目的 观察联合缩宫素与间苯三酚在基层医院分娩中疗效。方法 选用高明区人民医院2013年8月—2014年10月要求自然分娩的初产妇200例,随机分成两组,孕妇进入临产时,观察组予双管输液,予缩宫素2.5U+5%葡萄糖注射液静滴,另一静脉通路5%葡萄糖注射液250 mL+间苯三120 mg静滴;对照组仅予缩宫素2.5U+5%葡萄糖注射液静滴。比较两组产妇各产程时间、分娩方式、新生儿情况、产后出血量。结果 观察组第一产程、第二产程、第三产程时间均短于对照组(P＜0.01),剖宫产率3%及新生儿窒息率3%均低于对照组21%,和13%;P＜0.01;产后2小时出血量较对照组少(109.38±16.13)mL vs(185.00±30.71)mL, P＜0.01。结论 临产孕妇联合间苯三酚与缩宫素,可缩短产程,降低剖宫产率,降低新生儿窒息发生率,减少产后出血量,推荐基层医院使用。

Objective To investigate the effect of oxytocin combined with phloroglucinol in childbirth in primary hospital. Methods A total of 200 primiparas admitted to department of obstetrics in Gaoming people's hospital from August 2013 to October 2014　were selected as study subjects. The cases were randomly divided into observation group (100 cases) and control group (100 cases). In labor, cases in control group were given oxytocin 2.5 U and 5% glucose injection 500 mL, and were given 5% glucose injection 250 mL and phloroglucinol 120 mg by double tube intravenous infusion. Cases in observation group were only given oxytocin 2.5 U and 5% glucose injection 500 mL intravenous infusion. The duration of delivery、delivery mode、the condition of newborn and volume of bleeding after labor were compared between two groups. Results For the first、second and third stages of labor, duration of delivery in observation group were significantly shorter than that in control group (P＜0.01), Both cesarean delivery rate [3%(3/100)] and the incidence of neonatal asphyxia[3%(3/100)] in observation group were significantly lower than that in control group 21%(21/100)and 13%(13/100;P＜0.01). The volume of bleeding during two hours after labor in observation group was less than that in control group (109.38±16.13)mL vs 185.00±30.71 mL, P＜0.01. Conclusion In the stages of labor, the use of oxytocin combined with phloroglucinol can shorten the duration of delivery, reduce the cesarean delivery rate and the incidence of neonatal asphyxia and reduce the volume of bleeding after labor. It is worth recommending to use in primary hospital.

目的 对兰索拉唑肠溶片联合氟哌噻吨美利曲辛治疗焦虑糜烂性胃炎患者的治疗效果进行研究。方法 选取2013年1月—2015年1月在我院收治的伴有焦虑情绪的糜烂性胃炎患者106例。随机分为对照组,给予兰索拉唑肠溶片治疗,观察组,给予兰索拉唑肠溶片联合氟哌噻吨美利曲辛治疗,并且对疗效进行比较。结果 治疗前,两组患者在腹痛、腹胀、反酸、嗳气以及黏膜糜烂各指标评分比较,差异无统计学意义(P>0.05);治疗后,2组患者以上指标均有所改善,并且观察组患者同期指标改善均优于对照组(P<0.05);治疗前,两组患者胃黏膜中PGE2和MDA含量无差异(P>0.05);治疗后,两组患者的PGE2均上升,而MDA则下降,并且观察组患者PGE2含量比对照组高,MDA则比对照组低,差异均有统计学意义(P<0.05);治疗前,两组患者HAMA、HAMD评分差异不明显,无统计学意义(P>0.05);治疗后,两组患者焦虑情况均有所改善,并且观察组患者情绪改善程度优于对照组患者,差异均有统计学意义(P<0.05);观察组不良反应发生率为5.6%,对照组不良反应发生率5.6%,差异无统计学意义,P>0.05。结论 兰索拉唑与氟哌噻吨美利曲辛联合应用有助于改善糜烂性胃炎患者的病情,并且可以缓解患者的焦虑情绪,安全性高,值得临床推广。

