Objective:To investigate the effects of a single intravenous injection of low-dose esketamine during cesarean section on postpartum depression in primiparas.Methods:This study is a prospective randomized controlled trial involving 106 primiparas who underwent scheduled intrathecal anesthesia for cesarean section at Xi'an International Medical Center Hospital from January 2021 to December 2023. The participants were randomly assigned to either the control group or the observation group, with 53 women in each group, using a random number table method. Both groups received the same type and method of anesthesia. In the observation group, 5 minutes after the delivery of the fetus and the clamping of the umbilical cord, a low dose of esketamine (0.2 mg/kg, dissolved in 10 mL of 0.9% sodium chloride injection) was administered intravenously. The control group received an equivalent volume of 0.9% sodium chloride injection as a placebo. The score of the Edinburgh Postnatal Depression Scale at various postpartum time intervals (3, 7, 14, 30, and 42 days), the incidence of postpartum depression, and any adverse drug reactions occurring within 3 days postoperatively were compared between the two groups. Additionally, the score of the Visual Analog Scale (VAS) for contraction pain was assessed.Results:The scores of the Edinburgh Postnatal Depression Scale in the observation group at 3, 7, 14, 30, and 42 days postpartum were (6.23 ± 1.21), (5.82 ± 1.77), (6.14 ± 1.20), (5.33 ± 1.19), and (6.01 ± 1.23), respectively. These scores were significantly lower than those in the control group [(8.99 ± 1.28), (8.91 ± 2.11), (9.03 ± 1.94), (10.40 ± 2.68), (9.28 ± 1.84), t = 11.40, 8.16, 9.22, 12.58, 10.75, all P < 0.001]. The incidence of postpartum depression in the observation group at 7 and 14 days postpartum was significantly lower than that in the control group [3.77% (2/53) vs. 16.98% (9/53), 3.77% (2/53) vs. 15.09% (8/53), χ2 = 4.97, 3.97, P = 0.026, 0.046]. There was no statistically significant difference in the incidence of adverse drug reactions within 3 days postoperatively between the two groups of women who underwent scheduled intrathecal anesthesia for cesarean section [15.09% (8/53) vs. 11.32% (6/53), χ2 = 0.32, P = 0.566]. The scores of the Visual Analog Scale for contraction pain in the observation group at 3, 6, 12, and 24 hours postoperatively were (2.13 ± 0.28), (2.55 ± 0.33), (2.73 ± 0.35), and (3.06 ± 0.37), respectively. These scores were significantly lower than those in the control group [(4.35 ± 0.46), (5.43 ± 0.36), (5.68 ± 0.35), (5.26 ± 0.43), t = 30.01, 42.93, 43.38, 28.23, all P < 0.001]. Conclusions:A single intravenous injection of low-dose esketamine during cesarean section can effectively alleviate emotional distress in primiparas in the short term after surgery, which has significant clinical implications for reducing the incidence of postpartum depression.

Objective:To investigate the effects of a single intravenous injection of low-dose esketamine during cesarean section on postpartum depression in primiparas.Methods:This study is a prospective randomized controlled trial involving 106 primiparas who underwent scheduled intrathecal anesthesia for cesarean section at Xi'an International Medical Center Hospital from January 2021 to December 2023. The participants were randomly assigned to either the control group or the observation group, with 53 women in each group, using a random number table method. Both groups received the same type and method of anesthesia. In the observation group, 5 minutes after the delivery of the fetus and the clamping of the umbilical cord, a low dose of esketamine (0.2 mg/kg, dissolved in 10 mL of 0.9% sodium chloride injection) was administered intravenously. The control group received an equivalent volume of 0.9% sodium chloride injection as a placebo. The score of the Edinburgh Postnatal Depression Scale at various postpartum time intervals (3, 7, 14, 30, and 42 days), the incidence of postpartum depression, and any adverse drug reactions occurring within 3 days postoperatively were compared between the two groups. Additionally, the score of the Visual Analog Scale (VAS) for contraction pain was assessed.Results:The scores of the Edinburgh Postnatal Depression Scale in the observation group at 3, 7, 14, 30, and 42 days postpartum were (6.23 ± 1.21), (5.82 ± 1.77), (6.14 ± 1.20), (5.33 ± 1.19), and (6.01 ± 1.23), respectively. These scores were significantly lower than those in the control group [(8.99 ± 1.28), (8.91 ± 2.11), (9.03 ± 1.94), (10.40 ± 2.68), (9.28 ± 1.84), t = 11.40, 8.16, 9.22, 12.58, 10.75, all P < 0.001]. The incidence of postpartum depression in the observation group at 7 and 14 days postpartum was significantly lower than that in the control group [3.77% (2/53) vs. 16.98% (9/53), 3.77% (2/53) vs. 15.09% (8/53), χ2 = 4.97, 3.97, P = 0.026, 0.046]. There was no statistically significant difference in the incidence of adverse drug reactions within 3 days postoperatively between the two groups of women who underwent scheduled intrathecal anesthesia for cesarean section [15.09% (8/53) vs. 11.32% (6/53), χ2 = 0.32, P = 0.566]. The scores of the Visual Analog Scale for contraction pain in the observation group at 3, 6, 12, and 24 hours postoperatively were (2.13 ± 0.28), (2.55 ± 0.33), (2.73 ± 0.35), and (3.06 ± 0.37), respectively. These scores were significantly lower than those in the control group [(4.35 ± 0.46), (5.43 ± 0.36), (5.68 ± 0.35), (5.26 ± 0.43), t = 30.01, 42.93, 43.38, 28.23, all P < 0.001]. Conclusions:A single intravenous injection of low-dose esketamine during cesarean section can effectively alleviate emotional distress in primiparas in the short term after surgery, which has significant clinical implications for reducing the incidence of postpartum depression.

