Evidence map›Paper›PMID 35427184›Full record

ArticleJCO clinical cancer informatics2022

Feasibility and Prediction of Adverse Events in a Postoperative Monitoring Program of Patient-Reported Outcomes and a Wearable Device Among Gynecologic Oncology Patients.

Emma L Barber, Ravi Garg, Anna Strohl, Dario Roque, Edward Tanner

Open access · greenAbstract read
In one paragraph

Article in JCO clinical cancer informatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 15% of its field
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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 3 institutions in 1 country.

Emma L BarberDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Northwestern University, Chicago, IL.ORCID 0000-0002-8111-0767
Ravi GargSurgical Outcomes and Quality Improvement Center, Institute for Public Health in Medicine, Chicago, IL.
Anna StrohlDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, University Hospitals, Cleveland, OH.
Dario RoqueDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Northwestern University, Chicago, IL.ORCID 0000-0003-0991-2623
Edward TannerDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, Northwestern University, Chicago, IL.ORCID 0000-0003-0829-1642
Northwestern University · USAnesthesia Quality Institute · USUniversity Hospitals of Cleveland · US

Funding

Research Career Development in Obstetrics and GynecologyK12HD050121 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Serdar E. Bulun · 2005 to 2026
$7.2M
The Claude D. Pepper Older Americans Independence Center (OAIC) at Northwestern UniversityP30AG059988 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BRADLEY, SARA · 2020 to 2024
$7.1M
NIA NIH HHS P30 AG059988NICHD NIH HHS K12 HD050121
6 · The paper itself

Abstract

purposeThe objective of this study was to test the feasibility of implementing a postoperative monitoring program for women with gynecologic cancers composed of patient-reported outcomes (PROs) and a wearable activity monitor.

methodsWe prospectively enrolled patients undergoing gynecologic cancer surgery to this single-arm study. Enrolled patients completed PROs (Patient-Reported Outcomes Measurement Information System physical function, sleep disturbance, anxiety, fatigue, and pain intensity) at baseline and one-week intervals for 4 weeks. They also wore a wearable accelerometer device that measured steps, heart rate, and intensity of physical activity. The primary outcome was feasibility. The secondary outcome was prediction of unscheduled contacts with the health care system on a given postoperative day.

resultsWe enrolled 34 women. Three patients were unevaluable. The mean age was 58 years. The mean body mass index was 31 kg/m

conclusionImplementation of a postoperative monitoring program of patient-reported outcomes and a wearable device was feasible. The specific day of an unscheduled contact with the health care system was predicted with acceptable discrimination.

Indexed as

Genital Neoplasms, FemaleWearable Electronic DevicesFatigueFeasibility StudiesFemaleHumansMiddle AgedPatient Reported Outcome Measures

Identifiers

PMID35427184
PMCPMC9848580
OpenAlexW4223893181

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.