Objective To observe the clinical efficacy of lansoprazole enteric-coated tablets combined with flupentixol-melitracen in treating anxiety patients with erosive gastritis. Methods 106 patients with erosive gastritis and anxiety in our hospital from January 2013 to January 2015 were divided into an observation group and a control group, with 53 patients in each group. The control group was given lansoprazole enteric-coated tablets alone, and the observation group was treated with lansoprazole enteric-coated tablets and flupentixol-melitracen. Clinical symptoms and mucosal erosion were compared between the two groups of patients before and after treatment. Gastric mucosa malondialdehyde (MDA) and prostration E2 (PGE2) contents, anxiety and depression status were also assessed. Results After treatment, the scores of abdominal pain, bloating, acid reflux, belching, and mucosal erosions were significantly lower in the observation group than in the control group (P< 0.05). PGE2and MDA contents in the gastric mucosa in the observation group were different from those in the control group(P< 0.05). HAMA and HAMD scores were lower in the observation group than in the control group (P< 0.05). There was no difference of adverse reaction rate between the control group and the observation group (P>0.05). Conclusion Lansoprazole enteric-coated tablets combined with flupentixol-melitracen has better clinical efficacy than lansoprazole enteric-coated tablets only in patients with erosive gastritis and anxiety in terms of the improvement of clinical symptoms and mucosal erosion and the relief of negative emotions.

目的 评估CO₂激光治疗宫颈上皮内瘤变Ⅱ级（CIN2）病例的疗效。方法 收集2021年11月至2023年10月在本院行CO2激光治疗的92例CIN2患者的临床资料, 采用液基细胞学检查（LCT）和人乳头状瘤病毒（HPV）联合筛查随访,随访6~12个月, 任一结果异常者转诊阴道镜检查, 必要时行病理活组织检查（活检）观察鳞状上皮内病变情况。结果 92例CIN2患者中, 年龄25~45岁、有人工流产史、性伴侣人数3个及以上、因发现宫颈病变就诊者占比较多,患者均未生育。所有患者就诊时均发现HPV阳性, 20.65%患者报告HPV16阳性, HPV18阳性者占比1.09%, HPV其他12种阳性占60.87%, HPV16阳性伴其他12种阳性占17.39%。79例患者随访6个月后总HPV+LCT均阴率为74.68%（59/79）,LCT和HPV阴转率分别为92.41%（73/79）和74.68%（59/79）。所有患者术后12个月LCT均转阴。29例患者在术后12个月均无病变持续或病变发展。25岁以下患者术后6个月及12个月HPV持续率最低, 45~55岁患者术后HPV持续率最高,且多发生HPV16阳性及合并其他HPV亚型阳性的情况。结论 CO₂激光治疗可提高患者术后HPV与LCT阴转率, 所有患者术后6个月及12个月随访均无病变加重,且可明显改善年轻患者HPV感染情况。对于有生育要求且具备适应证的CIN2患者, 应积极采取CO₂激光治疗以获得更高健康收益。

Objective To evaluate the therapeutic efficacy of CO₂ laser treatment in cervical intraepithelial neoplasia grade 2（CIN2）patients. Methods We retrospectively analyzed data from 92 CIN2 patients who underwent CO₂ laser therapy at the institution from November 2021 to October 2023. Postoperative followed-up for 6-12 months, screening with liquid-based cytopathology test（LCT）and high-risk human papilloma virus（HPV）testing. Patients with abnormal results in either test were referred for colposcopy, with biopsy performed to evaluate residual or recurrent squamous intraepithelial lesions. Results Among total of 92 patients, most patients aged 25-45 years old, with a history of induced abortion, had three or more sexual partners, and visited hospital due to cervical lesions, and none of the patients gave birth. All patients were found to be HPV positive at hospital visits, with 20. 65% of HPV16 positive, 1. 09% of HPV18 positive, 60. 87% of other 12 kinds HPV positive, while HPV16 positive with other 12 kinds accounted for 17. 39%. Among the 79 patients after 6-month follow-up, the dual-negative conversion rate（HPV+LCT）was 74. 68%（59/79）, with LCT and HPV negative rates reaching 92. 41%（73/79）and 74. 68%（59/79）, respectively. After 12-month follow-up, all patients achieved LCT negativity, 29 patients with no documented lesion persistence or disease progression. Notably, patients aged <25 years exhibited the lowest postoperative HPV persistence rates between 6- to 12-month follow-up, whereas those aged 45-55 years demonstrated the highest persistence rates, frequently associated with HPV16 positivity or co-infection with other HPV subtypes. Conclusions CO₂ laser therapy significantly increases postoperative negative conversion rates for HPV and LCT. No lesion progression was observed in patients between 6- to 12-month follow-ups. The therapy also notably improves HPV clearance in younger patients. For patients with CIN2 who have fertility requirements and meet the indications, CO2 laser therapy should be actively adopted to achieve greater health benefits.

