Pulmonal hypertensjon (PH)
Sist revidert:
Sist revidert av:Ingard Løge
Definisjon:
Definert ved økt gjennomsnittlig hviletrykk i arteria pulmonalis (MAP) ≥ 20 mmHg i hvile. Kan være idiopatisk, eller som komplikasjon til en rekke ulike sykdommer som hjertesvikt, kroniske lungesykdommer, tromboemboli eller bindevevssykdommer
Forekomst:
Hyppigst sekundært til hjertesvikt eller kronisk lungesykdom. Idiopatisk form er sjelden: 1-2 nye tilfeller per million
Symptomer:
Symptomer er tung pust, slitenhet, synkope. Ev. symptomer på underliggende sykdom
Funn:
Ev. cyanose. EKG-forandringer forenlig med høyresidig belastning. Eventuelt ødemer, hepatomegali og halsvenestuvning ved høyresidig hjertesvikt.
Diagnostikk:
Diagnosen stilles ved ekkokardiografi og påfølgende hjertekateterisering med trykkmåling
Behandling:
Spesialistbehandling. Behandling av underliggende sykdom. Vasodilaterende behandling spesielt ved idiopatisk form. Ev. lungetransplantasjon
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- Ingard Løge, spesialist allmennmedisin, redaktør Norsk Elektronisk Legehåndbok