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Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension
OBJECTIVE: The aim of the research reported here was to compare pulmonary artery systolic pressure (PASP) and 6-minute walk distance after 1 year of follow-up in hemoglobin E/β thalassemia (E/β-Thal) with pulmonary arterial hypertension (PAH) patients who received chronic blood transfusions versus t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145826/ https://www.ncbi.nlm.nih.gov/pubmed/25170276 http://dx.doi.org/10.2147/IJGM.S66610 |
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author | Chueamuangphan, Nonlawan Patumanond, Jayanton Wongtheptien, Wattana Nawarawong, Weerasak Sukonthasarn, Apichard Chuncharunee, Suporn Tawichasri, Chamaiporn |
author_facet | Chueamuangphan, Nonlawan Patumanond, Jayanton Wongtheptien, Wattana Nawarawong, Weerasak Sukonthasarn, Apichard Chuncharunee, Suporn Tawichasri, Chamaiporn |
author_sort | Chueamuangphan, Nonlawan |
collection | PubMed |
description | OBJECTIVE: The aim of the research reported here was to compare pulmonary artery systolic pressure (PASP) and 6-minute walk distance after 1 year of follow-up in hemoglobin E/β thalassemia (E/β-Thal) with pulmonary arterial hypertension (PAH) patients who received chronic blood transfusions versus those who received occasional transfusions. METHODS: A nonrandomized clinical trial was conducted at the Hematological Outpatient Clinic of Chiang Rai Hospital, Thailand. All adult cases of E/β-Thal with PAH (defined as PASP >35 mmHg by Doppler echocardiography) were evaluated and followed for the next 12 months. The patients were classified into two groups by patient preference. Group 1 patients received chronic blood transfusions – one to two units of leukocyte-poor packed red cells every 2–4 weeks – over 1 year to maintain pre-transfusion hemoglobin levels of ≥7.0 g/dL. Group 2 patients received occasional transfusions over the course of 1 year, with more than 4 weeks between transfusions. All patients were treated with iron chelation when serum ferritin levels were ≥1,000 μg/dL. PASP and the 6-minute walk distance were evaluated at baseline and at 6 and 12 months. Propensity score adjustment was used to control for confounding by indication and contraindication. Multivariable regression analysis was used to evaluate the effects of chronic blood transfusion. RESULTS: There were 16 (53.3%) patients in Group 1 and 14 (46.7%) in Group 2. At 12 months, patients in Group 1 had a greater reduction in PASP than those in Group 1 (adjusted mean difference, −16.83; 95% confidence interval, −26.35 to −7.32; P=0.001). The 6-minute walk distance at 12 months in Group 1 patients was greater than that in Group 2 patients (adjusted mean difference, 46.55; 95% confidence interval, 18.08 to 75.02; P=0.001). CONCLUSION: This study found evidence that chronic blood transfusions may have beneficial effects in PAH in thalassemia patients over 1 year. |
format | Online Article Text |
id | pubmed-4145826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41458262014-08-28 Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension Chueamuangphan, Nonlawan Patumanond, Jayanton Wongtheptien, Wattana Nawarawong, Weerasak Sukonthasarn, Apichard Chuncharunee, Suporn Tawichasri, Chamaiporn Int J Gen Med Original Research OBJECTIVE: The aim of the research reported here was to compare pulmonary artery systolic pressure (PASP) and 6-minute walk distance after 1 year of follow-up in hemoglobin E/β thalassemia (E/β-Thal) with pulmonary arterial hypertension (PAH) patients who received chronic blood transfusions versus those who received occasional transfusions. METHODS: A nonrandomized clinical trial was conducted at the Hematological Outpatient Clinic of Chiang Rai Hospital, Thailand. All adult cases of E/β-Thal with PAH (defined as PASP >35 mmHg by Doppler echocardiography) were evaluated and followed for the next 12 months. The patients were classified into two groups by patient preference. Group 1 patients received chronic blood transfusions – one to two units of leukocyte-poor packed red cells every 2–4 weeks – over 1 year to maintain pre-transfusion hemoglobin levels of ≥7.0 g/dL. Group 2 patients received occasional transfusions over the course of 1 year, with more than 4 weeks between transfusions. All patients were treated with iron chelation when serum ferritin levels were ≥1,000 μg/dL. PASP and the 6-minute walk distance were evaluated at baseline and at 6 and 12 months. Propensity score adjustment was used to control for confounding by indication and contraindication. Multivariable regression analysis was used to evaluate the effects of chronic blood transfusion. RESULTS: There were 16 (53.3%) patients in Group 1 and 14 (46.7%) in Group 2. At 12 months, patients in Group 1 had a greater reduction in PASP than those in Group 1 (adjusted mean difference, −16.83; 95% confidence interval, −26.35 to −7.32; P=0.001). The 6-minute walk distance at 12 months in Group 1 patients was greater than that in Group 2 patients (adjusted mean difference, 46.55; 95% confidence interval, 18.08 to 75.02; P=0.001). CONCLUSION: This study found evidence that chronic blood transfusions may have beneficial effects in PAH in thalassemia patients over 1 year. Dove Medical Press 2014-08-19 /pmc/articles/PMC4145826/ /pubmed/25170276 http://dx.doi.org/10.2147/IJGM.S66610 Text en © 2014 Chueamuangphan et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Chueamuangphan, Nonlawan Patumanond, Jayanton Wongtheptien, Wattana Nawarawong, Weerasak Sukonthasarn, Apichard Chuncharunee, Suporn Tawichasri, Chamaiporn Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title | Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title_full | Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title_fullStr | Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title_full_unstemmed | Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title_short | Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension |
title_sort | benefits of chronic blood transfusion in hemoglobin e/β thalassemia with pulmonary arterial hypertension |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145826/ https://www.ncbi.nlm.nih.gov/pubmed/25170276 http://dx.doi.org/10.2147/IJGM.S66610 |
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