目的 探讨传统术式联合骶主韧带复合体交叉悬吊术与骶棘韧带悬吊术（SSLF）在前盆腔膨出方面的相对疗效与价值。方法 回顾性分析2019年1月—2021年3月安徽医科大学附属六安医院收治的80例重度盆腔器官脱垂（POP）患者临床资料。将接受传统经阴道子宫切除术、阴道前后壁修补术及骶棘韧带悬吊术的40例患者纳入对照组,在上述术式基础上加行骶主韧带复合体交叉悬吊术的40例患者纳入观察组。所有纳入研究的POP患者的盆腔器官脱垂定量评估（POP-Q）评分结果为Ⅱ~Ⅳ度。对比两组患者的围术期指标,包括手术时间、术中出血量、术后病率（定义为术后24 h内连续2次、相隔4 h体温超过38 ℃）、术后留置导尿时间、术后住院时间,以及术中和术后并发症等。此外,术后对患者分别进行了电话随访及门诊复查,随访时间为术后3个月、6个月、1年和2年。生活质量评价采用盆底功能障碍性疾病症状问卷（PFDI-20）和盆底疾病生命质量影响问卷（PFIQ-7）。结果 两组患者手术时间、术中出血量、术后留置导尿时间比较差异均有统计学意义（P<0.05）,观察组术中出血量少于对照组,手术时间短于对照组,尿管留置时间短于对照组;两组患者术后住院时间、术后病率（手术后24 h内连续2次、相隔4 h体温超过38℃）比较差异无统计学意义（P>0.05）。两组间术前PFIQ-7和PFDI-20评分比较差异无统计学意义（P>0.05）;术后2年评分观察组高于对照组（P<0.05）。结论 经阴道子宫切除+阴道前后壁修补+骶棘韧带悬吊术及在上述术式基础上行骶主韧带复合体交叉悬吊术,均为临床治疗重度POP的常用手术方式。后者在治疗重度POP的主、客观治愈率上高于传统修补术式,且复发率更低,疗效更加持久。此外,骶主韧带复合体交叉悬吊术在改善单纯SSLF术后前盆腔膨出方面具有显著优势,为临床上POP的治疗与预后提供了新的思路。

