Published ahead of print on October 11, 2007, doi:10.1164/rccm.200704-541OC
American Journal of Respiratory and Critical Care Medicine Vol 177. pp. 108-113, (2008)
© 2008 American Thoracic Society
doi: 10.1164/rccm.200704-541OC
Prevalence of HIV-related Pulmonary Arterial Hypertension in the Current Antiretroviral Therapy Era
Olivier Sitbon1,
Caroline Lascoux-Combe2,
Jean-François Delfraissy3,
Patrick G. Yeni4,
François Raffi5,
Dominique De Zuttere6,
Virginie Gressin7,
Pierre Clerson8,
Daniel Sereni2 and
Gérald Simonneau1
1 Service de Pneumologie et Reanimation, Hôpital Antoine Béclère, Clamart, France; 2 Service de Medecine Interne, Hôpital Saint Louis, Paris, France; 3 Service de Medecine Interne, Hôpital Bicêtre, Le Kremlin Bicêtre, France; 4 Service des Maladies Infectieuses et Tropicales A, Hôpital Bichat, Paris, France; 5 CISIH, Hôtel Dieu, Nantes, France; 6 Service de Medecine Interne, Hôpital du Perpétuel Secours, Levallois Perret, France; 7 Actelion Pharmaceuticals France, Paris, France; and 8 Orgamétrie, Roubaix, France
Correspondence and requests for reprints should be addressed to Olivier Sitbon, M.D., Ph.D., Service de Pneumologie Hôpital Antoine Béclère, 157 rue de la Porte de Trivaux, 92141 Clamart, France. E-mail: olivier.sitbon{at}abc.aphp.fr
Rationale: The prevalence of HIV-associated pulmonary arterial hypertension (PAH) has not been evaluated since introduction of combined, highly active antiretroviral treatments.
Objectives: To establish the current prevalence of PAH in a large HIV-positive population.
Methods: Prospective study conducted in 7,648 consecutive HIV-positive adults in 14 HIV clinics in France. PAH was identified through screening with a predefined algorithm. Patients with dyspnea unexplained by other causes underwent transthoracic Doppler echocardiography. PAH was suspected if peak velocity of tricuspid regurgitation was greater than 2.5 m/second and was confirmed by right heart catheterization.
Measurements and Main Results: PAH was diagnosed if mean pulmonary arterial pressure at rest was 25 mm Hg or greater (with pulmonary capillary wedge pressure 15 mm Hg) or 30 mm Hg or greater on exercise. A total of 739 patients had dyspnea, of which 312 met exclusion criteria and 150 refused to participate. Among the remaining 277, 30 had known PAH and 247 had unexplained dyspnea and underwent echocardiography; PAH was suspected in 18 and confirmed in 5, to give a total of 35 cases. The prevalence was thus 0.46% (95% confidence interval, 0.32–0.64%). All new cases had relatively milder PAH.
Conclusions: The prevalence of HIV-associated PAH is about the same as it was in the early 1990s. Given the current good long-term prognosis of patients with HIV, the severity of PAH in HIV-infected patients, and the absence of predictive factors, careful screening for PAH is warranted for patients with unexplained dyspnea.
Key Words: dyspnea echocardiography, Doppler epidemiologic studies HIV infection hypertension, pulmonary prevalence
| AT A GLANCE COMMENTARY
Scientific Knowledge on the Subject
One established risk factor for development of pulmonary arterial hypertension (PAH) is HIV infection, with the main symptom, progressive dyspnea, reported in about 85% of patients. In the early 1990s, when highly active antiretroviral treatments (HAART) were not available, prevalence of HIV-PAH was 0.5% (95% confidence interval, 0.10–0.90%).
What This Study Adds to the Field
The prevalence of HIV-associated PAH is about the same as it was in the early 1990s. Given the current good long-term prognosis of patients with HIV, the severity of PAH in HIV-infected patients, and the absence of predictive factors, careful screening for PAH is warranted for patients with unexplained dyspnea.
|
This article has been cited by other articles:

