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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...

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Autores principales: Chueamuangphan, Nonlawan, Patumanond, Jayanton, Wongtheptien, Wattana, Nawarawong, Weerasak, Sukonthasarn, Apichard, Chuncharunee, Suporn, Tawichasri, Chamaiporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
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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.
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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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