Objective To explore the relative efficacy and value of the combination of traditional surgical methods with cross suspension of the sacro–uterine ligament complex and sacrospinous ligament suspension（SSLF）in preventing the recurrence of anterior pelvic prolapse after surgery. Methods This study retrospectively analyzed the clinical data of 80 patients with severe pelvic organ prolapse in Lu’an Hospital Affiliated to Anhui Medical University from January 2019 to March 2021. In the control group,patients received traditional transvaginal hysterectomy,repair of the anterior and posterior vaginal walls,and sacrospinous ligament suspension, while in the observation group, cross suspension of the sacro–uterine ligament complex was added on the basis of traditional surgical methods. The patients participating in the study were divided into the observation group（40 cases）and the control group（40 cases）according to different surgical methods. All patients with pelvic organ prolapse（POP）included in this study had POP–Q scores of grade II to IV. We compared the perioperative indicators of the two groups,including operation time, intraoperative blood loss, postoperative morbidity （defined as a body temperature exceeding 38°C for two consecutive times within 24 hours after surgery,separated by 4 hours）, postoperative indwelling catheterization time, postoperative hospital stay, and intraoperative and postoperative complications. In addition, patients were followed up by telephone and outpatient reexamination after surgery at 3 months, 6 months, 1 year, and 2 years. The quality of life was evaluated using the Pelvic Floor Dysfunction Symptom Questionnaire （PFDI–20） and the Pelvic Floor Disease Quality of Life Impact Questionnaire （PFIQ–7）. Results Comparing the operation time, intraoperative blood loss, and postoperative indwelling catheterization time of the two groups, there were statistically significant differences, P<0. 05. The intraoperative blood loss in the observation group was less than that in the control group, the operation time was shorter than that in the control group, and the indwelling catheter time was shorter than that in the control group. There was no statistically significant difference in postoperative hospital stay and postoperative morbidity（within 24 hours after surgery, two consecutive times with a body temperature exceeding 38°C separated by 4 hours）between the two groups, P>0. 05. There was no statistically significant difference in preoperative PFIQ–7 and PFDI–20 scores between the two groups（P>0. 05）, however, the scores of the observation group were higher than those of the control group 2 years after surgery, and the difference was statistically significant（P<0. 05）. Conclusions Traditional transvaginal hysterectomy + repair of the anterior and posterior vaginal walls + sacrospinous ligament suspension and cross suspension of the sacro–uterine ligament complex based on traditional surgical methods are both common surgical methods for the clinical treatment of severe pelvic organ prolapse. Studies have shown that the latter has a higher subjective and objective cure rate and a lower recurrence rate in the treatment of severe pelvic organ prolapse, with a more durable therapeutic effect. In addition,cross suspension of the sacro–uterine ligament complex has significant advantages in improving anterior pelvic prolapse after simple SSLF, providing new ideas for the treatment and prognosis of pelvic organ prolapse in clinical practice.

        目的   比较鲁拉西酮与奥氮平用于治疗女性急性期精神分裂症患者的疗效，以及其对体质量、糖脂代谢风险的影响。以期为女性急性期的精神分裂症患者抗精神病药物的选择提供参考。方法   连续选取于2022年4月—2024年4月内江门市第三人民医院收治的女性急性期精神分裂症患者80例，采用计算机随机分组法将患者分为治疗组与阳性药物对照组进行对照。治疗组40例口服鲁拉西酮40~80 mg/d，阳性药物对照40例组口服奥氮平5~20 mg/d。分别测量两组治疗前（基线）以及连续用药治疗2、4、6周后的PANSS量表评分，以及治疗后的代谢指标［体质量指数（BMI）、血清空腹血糖（FPG）、甘油三酯（TG）、总胆固醇（TC）、高密度脂蛋白（HDL）、低密度脂蛋白（LDL）、载脂蛋白A（ApoA）、载脂蛋白B（ApoB）、载脂蛋白E（ApoE），并将治疗组与对照组前后疗效及各项代谢指标进行比较分析。结果   两组的总有效率比较差异无统计学意义（χ ² =1.569，P＞0.05）；两组治疗前后PANSS量表评分的时间-组别效应与组别效应均无统计学意义（χ ² =0.466、3.640，P=0.926、0.056），时间主效应显著（χ ² =363.24，P＜0.001）。两组TG、TC、HDL、ApoA、ApoB存在组别-时间交互效应（χ ² =7.562、5.991、6.163、6.958、4.397，P=0.006、0.014、0.013、0.008、0.036），两组TG、ApoA时间主效应显著（χ ² =33.473、8.846，P＜0.001、0.003），两组ApoA组别效应显著（χ ² =4.889，P=0.027）。结论   与奥氮平相比，鲁拉西酮治疗女性急性期精神分裂症的疗效相当，且对代谢指标影响更小。

