Evidence map›Paper›PMID 42131776›Full record

ArticleCrohn's & colitis 3602026

Evaluation of a pharmacist directed treat to target approach in patients with inflammatory bowel disease receiving upadacitinib or risankizumab.

Justin Han, Archariya Puangampai, Bernice Man, Huda-Marie Kandah, David T Rubin, David K Choi

Abstract read
In one paragraph

Article in Crohn's & colitis 360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Justin HanDepartment of Pharmacy, University of Chicago Medicine, Chicago, IL 60637, United States.ORCID https://orcid.org/0009-0003-9692-635X
Archariya PuangampaiDepartment of Pharmacy, University of Chicago Medicine, Chicago, IL 60637, United States.
Bernice ManDepartment of Pharmacy, University of Chicago Medicine, Chicago, IL 60637, United States.
Huda-Marie KandahDepartment of Pharmacy, University of Chicago Medicine, Chicago, IL 60637, United States.
David T RubinInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, IL 60637, United States.ORCID https://orcid.org/0000-0001-5647-1723
David K ChoiDepartment of Pharmacy, University of Chicago Medicine, Chicago, IL 60637, United States.ORCID https://orcid.org/0000-0002-2453-1784

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: An evolving strategy to enhance quality of life and remission rates in inflammatory bowel disease (IBD) is the treat-to-target approach. This approach offers a structured algorithm for therapeutic interventions, yet its implementation faces challenges, such as administrative burden and limited resources. This study elucidates the pharmacist's role in the treat-to-target approach. Methods: Retrospective chart review was conducted from August 7 to December 15, 2023. Patients ≥ 18 years of age, diagnosed with IBD, initiated on upadacitinib or risankizumab were included. "Treat-to-target" was defined as serial communication and monitoring of symptoms, clinical response, and laboratory values at predefined time points after starting therapy. A pharmacist-led follow-up protocol was conducted by an embedded IBD clinical pharmacist who assessed successful therapy initiation, medication adherence, steroid use, adverse effects, clinical disease activity, need for clinic visits, and lab monitoring at 2, 4, 8, 12 weeks, 6 months, and 12 months after therapy initiation. Results: It was found that 227 patients initiated upadacitinib, and 210 initiated risankizumab. The overall success rate in reaching patients for through the pharmacist-directed follow-up protocol was 84%. The IBD Pharmacist made 3512 interventions, the most common being therapy continuation and lab monitoring recommendations. Therapy discontinuations were observed, particularly between 12 weeks and 6 months post-initiation. Conclusions: We demonstrate a high participation rate to a pharmacist-led follow-up and monitoring protocol for patients receiving upadacitinib and risankizumab therapy. These findings underscore the importance of pharmacist-led interventions in ensuring continuity of care and tracking patient progress with IBD therapies, which are key elements of a successful treat-to-target strategy.

Indexed as

biologicsCrohn’s diseaseinflammatory bowel diseaselab monitoringpharmacistprior authorizationrisankizumabspecialty pharmacytherapeutic drug monitoringtreat-to-targetulcerative colitisupadacitinib

Identifiers

PMID42131776
PMCPMC13166866

What Socratic holds

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LicenceCC BY-NC
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.