UK-based real-time lymphoproliferative disorder diagnostic service to improve the management of patients in Ghana

dc.contributor.authorEkem, I.
dc.contributor.authorParkins, E.
dc.contributor.authorRoger, G.
dc.contributor.authorOwen, G.
dc.contributor.authorBedu-Addo, G.
dc.contributor.authorOhene Opare, S.
dc.contributor.authorAdomakoh, Y.
dc.contributor.authorBates, I.
dc.date.accessioned2012-05-16T13:14:55Z
dc.date.accessioned2017-10-19T11:54:36Z
dc.date.available2012-05-16T13:14:55Z
dc.date.available2017-10-19T11:54:36Z
dc.date.issued2009
dc.description.abstractThe objective of the study was to evaluate the feasibility of a UK-based real-time service to improve the diagnosis and management of lymphoproliferative disorders (LPDs) in Ghana. Adult patients reporting to hospital with a suspected LPD, during a 1 year period, were prospectively enrolled. Bone marrow and/or lymph node biopsies were posted to the Haematology Malignancy Diagnostic Service (HMDS), Leeds, UK and underwent morphological analysis and immunophenotyping. Results were returned by e-mail. The initial diagnoses made in Ghana were compared with the final HMDS diagnoses to assess the contribution of the HMDS diagnosis to management decisions. The study was conducted at the two teaching hospitals in Ghana-Komfo Anokye, Kumasi and Korle Bu, Accra. Participants comprised 150 adult patients (>/=12 years old), 79 women, median age 46 years. Bone marrow and lymph node biopsy samples from all adults presenting with features suggestive of a LPD, at the two teaching hospitals in Ghana, over 1 year were posted to a UK LPD diagnostic centre, where immunophenotyping was performed by immunohistochemistry. Molecular analysis was performed where indicated. Diagnostic classifications were made according to international criteria. Final diagnosis was compared to the initial Ghanaian diagnosis to evaluate discrepancies; implications for alterations in treatment decisions were evaluated. Median time between taking samples and receiving e-mail results in Ghana was 15 days. Concordance between initial and final diagnoses was 32% (48 of 150). The HMDS diagnosis would have changed management in 31% (46 of 150) of patients. It is feasible to provide a UK-based service for LPD diagnosis in Africa using postal services and e-mail. This study confirmed findings from wealthy countries that a specialised haematopathology service can improve LPD diagnosis. This model of Ghana-UK collaboration provides a platform on which to build local capacity to operate an international quality diagnostic service for LPDs.en_US
dc.identifier.urihttp://197.255.68.203/handle/123456789/1398
dc.language.isoenen_US
dc.publisherIndian Journal Dermatol 2(3): 143-149en_US
dc.titleUK-based real-time lymphoproliferative disorder diagnostic service to improve the management of patients in Ghanaen_US
dc.typeArticleen_US

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