        Objective  To compare the efficacy of lurasidone and olanzapine in the treatment of female patients with acute schizophrenia，as well as their effects on body mass，glucose and lipid metabolism risk．To provide  reference for the selection of antipsychotic drugs for female patients with acute schizophrenia．Methods  From April 2022 to April 2024，80 female patients with acute phase schizophrenia admitted to the Third People’s Hospital of Jiangmen City were selected as samples and included in the study．The patients were randomly divided into a treatment group and a positive drug control group using a computer randomization method for comparison．The treatment group took oral lorazepine tablets（40 cases；40-80 mg/d），while the positive drug control group took oral olanzapine tablets（40 cases；5-20 mg/d）．The Positive and Negative Symptom Scale（PANSS）scores of two groups before treatment（baseline）and after 2，4，and 6 weeks of continuous medication treatment were measured，as well as metabolic indicators after treatment （body mass index［BMI］，serum fasting blood glucose［FPG］，total cholesterol［TC］，triglycerides［TG］，high-density lipoprotein［HDL］，low-density lipoprotein［LDL］，apolipoprotein A［ApoA］，apolipoprotein B［ApoB］，apolipoprotein E［ApoE］），and the efficacy and various metabolic indicators between the treatment group and the control group before and after treatment were compared and analyzed．Results  The total effective  rate of the two groups was not statistically significant（χ ² =1.569，P＞0.05）．The time-group effect and group effect of PANSS scores before and after treatment in both groups were not statistically significant（χ ² =0.466，3.640，P=0.926，0.056），while the time main effect was significant（χ ² =363.24，P＜0.001）．There was a group-time interaction effect between two groups of TG，TC，HDL，ApoA，and ApoB（χ ² =7.562，5.991，6.163，6.958，4.397，P=0.006，0.014，0.013，0.008，0.036）．The time main effect of TG and ApoA was significant in both groups（χ ² =33.473，8.846，P＜0.001，0.003），and the group effect of ApoA was significant in both groups（χ ² =4.889，P=0.027）．Conclusions  Compared with olanzapine，the efficacy of lurasidone in the treatment of acute phase schizophrenia in women is comparable，and it has a smaller impact on metabolic indicators．

        目的   分析达格列净联合沙库巴曲缬沙坦治疗射血分数降低的心力衰竭（HFrEF）效果。方法  连续抽取2021年1月—2023年6月在广州市第一人民医院心内科住院的射血分数降低的心力衰竭（HFrEF）患者203例，随访至少6个月，按照接受的治疗进行分组。对照组予常规治疗和沙库巴曲缬沙坦治疗；观察组予常规治疗、沙库巴曲缬沙坦和达格列净治疗；对比两组疗效，观察指标包括住院时间，入院及出院后6个月的心功能状态（NYHA纽约心脏病协会心功能分级）、心脏超声指标左室射血分数（LVEF）、左室舒张末内径（LVEDD）、左室收缩末内径（LVSDD）、血液指标-端脑钠肽前体（NT-proBNP N）、糖化血红蛋白（HBA1c）、血肌酐（Cr）、6个月时的再住院率及全因死亡率。结果   观察组心脏监护病房（CCU）停留时间（2.54±1.26）d，短于对照组的（3.73±1.21）d；观察组6个月时观察组心功能NYHA改善≥2级比例为95.05%高于对照组的86.27%，差异有统计学意义（P＜0.05）；观察组6个月时的LVEDD、LVESD水平分别为（48.22±7.35）（34.61±4.32）mm，低于对照组的（51.47±8.02）（43.07±5.33）mm，LVEF为（51.49±5.40）%，高于对照组的（46.18±4.21）%，差异有统计学意义（P＜0.05）；6个月时观察组的NT-proBNP为（415.58±31.57）pg/mL，低于对照组的（520.23±385.56）pg/mL，差异有统计学意义（P＜0.05）；两组的住院时间、血清肌酐（Cr）、HBA1c、6个月时的再住院率、全因病死率对比，差异不显著（P＞0.05）。观察组HBA1c值为（6.04±0.66）mmol/L，高于对照组的（5.20±0.56）mmol/L（P＜0.05）。结论  HFrEF患者采取达格列净+沙库巴曲缬沙坦治疗，可通过协同作用，缩短CCU停留时间，改善患者6个月时的心功能状态，降低NT-proBNP值，减少心脏扩大趋势，提高LVEF水平。

