Evidence map›Paper›PMID 30339657›Full record

ArticleJournal of pediatric hematology/oncology2019

Acceptability and Feasibility of a Disease-specific Patient Portal in Adolescents With Sickle Cell Disease.

Katherine M Kidwell, James Peugh, Emilie Westcott, Cara Nwankwo, Maria T Britto, Charles T Quinn, Lori E Crosby

Abstract readMulticenter Study
In one paragraph

Article in Journal of pediatric hematology/oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  8. Article
  9. A program of transition to adult care for sickle cell disease.Hematology. American Society of Hematology. Education Program · 2019
    Review
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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

7 authors.

Katherine M KidwellDivision of Behavioral Medicine.
James PeughDivision of Behavioral Medicine.
Emilie WestcottDivision of Behavioral Medicine.
Cara NwankwoDivision of Behavioral Medicine.
Maria T BrittoCenter for Innovation in Chronic Disease Care.
Charles T QuinnDivision of Hematology, Cincinnati Children's Hospital Medical Center.
Lori E CrosbyDivision of Behavioral Medicine.

Funding

Patient-Provider Interventions to Improve Transition to Adult Care in SCDK07HL108720 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI CROSBY, LORI E · 2011 to 2014
$1.6M
NHLBI NIH HHS K07 HL108720
6 · The paper itself

Abstract

objectiveTo examine the acceptability, feasibility, and efficacy of a health care portal. OBSERVATIONS: Adolescents and young adults with sickle cell disease were taught how to use sickle cell disease conditions page in MyChart and completed questionnaires at baseline, postintervention (T2, 6 wk after baseline) and after 3 months (T3). In total, 44 participants (M age=18.82, SD=2.72) viewed an average of 58.07 pages from T1 to T2. The portal was highly accepted (90.32%). Efficacy data indicated that portal use was associated with improved patient-provider communication.

conclusionsElectronic portals are promising tools for improving medical self-management.

Indexed as

Anemia, Sickle CellPatient Acceptance of Health CarePatient PortalsAdolescentFeasibility StudiesFemaleHumansMaleSelf-ManagementYoung Adult

Identifiers

PMID30339657
PMCPMC6472992

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.