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Treatment of IBS in Primary Health Care.

Treatment of IBS in Primary Health Care: Adherence to Guidelines

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05144581
Enrollment
3000
Registered
2021-12-03
Start date
2021-11-29
Completion date
2024-05-31
Last updated
2021-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritable Bowel Syndrome

Keywords

Irritable bowel syndrome, Functional gastrointestinal disorders

Brief summary

The purpose of this study is to retrospectively evaluate treatment strategies for IBS used within primary Health care in Örebro Region.

Detailed description

The defining features of IBS comprise the presence of recurrent abdominal pain in association with altered bowel habits (diarrhea, constipation or both), as stated in the Rome IV criteria. The spectrum, duration and severity of symptoms can range from inconvenient to incapacitating, and can prevent individuals from participating in everyday activities. Despite the prevalence of IBS, its management remains a challenge for global healthcare systems. Treatment of IBS comprises, in summary, information to patients, dietary treatment, pharmacological treatment and psychological treatment. Pharmacological treatment includes antidepressants, bulking agents or fiber supplements, rifaximin, linaclotide, eluxadoline, loperamide, antispasmodics, prokinetics and probiotics. Since the majority of patients with irritable bowel syndrome (IBS) are diagnosed and treated in primary care, the aim of this project is to investigate the adherence of general practitioners (GPs) to recommended therapeutic approaches for IBS. In this study, data regarding therapeutic approaches will be collected retrospectively over the period of 2013-2019 by using the electronic patient register in Örebro Region. Patients will be identified by ICD-code K.58. The used treatments will be categorized in grade of recommendation as well as in strength of evidence. The efficacy of the used treatments will be evaluated, if possible. Over the counter agents, and lifestyle adjustments will not be evaluated. The used treatments will be categorized in grade of recommendation (weak and strong) as well as in strength of evidence /very low, low, moderate and high). The eventual use of inappropriate treatments will be recorded as well. The efficacy of the used treatments will be, if possible, evaluated from the patient registers. The standardized and validated questionnaires IBS-Symptom Severity Score and IBS-Quality of Life scores are not routinely used within the primary health care. For this reason, the efficacy of the treatments will be categorized in no effect, moderate effect and good effect. Descriptive statistics will be used.

Interventions

None listed

Sponsors

Region Örebro County
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years

Inclusion criteria

* All adult patients (both sexes) who were diagnosed with IBS according to ICD-10 in Region Örebro County 2013-2017.

Exclusion criteria

* Patients \< 18 years or \> 65 years.

Design outcomes

Primary

MeasureTime frameDescription
Adherence to guidelines of pharmacological treatment of IBS within primary care2013-2017The proportion of patients that have received pharmacological treatment according to guidelines for IBS within primary care.
Adherence to guidelines of non-pharmacological treatment of IBS within primary care2013-2017The proportion of patients that have received non-pharmacological treatment according to guidelines for IBS within primary care.

Secondary

MeasureTime frameDescription
Efficacy of treatment of IBS2013-2017Used treatments of IBS will be categorized in grade of recommendation as well as in strenght of evidence.
Use of inappropriate treatments of IBS2013-2017The prevalence of inappropriate treatment strategies of IBS within primary care will be recorded.

Contacts

Primary ContactJussi Rauma, M.D.
jussi.rauma@regionorebrolan.se+460702484167

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026