Pulmonary hypertension natural history: Difference between revisions
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==Natural History== | ==Natural History== | ||
*The National Institutes of Health (NIH) Registry estimated a median survival of 2.8 years for symptomatic patients with idiopathic pulmonary hypertension who do not recieve any treatment, with the cause of death usually being right ventricular failure ([[cor pulmonale]]). | *The National Institutes of Health (NIH) Registry estimated a median survival of 2.8 years for symptomatic patients with idiopathic pulmonary hypertension who do not recieve any treatment, with the cause of death usually being right ventricular failure ([[cor pulmonale]]).<ref name="pmid3605900">{{cite journal| author=Rich S, Dantzker DR, Ayres SM, Bergofsky EH, Brundage BH, Detre KM et al.| title=Primary pulmonary hypertension. A national prospective study. | journal=Ann Intern Med | year= 1987 | volume= 107 | issue= 2 | pages= 216-23 | pmid=3605900 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3605900 }} </ref> The 1, 3,and 5-year survival rates for untreated patients with idiopathic pulmonary hypertension were 68%, 48%, and 34%, respectively. Studies from Japan,India and Mexico have suggested similar results.<ref name="pmid3605900">{{cite journal| author=Rich S, Dantzker DR, Ayres SM, Bergofsky EH, Brundage BH, Detre KM et al.| title=Primary pulmonary hypertension. A national prospective study. | journal=Ann Intern Med | year= 1987 | volume= 107 | issue= 2 | pages= 216-23 | pmid=3605900 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3605900 }} </ref> | ||
*The median survival duration was even lower for patients with pulmonary hypertension that was associated with other diseases like [[portal hypertension]], and [[Scleroderma]] (2-year survival of 40% if untreated). | |||
*The median survival duration was even lower for patients with pulmonary hypertension that was associated with other diseases like [[portal hypertension]], and [[Scleroderma]](2-year survival of 40% if untreated). | |||
*A recent outcome study of those patients who had started treatment with [[bosentan]] (Tracleer®) showed that 86% patients were alive at 3 years. | *A recent outcome study of those patients who had started treatment with [[bosentan]] (Tracleer®) showed that 86% patients were alive at 3 years. | ||
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*It would not be unreasonable to expect median survival to extend past 10 years in the near future. | *It would not be unreasonable to expect median survival to extend past 10 years in the near future. | ||
==Complications== | ==Complications== | ||
* [[Right-sided heart failure]] ([[cor pulmonale]]). | * [[Right-sided heart failure]] ([[cor pulmonale]]). | ||
Revision as of 19:18, 28 August 2014
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Pulmonary hypertension natural history On the Web |
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American Roentgen Ray Society Images of Pulmonary hypertension natural history |
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Risk calculators and risk factors for Pulmonary hypertension natural history |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor(s)-in-Chief: Ralph Matar
Overview
In the NHLBI registry for primary pulmonary hypertension, the mean interval from the onset of symptoms to diagnosis was 2 years, and the most common initial symptoms were dyspnea, fatigue, and syncope. There was an estimated median survival of 2.8 years for symptomatic patients who do not recieve any treatment, with the most common cause of death as cor pulmonale.
Natural History
- The National Institutes of Health (NIH) Registry estimated a median survival of 2.8 years for symptomatic patients with idiopathic pulmonary hypertension who do not recieve any treatment, with the cause of death usually being right ventricular failure (cor pulmonale).[1] The 1, 3,and 5-year survival rates for untreated patients with idiopathic pulmonary hypertension were 68%, 48%, and 34%, respectively. Studies from Japan,India and Mexico have suggested similar results.[1]
- The median survival duration was even lower for patients with pulmonary hypertension that was associated with other diseases like portal hypertension, and Scleroderma (2-year survival of 40% if untreated).
- A recent outcome study of those patients who had started treatment with bosentan (Tracleer®) showed that 86% patients were alive at 3 years.
- With multiple agents now available, combination therapy is increasingly used. Impact of these agents on survival is not known, since many of them have been developed only recently.
- It would not be unreasonable to expect median survival to extend past 10 years in the near future.
Complications
- Right-sided heart failure (cor pulmonale).
- Blood clots.
- Arrhythmia (irregular heart beats).
- Bleeding into the lungs and coughing up blood.
Prognosis
- The long-term prognosis has been known to be poor, however outcomes have changed dramatically over the last two decades. This may be attributed to the use of newer drug therapy, better overall care, and earlier diagnosis (lead time bias).
- Some people with this condition may have heart failure that could lead to death. Assessment of prognosis in patients with pulmonary arterial hypertension (PAH) is important since it influences both medical therapy and referral for transplantation.
- Surprisingly, patients with Eisenmenger syndrome have a more favorable hemodynamic profile and prognosis than adults with idiopathic or primary pulmonary hypertension.[2]
- Indicators of Poor Prognosis:
- Age>45 at presentation.
- Poor exercise capacity.
- Elevated Brain Natriuretic Peptide.
- Pericardial effusion.
- Elevated right atrial size and pressure.
- Significant right ventricular dysfunction or failure.
- Low cardiac index.
- Decreased pulmonary arterial capacitance.
- Underlying Scleroderma or liver disease.
ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death (DO NOT EDIT) [3]
Recommendations for Pulmonary Arterial Hypertension
| Class III |
| "1. Prophylactic antiarrhythmic therapy generally is not indicated for primary prevention of SCD in patients with pulmonary arterial hypertension (PAH) or other pulmonary conditions.(Level of Evidence: C)" |
References
- ↑ 1.0 1.1 Rich S, Dantzker DR, Ayres SM, Bergofsky EH, Brundage BH, Detre KM; et al. (1987). "Primary pulmonary hypertension. A national prospective study". Ann Intern Med. 107 (2): 216–23. PMID 3605900.
- ↑ Hopkins WE,Ochoa LL, Richardson GW, Trulock EP(1996) Comparison of the hemodynamics and survival or patients with severe pulmonary hypertension or Eisenmenger Syndrome.
- ↑ Zipes DP, Camm AJ, Borggrefe M, Buxton AE, Chaitman B, Fromer M; et al. (2006). "ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (writing committee to develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society". Circulation. 114 (10): e385–484. doi:10.1161/CIRCULATIONAHA.106.178233. PMID 16935995.