       Objective  To analyze the efficacy of  dapagliflozin combined with  sacubitril/valsartan in the treatment of heart failure with reduced ejection fraction（HFrEF）．Methods  A total of 203 patients with HFrEF who were hospitalized in the cardiology department of the hospital between January 2021 and June 2023 were enrolled and followed up for at least six months．Patients were divided into groups based on their treatment regimens：the control group received conventional treatment plus sacubitril/valsartan，while the observation group received conventional treatment plus sacubitril/valsartan and dapagliflozin．The two groups were compared for clinical outcomes，including length of hospital stay，cardiac function（NYHA classification）at admission and six months after discharge，echocardiographic indicators（LVEF，LVEDD，LVESD），blood indicators（NT-proBNP，HbA1c，creatinine），six-month rehospitalization rate，and all-cause mortality．Results  The observation group had a shorter CCU stay（2.54±1.26 days）compared to the control group（3.73±1.21 days）．At sixth month，the proportion of patients in the observation group with an NYHA improvement ≥2 grades（95.05%）was significantly higher than that in the control group（86.27%）（P＜0.05）．The observation group demonstrated lower LVEDD（48.22±7.35 mm）and LVESD（34.61±4.32 mm）levels and higher LVEF（51.49±5.40%）compared to the control group（LVEDD：［51.47±8.02］ mm，LVESD：［43.07±5.33］mm，LVEF：［46.18±4.21］%）（P＜0.05）．NT-proBNP levels in the observation group（［415.58±31.57］ pg/mL）were significantly lower than those in the control group（［520.23±385.56］ pg/ml）（P＜0.05）．There were no significant differences between the two groups in length of total hospital stay，serum creatinine，HbA1c，six-month rehospitalization rate，or all-cause mortality（P＞0.05）．However，HbA1c levels in the observation group（［6.04±0.66］ mmol/L）were higher than those in the control group（［5.20±0.56］ mmol/L）（P＜0.05）．Conclusions  The combination of dapagliflozin and sacubitril/valsartan in the treatment of HFrEF patients can exert a synergistic effect，shorten CCU stay，improve cardiac function at sixth month，reduce NT-proBNP levels，mitigate cardiac dilation，and increase LVEF．

       目的   探究腕踝针联合揿针治疗带状疱疹后遗痛的临床疗效观察。方法   选取上海市黄浦区中西医结合医院2021年10月—2024年4月收治的80例带状疱疹后遗神经痛患者为研究对象，按随机数表法分为研究组、对照组，各40例。对照组采用口服甲钴胺治疗；研究组采用腕踝针联合揿针治疗。比较两组治疗疗效；治疗前后采用视觉模拟评分（VAS）与阿森斯失眠量表评分（AIS）、皮肤病生活质量指数（DLQI）、汉密尔顿抑郁量表评分（HAMD）、汉密尔顿焦虑量表评分（HAMA）。结果   研究组治疗总有效率为92.5%，对照组治疗总有效率为75%。比较差异有统计学意义（P＜0.05）。两组患者治疗后VAS、AIS均比治疗前改善，研究组VAS评分为（1.00±0.45）、AIS评分为（7.15±0.89），优于对照组VAS（2.15±0.36）和AIS（5.65±0.70），比较差异有统计学意义（P＜0.05）。相较于治疗前，两组患者DLQI评分均有改善，研究组［休闲活动评分（1.73±0.45）、人际交往评分（1.13±0.34）、工作学习评分（0.94±0.25）、自觉症状评分（1.83±0.38）、日常活动评分（0.98±0.28）］优于对照组［休闲活动评分（2.06±0.40）、人际交往评分（1.81±0.39）、工作学习评分（1.08±0.38）、自觉症状评分（2.01±0.34）、日常活动评分（1.10±0.30）］，差异有统计学意义（P＜0.05）。两组患者HAMD评分、HAMA评分，相较于治疗前均有改善，研究组HAMD评分为（34.63±2.61）、HAMA评分为（35.75±2.48），优于对照组HAMD评分（47.68±3.21）和HAMA评分（46.90±3.31），差异有统计学意义（P＜0.05）。结论   腕踝针联合揿针治疗带状疱疹后遗神经痛的临床疗效显著，可有效改善患者生活质量、疼痛程度、焦虑及抑郁程度，提升患者睡眠质量。

