Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar
Sickle cell disease (SCD) is an orphan and extremely rare condition in Colombia and worldwide. However, a significant number of cases were identified in San Basilio de Palenque, Bolívar, enabling a pharmacotherapeutic follow-up study. This population represents a genetic bottleneck with limited admi...
- Autores:
-
Alviz Amador Antistio
Gonzalez Cervera Tulia
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2025
- Institución:
- Universidad de Cartagena
- Repositorio:
- Repositorio Universidad de Cartagena
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.unicartagena.edu.co:11227/19734
- Acceso en línea:
- https://hdl.handle.net/11227/19734
- Palabra clave:
- Education - Research
pharmacotherapeutic
hemoglobinopathy
- Rights
- openAccess
- License
- Derechos reservados Universidad de Cartagena.
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Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| title |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| spellingShingle |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar Education - Research pharmacotherapeutic hemoglobinopathy |
| title_short |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| title_full |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| title_fullStr |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| title_full_unstemmed |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| title_sort |
Evaluation of pharmacotherapy in sickle cell disease in an AfroColombian community: A cross-sectional analytical study in San Basilio de Palenque, Bolívar |
| dc.creator.fl_str_mv |
Alviz Amador Antistio Gonzalez Cervera Tulia |
| dc.contributor.author.none.fl_str_mv |
Alviz Amador Antistio Gonzalez Cervera Tulia |
| dc.contributor.educationalvalidator.none.fl_str_mv |
Antistio Alviz Amador |
| dc.subject.armarc.none.fl_str_mv |
Education - Research pharmacotherapeutic hemoglobinopathy |
| topic |
Education - Research pharmacotherapeutic hemoglobinopathy |
| description |
Sickle cell disease (SCD) is an orphan and extremely rare condition in Colombia and worldwide. However, a significant number of cases were identified in San Basilio de Palenque, Bolívar, enabling a pharmacotherapeutic follow-up study. This population represents a genetic bottleneck with limited admixture, making it crucial for further genetic and clinical research. Despite being largely unexplored due to lack of awareness and state neglect, SCD persists in this community. This study aimed to characterize and follow up pharmacotherapeutically on patients with SCD and traits. An observational, cross-sectional analytical study was conducted in 20 patients, assessing sociodemographic factors, pharmacotherapeutic follow-up, and pharmaceutical interventions. Results showed that 75% of patients were female, and 40% were homozygous. The most commonly used medications included folic acid, analgesics (paracetamol, tramadol, naproxen, codeine, ibuprofen, morphine), L-glutamine, and enalapril. Pain from vaso-occlusive crises and hemolytic episodes was the main reason for analgesic use. Notably, 62% of homozygous patients were not receiving baseline treatment with hydroxycarbamide, increasing their risk of complications. Addressing this gap through pharmaceutical interventions was one of the study's key contributions. In conclusion, this research highlights the need for a multidisciplinary approach to optimize treatment and improve the quality of life of affected patients. Given its genetic significance, San Basilio de Palenque represents a unique setting for further studies on SCD. |
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2025 |
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2025-07-09T15:04:54Z |
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2025-07-09T15:04:54Z |
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2025 |
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Trabajo de grado - Maestría Articulo de Revista |
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eng |
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eng |
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Intractable & Rare Diseases Research |
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127 |
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122 |
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1. Roldán-Isaza M, Herrera-Almanza L, HernándezMartínez A, Martínez-Sánchez LM. Sickle cell disease and resistance to malaria. Narrative review. Revista de la Facultad de Ciencias de la Salud Universidad del Cauca. 2020; 22:34-42. (in Spanish) 2. Mañú Pereira MDM, Colombatti R, Alvarez F, et al. Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective. Lancet Haematol. 2023; 10:e687-e694. 3. Acuña C, Cuero K, Espitia K, Rojas R, Torres R. Sickle cell disease and situation in Colombia: Review. Bioscience. 2017; 3: 65-75. (in Spanish) 4. Pharmaceutical Care Research Group, University of Granada (Spain). Pharmacotherapy follow-up: The Dader method (3rd revision: 2005). Pharmacy Practice. 2006; 4:44-53. (in Spanish) |
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Derechos reservados Universidad de Cartagena. |
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Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0) |
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Derechos reservados Universidad de Cartagena. https://creativecommons.org/licenses/by-nc/4.0/ Atribución-NoComercial 4.0 Internacional (CC BY-NC 4.0) http://purl.org/coar/access_right/c_abf2 |
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Alviz Amador AntistioGonzalez Cervera TuliaAntistio Alviz Amador2025-07-09T15:04:54Z2025-07-09T15:04:54Z20252186-361https://hdl.handle.net/11227/19734Sickle cell disease (SCD) is an orphan and extremely rare condition in Colombia and worldwide. However, a significant number of cases were identified in San Basilio de Palenque, Bolívar, enabling a pharmacotherapeutic follow-up study. This population represents a genetic bottleneck with limited admixture, making it crucial for further genetic and clinical research. Despite being largely unexplored due to lack of awareness and state neglect, SCD persists in this community. This study aimed to characterize and follow up pharmacotherapeutically on patients with SCD and traits. An observational, cross-sectional analytical study was conducted in 20 patients, assessing sociodemographic factors, pharmacotherapeutic follow-up, and pharmaceutical interventions. Results showed that 75% of patients were female, and 40% were homozygous. The most commonly used medications included folic acid, analgesics (paracetamol, tramadol, naproxen, codeine, ibuprofen, morphine), L-glutamine, and enalapril. Pain from vaso-occlusive crises and hemolytic episodes was the main reason for analgesic use. Notably, 62% of homozygous patients were not receiving baseline treatment with hydroxycarbamide, increasing their risk of complications. Addressing this gap through pharmaceutical interventions was one of the study's key contributions. In conclusion, this research highlights the need for a multidisciplinary approach to optimize treatment and improve the quality of life of affected patients. Given its genetic significance, San Basilio de Palenque represents a unique setting for further studies on SCD.application/pdfengIntractable & Rare Diseases Research1271221. Roldán-Isaza M, Herrera-Almanza L, HernándezMartínez A, Martínez-Sánchez LM. Sickle cell disease and resistance to malaria. Narrative review. Revista de la Facultad de Ciencias de la Salud Universidad del Cauca. 2020; 22:34-42. (in Spanish)2. Mañú Pereira MDM, Colombatti R, Alvarez F, et al. Sickle cell disease landscape and challenges in the EU: the ERN-EuroBloodNet perspective. Lancet Haematol. 2023; 10:e687-e694.3. Acuña C, Cuero K, Espitia K, Rojas R, Torres R. Sickle cell disease and situation in Colombia: Review. Bioscience. 2017; 3: 65-75. (in Spanish)4. Pharmaceutical Care Research Group, University of Granada (Spain). Pharmacotherapy follow-up: The Dader method (3rd revision: 2005). Pharmacy Practice. 2006; 4:44-53. 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