Evidence mapPaperPMID 41001605Full record

ArticleO&G open2024

Opportunities to Improve Recognition of Diabetic Ketoacidosis in Pregnancy.

Tiffany Corlin, Sereen K Nashif, Katelyn M Tessier, Megan Kristan, W Kirke Rogers, Sarah A Wernimont

Abstract read
In one paragraph

Article in O&G open, 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
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.

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.

Tiffany CorlinDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.
Sereen K NashifDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.
Katelyn M TessierDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.
Megan KristanDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.
W Kirke RogersDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.
Sarah A WernimontDivision of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology and Women's Health, the Masonic Cancer Center, Biostatistics Core, the Division of Endocrinology, Department of Medicine, and the Department Anesthesiology and Critical Care, University of Minnesota, Minneapolis, Minnesota.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of ketosis and anion gap metabolic acidosis in individuals with diabetes indicates diabetic ketoacidosis (DKA). The incidental detection of such laboratory abnormalities in persons with diabetes should trigger an intentional evaluation for DKA. The objective of this retrospective cohort study was to assess the frequency with which pregnant individuals with diabetes and a laboratory abnormality potentially indicative of DKA underwent a complete laboratory assessment and to identify factors associated with completion of the appropriate laboratory testing. Clinical characteristics were evaluated for patients with complete and incomplete workups. Workup for DKA was completed in only 30.0% of individuals with laboratory evidence of acidosis or ketosis; 64.0% (57/89) of those with complete workups did not meet criteria for DKA. This study highlights opportunities to ensure complete laboratory workup for DKA, especially in patients with non-type 1 diabetes, obstetric conditions such as labor, and lower glucose on presentation.

Identifiers

PMID41001605
PMCPMC12456582

What Socratic 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 Socratic graph.