       Objective  To investigate the clinical efficacy of wrist and ankle acupuncture combined with thumbtack needle in the treatment of postherpetic herpes zoster pain．Methods  Eighty patients with postherpetic neuralgia admitted to Shanghai Huangpu District Hospital of Integrative Medicine from October 2021 to April 2024 were selected for the study，and were divided into a study group and a control group of 40 cases each according to the random number table method．The control group was treated with oral mecoblamin tables；the study group was treated with wrist and ankle acupuncture combined with thumbtack needle．The efficacy of treatment between the two groups was compared；before and after treatment，the visual analogue score（VAS）and Asens Insomnia Scale（AIS），Dermatological Quality of Life Index（DLQI），Hamilton Depression Scale（HAMD），Hamilton Anxiety Scale（HAMA）were compared．Results  The treatment efficiency was 92.5% in the study group and 75% in the control group．The difference was statistically significant（P＜0.05）．VAS scores and AIS scores of patients in both groups improved after treatment，and VAS score（1.00±0.45），AIS score（7.15±0.89）of the study group were better than VAS score（2.15±0.36），AIS score（5.65±0.70）of the control group．The differences were statistically significant（P＜0.05）．The DLQI scores of both groups improved after treatment，and the score of study group（leisure activity score［1.73±0.45］，interpersonal interaction score［1.13±0.34］，work-study score［0.94±0.25］，self-perceived symptom score［1.83±0.38］，daily activities score［0.98±0.28］）were higher than those of the control group（leisure activity score［2.06±0.40］，interpersonal score［1.81±0.39］，work-study score［1.08±0.38］，conscious symptom score［2.01±0.34］，daily activity score［1.10±0.30］）．The differences were statistically significant（P＜0.05）．HAMD scores and HAMA scores of patients in both groups，showed significant improvement after treatment，and HAMD scores（34.63±2.61）and HAMA scores（35.75±2.48）of the study group were better than HAMD scores（47.68±3.21）and HAMA scores（46.90±3.31）of the control group．The difference was statistically significant（P＜0.05）．Conclusions  The clinical efficacy of wrist and ankle acupuncture combined with thumbtack needle in the treatment of postherpetic pain is remarkable，effectively improving the quality of life，pain，anxiety and depression，and enhancing the quality of sleep of patients．

       目的 评价不同间变性淋巴瘤激酶（ALK）抑制剂联合安罗替尼治疗非小细胞肺癌（NSCLC）的疗效。方法 收集ALK突变阳性NSCLC患者的临床资料，筛选服用ALK抑制剂疗效不佳再加用安罗替尼的病例。根据不同的用药方案分为阿来替尼+安罗替尼，塞瑞替尼+安罗替尼和克唑替尼+安罗替尼三个组别。记录患者联合用药前最近一次的影像学检查结果，并以此为基线按Recist1.1评价疗效，以病情进展、患者死亡、停药、改变治疗方案为终点计算各组患者的无事件生存期（EFS），收集肿瘤标志物、血常规和肝功、心功能、肾功能生化检测等指标数据，统计分析患者联合用药前后各项指标的变化。结果 经筛选，共纳入49例患者的临床数据。阿来替尼+安罗替尼组有23例，疾病控制率（DCR）为86.96%；平均EFS为（10.8±3.6）个月，中位EFS为8.3个月；塞瑞替尼+安罗替尼组有14例，DCR为71.43%；平均EFS为（6.5±2.9）个月，中位EFS为5.6个月；克唑替尼+安罗替尼组有12列，DCR为66.67%；平均EFS为（7.7±3.2）个月，中位EFS为7.2个月。阿来替尼+安罗替尼组的平均EFS长于另外两组（P＜0.05）。各研究组肿瘤标志物仅有CyFra21-1在克唑替尼+安罗替尼组在联合用药后升高（P＜0.05），生化检测和血常规指标在用药前后差异无统计学意义（P＞0.05）。结论  ALK抑制剂与安罗替尼联用，疗效最好为阿来替尼，其次为塞瑞替尼，最后为克唑替尼。三种ALK抑制剂与安罗替尼联用后，均未导致心、肝、肾功能和血细胞损害。

