Evidence map›Paper›PMID 41032167›Full record

ArticleClinical rheumatology2025

Prevalence, clinical characteristics, and hospital course of systemic sclerosis-associated pseudo-obstruction.

Laura Ross, Lyman Lin, Dylan Hansen, Alannah Quinlivan, Wendy Stevens, Susanna Proudman, Jennifer Walker, Joanne Sahhar, Gene-Siew Ngian, Lauren Host and 2 more

Abstract read
In one paragraph

Article in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Laura RossDepartment of Medicine, University of Melbourne at St Vincent's Hospital, Fitzroy, Australia. laura.ross@unimelb.edu.au.ORCID http://orcid.org/0000-0003-4636-729X
Lyman LinDepartment of Gastroenterology, St Vincent's Hospital Melbourne, Fitzroy, Australia.
Dylan HansenDepartment of Rheumatology, St Vincent's Hospital Melbourne, 41 Victoria Pde Fitzroy VIC, Fitzroy, 3065, Australia.
Alannah QuinlivanDepartment of Medicine, University of Melbourne at St Vincent's Hospital, Fitzroy, Australia.
Wendy StevensDepartment of Medicine, University of Melbourne at St Vincent's Hospital, Fitzroy, Australia.
Susanna ProudmanRheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia.
Jennifer WalkerDepartment of Rheumatology, Flinders Medical Centre, Bedford Park, Australia.
Joanne SahharDepartment of Rheumatology, Monash Health, Clayton, Australia.
Gene-Siew NgianDepartment of Rheumatology, Monash Health, Clayton, Australia.
Lauren HostDepartment of Rheumatology, Fiona Stanley Hospital, Murdoch, Australia.
Mandana NikpourSchool of Public Health, University of Sydney, Sydney, Australia.
Chamara BasnayakeDepartment of Medicine, University of Melbourne at St Vincent's Hospital, Fitzroy, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGastrointestinal involvement is almost universal in patients with systemic sclerosis (SSc). Enteric dysmotility, at its most severe, can present with pseudo-obstruction. In this study, we aimed to quantify the prevalence of SSc pseudo-obstruction and evaluate risk factors for its development. In a subgroup of patients requiring admission to hospital for acute episodes of pseudo-obstruction, we evaluated the clinical course and treatments administered.

methodsUsing data from 1969 Australian Scleroderma Cohort Study (ASCS) participants, we performed multivariable logistic regression analysis to identify SSc-specific risk factors for pseudo-obstruction. Descriptive statistics were used to examine the clinical course of patients admitted with pseudo-obstruction at a single ASCS centre.

resultsPseudo-obstruction occurred uncommonly, affecting 70 (3.56%) ASCS participants. Records of 14 participants with a total of 39 admissions for acute pseudo-obstruction were identified. Pseudo-obstruction was associated with longer disease duration (OR 1.03, p = 0.03), bowel dysmotility (OR 4.51, p < 0.01), small intestinal bacterial overgrowth (OR 2.81, 95% CI (1.00-1.05), p < 0.01), and gastric antral vascular ectasia (OR 2.52, 95% CI 1.28-4.94, p < 0.01). Severe diarrhoea, as measured by the UCLA Gastrointestinal 2.0 questionnaire, was the only clinical symptom significantly associated with episodes of pseudo-obstruction (OR 3.39, 95% CI 1.56-7.38, p < 0.01). Opioids were more commonly prescribed in patients with pseudo-obstruction but were not significantly associated with pseudo-obstruction in multivariable analysis (OR 1.24, 95% CI 0.62-2.48, p = 0.54). Patients with a history of pseudo-obstruction were more likely to require enteral (4.29% vs. 0.21%, p < 0.01) or parenteral nutrition (7.14% vs. 0.16%, p < 0.01).

conclusionPseudo-obstruction is associated with other severe gastrointestinal manifestations and is associated with malnutrition in SSc patients. Future studies are required to assess the impact of treatment of SSc-associated enteric dysmotility to prevent progression to pseudo-obstruction. Key Points • Pseudo-obstruction is an uncommon manifestation of systemic sclerosis but frequently recurs and is associated with increased mortality. • Severe diarrhoea and long disease duration are associated with an increased risk of pseudo-obstruction. • Pseudo-obstruction occurs more commonly in patients with severe enteric dysmotility and gastric antral vascular ectasia (GAVE).

Indexed as

Intestinal Pseudo-ObstructionScleroderma, SystemicAdultAgedAustraliaFemaleHospitalizationHumansLogistic ModelsMaleMiddle AgedPrevalenceRisk FactorsEnteric dysmotilityGastrointestinalPseudo-obstructionSystemic sclerosis

Identifiers

PMID41032167
PMCPMC12568857

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.