Pulmonary hypertension resident survival guide: Difference between revisions

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==Definition==
==Definition==
Pulmonary hypertension (PH) is defined by mean pulmonary artery pressure > 25 mm Hg at rest.
Pulmonary hypertension (PH) is defined by mean pulmonary artery pressure > 25 mm Hg at rest.<ref name="Kiely-2013">{{Cite journal  | last1 = Kiely | first1 = DG. | last2 = Elliot | first2 = CA. | last3 = Sabroe | first3 = I. | last4 = Condliffe | first4 = R. | title = Pulmonary hypertension: diagnosis and management. | journal = BMJ | volume = 346 | issue =  | pages = f2028 | month =  | year = 2013 | doi =  | PMID = 23592451 }}</ref>
 


==Causes==
==Causes==
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The following guideline is based on Expert consensus document on pulmonary hypertension published by ACCF/AHA in 2009.<ref name="pmid19332472">{{cite journal| author=McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR et al.| 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 | year= 2009 | volume= 119 | issue= 16 | pages= 2250-94 | pmid=19332472 | doi=10.1161/CIRCULATIONAHA.109.192230| pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19332472  }} </ref>


==Do's==
==Do's==


==Don'ts==
==Don'ts==
<ref name="pmid19332472">{{cite journal| author=McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR et al.| 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 | year= 2009 | volume= 119 | issue= 16 | pages= 2250-94 | pmid=19332472 | doi=10.1161/CIRCULATIONAHA.109.192230 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19332472  }} </ref>
 


==References==
==References==

Revision as of 18:05, 7 January 2014

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Abdurahman Khalil, M.D. [2]

Definition

Pulmonary hypertension (PH) is defined by mean pulmonary artery pressure > 25 mm Hg at rest.[1]


Causes

Life threatening causes

Life threatening conditions which may cause death or permanent disability within 24 hours if left untreated.

  • Pulmonary veno-occlusive disease (PE)

Common causes

Management

 
 
 
 
Characterize the symptoms:
❑ Progressive dyspnea
❑ Exertional dizziness and syncope
❑ Edema of the extremities
Anginal pain
❑ Palpitations
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:
❑ Loud P2 (Pulmonary second heart sound)
Systolic murmur from Tricuspid regurgitation
❑ Raised JVP (Jugular venous pressure)
Peripheral edema
Ascites
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Consider alternative diagnosis:
Left sided heart failure
Coronary artery disease
❑ Liver disease
Budd-chiari syndrome
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Anticoagulation ±
Diuretics ±
❑ Oxygen ±
Digoxin
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Acute vasoreactivity testing
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Positive
 
 
 
 
 
Negative
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Oral Calcium channel blocker (CCB)
 
 
Lower risk
 
 
 
Higher risk
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Sustained response
 
 
Endothelin receptor antagonsists (ERA's) or
Phospodiesterase-5 inhibitors (PDE-5 Is) ((Oral)
Epoprostenol or Treprostinil (IV)
Illoprost (inhaled)
❑ Treprostinil (SC)
 
 
 
❑ Epoprostenol or Treprostinil (IV)
❑ Illoprost (inhaled)
❑ ERAs or PDE-5 Is ((Oral)
❑ Treprostinil (SC)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Continue CCB
 
 
Reassess consider combo-therapy
 
 
 
 
Atrial septostomy
Lung transplant
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Investigational protocols
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

The following guideline is based on Expert consensus document on pulmonary hypertension published by ACCF/AHA in 2009.[2]

Do's

Don'ts

References

  1. Kiely, DG.; Elliot, CA.; Sabroe, I.; Condliffe, R. (2013). "Pulmonary hypertension: diagnosis and management". BMJ. 346: f2028. PMID 23592451.
  2. McLaughlin VV, Archer SL, Badesch DB, Barst RJ, Farber HW, Lindner JR; et al. (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.