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1.
Front Endocrinol (Lausanne) ; 15: 1403754, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-39165509

RESUMEN

Objective: For elective cesarean section patients with gestational diabetes mellitus (GDM), there is a lack of evidence-based research on the use of enhanced recovery after surgery (ERAS). This study aims to compare the ERAS after-surgery protocol and traditional perioperative management. Research design and methods: In this retrospective cohort study, singleton pregnancies with good glucose control GDM, delivered by elective cesarean sections under intravertebral anesthesia at least 37 weeks from January 1 to December 31, 2022, were collected at the Third Affiliated Hospital of Sun Yat-sen University. We divided all enrolled pregnant women and newborns into an ERAS group and a control group (the traditional perioperative management group) based on their adherence to the ERAS protocol. The primary outcome was the preoperative blood glucose level, with an increase of more than 1 mmol/L indicating clinical significance when compared to the control group. The secondary outcome was centered around an adverse composite outcome that affected both mothers and newborns. Results: We collected a total of 161 cases, with 82 in the ERAS group and 79 in the control group. Although the mean preoperative blood glucose level in the ERAS group was significantly higher than in the control group (5.01 ± 1.06 mmol/L vs. 4.45 ± 0.90 mmol/L, p<0.001), the primary outcome revealed that the mean glycemic difference between the groups was 0.47 mmol/L (95% CI 0.15-0.80 mmol/L), which was below the clinically significant difference of 1 mmol/L. For the secondary outcomes, the ERAS group had an 86% lower risk of a composite adverse outcome compared to the control group. This included a 73% lower risk of perioperative maternal hypoglycemia and a 92% lower rate of neonatal hypoglycemia, all adjusted by age, hypertensive disorder of pregnancy, BMI, gestational weeks, primigravidae, primary pregnancy, GDM, surgery duration, and fasting glucose. Conclusion: Implementing a low-dose carbohydrate ERAS in pregnant women with GDM prior to elective cesarean section, compared to traditional perioperative management, does not lead to clinically significant maternal glucose increases and thus glucose-related maternal or neonatal perioperative complications.


Asunto(s)
Glucemia , Cesárea , Diabetes Gestacional , Procedimientos Quirúrgicos Electivos , Recuperación Mejorada Después de la Cirugía , Humanos , Femenino , Embarazo , Cesárea/efectos adversos , Estudios Retrospectivos , Adulto , Recién Nacido , Procedimientos Quirúrgicos Electivos/efectos adversos , Glucemia/metabolismo , Glucemia/análisis , Complicaciones Posoperatorias/etiología , Complicaciones Posoperatorias/prevención & control , Complicaciones Posoperatorias/epidemiología
2.
Int J Clin Exp Pathol ; 10(10): 10383-10391, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-31966374

RESUMEN

Preeclampsia (PE), a complication of pregnancy, is the leading cause of maternal and perinatal morbidity and mortality and seriously impacts maternal and child health. This study aimed to characterize biomarkers for the early diagnosis of PE. We performed a comparative proteomic analysis on the plasma obtained from PE and healthy pregnant women. We analyzed the plasma samples using two-dimensional differential gel electrophoresis (2D-DIGE) coupled with Ultraflex III, a MALDI-TOF-TOF (matrix-assisted laser desorption/ionization-time-of-flight) mass spectrometer and identified differentially expressed proteins (DEPs). We analyzed the abundance levels of these DEPs by enzyme-linked immunosorbent assay (ELISA) to further confirm their role as putative PE biomarkers. We identified a total of 56 DEPs, of which 48 were down-regulated and 8 were up-regulated in women with PE. The identities of 8 of these DEPs were characterized by mass spectrum analysis, including LG3BP (lectin, galactoside-binding, soluble, 3 binding protein), APOA1 (apolipoprotein A-I), FETUA (alpha-2-HS-glycoprotein), CFAI (complement factor I), CD5L (CD5 antigen-like), K2C6A (keratin, type II cytoskeletal 6A), PON1 (paraoxonase/arylesterase 1) and HP1 (haptoglobin). Finally, the differential expression of these 8 proteins was verified by ELISA. In summary, we applied the 2D-DIGE and Ultraflex III-TOF/TOF platform to identify potential plasma biomarkers of PE. Of these, plasma LG3BP, APOA1, FETUA, CFAI, CD5L, K2C6A, PON1 and HP1 were promising candidates for predicting PE.

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