BackgroundConcomitant pulmonary hypertension and interstitial lung disease in systemic sclerosis (SSc-PH-ILD) represents a distinct subpopulation of SSc with poorer prognosis in Western studies. In Asian patients, characterisation of SSc-PH-ILD is still lacking.ObjectivesTo analyse hospital admissions, survival and prognostic markers among SSc patients with PH, ILD or concomitant PH-ILD in the Scleroderma Cohort Singapore.MethodsIn this study involving 3 tertiary Rheumatology institutions Jan 2008 to , Oct 2016 SSc patients with significant pulmonary involvement were included. ILD was based on high resolution computed tomography and predicted FVC <70%. PH was based on either echocardiographic systolic pulmonary arterial pressure (sPAP) ≥50 mmHg, or right heart catheterization (RHC) findings of mean PAP≥25 mmHg. Hospitalisation rates and survival of SSc patients with PH, ILD or PH-ILD were compared. Risk factors of poor outcomes were identified by multivariate stepwise Cox regression analysis.ResultsAmong 490 patients, 92 had ILD, 50 PH and 43 PH-ILD (table 1). Of 93 patients with PH or PH-ILD, 56 were based on echocardiography and 37 on RHC. The 5 year survival was 79%, 87% and 90% in PH, PH-ILD and ILD subgroup, respectively (figure 1). In multivariable analysis, PH was significantly associated with 2.8-fold increased risk of death. Male gender, malabsorption, digital ulcerations and renal crisis were also significantly associated with mortality (table 2). No significant difference in hospital admissions/year among different subgroups. Increased hospital admissions were associated with renal crisis, right heart failure and use of PH medications.Abstract FRI0453 – Table 1Clinical characteristicsPH (n=50)ILD (n=92)PH-ILD (n=43)No PH/ILD (n=305) Female, n447638270Follow up duration (months±SD)53.46±55.76101.5±80.0488.71±65.5364.66±36.27Age at SSc diagnosis (years±SD)51.08±16.4446.87±12.453.84±15.1746.44±14.59Duration of SSc at entry (years±SD)5.85±6.956.93±7.456.14±7.985.20±8.24Dc-SSc, n134511100PH specific treatments+, n28N/A26N/AImmunosuppressants++, n256427176+Prostacyclin, phosphodiesterase type 5 inhibitors, endothelin receptor antagonist;++Methotrexate, cyclophosphamide, mycophenolate mofetil.Abstract FRI0453 – Table 2Survival analysisHazard Ratio (95% CI)P Value Male gender2.85 (1.53–5.33)0.0010Malabsorption2.89 (1.67–5.01)0.0002Renal crisis2.00 (1.00–3.99)0.0490Digital ulcerations2.06 (1.21–3.50)0.0076Abstract FRI0453 – Figure 1Adjusted survival curve comparing survival of SSc patients with PH, ILD, and concomittant PH-ILD. X-axis shows years of survival from diagnosis of PH or ILD.ConclusionsCompared to those with ILD or PH-ILD, SSc-PH patients had increased mortality, but not hospitalisation rates. This could be due to small sample size or short follow up duration. We identified risk factors associated with worse outcomes in SSc patients with significant pulmonary involvement.Disclosure of InterestNone declared