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Patient ar risk of developing Pulmonary Hypertension are:
__NOTOC__
*Those who havefamily history of the condition.
{{Pulmonary hypertension}}
*Those who have certain diseases or conditions, such as heart and lung diseases, liver disease, HIV infection.
{{CMG}}; '''Assistant Editor(s)-in-Chief:''' [[User:Ralph Matar|Ralph Matar]]; {{Rim}}
*Those who are prone to have recurrent Pulmonary Embolism.
 
*Those who use street drugs (such as cocaine) or certain diet medicines.
==Overview==
*Those who live at high altitudes(hypoxemia).
Pulmonary hypertension (PH) is a multifactorial disease involving genetic and environmental risk factors. Risk factors for pulmonary arterial hypertension include [[BMPR2]] [[mutation]], [[connective tissue disease]], [[HIV infection]], [[portal hypertension]], [[fenfluramine]] use, and [[congenital heart disease]] with a [[shunt]]. [[Left heart]] and [[lung]] diseases are risk factors for PH. Patients with a [[hypercoagulable state]] (such as the presence of [[lupus anticoagulant]], deficiency of [[protein C]], [[protein S]], or [[antithrombin III]], [[inflammation#Chronic inflammation|chronic inflammatory disorders]], [[myeloproliferative syndrome]]s, and [[splenectomy]]) are at an increased risk for chronic [[thromboembolic]] pulmonary hypertension.
 
==Risk Factors==
Risk factors of pulmonary hypertension are divided as follows:<ref name="McLaughlin-2009">{{Cite journal  | last1 = McLaughlin | first1 = VV. | last2 = Archer | first2 = SL. | last3 = Badesch | first3 = DB. | last4 = Barst | first4 = RJ. | last5 = Farber | first5 = HW. | last6 = Lindner | first6 = JR. | last7 = Mathier | first7 = MA. | last8 = McGoon | first8 = MD. | last9 = Park | first9 = MH. | title = 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. | journal = Circulation | volume = 119 | issue = 16 | pages = 2250-94 | month = Apr | year = 2009 | doi = 10.1161/CIRCULATIONAHA.109.192230 | PMID = 19332472 }}</ref>
 
===Pulmonary Arterial Hypertension===
* [[BMPR2]] gene mutation
* [[ALK1]] gene mutation
* [[Connective tissue disease]]
* [[HIV]] infection
* [[Portal hypertension]]
* [[Congenital heart disease]]
* [[Schistosomiasis]]
* Chronic [[hemolytic anemia]]
* [[Drug]]s and [[toxin]]s
 
Shown below is a table summarizing the list of drugs associated with PAH:
 
{| style="cellpadding=0; cellspacing= 0; width: 600px;"
|-
| style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF; width: 25%" align="center" |Definite risk || style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF; width: 25%" align="center" |Possible risk || style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF; width: 25%" align="center" |Likely risk || style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF; width: 25%" align="center" |Unlikely risk
|-
| style="font-size: 100; padding: 0 5px; background: #F5F5F5" align="left" |
* [[Aminorex]]
* [[Fenfluramine]]
* [[Dexfenfluramine]]
* Toxic rapeseed oil
* [[Benfluorex]]
| style="font-size: 100; padding: 0 5px; background: #F5F5F5" align="left" |
* [[Cocaine]]
* [[Phenylpropanolamine]]
* [[St John's wort]]
* [[Chemotherapy]]
* [[Selective serotonin reuptake inhibitor]]s
* [[Pergolide]]
| style="font-size: 100; padding: 0 5px; background: #F5F5F5" align="left" |
* [[Amphetamine]]
* [[L-tryptophan]]
* [[Methamphetamine]]
| style="font-size: 100; padding: 0 5px; background: #F5F5F5" align="left" |
* [[Oral contraceptive]]
* [[Estrogen|Estrogen therapy]]
* [[Smoking]]
|}
 
===Pulmonary hypertension due to Left Heart Disease===
* [[Systolic dysfunction]]
* [[Diastolic dysfunction]]
* Left [[valvular disease]]
 
===Pulmonary Hypertension due to Lung Diseases and/or Hypoxia===
* Alveolar [[hypoventilation]] disorders
* Chronic exposure to high altitude
* [[Chronic obstructive pulmonary disease]]
* Developmental abnormalities
* [[Interstitial lung disease]]
* Pulmonary diseases with mixed restrictive and obstructive pattern
* Sleep related breathing problems
 
===Chronic Thromboembolic Pulmonary Hypertension===
* [[Pulmonary embolism]]
* [[Hypercoagulability]] ([[lupus anticoagulant]], deficiency of [[protein C]], [[protein S]], or [[antithrombin III]], [[inflammation|chronic inflammatory disorder]]s, [[myeloproliferative syndrome]]s, and [[splenectomy]])
 
===PH with Unclear and/or Multifactorial Mechanisms===
* [[Myeloproliferative disease]]
* [[Splenectomy]]
* [[Sarcoidosis]]
* [[Histiocytosis]]
* [[Lymphangioleiomyomatosis]]
* [[Neurofibromatosis]]
* [[Vasculitis]]
* [[Glycogen storage disease]]
* [[Gaucher disease]]
* [[Thyroid]] disorder
* Obstruction by [[tumor]]
* Fibrosing [[mediastinitis]]
* [[Chronic renal failure]] on [[dialysis]]
 
==References==
{{Reflist|2}}
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{{WikiDoc Sources}}
[[Category:Medicine]]
[[Category:Cardiology]]
[[Category:Pulmonology]]
[[Category:Emergency medicine]]
[[Category:Up-To-Date]]

Latest revision as of 17:20, 9 June 2021

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Assistant Editor(s)-in-Chief: Ralph Matar; Rim Halaby, M.D. [2]

Overview

Pulmonary hypertension (PH) is a multifactorial disease involving genetic and environmental risk factors. Risk factors for pulmonary arterial hypertension include BMPR2 mutation, connective tissue disease, HIV infection, portal hypertension, fenfluramine use, and congenital heart disease with a shunt. Left heart and lung diseases are risk factors for PH. Patients with a hypercoagulable state (such as the presence of lupus anticoagulant, deficiency of protein C, protein S, or antithrombin III, chronic inflammatory disorders, myeloproliferative syndromes, and splenectomy) are at an increased risk for chronic thromboembolic pulmonary hypertension.

Risk Factors

Risk factors of pulmonary hypertension are divided as follows:[1]

Pulmonary Arterial Hypertension

Shown below is a table summarizing the list of drugs associated with PAH:

Definite risk Possible risk Likely risk Unlikely risk

Pulmonary hypertension due to Left Heart Disease

Pulmonary Hypertension due to Lung Diseases and/or Hypoxia

Chronic Thromboembolic Pulmonary Hypertension

PH with Unclear and/or Multifactorial Mechanisms

References

  1. McLaughlin, VV.; Archer, SL.; Badesch, DB.; Barst, RJ.; Farber, HW.; Lindner, JR.; Mathier, MA.; McGoon, MD.; Park, MH. (2009). "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. 119 (16): 2250–94. doi:10.1161/CIRCULATIONAHA.109.192230. PMID 19332472. Unknown parameter |month= ignored (help)

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