KEGG DISEASE: Acute heart failure

KEGG

DISEASE: Acute heart failure

Entry

H01631                      Disease

Name

Acute heart failure

Subgroup

Sudden cardiac failure, infantile (SCFI)
Sudden cardiac failure, alcohol-induced (SCFAI)

Description

Acute heart failure (AHF) can be defined as a heterogeneous syndrome of signs and symptoms of new-onset or gradual/rapidly worsening heart failure (HF), requiring urgent therapy. Intrinsic cardiac abnormalities and comorbid conditions, including lung and renal disease, and sleep-disordered breathing, can contribute to the development of AHF. Factors triggering AHF may include ischemia, hypertension, arrhythmias, noncardiac comorbidities, and administered drugs, etc. Because of the poor clinical outcome and the relevant associated morbidity and mortality, it remains a major public health issue with a substantial socioeconomic burden.

Category

Cardiovascular disease

Brite

Human diseases in ICD-11 classification [BR:br08403]
11 Diseases of the circulatory system
  Heart failure
   BD1Y  Other specified heart failure
    H01631  Acute heart failure

Gene

PPA2 [HSA:27068] [KO:K01507]

Drug

Milrinone lactate [DR:D02085]
Sodium nitroprusside [DR:D00614]

Other DBs

ICD-11:

MeSH:

OMIM:

Reference

Authors

Mentz RJ, O'Connor CM

Title

Pathophysiology and clinical evaluation of acute heart failure.

Journal

Nat Rev Cardiol 13:28-35 (2016)
DOI:10.1038/nrcardio.2015.134

Reference

Authors

Ponikowski P, Jankowska EA

Title

Pathogenesis and clinical presentation of acute heart failure.

Journal

Rev Esp Cardiol (Engl Ed) 68:331-7 (2015)
DOI:10.1016/j.rec.2015.02.001

Reference

Authors

Chowdhury P, Kehl D, Choudhary R, Maisel A

Title

The use of biomarkers in the patient with heart failure.

Journal

Curr Cardiol Rep 15:372 (2013)
DOI:10.1007/s11886-013-0372-4

Reference

PMID:27523597 (SCFI_SCFAI)

Authors

Kennedy H, Haack TB, Hartill V, Matakovic L, Baumgartner ER, Potter H, Mackay R, Alston CL, O'Sullivan S, McFarland R, Connolly G, Gannon C, King R, Mead S, Crozier I, Chan W, Florkowski CM, Sage M, Hofken T, Alhaddad B, Kremer LS, Kopajtich R, Feichtinger RG, Sperl W, Rodenburg RJ, Minet JC, Dobbie A, Strom TM, Meitinger T, George PM, Johnson CA, Taylor RW, Prokisch H, Doudney K, Mayr JA

Title

Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.

Journal

Am J Hum Genet 99:674-682 (2016)
DOI:10.1016/j.ajhg.2016.06.027

Reference

PMID:27523598 (SCFI)

Authors

Guimier A, Gordon CT, Godard F, Ravenscroft G, Oufadem M, Vasnier C, Rambaud C, Nitschke P, Bole-Feysot C, Masson C, Dauger S, Longman C, Laing NG, Kugener B, Bonnet D, Bouvagnet P, Di Filippo S, Probst V, Redon R, Charron P, Rotig A, Lyonnet S, Dautant A, de Pontual L, di Rago JP, Delahodde A, Amiel J

Title

Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy.

Journal

Am J Hum Genet 99:666-673 (2016)
DOI:10.1016/j.ajhg.2016.06.021

LinkDB

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