Evidence map›Paper›PMID 35213607›Full record

SynthesisPloS one2022

Pediatric growth hormone treatment in Italy: A systematic review of epidemiology, quality of life, treatment adherence, and economic impact.

Massimiliano Orso, Barbara Polistena, Simona Granato, Giuseppe Novelli, Roberto Di Virgilio, Daria La Torre, Daniela d'Angela, Federico Spandonaro

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 21 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

8 authors at 3 institutions in 1 country.

Massimiliano OrsoC.R.E.A. Sanità (Centre for Applied Economic Research in Healthcare), Rome, Italy.ORCID 0000-0003-0200-1202
Barbara PolistenaC.R.E.A. Sanità (Centre for Applied Economic Research in Healthcare), Rome, Italy.
Simona GranatoMedical Department, Pfizer Italia, Rome, Italy.
Giuseppe NovelliHealth Economics & Outcomes Research, Pfizer Italia, Rome, Italy.
Roberto Di VirgilioHealth Economics & Outcomes Research, Pfizer Italia, Rome, Italy.
Daria La TorreGlobal Medical Affairs, Pfizer Rare Disease, Rome, Italy.
Daniela d'AngelaC.R.E.A. Sanità (Centre for Applied Economic Research in Healthcare), Rome, Italy.
Federico SpandonaroC.R.E.A. Sanità (Centre for Applied Economic Research in Healthcare), Rome, Italy.ORCID 0000-0003-1388-2850
Pfizer (Italy) · ITUniversity of Rome Tor Vergata · ITSan Raffaele University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis systematic review aims to describe 1) the epidemiology of the diseases indicated for treatment with growth hormone (GH) in Italy; 2) the adherence to the GH treatment in Italy and factors associated with non-adherence; 3) the economic impact of GH treatment in Italy; 4) the quality of life of patients treated with GH and their caregivers in Italy.

methodsSystematic literature searches were performed in PubMed, Embase and Web of Science from January 2010 to March 2021. Literature selection process, data extraction and quality assessment were performed by two independent reviewers. Study protocol has been registered in PROSPERO (CRD42021240455).

resultsWe included 25 studies in the qualitative synthesis. The estimated prevalence of growth hormone deficiency (GHD) was 1/4,000-10,000 in the general population of children; the prevalence of Short Stature HOmeoboX Containing gene deficiency (SHOX-D) was 1/1,000-2,000 in the general population of children; the birth prevalence of Turner syndrome was 1/2,500; the birth prevalence of Prader-Willi syndrome (PWS) was 1/15,000. Treatment adherence was suboptimal, with a range of non-adherent patients of 10-30%. The main reasons for suboptimal adherence were forgetfulness, being away from home, pain/discomfort caused by the injection. Economic studies reported a total cost for a complete multi-year course of GH treatment of almost 100,000 euros. A study showed that drug wastage can amount up to 15% of consumption, and that in some Italian regions there could be a considerable over- or under-prescribing. In general, patients and caregivers considered the GH treatment acceptable. There was a general satisfaction among patients with regard to social and school life and GH treatment outcomes, while there was a certain level of intolerance to GH treatment among adolescents. Studies on PWS patients and their caregivers showed a lower quality of life compared to the general population, and that social stigma persists.

conclusionGrowth failure conditions with approved GH treatment in Italy constitute a significant burden of disease in clinical, social, and economic terms. GH treatment is generally considered acceptable by patients and caregivers. The total cost of the GH treatment is considerable; there are margins for improving efficiency, by increasing adherence, reducing drug wastage and promoting prescriptive appropriateness.

Indexed as

Human Growth HormonePrader-Willi SyndromeQuality of LifeTreatment Adherence and ComplianceTurner SyndromeAdolescentChildChild, PreschoolFemaleHumansItalyMalePrevalenceHuman Growth Hormone

Identifiers

PMID35213607
PMCPMC8880399
OpenAlexW4214602326

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.