Evidence map›Paper›PMID 41757229›Full record

ReviewFrontiers in endocrinology2026

The SGLT2 inhibitor checklist: a comprehensive review of perioperative and acute phase safety management.

Bin Deng, Wenhua Liu, Qingmin Chu

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2026. 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

3 authors.

Bin DengDepartment of Cardiology, Shenzhen Bao'an Chinese Medicine Hospital, Shenzhen, China.
Wenhua LiuDepartment of Endocrinology, Bao'an Authentic TCM Therapy Hospital, Shenzhen, China.
Qingmin ChuDepartment of Cardiology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sodium-glucose cotransporter-2 (SGLT2) inhibitors have transcended their initial designation as mere glucose-lowering agents to become a foundational pillar in the management of cardiorenal metabolic syndrome. Their cardiorenal benefits have made them ubiquitous in surgical patients, including those without diabetes. However, this therapeutic triumph has introduced a unique and deceptive perioperative challenge: euglycemic diabetic ketoacidosis (euDKA). This metabolic emergency, characterized by severe metabolic acidosis and ketosis in the absence of significant hyperglycemia, poses a diagnostic dilemma that continues to jeopardize patient safety. This comprehensive review synthesizes the rapidly evolving landscape of perioperative SGLT2 inhibitor management as of 2025. We provide an exhaustive dissection of the endocrine mechanisms driving ketogenesis, challenging the canonical "insulin-deficiency" model by integrating novel data on human pancreatic α-cell SGLT1 expression, renal sodium-monocarboxylate transporter (SMCT) upregulation, and the newly elucidated arginine vasopressin (AVP)-V1b receptor axis which mechanistically links dehydration to hyperglucagonemia. Furthermore, we critically adjudicate the conflicting clinical evidence emerging in 2024-2025, juxtaposing the reassuring "natural experiment" data from JAMA Surgery against the persistent safety signals in BMJ Open and anesthesia literature. We analyze the risks of "rebound" heart failure associated with medication withdrawal-citing specific hazard ratios for readmission-and provide a comparative analysis of divergent international guidelines (FDA, EMA, ANZCA, JBDS). Finally, we propose a physiologically grounded, risk-stratified clinical decision framework to guide the perioperative suspension and resumption of these potent agents.

Indexed as

Diabetic KetoacidosisPerioperative CareSodium-Glucose Transporter 2 InhibitorsHumansSodium-Glucose Transporter 2 Inhibitorsarginine vasopressin (AVP) axiseuglycemic diabetic ketoacidosis (euDKA)ketogenesisperioperative managementrisk stratificationSGLT2 inhibitorssodium-monocarboxylate transporters (SMCT)

Identifiers

PMID41757229
PMCPMC12932149

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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.