Literature DB >> 34127030

Survival of patients with rare diseases: a population-based study in Tuscany (Italy).

Francesca Gorini1, Alessio Coi2, Lorena Mezzasalma2, Silvia Baldacci2, Anna Pierini2,3, Michele Santoro2.   

Abstract

BACKGROUND: Rare diseases (RDs) encompass a heterogeneous group of life-threatening or chronically debilitating conditions that individually affect a small number of subjects but overall represent a major public health issue globally. There are still limited data on RD burden due to the paucity of large population-based epidemiological studies. The aim of this research was to provide survival estimates of patients with a RD residing in Tuscany, Italy.
METHODS: Cases collected in the Rare Diseases Registry of Tuscany with diagnosis between 1st January 2000 and 31th December 2018 were linked to the regional health databases in order to retrieve information on mortality of all subjects. Survival at 1, 5 and 10 years from diagnosis with 95% confidence intervals (CI) was estimated by sex, age class, nosological group and subgroup using the Kaplan-Meier method. The effect of sex, age and period of diagnosis (years 2000-2009 or 2010-2018) on survival was estimated using Cox proportional hazards regression.
RESULTS: Survival at 1, 5 and 10 years from diagnosis was 97.3%, 88.8% and 80.8%, respectively. Respiratory diseases and peripheral and central nervous system disorders were characterized by the lowest survival at 5 and 10 years. Despite a modest higher prevalence of RDs among females (54.0% of the total), male cases had a significant increased risk of death (hazard ratio, HR 1.48, 95% CI 1.38-1.58). Cases diagnosed during 2010-2018 period had a risk of death significantly lower than those diagnosed during 2000-2009 (HR 0.81, 95% CI 0.82-0.96), especially for immune system disorders (HR 0.48, 95% CI 0.26-0.87), circulatory system diseases (HR 0.61, 95% CI 0.45-0.84) and diseases of the musculoskeletal system and connective tissue (HR 0.64, 95% CI 0.49-0.84).
CONCLUSIONS: An earlier diagnosis as well as the improvement in the efficacy of treatment resulted in a decreased risk of death over the years for specific RDs. The linkage between a population-based registry and other regional databases exploited in this study provides a large and accurate mass of data capable of estimating patients' life-expectancy and increasing knowledge on the collective burden of RDs.

Entities:  

Keywords:  Disease registry; Mortality risk; Rare disease; Survival

Year:  2021        PMID: 34127030     DOI: 10.1186/s13023-021-01907-0

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  18 in total

Review 1.  Why rare diseases are an important medical and social issue.

Authors:  Arrigo Schieppati; Jan-Inge Henter; Erica Daina; Anita Aperia
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Authors:  Carlos R Ferreira
Journal:  Am J Med Genet A       Date:  2019-03-18       Impact factor: 2.802

3.  How many rare diseases are there?

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Journal:  Nat Rev Drug Discov       Date:  2020-02       Impact factor: 84.694

Review 4.  Rare Diseases: Joining Mainstream Research and Treatment Based on Reliable Epidemiological Data.

Authors:  Stephen C Groft; Manuel Posada de la Paz
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

Review 5.  Rare Disease Terminology and Definitions-A Systematic Global Review: Report of the ISPOR Rare Disease Special Interest Group.

Authors:  Trevor Richter; Sandra Nestler-Parr; Robert Babela; Zeba M Khan; Theresa Tesoro; Elizabeth Molsen; Dyfrig A Hughes
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Review 6.  Epidemiology of amyotrophic lateral sclerosis: an update of recent literature.

Authors:  Elisa Longinetti; Fang Fang
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7.  A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region's rare diseases registry.

Authors:  Monica Mazzucato; Laura Visonà Dalla Pozza; Silvia Manea; Cinzia Minichiello; Paola Facchin
Journal:  Orphanet J Rare Dis       Date:  2014-03-19       Impact factor: 4.123

8.  Public Health and Rare Diseases: Oxymoron No More.

Authors:  Rodolfo Valdez; Lijing Ouyang; Julie Bolen
Journal:  Prev Chronic Dis       Date:  2016-01-14       Impact factor: 2.830

9.  The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort.

Authors:  Caroline E Walker; Trinity Mahede; Geoff Davis; Laura J Miller; Jennifer Girschik; Kate Brameld; Wenxing Sun; Ana Rath; Ségolène Aymé; Stephen R Zubrick; Gareth S Baynam; Caron Molster; Hugh J S Dawkins; Tarun S Weeramanthri
Journal:  Genet Med       Date:  2016-09-22       Impact factor: 8.822

10.  Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database.

Authors:  Stéphanie Nguengang Wakap; Deborah M Lambert; Annie Olry; Charlotte Rodwell; Charlotte Gueydan; Valérie Lanneau; Daniel Murphy; Yann Le Cam; Ana Rath
Journal:  Eur J Hum Genet       Date:  2019-09-16       Impact factor: 4.246

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  4 in total

1.  Healthcare Burden of Rare Diseases: A Population-Based Study in Tuscany (Italy).

Authors:  Silvia Baldacci; Michele Santoro; Anna Pierini; Lorena Mezzasalma; Francesca Gorini; Alessio Coi
Journal:  Int J Environ Res Public Health       Date:  2022-06-21       Impact factor: 4.614

2.  Criteria to define rare diseases and orphan drugs: a systematic review protocol.

Authors:  Ghada Mohammed Abozaid; Katie Kerr; Amy McKnight; Hussain A Al-Omar
Journal:  BMJ Open       Date:  2022-07-29       Impact factor: 3.006

3.  Real-world use of orphan medicinal products (OMPs) in rare disease (RD) patients: A population-based registry study.

Authors:  Monica Mazzucato; Cinzia Minichiello; Andrea Vianello; Laura Visonà Dalla Pozza; Ema Toto; Paola Facchin
Journal:  Front Pharmacol       Date:  2022-09-30       Impact factor: 5.988

4.  Characteristics and factors associated with mortality due to rare diseases in Chile, 2002-2017

Authors:  Jahir Andrés Ávila; Julio César Martínez
Journal:  Biomedica       Date:  2022-09-02       Impact factor: 1.173

  4 in total

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