PMID- 34622787 OWN - NLM STAT- MEDLINE DCOM- 20211018 LR - 20231107 IS - 2149-2271 (Electronic) IS - 2149-2263 (Print) IS - 2149-2263 (Linking) VI - 25 IP - 10 DP - 2021 Oct TI - Clinical efficacy, safety, tolerability, and survival outcome of long-term inhaled iloprost treatment in the management of pulmonary arterial hypertension: Data from prospective multicenter observational OPTION study. PG - 721-732 LID - 10.5152/AnatolJCardiol.2021.03009 [doi] AB - OBJECTIVE: To evaluate clinical efficacy, safety and tolerability of long-term inhaled iloprost treatment in the daily practice for the management of pulmonary arterial hypertension (PAH). METHODS: A total of 115 patients with PAH on inhaled iloprost treatment were included. New York Heart Association (NYHA) functional class, brain natriuretic peptide (BNP) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels, and 6-minute walk distance (6MWD) were recorded at baseline and at 3rd to 24th month visits. Safety and tolerability of iloprost treatment were also evaluated during follow-up, as were the survival, clinical worsening, and the related risk factors. RESULTS: The treatment was associated with an increase in the percentage NYHA functional class II (from 0.0% at enrolment to 36.2% at 24th month visit) patients but no significant difference was noted in 6MWD values. Clinical worsening was observed in 63.5% patients, while survival rate was 69.6%. NT-proBNP levels were significantly higher in non-survivors than in survivors (p=0.042). Cox regression analysis revealed the association of female sex [odds ratio (OR)=0.318; 95% confidence interval (CI), 0.128-0.792; p=0.014] and scleroderma-related PAH (OR=0.347; 95% CI, 0.140-0.860; p=0.022) with significantly lower risk (3.14 fold and 2.88 fold, respectively) of mortality. CONCLUSION: Our findings indicate favorable efficacy, safety, and tolerability of long-term iloprost treatment in the management of PAH, whereas improved NYHA functional class was not accompanied with a significant change in 6MWD values. Patient age was a risk factor for clinical worsening, while female sex, scleroderma subtype, and lower NT-proBNP levels were associated with significantly lower mortality risk. FAU - Kucukoglu, Mehmet Serdar AU - Kucukoglu MS AD - Department of Cardiology, Istanbul University Cardiology Institute, Istanbul, Turkey. FAU - Hanta, Ismail AU - Hanta I AD - Department of Chest Diseases, Cukurova University Faculty of Medicine, Adana, Turkey. FAU - Akdeniz, Bahri AU - Akdeniz B AD - Department of Cardiology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey. FAU - Gullulu, Sumeyye AU - Gullulu S AD - Department of Cardiology, Uludag University Faculty of Medicine, Bursa, Turkey. FAU - Atahan, Ersan AU - Atahan E AD - Department of Chest Diseases, Istanbul University Cerrahpasa Faculty of Medicine, Istanbul, Turkey. FAU - Sayin, Tamer AU - Sayin T AD - Department of Cardiology, Ankara University Faculty of Medicine, Ankara, Turkey. FAU - Okumus, Gulfer AU - Okumus G AD - Department of Chest Diseases, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey. FAU - Onen, Zeynep Pinar AU - Onen ZP AD - Department of Chest Diseases, Ankara University Faculty of Medicine, Ankara, Turkey. FAU - Yokusoglu, Mehmet AU - Yokusoglu M AD - Department of Cardiology, Gulhane Military Medical Academy, Ankara, Turkey. FAU - Baygul, Arzu AU - Baygul A AD - Department of Biostatistics, Koc University School of Medicine, Istanbul, Turkey. LA - eng PT - Journal Article PT - Multicenter Study PT - Observational Study PL - Turkey TA - Anatol J Cardiol JT - Anatolian journal of cardiology JID - 101652981 RN - JED5K35YGL (Iloprost) SB - IM MH - Female MH - Humans MH - *Hypertension, Pulmonary/drug therapy MH - Iloprost/therapeutic use MH - Prospective Studies MH - *Pulmonary Arterial Hypertension MH - Treatment Outcome PMC - PMC8504660 COIS- Conflict of interest: None declared. EDAT- 2021/10/09 06:00 MHDA- 2021/10/21 06:00 PMCR- 2021/09/16 CRDT- 2021/10/08 08:43 PHST- 2021/10/08 08:43 [entrez] PHST- 2021/10/09 06:00 [pubmed] PHST- 2021/10/21 06:00 [medline] PHST- 2021/09/16 00:00 [pmc-release] AID - ajc-25-10-721 [pii] AID - 10.5152/AnatolJCardiol.2021.03009 [doi] PST - ppublish SO - Anatol J Cardiol. 2021 Oct;25(10):721-732. doi: 10.5152/AnatolJCardiol.2021.03009.