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Abstract Number: 723

Early Mortality in Australian, Canadian and Spanish Scleroderma Patients: Rationale for Establishing a Multi-National Inception Cohort of Patients with Systemic Sclerosis

YanJie Hao1, Marie Hudson2,3, Patricia Carreira4, Wendy Stevens1,5, Candice Rabusa6, Solene Tatibouet7,8, Loreto Carmona9, Beatriz E Joven10, Susanna Proudman11,12, Murray Baron7,8 and Mandana Nikpour1,13, 1Rheumatology, St. Vincent’s Hospital Melbourne, Melbourne, Australia, 2Rheumatology, Lady David Institute for Medical Research and Jewish General Hospital, Montreal, QC, Canada, 3Division of Rheumatology, McGill University, Montreal, QC, Canada, 4Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain, 5The University of Melbourne Department of Medicine at St. Vincent’s Hospital Melbourne, Melbourne, Australia, 6Rheumatology, The University of Melbourne at St Vincent’s Hospital, Melbourne, Australia, 7Rheumatology, Jewish General Hospital, Montreal, QC, Canada, 8Rheumatology, Lady David Research Institute, Montreal, QC, Canada, 9Instituto de Salud Musculoesqueletica, Madrid, Spain, 10Rheumatology, Hospital Universitario, Madrid, Spain, 11Rheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia, 12Discipline of Medicine, University of Adelaide, Adelaide, Australia, 13Medicine, The University of Melbourne at St. Vincent’s Hospital, Melbourne, Australia

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Morbidity and mortality and systemic sclerosis

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Session Information

Title: Systemic Sclerosis, Fibrosing Syndromes and Raynaud's - Clinical Aspects and Therapeutics: Systemic Sclerosis Measures and Outcomes

Session Type: Abstract Submissions (ACR)

Background/Purpose Studies of ‘prevalent’ cohorts wherein most patients have longstanding disease at recruitment may underestimate mortality in systemic sclerosis (SSc) due to survivor bias. The aim of this study was to quantify mortality in Australian, Canadian and Spanish patients with SSc and to compare patients with prevalent and incident disease.

Methods We quantified mortality as Standardized Mortality Ratio (SMR) and Years of Life Lost (YLL) in each of the cohorts based on Australian Bureau of Statistics, Statistics Canada and Spain National Statistics Institute data for the general population, and percentage survival in the first decade of disease in the whole combined ‘prevalent’ cohort and a subset of patients recruited within 4 years of onset of disease (the combined ‘incident’ cohort). We determined a single primary cause of death (SSc or non-SSc related) and all other SSc organ involvement that contributed to death.

Results In the combined prevalent cohort of 3218 patients (1411 Australian, 1465 Canadian and 342 Spanish), 53% of the primary causes of 440 deaths (157 Australian, 213 Canadian and 70 Spanish) recorded were SSc related; the most common cause of SSc-related death was heart-lung disease (Table 1). Malignancy, atherosclerotic vascular disease and sepsis were the most common non-SSc related causes. SSc organ involvement contributed to 31% of these non-SSc related deaths. In multivariable regression, the predictors of mortality were male sex, older age at disease onset, diffuse subtype and presence of PAH, ILD, myocardial involvement, or renal crisis. The SMR and YLL were higher (Table 2) in Australian and Canadian incident cohorts compared with the respective prevalent cohorts. Survival was lower (Figure 1) in the combined incident cohort than the prevalent cohort.

 

Conclusion Mortality in Canadian, Spanish and Australian SSc patients is substantial. Our results suggest that prevalent cohorts underestimate mortality in SSc by failing to capture early deaths, particularly in diffuse disease. These findings provide a compelling rationale for establishing a large multi-national inception cohort of patients with SSc to more accurately quantify early mortality in this disease.

Table 1 Causes of SSc-related death

 

Organ system

Australian Cohort

01/2007-03/2014

Canadian Cohort

01/2005-03/2014

Spanish Cohort

01/2000-03/2014

Combined cohort

 

 

Principal

Cause

N=87

n(%)

Contribu-ting cause

N=157

n (%)

Principal

Cause

N=94

n (%)

Contribu-ting cause

N=213

n (%)

Principal cause

N=52

n (%)

Contribu-ting cause

N=70

n (%)

Principal cause

N=233

n (%)

Contribu

-ting

cause

N=440

n (%)

Heart and Lung

74(85.0)

44(28.0)

57(60.6)

55(25.8)

35(67.3)

12(17.1)

166(71.2)

111(25.2)

 PAH

41(47.1)

24(15.3)

30(31.9)

22(10.3)

14(26.9)

3(4.3)

85(36.5)

49(11.1)

 ILD

19(21.8)

20(12.7)

17(18.1)

33(15.5)

14(26.9)

9(12.9)

50(21.5)

62(14.1)

 PAH and ILD

14(16.1)

 

10(10.6)

 

7(13.5)

 

31(13.3)

 

Myocardial involvement

2(2.3)

0(0)

8(8.5)

7(3.3)

10(19.2)

8(11.4)

20(8.6)

15(3.4)

Pericardial involvement

0(0)

3(1.9)

4(4.3)

5(2.3)

0(0)

3(4.3)

4(1.7)

11(2.5)

Renal crisis

4(4.6)

1(0.6)

9(9.6)

6(2.7)

2(3.8)

3(4.3)

15(6.4)

10(2.3)

Gut involvement

6(6.9)

14(8.9)

14(14.9)

17(8.0)

4(7.7)

13(18.6)

24(10.3)

44(10.0)

Sepsis due to ischemic digit or decubitus ulcer

2(2.3)

22(14.0)

1(1.1)

6(2.8)

1(1.9)

13(18.6)

4(1.7)

41(9.3)

Table 2 A comparison of mortality in ‘prevalent’ and ‘incident’ cohorts

 

Australian Patients

01/2007-12/2012

Canadian Patients

01/2005-12/2012

Spanish Patients

01/2000-12/2012

 

‘Prevalent’

cohort

n=1252

‘Incident’

cohort

n=339

‘Prevalent’

cohort

n=1132

‘Incident’

cohort

n=405

‘Prevalent’

cohort

n=342

‘Incident’

cohort

n=183

Number

of deaths

110

27

151

53

58

32

SMR(95%CI)

Women

Men

Overall

2.6(2.1-3.1)

 4.2(2.4-5.9)

 2.8(2.4-3.3)

2.4(1.2-3.5)

 9.1(3.7-14.5)

3.4(2.3-4.5)

3.3 (2.7-3.9)

5.9 (3.9-7.9)

3.7 (3.2-4.2)

4.2 (2.9-5.5)

 6.8 (3.1-10.4)

4.7 (3.6-5.7)

4.1(3.0–5.3)

 9.5(3.6–15.4)

4.6(3.7–5.5)

3.3(2.0–4.5)

 8.4(1.7–15.1)

3.8(2.8–4.9)

YLL (years)

Women

Men

11.9

17.2

11.3

25.8

19.8

16.7

21.1

19.7

22.4

24.4

16.4

25.7

 

 

Figure 1 Survival curves in combined cohorts

 


Disclosure:

Y. Hao,
None;

M. Hudson,
None;

P. Carreira,
None;

W. Stevens,
None;

C. Rabusa,
None;

S. Tatibouet,
None;

L. Carmona,
None;

B. E. Joven,
None;

S. Proudman,
None;

M. Baron,
None;

M. Nikpour,
None.

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