PMID- 29642071 OWN - NLM STAT- MEDLINE DCOM- 20181221 LR - 20181221 IS - 1423-0356 (Electronic) IS - 0025-7931 (Linking) VI - 96 IP - 2 DP - 2018 TI - Risk Factor Profiles Achieved with Medical Therapy in Prevalent Patients with Pulmonary Arterial and Distal Chronic Thromboembolic Pulmonary Hypertension. PG - 127-137 LID - 10.1159/000488000 [doi] AB - BACKGROUND: The latest pulmonary hypertension (PH) guidelines define therapeutic goals in terms of symptoms, exercise capacity, and haemodynamics for patients with pulmonary arterial hypertension (PAH) and recommend advanced combined medical therapy. For inoperable or post-surgical residual distal chronic thromboembolic PH (CTEPH) medical treatment is similarly advised. OBJECTIVES: We analysed whether risk factor goals are achieved and combination therapy is used in prevalent patients with PAH or distal CTEPH. METHODS: PAH or distal CTEPH patients who were seen at the University Hospital Zurich during the last year were analysed in terms of demography, clinical data, medication, and therapeutic goals. Achievement of therapeutic goals was defined as New York Heart Association (NYHA) class 440 m. RESULTS: A total of 108 PAH patients (age 59 +/- 18 years, 62% female, 64% idiopathic, 36% associated) and 38 distal CTEPH patients (age 69 +/- 14 years, 55% female) were included. They had been diagnosed on average 66 +/- 48 months (+/-SD) previously. The percentage of PAH/CTEPH patients with NYHA 440 m 63/50. Overall, 33/31% fulfilled 3 and 29/35% fulfilled 2 of these goals. Regarding therapy, 43% of PAH patients were on double and 10% on triple combination therapy, whereas 16% of distal CTEPH patients were on double and 3% on triple combination therapy. CONCLUSIONS: In this real-life cohort of prevalent patients with PAH or distal CTEPH, targeted drug therapy resulted in an achievement of >/=2/3 predefined therapeutic goals in 2/3 of patients. Patients with PAH were more likely to receive combination therapy compared to CTEPH patients. CI - (c) 2018 S. Karger AG, Basel. FAU - Bartenstein, Philipp AU - Bartenstein P FAU - Saxer, Stephanie AU - Saxer S FAU - Appenzeller, Paula AU - Appenzeller P FAU - Lichtblau, Mona AU - Lichtblau M FAU - Schwarz, Esther I AU - Schwarz EI FAU - Ulrich, Silvia AU - Ulrich S LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20180411 PL - Switzerland TA - Respiration JT - Respiration; international review of thoracic diseases JID - 0137356 RN - 0 (Antihypertensive Agents) RN - 0 (Peptide Fragments) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) SB - IM MH - Adult MH - Aged MH - Antihypertensive Agents/*therapeutic use MH - Body Mass Index MH - Chronic Disease MH - Female MH - Humans MH - Hypertension, Pulmonary/*drug therapy/etiology/physiopathology MH - Male MH - Middle Aged MH - Natriuretic Peptide, Brain/blood MH - Peptide Fragments/blood MH - Risk Factors MH - Thromboembolism/*complications MH - Treatment Outcome MH - Walk Test OTO - NOTNLM OT - Chronic thromboembolic pulmonary hypertension OT - Combination therapy OT - Pulmonary arterial hypertension OT - Risk stratification OT - Therapeutic goals EDAT- 2018/04/12 06:00 MHDA- 2018/12/24 06:00 CRDT- 2018/04/12 06:00 PHST- 2018/01/10 00:00 [received] PHST- 2018/02/26 00:00 [accepted] PHST- 2018/04/12 06:00 [pubmed] PHST- 2018/12/24 06:00 [medline] PHST- 2018/04/12 06:00 [entrez] AID - 000488000 [pii] AID - 10.1159/000488000 [doi] PST - ppublish SO - Respiration. 2018;96(2):127-137. doi: 10.1159/000488000. Epub 2018 Apr 11.