      Objective  To evaluate the efficacy of different anaplastic lymphoma kinase（ALK）inhibitors combined with anlotinib in the treatment of non-small cell lung cancer（NSCLC）．Methods  Clinical data of drug resistant NSCLC patients with ALK positive mutation was collected who were treated with ALK inhibitors and anlotinib synchronously．According to different regimens，three groups were set，alectinib+anlotinib，ceritinib+anlotinib，and crizotinib+anlotinib．The latest imageological examination  results of the patient before the synchronous therapy was set as the baseline to evaluate the therapeutic effect according to Recist1.1．The event free survival（EFS）of each group was calculated with disease progression，patient death，treatment discontinuation and changing regimen as endpoints．Data of tumor markers，hematology test，liver function，cardiac function，renal function biochemical examination was collected and analyzed statistically before and after the combination therapy，with P＜0.05 as the statistically significant difference．Results  After screening，clinical data of 49 patients were collected．Twenty-three patients in the alectinib+anlotinib group，with a disease control rate（DCR） of 86.96%；mean EFS was（10.8±3.6）months，median EFS of 8.3 months；14 patients in the ceritinib+anlotinib group，with a DCR of 71.43%，mean EFS was（6.5±2.9）months，median EFS was 5.6 months；12 patients in the crizotinib+anlotinib group，with a DCR of 66.67%，mean EFS was（7.7±3.2）months，median EFS was 7.2 months．EFS of alectinib+anlotinib group was longer significantly than the other two groups（P＜0.05）．Only CyFra21-1，increased significantly after the combination of crizotinib and anlotinib（P＜0.05）．No statistically significant difference in biochemical test and hematology test before and after the treatment（P＞0.05）．Conclusions  The therapeutic effect of ALK inhibitors with anlotinib was ordered，alectinib being the most effective，followed by ceritinib and finally crizotinib．The combination of ALK inhibitors with anlotinib did not cause any abnormal results in the examination of heart，liver，kidney and blood cells．

       目的 探讨术中未恢复窦性心律需要行电复律的心房颤动（房颤）患者在清醒和镇静两种状态下的安全性及有效性。方法 选择2022年1月—2023年12月100例接受射频消融术中行同步直流电复律的持续性房颤患者进行研究，采用随机数字表法将患者分为观察组（清醒状态）和对照组（镇静状态），其中观察组和对照组各为50例。观察两组患者接受电复律的成功率、复发率和不良事件发生率（呼吸抑制、低血压、谵妄、肺水肿、心律失常）等指标。结果 观察组和对照组首次电复律成功分别有48、49例，成功率分别为96%、98%，组间比较差异无统计学意义（P=0.558）。观察组术后30 min内有2例复发，对照组术后30 min内无复发，组间比较差异无统计学意义（P=0.153）。在不良反应方面，观察组共发生1例心律失常事件，1例低血压事件，不良反应的总发生率为4%。对照组共发生3例呼吸抑制事件、2例谵妄事件、1例心律失常事件、2例低血压事件，不良反应的总发生率为16%，组间比较差异有统计学意义（P=0.046）。结论 对持续性房颤患者在射频消融术中，处于清醒状态下行电复律也具有良好的临床疗效，可以减少不良事件的发生，安全性更高。

  Objective  To compare the safety and efficacy of awake state and sedation state in patients with atrial fibrillation（AF）who did not recover sinus rhythm and needed electrical cardioversion during operation．Methods  A total of 100 patients with persistent atrial fibrillation who underwent synchronous direct current cardioversion during radiofrequency ablation from January 2022 to December 2023 were selected and divided into the observation group（awake state）and the control group（sedation state）according to the random number table method，with 50 cases in each group．The success rate of electrical cardioversion，recurrence rate and incidence of adverse events（respiratory depression，hypotension，delirium，pulmonary edema，arrhythmia）were observed．Results  The first electrical cardioversion was successful in 48 and 49 patients in the observation group and the control group，and the success rates were 96% and 98%，respectively．There was no significant difference between the two groups（P=0.558）．There were 2 cases of  recurrence in the observation group and no  recurrence in the control group within 30 minutes after operation，and there was no significant difference between the two groups（P=0.153）．In terms of adverse reactions，there were 1 case of arrhythmia event and 1 case of hypotension event in the observation group，and the total incidence of adverse reactions was 4%．There were 3 cases of respiratory depression events，2 cases of delirium events，1 case of arrhythmia events，and 2 cases of hypotension events in the control group．The total incidence of adverse reactions was 16%，and the difference between the two groups was statistically significant（P=0.046）．Conclusions  Electrical cardioversion in awake state during  radiofrequency ablation of persistent atrial fibrillation has a good clinical efficacy and safety，which can reduce the occurrence of adverse events．