Evidence map›Paper›PMID 37144265›Full record

ArticleTurkish archives of pediatrics2023

Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience.

Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Firdevs Baş, Şükran Poyrazoğlu, Neşe Akcan, Rejin Kebudi, Ayça İribaş Çelik, Rüveyde Bundak, Feyza Darendeliler

Open access · diamondAbstract read
In one paragraph

Article in Turkish archives of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
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

9 authors at 2 institutions in 2 countries.

Zehra Yavaş AbalıDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Ayşe Pınar ÖztürkDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Firdevs BaşDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Şükran PoyrazoğluDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Neşe AkcanDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey; Department of Pediatric Endocrinology, Near East University Faculty of Medicine, Nicosia, Turkish Republic of Northern Cyprus.
Rejin KebudiDepartment of Pediatric Hematology-Oncology, İstanbul University Institute of Oncology, İstanbul, Turkey.
Ayça İribaş ÇelikDepartment of Radiation Oncology, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Rüveyde BundakDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey; Department of Pediatric Endocrinology, University of Kyrenia Faculty of Medicine, Kyrenia, Turkish Republic of Northern Cyprus.
Feyza DarendelilerDepartment of Pediatric Endocrinology and Diabetes, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Istanbul University · TRUniversity of Kyrenia · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBrain tumors in childhood carry a high risk for endocrine disorders due to the direct effects of the tumor and/or surgery and radiotherapy. Somatotropes are vulnerable to pressure and radiotherapy; therefore, growth hormone deficiency is one of the most frequent abnormalities. This study aimed to evaluate endocrine disorders and recombinant growth hormone treatment outcomes in brain tumor survivors. MATERIALS AND

methodsIn this study, 65 (27 female) patients were classified into 3 groups as craniopharyngioma (n = 29), medulloblastoma (n = 17), and others (n = 19). "Others" group included astrocytoma, ependymoma, germinoma, pineoblastoma, and meningioma patients. Anthropometric data and endocrine parameters of patients and their growth outcome with/without recombinant growth hormone therapy were collected from medical records, retrospectively.

resultsMean age at the first endocrinological evaluation was 8.7 ± 3.6 years (range: 1.0- 17.1 years). Height, weight, and body mass index standard deviation score, mean ± standard deviation (median) values were -1.7 ± 1.7 (-1.5), -0.8 ± 1.9 (-0.8), and 0.2 ± 1.5 (0.4), respectively. Hypothyroidism (central 86.9%, primary 13.1%) was detected during follow-up in 81.5% of patients. Primary hypothyroidism in medulloblastoma (29.4%) was significantly higher compared to other groups (P = .002). The frequency of hypogonadotropic hypogonadism, central adrenal insufficiency, and diabetes insipidus was significantly high in the craniopharyngioma cases.

conclusionIn our study, endocrine disorders other than growth hormone deficiency were also frequently observed. In craniopharyngioma cases, the response to recombinant growth hormone therapy was satisfactory. However, there was no improvement in height prognosis during recombinant growth hormone therapy in medulloblastoma patients. A multidisciplinary approach to the care of these patients, referral for endocrine complications, and guidelines on when recombinant growth hormone therapy is required.

Identifiers

PMID37144265
PMCPMC10210600
OpenAlexW4367849258

What OpenQuestion holds

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Registered trials

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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.