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Pulmonary hypertension (PH or PHTN) is a condition of increased blood pressure in the arteries of the lungs. [7] Symptoms include shortness of breath, fainting, tiredness, chest pain, swelling of the legs, and a fast heartbeat. [7] [1] The condition may make it difficult to exercise. [7] Onset is typically gradual. [8]
A pulmonary artery wedge pressure being less than 15 mmHg (also measured by right heart catheterization) excludes post-capillary bed (in the veins distal to the capillary bed) pulmonary hypertension. Pulmonary arterial hypertension is a subgroup of pulmonary hypertension and is categorized as World Health Organization as group 1. [3]
A review of the program was enacted in 2009. USMLE claimed it was done with the intention of orienting the examination to support the licensing decisions made by medical boards, transitioning the exam to a competencies schema and emphasizing the importance of scientific foundations of medicine throughout the examination sequence.
The Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) is a disease specific patient-reported outcome measure which assesses quality of life of patients with pulmonary hypertension (PH). [1] It was the first pulmonary hypertension specific questionnaire for assessing patient reported symptoms, quality of life and functioning. [2]
Physical exam findings often found in patients with respiratory failure include findings indicative of impaired oxygenation (low blood oxygen level). These include, but are not limited to, the following: Accessory muscle use in breathing or other signs of respiratory distress [6] Altered mental status (eg. confusion, lethargy) [6]
Rapid Review, Laboratory Testing in Clinical Medicine He has been teaching USMLE preparation since 1991. One of the reasons Goljan is particularly renowned among medical student circles is the bootleg Goljan pathology lectures (audio recordings and printed materials) commonly passed down from upperclassmen or downloaded from the Internet.
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