|
 |

|
 |
 
A. Barnier, I. Frachon, J. Dewilde, C. Gut-Gobert, Y. Jobic, and C. Leroyer
Improvement of HIV-related pulmonary hypertension after the introduction of an antiretroviral therapy
Eur. Respir. J.,
July 1, 2009;
34(1):
277 - 278.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. M. Hassoun, L. Mouthon, J. A. Barbera, S. Eddahibi, S. C. Flores, F. Grimminger, P. L. Jones, M. L. Maitland, E. D. Michelakis, N. W. Morrell, et al.
Inflammation, growth factors, and pulmonary vascular remodeling.
J. Am. Coll. Cardiol.,
June 30, 2009;
54(1 Suppl):
S10 - S19.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Simonneau, I. M. Robbins, M. Beghetti, R. N. Channick, M. Delcroix, C. P. Denton, C. G. Elliott, S. P. Gaine, M. T. Gladwin, Z.-C. Jing, et al.
Updated clinical classification of pulmonary hypertension.
J. Am. Coll. Cardiol.,
June 30, 2009;
54(1 Suppl):
S43 - S54.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. B. Badesch, H. C. Champion, M. A. Gomez Sanchez, M. M. Hoeper, J. E. Loyd, A. Manes, M. McGoon, R. Naeije, H. Olschewski, R. J. Oudiz, et al.
Diagnosis and assessment of pulmonary arterial hypertension.
J. Am. Coll. Cardiol.,
June 30, 2009;
54(1 Suppl):
S55 - S66.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
V. V. McLaughlin, S. L. Archer, D. B. Badesch, R. J. Barst, H. W. Farber, J. R. Lindner, M. A. Mathier, M. D. McGoon, M. H. Park, R. S. Rosenson, et al.
ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension: A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association Developed in Collaboration With the American College of Chest Physicians; American Thoracic Society, Inc.; and the Pulmonary Hypertension Association
J. Am. Coll. Cardiol.,
April 28, 2009;
53(17):
1573 - 1619.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
Writing Committee Members, V. V. McLaughlin, S. L. Archer, D. B. Badesch, R. J. Barst, H. W. Farber, J. R. Lindner, M. A. Mathier, M. D. McGoon, M. H. Park, et al.
ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension: A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association: Developed in Collaboration With the American College of Chest Physicians, American Thoracic Society, Inc., and the Pulmonary Hypertension Association
Circulation,
April 28, 2009;
119(16):
2250 - 2294.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Humbert
Update in Pulmonary Hypertension 2008
Am. J. Respir. Crit. Care Med.,
April 15, 2009;
179(8):
650 - 656.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Lapa, B. Dias, C. Jardim, C. J.C. Fernandes, P. M.M. Dourado, M. Figueiredo, A. Farias, J. Tsutsui, M. Terra-Filho, M. Humbert, et al.
Cardiopulmonary Manifestations of Hepatosplenic Schistosomiasis
Circulation,
March 24, 2009;
119(11):
1518 - 1523.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
R. Souza and C. Jardim
Trends in pulmonary arterial hypertension
Eur. Respir. Rev.,
March 1, 2009;
18(111):
7 - 12.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. Degano, A. Yaici, J. Le Pavec, L. Savale, X. Jais, B. Camara, M. Humbert, G. Simonneau, and O. Sitbon
Long-term effects of bosentan in patients with HIV-associated pulmonary arterial hypertension
Eur. Respir. J.,
January 1, 2009;
33(1):
92 - 98.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Humbert
Update in Pulmonary Arterial Hypertension 2007
Am. J. Respir. Crit. Care Med.,
March 15, 2008;
177(6):
574 - 579.
[Full Text]
[PDF]
|
 |
|
Copyright © 2008 American Thoracic Society
|
|
|