4.7 Article

Contemporary Trends in the Diagnosis and Management of Pulmonary Arterial Hypertension An Initiative to Close the Care Gap

Journal

CHEST
Volume 143, Issue 2, Pages 324-332

Publisher

ELSEVIER
DOI: 10.1378/chest.11-3060

Keywords

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Funding

  1. Actelion Pharmaceuticals US, Inc
  2. Gilead
  3. Novartis AG
  4. United Therapeutics Corporation
  5. Lung LLC
  6. Pfizer, Inc
  7. GlaxoSimithKline plc
  8. Ikaria, Inc
  9. Bayer AG

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Background: The Pulmonary Arterial Hypertension-Quality Enhancement Research Initiative (PAH-QuERI) was created to help clinicians to implement a guidelines-based approach to the diagnosis and management of pulmonary arterial hypertension (PAR). Patients with PAR represent a heterogeneous population, and physician evaluation and treatment paradigms may vary considerably. Methods: Using an electronic data management system, participating physicians recorded data on diagnostic workup, disease management, and outcomes of patients with PAH. Queries were generated automatically following each follow-up visit if the tests recommended by the American College of Chest Physicians (ACCP) were not performed at least once. Results: Of 791 patients enrolled in PAH-QuERI, 77% were women; 64% received a diagnosis >3 months prior to enrollment; 9% were in New York Heart Association functional class I, 39% in II, 48% in III, and 5% in IV; and the median age was 55 years (interquartile range, 45-66 years). At enrollment, all ACCP-recommended tests had been performed in only 6% of patients. The automated program generated 1,530 reminders for 642 patients (81%) with validated enrollment data. The proportion of recommended tests performed was 91% for CBC count, 91% for liver function test, 50% for connective tissue disease screen, 29% for HIV screen, 88% for chest radiograph, 82% for ECG, 97% for two-dimensional echocardiogram, 83% for pulmonary function tests, 41% for oximetry, 57% for ventilation/perfusion scan, 79% for 6-min walk distance, and 90% for right-sided heart catheterization. Regarding management, 78% of patients were on disease-specific therapy, and the use of these therapies tended to increase with the functional disability of the patient. One hundred seventy patients were taking calcium channel blockers, 91 specifically for PAR. Only six of 91 patients (7%) who received calcium channel blockers specifically for PAH had met the current guideline for acute vasoreactivity. Conclusions: When comparing reported clinical practice with ACCP guidelines-recommended strategies, a diagnostic care gap is apparent such that certain essential and recommended diagnostic tests may be underused despite the availability of detailed guidelines and reminders. CHEST 2013; 143(2):324-332

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