Objective To investigate the correlations of serum cystatin C level with severity of stroke and short-term outcome in patients with acute ischemic stroke.Methods Patients with first-ever acute ischemic stroke aged ≥50 years who did not receive thrombolysis and took a visit within 3 d after onset were selected prospectively.The serum cystatin C level was detected within 24 h after admission and various clinical data were collected.The National Institutes of Health Stroke Scale (NIHSS) was used to assess the neurological deficits on the day of admission.The NIHSS score ＜8 was defined as mild stroke and ≥8 was defined as moderate to severe stroke.The modified Rankin Scale (mRS) was used to evaluate the short-term outcome at discharge or 14 d after onset,0-2 was defined as good outcome and ＞2 was defined as poor outcome.Results A total of 188 patients were enrolled,including 93 (49.5％) females and 95 (50.5％) males,their mean age was 65.4 ±9.2 years old (range 50-87).There were 120 patients with mild stroke (63.8％),68 with moderate to severe stroke (36.2％);106 patients (56.4％) had good outcome and 82 (43.6％) had poor outcome.Univariate analysis showed that serum cystatin C level in the moderate to severe stroke group was significantly higher than that in the mild stroke group (1.36 ± 0.29 mg/L vs.1.21 ±0.23 mg/L;t =3.902,P ＜ 0.001),the serum cystatin C level in the poor outcome group was significantly higher than that in the good outcome group (1.38 ± 0.25 mg/L vs.1.22 ± 0.25 mg/L;t =4.101,P =0.001).Multivariate logistic regression analysis showed that the serum cystatin C level was an independent risk factor for stroke severity (odds ratio 12.182,95％ confidence interval 11.163-13.202;P ＜ 0.001) and short-term poor outcome (odds ratio 9.025,95 ％ confidence interval 8.202-9.848;P ＜ 0.001).Conclusion The serum cystatin C level is significantly correlated with the severity of stroke and the short-term outcome in patients with acute ischemic stroke.

Objective To investigate the relationship betw een the serum bilirubin level and the severity of disease and short-term outcome in patient w ith acute ischemic stroke. Methods A total of 120 consecutive inpatients w ith acute ischemic stroke w ere enroled and 105 healthy subjects at the same time w ere used as a control group. The biochemical indicators, such as serum total bilirubin, direct bilirubin, indirect bilirubin, blood lipid, and blood glucose w ere measured w ithin 24 h after admission. The National Institutes of Health Stroke Scale ( NIHSS ) w as used to assess the neurological deficits on the day of admission. The NIHSS score <8 w as defined as mild stroke and ≥8 w as defined as moderate to severe stroke. At discharge or 14 d after onset, the modified Rankin Scale (mRS) w as used to evaluate the clinical outcomes, 0-2 w as defined as good outcome and > 2 w as defined as poor outcome. The levels of serum total bilirubin, direct bilirubin, and indirect bilirubin w ere measured again. Results The levels of serum total bilirubin, direct bilirubin, and indirect bilirubin in the moderate to severe stroke group w ere significantly higher than those in the mild stroke group ( P <0.01) and the control group ( P <0.01). Multivariate logistic regression analysis show ed that the increased levels of serum total bilirubin (odds ratio [OR] 1.855,95%confidence interval [CI] 1.390-2.475; P <0.01), indirect bilirubin ( OR 3.380, 95%CI 1.271-11.901; P <0.05), and direct bilirubin ( OR 3.51, 95%CI 1.062-11.473; P <0.01) had significantly independent correlation w ith baseline disease severity. Univariate analysis show ed that the increased serum total bilirubin level on admission w as associated w ith the short-term poor outcome ( P <0.05), but after adjustment for other confounding factors, there w as no statistical significance ( OR 2.411, 95%CI 0.803-7.243, P >0.05). Conclusions The serum bilirubin level show ed stress increase in patients w ith cerebral infarction in acute phase; and it w as significantly associated w ith the degree of neurological deficit, but it w as not associated w ith short-term outcome. It might be a defense response to the body for stroke events.

Objective To investigate the clinical features and the mechanism of falciparum malaria in several patients between Chinese and Malian.Methods The data of Chinese (n =28) and Malian patients (n =35) including general condition,Glasgow Coma Scale (GCS),APACHE Ⅱ,the time of applying ventilator and days of stay in ICU,laboratory examination (plasmodium test,routine blood test,liver and kidney function and C-reactive protein (CRP) assayed before treatment and 1d,3d,7d after treatment,cranial computed tomography and mortality were recorded for investigating the clinical features of the disease.Results There was difference in age range between Chinese patients (ranged from 32 to 50 years old) and Malian patients (ranged from 8 to 72 years old),and difference in severity of the disease between patients of two countries was found and Malian patients were more severely infected than Chinese patients.The results of plasmodium test,routine blood test,liver and kidney function and level of CRP often varied greatly during the entire course of the disease,and the changes were greater in Malian patients.The correlation between APACHE Ⅱ and CRP was found (P ＜ 0.05).The cranial CT displayed ischemia focus in brain.The mortality of Chinese patients was 16.7％ and that of Malian was 25.0％.Conclusions There was difference in composition of residents between Chinese patients and Malian patients.Malian patients were more severely infected with Plasmodium falciparum than Chinese patients,and this difference might be due to the potential correlation between the disease virulence and immune response of patients.