Sökning: "pulmonell hypertension"
Visar resultat 1 - 5 av 9 uppsatser innehållade orden pulmonell hypertension.
1. Physiology-Guided Machine Learning for Improved Reliability of Non-Invasive Assessment of Pulmonary Hypertension
Master-uppsats, Linköpings universitet/Avdelningen för medicinsk teknikSammanfattning : Diagnosing pulmonary hypertension (PH) with right heart catheterization (RHC) is associated with a risk for complications and high expenses, leading to late diagnoses [1]. Transthoracic echocardiography can be used to assess non-invasive indicators for PH such as right ventricular systolic pressure (RVSP), which can be estimated by combining the peak tricuspid regurgitation velocity (TRV) with the estimated right arterial pressure (RAP). LÄS MER
2. Comparison of direct Fick's principle and thermodilution for calculating cardiac output in patients with pulmonary arterial hypertension.Does the assessment of cardiac index and pulmonary vascular resistance differ depending on which method is chosen?
Master-uppsats, Örebro universitet/Institutionen för hälsovetenskaperSammanfattning : Pulmonary arterial hypertension (PAH) is an uncommon but serious disease that causes increased pressure in the pulmonary vessels and increased pulmonary vascular resistance (PVR), which in turn leads to right heart failure. At diagnosis, mean pulmonary artery pressure (mPAP) must be >20 mmHg, pulmonary artery wedge pressure (PAWP) ≤15 mmHg and PVR >2 Wood units (WU). LÄS MER
3. RIGHT VENTRICULAR STROKE WORK INDEX MED EKOKARDIOGRAFI HOS PATIENTER MED PULMONELL ARTERIELL HYPERTENSION, EN JÄMFÖRELSE MED HÖGERSIDIG HJÄRTKATETERISERING.
Kandidat-uppsats, Malmö universitet/Fakulteten för hälsa och samhälle (HS)Sammanfattning : Pulmonell hypertension (PH) är en sjukdom med flera olika etiologier som bidrar till ett förhöjt tryck i lungkretsloppet. PH definieras som ett medelartärtryck i lungpulsådern 25mm Hg i vila uppmätt vid högersidig hjärtkateterisering (RHC). De olika orsakerna till PH delas in i fem grupper. LÄS MER
4. Samband mellan gångsträcka, dyspné och desaturation i 6 minuters gångtest hos en grupp individer med pulmonell arteriell hypertension (PAH) - en registerbaserad pilotstudie.
Magister-uppsats, Uppsala universitet/Åsenlöf: FysioterapiSammanfattning : Background: Pulmonary arterial hypertension (PAH) is a rare but serious disease with symptoms as dyspnea, fatigue and intolerance to exercise. The treatment is mainly pharmacological with physical exercise as an important complement. The 6 minutes walking test (6MWT) is used today worldwide for assessment and follow-up of the PAH patient. LÄS MER
5. Läkemedelsbehandling vid CTEPH : Behandling med bosentan och sildenafil vid pulmonell hypertension vid kronisk lungemboli
Kandidat-uppsats, Umeå universitet/FarmakologiSammanfattning : .... LÄS MER