Evidence map›Paper›PMID 31117051›Full record

ArticleEndocrinology, diabetes & metabolism case reports2019

Octreotide use for rescue of vision in a pregnant patient with acromegaly.

Anne Marie Hannon, Isolda Frizelle, George Kaar, Steven J Hunter, Mark Sherlock, Christopher J Thompson, Domhnall J O'Halloran, Irish Pituitary Database Group

Open access · goldAbstract read
In one paragraph

Article in Endocrinology, diabetes & metabolism case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Approach of Acromegaly during Pregnancy.Diagnostics (Basel, Switzerland) · 2022
    Review
  4. Review
  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

8 authors at 3 institutions in 2 countries.

Anne Marie HannonDepartments of Endocrinology and Diabetes, Cork University Hospital, Cork, Ireland.
Isolda FrizelleDepartments of Endocrinology and Diabetes, Cork University Hospital, Cork, Ireland.
George KaarDepartments of Neurosurgery, Cork University Hospital, Cork, Ireland.
Steven J HunterDepartment of Endocrinology and Diabetes, Royal Victoria Hospital, Belfast, UK.
Mark SherlockDepartment of Endocrinology and Diabetes, Beaumont Hospital, Dublin, Ireland.
Christopher J ThompsonDepartment of Endocrinology and Diabetes, Beaumont Hospital, Dublin, Ireland.
Domhnall J O'HalloranDepartments of Endocrinology and Diabetes, Cork University Hospital, Cork, Ireland.
Irish Pituitary Database Group
Cork University Hospital · IEBeaumont Hospital · IEUniversity of Ulster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pregnancy in acromegaly is rare and generally safe, but tumour expansion may occur. Managing tumour expansion during pregnancy is complex, due to the potential complications of surgery and side effects of anti-tumoural medication. A 32-year-old woman was diagnosed with acromegaly at 11-week gestation. She had a large macroadenoma invading the suprasellar cistern. She developed bitemporal hemianopia at 20-week gestation. She declined surgery and was commenced on 100 µg subcutaneous octreotide tds, with normalisation of her visual fields after 2 weeks of therapy. She had a further deterioration in her visual fields at 24-week gestation, which responded to an increase in subcutaneous octreotide to 150 µg tds. Her vision remained stable for the remainder of the pregnancy. She was diagnosed with gestational diabetes at 14/40 and was commenced on basal bolus insulin regimen at 22/40 gestation. She otherwise had no obstetric complications. Foetal growth continued along the 50th centile throughout pregnancy. She underwent an elective caesarean section at 34/40, foetal weight was 3.2 kg at birth with an APGAR score of 9. The neonate was examined by an experienced neonatologist and there were no congenital abnormalities identified. She opted not to breastfeed and she is menstruating regularly post-partum. She was commenced on octreotide LAR 40 mg and referred for surgery. At last follow-up, 2 years post-partum, the infant has been developing normally. In conclusion, our case describes a first presentation of acromegaly in pregnancy and rescue of visual field loss with somatostatin analogue therapy. Learning points: Tumour expansion may occur in acromegaly during pregnancy. Treatment options for tumour expansion in pregnancy include both medical and surgical options. Somatostatin analogues may be a viable medical alternative to surgery in patients with tumour expansion during pregnancy.

Indexed as

2019AcromegalyCaesarean sectionCortisolCortisol (9am)CT scanDiabetes insipidus - gestationalDietFemaleGHGlucose (blood, fasting)Haemoglobin A1cHands - enlargementHeadacheHemianopiaIGF1InsulinIrelandMayMRINovel treatmentOctreotidePituitaryPituitary adenomaPregnant adultPrognathismProlactinSomatostatin analoguesTeeth gappingThyroid functionThyroxine (T4)Total T4TSHVisual field defectWhite

Identifiers

PMID31117051
PMCPMC6528404
OpenAlexW2946328968

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.