Evidence map›Paper›PMID 24039458›Full record

ArticleMedical devices (Auckland, N.Z.)2013

Validation and ease of use of a new pen device for self-administration of recombinant human growth hormone: results from a two-center usability study.

Robert Rapaport, Paul Saenger, Heinrich Schmidt, Yukihiro Hasegawa, Michel Colle, Sandro Loche, Sandra Marcantonio, Walter Bonfig, Markus Zabransky, Fima Lifshitz

Open access · goldAbstract read
In one paragraph

Article in Medical devices (Auckland, N.Z.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 18% 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, 13 citations in OpenAlex.

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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

10 authors at 9 institutions in 6 countries.

Robert RapaportDivision of Pediatric Endocrinology and Diabetes, Mount Sinai School of Medicine, Mineola, NY, USA.
Paul Saenger
Heinrich Schmidt
Yukihiro Hasegawa
Michel Colle
Sandro Loche
Sandra Marcantonio
Walter Bonfig
Markus Zabransky
Fima Lifshitz
Icahn School of Medicine at Mount Sinai · USOspedale Microcitemico · ITSanden (Japan) · JPSciences Po Bordeaux · FRTechnical University of Munich · DETokyo Metropolitan Children's Medical Center · JPUniversidade Estadual de Londrina · BRUniversity Children's Hospital Tübingen · DEWinthrop-University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Close adherence to the recommended treatment regimen is important for the success of recombinant human growth hormone therapy, although nonadherence can be common. Ease of use and safety during use/storage are among several important factors in the design of a growth hormone injection device intended for long-term use. This study was performed to validate the usability and assess the ease of use of a new pen device (SurePal™) that has been developed to support daily administration of the recombinant human growth hormone product, Omnitrope® (somatropin). The primary objectives of the study were to assess if study participants, representing intended users of the pen in clinical practice, were able to perform an injection procedure into an injection pad effectively and safely and disassemble the pen without receiving a needlestick injury. A total of 106 participants (61 adults and 45 children/adolescents) were enrolled at two study centers (one in the US, one in Germany). Results for both primary usability tasks met the predefined acceptance criteria, with >85% of participants successfully performing each task. All of the other tasks/handling steps assessed were also successfully performed by most participants, with high success rates reflected in the high proportion of participants who classified each task as "very easy" or "easy". After a second use of the device, 87%-97% of participants rated it as "very easy" or "easy" to use. In summary, the new pen device is safe and easy to use for both adults and children, and will help to support effective, long-term daily administration of the recombinant human growth hormone product, Omnitrope®.

Indexed as

ease of usegrowth hormoneOmnitrope®pen deviceSurePal™

Identifiers

PMID24039458
PMCPMC3770891
OpenAlexW2036062750

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.