ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 145

Cause-Specific Mortality in a Large Population-Based Cohort of Rheumatoid Arthritis Patients in Italy

Francesca Ometto1, UGO FEDELI2, ELENA SCHIEVANO2, Costantino Botsios3, MARIA CHIARA CORTI2 and Leonardo Punzi4, 1Rheumatology Unit, Department of Medicine - DIMED, University of Padova, PADOVA, Italy, 2Epidemiological Department, Veneto Region, VENETO, Italy, 3Rheumatology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy, 4Rheumatology Unit, Department of Medicine DIMED, University of Padova, Padova, Italy

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Cardiovascular disease, Epidemiologic methods, morbidity and mortality, respiratory disease and rheumatoid arthritis (RA)

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 5, 2017

Title: Epidemiology and Public Health Poster I: Rheumatoid Arthritis

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Studies on mortality in RA from Italy are completely lacking. The aim of our study was to investigate cause-specific mortality in RA subjects living in the Veneto Region (Italy).

Methods: We identified in the electronic archive of the Veneto Region patients aged 20Ð89 years who were exempt from copayment for RA in January 2010, and linked them with the archive of causes of deaths of the period 2010-2015. Causes of death were coded according to the International Classification of Diseases, 10th Edition. The selection of the underlying cause of death (UCOD) was performed by means of the Automated Classification of Medical Entities (US National Center for Health Statistics). Each subject was followed from 1st January 2010 either until death, or 90 years of age, or 31st December 2015, whichever came first. Standardized Mortality Ratios (SMRs) with 95% confidence intervals were computed as the ratios between deaths observed in the cohort, and those expected according to age- and gender-specific regional mortality rates.

Results: Overall 16,098 residents diagnosed with RA and aged 20-89 years were enrolled in the cohort (Figure 1). The overall follow-up amounted to 88,599 person-years, with 2,142 registered decedents. The most common causes of death were circulatory diseases (36.6%), neoplasms (24.2%), and respiratory diseases (8.3%). Overall SMR in RA subjects was 1.42 (1.36-1.48). Mortality was significantly increased from circulatory (SMR=1.56, 1.45-1.67), respiratory (SMR=1.83, 1.57-2.12), digestive (SMR=1.93, 1.60-2.32), infectious (SMR=2.34, 1.88-2.89), and hematological diseases (SMR=3.22, 2.04-4.83), and falls (SMR=1.95, 1.19-3.01) (Table I). Particularly SMR for circulatory diseases was higher in patients aged <65 years: SMR 1.86 (1.06-3.02) in males, and 2.07 (1.23-3.28) in females. RA was selected as the UOCD in 6.1% of all deaths in the cohort and was mentioned in 25.4% of death certificates. Diseases often reported in the certificate without being selected as the UCOD where sepsis, pneumonia, diabetes mellitus, and hypertensive diseases (Table II).

Conclusion : In the Veneto Region, a 42% excess risk of death was observed among subjects with RA compared to the general population. Adverse effects of therapy and comorbidities should be identified and adequately monitored in RA subjects.

../Screen%20Shot%202017-06-14%20at%2011.54.21.png

Table 1. Number of deaths and standardized mortality ratio (SMR) with 95% Confidence Interval (CI).

n. deaths

SMR (CI)

Certain infectious and parasitic diseases (A00-B99)

88

2.34 (1.88-2.89)

Septicemia (A40ÐA41)

66

3.07 (2.37-3.90)

Neoplasms (C00-D48)

519

0.98 (0.90-1.07)

Malignant neoplasm of stomach (C16)

25

1.04 (0.67-1.54)

Malignant neoplasms of colon, rectum and anus (C18-C21)

51

0.96 (0.71-1.26)

Malignant neoplasm of pancreas (C25)

45

1.04 (0.76-1.39)

Malignant neoplasms of trachea, bronchus and lung (C33-C34)

102

1.10 (0.89-1.33)

Malignant neoplasm of breast (C50)

44

0.87 (0.63-1.16)

Non-HodgkinÕs lymphoma (C82-C85)

21

1.36 (0.84-2.08)

Leukemia (C91-C95)

22

1.31 (0.82-1.99)

Diseases of the blood and blood-forming organs (D50-D89)

23

3.22 (2.04-4.83)

