Development and Validation of Algorithms to Identify Pulmonary Arterial Hypertension in Administrative Data
Pulmonary arterial hypertension (PAH) is a rare disease, and much of our understanding stems from single-center studies, which are limited by sample size and generalizability. Administrative data offer an appealing opportunity to inform clinical, research, and quality improvement efforts for PAH. Ye...
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Veröffentlicht in: | Chest 2021-05, Vol.159 (5), p.1986-1994 |
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