Evidence map›Paper›PMID 36377209›Full record

ArticleThe American journal of case reports2022

Late-Onset Ornithine Transcarbamylase Deficiency Complicated with Extremely High Serum Ammonia Level: Prompt Induction of Hemodialysis as the Key to Successful Treatment.

Satsuki Yamamoto, Shun Yamashita, Toshihiko Kakiuchi, Kazuya Kurogi, Tomoyo M Nishi, Masaki Tago, Shu-Ichi Yamashita

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 3 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

7 authors at 1 institution in 1 country.

Satsuki YamamotoDepartment of General Medicine, Saga University Hospital, Saga, Japan.
Shun YamashitaDepartment of General Medicine, Saga University Hospital, Saga, Japan.ORCID 0000-0002-5143-8665
Toshihiko KakiuchiDepartment of Pediatrics, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-9995-5522
Kazuya KurogiDepartment of General Medicine, Saga University Hospital, Saga, Japan.
Tomoyo M NishiDepartment of General Medicine, Saga University Hospital, Saga, Japan.
Masaki TagoDepartment of General Medicine, Saga University Hospital, Saga, Japan.ORCID 0000-0003-1092-1834
Shu-Ichi YamashitaDepartment of General Medicine, Saga University Hospital, Saga, Japan.
Saga University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Ornithine transcarbamylase deficiency (OTCD) is an X-linked semi-dominant disorder, causing possible fatal hyperammonemia. Late-onset OTCD can develop at any time from 2 months after birth to adulthood, accounting for 70% of all OTCDs. CASE REPORT A 35-year-old man with chronic headaches stated that since childhood he felt sick after eating meat. Fourteen days before hospital admission, he began receiving 60 mg/day of intravenous prednisolone for sudden deafness. The prednisolone was stopped 5 days before hospital admission. Four days later, he was transferred to our hospital because of confusion. On admission, he had hyperammonemia of 393 µmol/L. Because he became comatose 7 hours after admission, and his serum ammonia increased to 1071 µmol/L, we promptly started hemodialysis. Because his family history included 2 deceased infant boys, we suspected late-onset OTCD. On day 2 of hospitalization, we began administering ammonia-scavenging medications. Because he gradually regained consciousness, we stopped his hemodialysis on day 6. After his general condition improved, he was transferred to the previous hospital for rehabilitation on day 32. We definitively diagnosed him with late-onset OTCD due to the low plasma citrulline and high urinary orotic acid levels found during his hospitalization. CONCLUSIONS Clinicians should suspect urea cycle disorders, such as OTCD, when adult patients present with marked hyperammonemia without liver cirrhosis. Adult patients with marked hyperammonemia should immediately undergo hemodialysis to remove ammonia, regardless of causative diseases.

Indexed as

HyperammonemiaOrnithine Carbamoyltransferase Deficiency DiseaseAdultAmmoniaChildHumansInfantMaleOrnithine CarbamoyltransferasePrednisoloneRenal DialysisAmmoniaOrnithine CarbamoyltransferasePrednisolone

Identifiers

PMID36377209
PMCPMC9676062
OpenAlexW4306385704

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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.