Endocrine, nutritional and metabolic diseases (E00-E90)

57

0.96 (0.73-1.25)

Diabetes mellitus (E10-E14)

43

0.93 (0.67-1.26)

Mental and behavioural disorders (F00-F99)

50

0.90 (0.67-1.18)

Dementia (F00-F03)

44

0.86 (0.62-1.15)

Diseases of the nervous system (G00-G99)

61

0.89 (0.68-1.14)

AlzheimerÕs disease (G30)

27

0.90 (0.59-1.31)

Diseases of the circulatory system (I00-I99)

783

1.56 (1.45-1.67)

Hypertensive diseases (I10-I15)

101

1.51 (1.23-1.83)

Ischemic heart diseases (I20-I25)

247

1.51 (1.33-1.71)

Other heart diseases (I00-I09, I26-I51)

201

1.64 (1.42-1.88)

Cerebrovascular diseases (I60-I69)

182

1.43 (1.23-1.65)

Diseases of the respiratory system (J00-J99)

177

1.83 (1.57-2.12)

Pneumonia (J12-J18)

61

2.22 (1.70-2.86)

Chronic lower respiratory diseases  (J40ÐJ47)

54

1.47 (1.10-1.92)

Interstitial pulmonary diseases (J84)

20

3.47 (2.12-5.36)

Diseases of the digestive system (K00-K93)

117

1.93 (1.60-2.32)

Vascular disorders of intestine (K55)

21

2.40 (1.48-3.66)

Diseases of liver (K70-K76)

20

0.95 (0.58-1.47)

Diseases of the musculoskeletal system (M00-M99)

149

17.3 (14.7-20.4)

Rheumatoid arthritis (M05-M06)

130

63.3 (52.9-75.2)

Diseases of the genitourinary system (N00-N95)

27

1.29 (0.85-1.88)

External causes of mortality (V01-Y84)

70

1.65 (1.28-2.08)

Falls (W00-W19)

20

1.95 (1.19-3.01)

All causes

2142

1.42 (1.36-1.48)

 

Table 2. Number of deaths and standardized mortality ratio (SMR) with 95% Confidence Interval (CI), by gender and age class.

 

Males

Females

 

n

SMR (CI)

n

SMR (CI)

All causes

 

 

 

 

20-64 yrs

62

1.50 (1.15-1.93)

106

1.54 (1.26-1.86)

65-74 yrs

141

1.30 (1.10-1.54)

235

1.41 (1.23-1.60)

75-89 yrs

452

1.32 (1.20-1.45)

1146

1.47 (1.39-1.56)

Neoplasms (C00-D48)

 

 

 

 

20-64 yrs

21

1.03 (0.64-1.58)

52

1.17 (0.87-1.53)

65-74 yrs

50

0.91 (0.67-1.20)

79

0.87 (0.69-1.09)

75-89 yrs

117

1.03 (0.85-1.23)

200

0.98 (0.85-1.12)

Circulatory system (I00-I99)

 

 

 

 

20-64 yrs

16

1.86 (1.06-3.02)

18

2.07 (1.23-3.28)

65-74 yrs

43

1.62 (1.17-2.18)

62

1.80 (1.38-2.30)

75-89 yrs

179

1.48 (1.27-1.71)

465

1.53 (1.40-1.68)

Respiratory system (J00-J99)

 

 

 

 

20-64 yrs

3

2.94 (0.59-8.59)

4

2.62 (0.71-6.71)

65-74 yrs

6

1.31 (0.48-2.85)

14

2.23 (1.22-3.74)

75-89 yrs

54

1.76 (1.33-2.30)

96

1.82 (1.47-2.30)

 


Disclosure: F. Ometto, None; U. FEDELI, None; E. SCHIEVANO, None; C. Botsios, None; M. C. CORTI, None; L. Punzi, None.

To cite this abstract in AMA style:

Ometto F, FEDELI U, SCHIEVANO E, Botsios C, CORTI MC, Punzi L. Cause-Specific Mortality in a Large Population-Based Cohort of Rheumatoid Arthritis Patients in Italy [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/cause-specific-mortality-in-a-large-population-based-cohort-of-rheumatoid-arthritis-patients-in-italy/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/cause-specific-mortality-in-a-large-population-based-cohort-of-rheumatoid-arthritis-patients-in-italy/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology