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Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction

RATIONALE: The demographics of patients with idiopathic pulmonary arterial hypertension (IPAH) are changing and this diagnosis is increasingly being made in older patients. However, diagnostic misclassifications are common as it may be difficult to differentiate between IPAH and pulmonary hypertensi...

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Autores principales: Olsson, Karen M, Sommer, Lisa, Fuge, Jan, Welte, Tobias, Hoeper, Marius M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358848/
https://www.ncbi.nlm.nih.gov/pubmed/25853979
http://dx.doi.org/10.1186/s12931-015-0194-6
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author Olsson, Karen M
Sommer, Lisa
Fuge, Jan
Welte, Tobias
Hoeper, Marius M
author_facet Olsson, Karen M
Sommer, Lisa
Fuge, Jan
Welte, Tobias
Hoeper, Marius M
author_sort Olsson, Karen M
collection PubMed
description RATIONALE: The demographics of patients with idiopathic pulmonary arterial hypertension (IPAH) are changing and this diagnosis is increasingly being made in older patients. However, diagnostic misclassifications are common as it may be difficult to differentiate between IPAH and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF). We investigated the hypothesis that the capillary pCO(2) (p(c)CO(2)) may help distinguishing between idiopathic pulmonary arterial hypertension (IPAH) and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF). METHODS: In a cross-sectional study, we retrospectively assessed p(c)CO(2) levels (obtained from arterialized capillary blood at the time of diagnosis) from patients with IPAH or PH-HFpEF, respectively. Receiver operated characteristics (ROC) were used to determine the p(c)CO(2) level providing the best discrimination between these two conditions. P(c)CO(2) values were considered helpful if they were associated with a negative predictive value >0.9 to excluded either IPAH or PH-HFpEF. RESULTS: The study enrolled 185 patients, 99 with IPAH (74% female; age 47 ± 17 years; body mass index 26 ± 5 kg/m(2), PAPm 53 ± 12 mmHg, PAWP 8 ± 3 mmHg), and 86 with PH-HFpEF (64% female; age 69 ± 10 years; body mass index 30 ± 6 kg/m(2), PAPm 47 ± 10 mmHg, PAWP 21 ± 5 mmHg). P(c)CO(2) at time of diagnosis was 33 ± 4 mmHg in the IPAH group and 40 ± 5 mmHg in the PH-HFpEF group (p < 0.001), respectively. According to ROC analysis, a p(c)CO(2) of 36 mmHg was the best discriminator between both entities with an area under curve of 0.87 (p < 0.001). The likelihood of PH-HFpEF was <10% in patients with a P(c)CO(2) < 34 mmHg, whereas the likelihood of IPAH was <10% in patients with a P(c)CO(2) > 41 mmHg. CONCLUSIONS: P(c)CO(2) levels were significantly lower in IPAH compared to PH-HFpEF and may provide useful information in differentiating between both conditions.
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spelling pubmed-43588482015-03-14 Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction Olsson, Karen M Sommer, Lisa Fuge, Jan Welte, Tobias Hoeper, Marius M Respir Res Research RATIONALE: The demographics of patients with idiopathic pulmonary arterial hypertension (IPAH) are changing and this diagnosis is increasingly being made in older patients. However, diagnostic misclassifications are common as it may be difficult to differentiate between IPAH and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF). We investigated the hypothesis that the capillary pCO(2) (p(c)CO(2)) may help distinguishing between idiopathic pulmonary arterial hypertension (IPAH) and pulmonary hypertension due to heart failure with preserved ejection fraction (PH-HFpEF). METHODS: In a cross-sectional study, we retrospectively assessed p(c)CO(2) levels (obtained from arterialized capillary blood at the time of diagnosis) from patients with IPAH or PH-HFpEF, respectively. Receiver operated characteristics (ROC) were used to determine the p(c)CO(2) level providing the best discrimination between these two conditions. P(c)CO(2) values were considered helpful if they were associated with a negative predictive value >0.9 to excluded either IPAH or PH-HFpEF. RESULTS: The study enrolled 185 patients, 99 with IPAH (74% female; age 47 ± 17 years; body mass index 26 ± 5 kg/m(2), PAPm 53 ± 12 mmHg, PAWP 8 ± 3 mmHg), and 86 with PH-HFpEF (64% female; age 69 ± 10 years; body mass index 30 ± 6 kg/m(2), PAPm 47 ± 10 mmHg, PAWP 21 ± 5 mmHg). P(c)CO(2) at time of diagnosis was 33 ± 4 mmHg in the IPAH group and 40 ± 5 mmHg in the PH-HFpEF group (p < 0.001), respectively. According to ROC analysis, a p(c)CO(2) of 36 mmHg was the best discriminator between both entities with an area under curve of 0.87 (p < 0.001). The likelihood of PH-HFpEF was <10% in patients with a P(c)CO(2) < 34 mmHg, whereas the likelihood of IPAH was <10% in patients with a P(c)CO(2) > 41 mmHg. CONCLUSIONS: P(c)CO(2) levels were significantly lower in IPAH compared to PH-HFpEF and may provide useful information in differentiating between both conditions. BioMed Central 2015-03-10 2015 /pmc/articles/PMC4358848/ /pubmed/25853979 http://dx.doi.org/10.1186/s12931-015-0194-6 Text en © Olsson et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Olsson, Karen M
Sommer, Lisa
Fuge, Jan
Welte, Tobias
Hoeper, Marius M
Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title_full Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title_fullStr Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title_full_unstemmed Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title_short Capillary pCO(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
title_sort capillary pco(2) helps distinguishing idiopathic pulmonary arterial hypertension from pulmonary hypertension due to heart failure with preserved ejection fraction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358848/
https://www.ncbi.nlm.nih.gov/pubmed/25853979
http://dx.doi.org/10.1186/s12931-015-0194-6
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