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A comprehensive framework for navigating patient care in systemic sclerosis: A global response to the need for improving the practice of diagnostic and preventive strategies in SSc.

Authors :
Saketkoo LA
Frech T
Varjú C
Domsic R
Farrell J
Gordon JK
Mihai C
Sandorfi N
Shapiro L
Poole J
Volkmann ER
Lammi M
McAnally K
Alexanderson H
Pettersson H
Hant F
Kuwana M
Shah AA
Smith V
Hsu V
Kowal-Bielecka O
Assassi S
Cutolo M
Kayser C
Shanmugam VK
Vonk MC
Fligelstone K
Baldwin N
Connolly K
Ronnow A
Toth B
Suave M
Farrington S
Bernstein EJ
Crofford LJ
Czirják L
Jensen K
Hinchclif M
Hudson M
Lammi MR
Mansour J
Morgan ND
Mendoza F
Nikpour M
Pauling J
Riemekasten G
Russell AM
Scholand MB
Seigart E
Rodriguez-Reyna TS
Hummers L
Walker U
Steen V
Source :
Best practice & research. Clinical rheumatology [Best Pract Res Clin Rheumatol] 2021 Sep; Vol. 35 (3), pp. 101707. Date of Electronic Publication: 2021 Sep 15.
Publication Year :
2021

Abstract

Systemic sclerosis (SSc), the most lethal of rheumatologic conditions, is the cause of death in >50% of SSc cases, led by pulmonary fibrosis followed by pulmonary hypertension and then scleroderma renal crisis (SRC). Multiple other preventable and treatable SSc-related vascular, cardiac, gastrointestinal, nutritional and musculoskeletal complications can lead to disability and death. Vascular injury with subsequent inflammation transforming to irreversible fibrosis and permanent damage characterizes SSc. Organ involvement is often present early in the disease course of SSc, but requires careful history-taking and vigilance in screening to detect. Inflammation is potentially reversible provided that treatment intensity quells inflammation and other immune mechanisms. In any SSc phenotype, opportunities for early treatment are prone to be under-utilized, especially in slowly progressive phenotypes that, in contrast to severe progressive ILD, indolently accrue irreversible organ damage resulting in later-stage life-limiting complications such as pulmonary hypertension, cardiac involvement, and malnutrition. A single SSc patient visit often requires much more physician and staff time, organization, vigilance, and direct management for multiple organ systems compared to other rheumatic or pulmonary diseases. Efficiency and efficacy of comprehensive SSc care enlists trending of symptoms and bio-data. Financial sustainability of SSc care benefits from understanding insurance reimbursement and health system allocation policies for complex patients. Sharing care between recognised SSc centers and local cardiology/pulmonary/rheumatology/gastroenterology colleagues may prevent complications and poor outcomes, while providing support to local specialists. As scleroderma specialists, we offer a practical framework with tools to facilitate an optimal, comprehensive and sustainable approach to SSc care. Improved health outcomes in SSc relies upon recogntion, management and, to the extent possible, prevention of SSc and treatment-related complications.<br />Competing Interests: Declaration of competing interest None of the authors have conflicts of interest to report that are related to the reported content of this paper.<br /> (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1532-1770
Volume :
35
Issue :
3
Database :
MEDLINE
Journal :
Best practice & research. Clinical rheumatology
Publication Type :
Academic Journal
Accession number :
34538573
Full Text :
https://doi.org/10.1016/j.berh.2021.101707