Evidence map›Paper›PMID 39110966›Full record

Observational studyJMIR human factors2024

Effects of a Digital Care Pathway for Multiple Sclerosis: Observational Study.

Märt Vesinurm, Anna Maunula, Päivi Olli, Paul Lillrank, Petra Ijäs, Paulus Torkki, Laura Mäkitie, Sini M Laakso

Abstract readObservational Study
In one paragraph

Observational study in JMIR human factors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

8 authors.

Märt VesinurmInstitute of Healthcare Engineering and Management, Department of Industrial Engineering and Management, Aalto University School of Science, Espoo, Finland.ORCID 0000-0001-7351-7834
Anna MaunulaBrain Center, Department of Neurology, Hyvinkää Hospital, Hyvinkää, Finland.ORCID 0000-0003-1499-0554
Päivi OlliBrain Center, Department of Neurology, Helsinki University Hospital, Helsinki, Finland.ORCID 0009-0009-9738-3581
Paul LillrankInstitute of Healthcare Engineering and Management, Department of Industrial Engineering and Management, Aalto University School of Science, Espoo, Finland.ORCID 0000-0001-6438-4363
Petra IjäsBrain Center, Department of Neurology, Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-7292-1971
Paulus TorkkiDepartment of Public Health, Faculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-1127-4205
Laura MäkitieBrain Center, Department of Neurology, Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-4063-6674
Sini M LaaksoBrain Center, Department of Neurology, Helsinki University Hospital, Helsinki, Finland.ORCID 0000-0002-0104-2849

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHelsinki University Hospital has developed a digital care pathway (DCP) for people with multiple sclerosis (MS) to improve the care quality. DCP was designed for especially newly diagnosed patients to support adaptation to a chronic disease.

objectiveThis study investigated the MS DCP user behavior and its impact on patient education-mediated changes in health care use, patient-perceived impact of MS on psychological and physical functional health, and patient satisfaction.

methodsWe collected data from the service launch in March 2020 until the end of 2022 (observation period). The number of users, user logins, and their timing and messages sent were collected. The association of the DCP on health care use was studied in a case-control setting in which patients were allowed to freely select whether they wanted to use the service (DCP group n=63) or not (control group n=112). The number of physical and remote appointments either to a doctor, nurse, or other services were considered in addition to emergency department visits and inpatient days. The follow-up time was 1 year (study period). Furthermore, a subgroup of 36 patients was recruited to fill out surveys on net promoter score (NPS) at 3, 6, and 12 months, and their physical and psychological functional health (Multiple Sclerosis Impact Scale) at 0, 3, 6, and 12 months.

resultsDuring the observation period, a total of 225 patients had the option to use the service, out of whom 79.1% (178/225) logged into the service. On average, a user of the DCP sent 6.8 messages and logged on 7.4 times, with 72.29% (1182/1635) of logins taking place within 1 year of initiating the service. In case-control cohorts, no statistically significant differences between the groups were found for physical doctors' appointments, remote doctors' contacts, physical nurse appointments, remote nurse contacts, emergency department visits, or inpatient days. However, the MS DCP was associated with a 2.05 (SD 0.48) visit increase in other services, within 1 year from diagnosis. In the prospective DCP-cohort, no clinically significant change was observed in the physical functional health between the 0 and 12-month marks, but psychological functional health was improved between 3 and 6 months. Patient satisfaction improved from the NPS index of 21 (favorable) at the 3-month mark to the NPS index of 63 (excellent) at the 12-month mark.

conclusionsThe MS DCP has been used by a majority of the people with MS as a complementary service to regular operations, and we find high satisfaction with the service. Psychological health was enhanced during the use of MS DCP. Our results indicate that DCPs hold great promise for managing chronic conditions such as MS. Future studies should explore the potential of DCPs in different health care settings and patient subgroups.

Indexed as

Multiple SclerosisAdultCase-Control StudiesCritical PathwaysFemaleFinlandHumansMaleMiddle AgedPatient SatisfactionSurveys and QuestionnairesTelemedicinecaregiverchronic conditioncommunicationdigital caredigital care pathwaydigital health servicelong-termmultiple sclerosisoutcomeoutpatient clinicpatient engagementpatient reported outcome measurespatient satisfactionquality of carequality of liferesource usagestrategytelemedicine

Identifiers

PMID39110966
PMCPMC11339567

What OpenQuestion holds

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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 OpenQuestion graph.