalid, S.K.; Zhara, T.; Ansari, S.; Farzana, T.; Shamsi, T. Transplantation in Low Resource Countries. Thalass. Rep. 2011, 1, e9. https://doi.org/10.4081/thal.2011.s2.e9

AMA Style

Faulkner L, Yaqub N, Khalid SK, Zhara T, Ansari S, Farzana T, Shamsi T. Transplantation in Low Resource Countries. Thalassemia Reports. 2011; 1(s2):e9. https://doi.org/10.4081/thal.2011.s2.e9

Chicago/Turabian Style

Faulkner, L., N. Yaqub, S. Khalid Khalid, T. Zhara, S. Ansari, T. Farzana, and T. Shamsi. 2011. "Transplantation in Low Resource Countries" Thalassemia Reports 1, no. s2: e9. https://doi.org/10.4081/thal.2011.s2.e9

APA Style

Faulkner, L., Yaqub, N., Khalid, S. K., Zhara, T., Ansari, S., Farzana, T., & Shamsi, T. (2011). Transplantation in Low Resource Countries. Thalassemia Reports, 1(s2), e9. https://doi.org/10.4081/thal.2011.s2.e9

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