Evidence map›Paper›PMID 38606228›Full record

ReviewCureus2024

Alkindi Sprinkle for Pediatric Patients With Primary Adrenocortical Insufficiency: A Narrative Review.

Alan D Kaye, Munira E Khaled, Kristin Nicole Bembenick, John Lacey, Anamika Tandon, Rucha A Kelkar, Alyssa G Derouen, Corrado Ballaera, Debbie Chandler, Shahab Ahmadzadeh and 2 more

Open access · diamondAbstract readReview
In one paragraph

Review in Cureus, 2024. 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
–field-weighted citation impact, top 96% 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, 0 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

12 authors at 1 institution in 2 countries.

Alan D KayeAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Munira E KhaledSchool of Medicine, Louisiana State University Health Sciences Center, Shreveport, USA.
Kristin Nicole BembenickSchool of Medicine, Louisiana State University Health Sciences Center, Shreveport, USA.
John LaceySchool of Medicine, Louisiana State University Health Sciences Center at New Orleans, New Orleans, USA.
Anamika TandonSchool of Medicine, Louisiana State University Health Sciences Center at New Orleans, New Orleans, USA.
Rucha A KelkarSchool of Medicine, Medical University of South Carolina, Charleston, USA.
Alyssa G DerouenAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Corrado BallaeraAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Debbie ChandlerAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Shahab AhmadzadehAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Sahar ShekoohiAnesthesiology, Louisiana State University Health Sciences Center, Shreveport, USA.
Giustino VarrassiPain Medicine, Paolo Procacci Foundation, Rome, ITA.
Medical University of South Carolina · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenocortical insufficiency, also known as adrenal insufficiency (AI), is an endocrine disorder characterized by inadequate production of adrenal hormones, including glucocorticoids and mineralocorticoids (MCs). The condition can be categorized as primary, secondary, or tertiary AI, depending on the location of the defect. Classical symptoms of AI include weakness, fatigue, abdominal pain, tachycardia, hypotension, electrolyte imbalances, and hyperpigmentation. In children, the most common cause of AI is classical congenital adrenal hyperplasia, which results from a deficiency in the 21-hydroxylase enzyme. The 21-hydroxylase enzyme produces all steroids, such as cortisol and aldosterone. AI management primarily involves hormone replacement therapy, typically with oral hydrocortisone and MC supplementation. However, the administration of hydrocortisone to pediatric patients presents challenges related to the lack of available dose-appropriate formulations. Historically, crushed or split adult tablets were used for the pediatric treatment of AI, although this poses an increased risk of under- or overtreatment. Inadequate dosing in the pediatric population can adversely affect growth, development, and metabolic health. Alkindi Sprinkle is a pediatric-specific hydrocortisone oral granule preparation that manages cortisol levels to help facilitate accurate therapeutic dosing. Alkindi offers several advantages, including accurate dosing, taste masking, and ease of administration. The present investigation describes AI, the management of AI, and the treatment of pediatric AI using Alkindi Sprinkle, including clinical efficacy.

Indexed as

adrenal crisisadrenocortical insufficiencyalkindi sprinkleglucocorticoid replacementmineralocorticoid deficiencypediatric adrenal insufficiencypediatric endocrinology

Identifiers

PMID38606228
PMCPMC11007452
OpenAlexW4392702542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.