Evidence map›Paper›PMID 36734395›Full record

ReviewPediatric endocrinology, diabetes, and metabolism2023

Audit of management of children and adolescents with congenital adrenal hyperplasia as per recent Endocrine Society guidelines.

Lalitha S, Hemchand Krishna Prasad, Bharath Ramjee, Lakshmi Venugopalan, Nandhini Ganapathy, Balamourougane Paramasamy

Open access · diamondAbstract readReview
In one paragraph

Review in Pediatric endocrinology, diabetes, and metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 1 institution in 1 country.

Lalitha SDepartment of Pediatrics, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Hemchand Krishna PrasadDepartment of Pediatric Endocrinology, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Bharath RamjeeDepartment of Endocrinology, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Lakshmi VenugopalanDepartment of Neonatology, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Nandhini GanapathyDepartment of Pediatric Surgery, Mehta Multispeciality Hospitals India Pvt Ltd, India.
Balamourougane ParamasamyDepartment of Pediatric Surgery, Mehta Multispeciality Hospitals India Pvt Ltd, India.
CARE Hospitals · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIn view of the modifications in the endocrine society guidelines on evaluation and management of children with congenital adrenal hyperplasia (CAH), we performed a review of children and adolescents with CAH. MATERIAL AND

methodsAn audit of 35 children with CAH presenting to the pediatric endocrinology clinic between January 2014 to November 2021 was conducted by formulating ten audit questions. The areas of focus included: genital reconstructive surgery, neonatal screening for CAH, stress dosing, need for adrenocorticotrophic hormone (ACTH) stimulation test, growth promoting therapy, bone age assessment, adrenal imaging, bone mineral density assessment, adequacy of hormone replacement and appropriate management of non-classical CAH.

resultsConservative approach to genitoplasty in female children increased from 42.9% to 88.9%. Newborn screening identified 4 babies including two asymptomatic males averting saltwasting crisis. Stress dosing of steroids were advised in all and emergency usage of injectable glucocorticoids was warranted in two children. Gonadotropin-releasing hormone (GnRH) analogue therapy improved the final median predicted height by 7 cm in 5 children. Twenty-three (65.7%) had bone age assessment with 14 (40%) having advanced bone age. ACTH stimulation test, Adrenal imaging, dual energy X-ray absorptiometry (DEXA) scan were done in accordance with the guideline. One child with nonclassical CAH was initiated on hydrocortisone replacement for advanced bone age.

conclusionsA shift to conservative surgical management of females, utility of neonatal screening for CAH, judicious use of growth promoting therapy is highlighted. Need for bone age testing, emergency hydrocortisone provision is warranted in our series.

Indexed as

Adrenal Hyperplasia, CongenitalAdolescentAdrenocorticotropic HormoneBone DensityChildFemaleGlucocorticoidsHumansHydrocortisoneInfantInfant, NewbornMaleAdrenocorticotropic HormoneGlucocorticoidsHydrocortisoneauditcongenital adrenal hyperplasiagenitoplastyscreening

Identifiers

PMID36734395
PMCPMC10226460
OpenAlexW4313433644

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.