双支架Nuss手术治疗青少年漏斗胸

目的 探讨使用双支架治疗青少年大范围漏斗胸微创Nuss手术的适应证、可行性和手术方法及效果.方法 31例中男24例,女7例;年龄14～18岁,平均(15.32±3.12)岁.根据Hallar指数均评价为中到重度,凹陷范围为4个肋间以上.选择胸腔镜辅助Nuss手术两点或者多点双支架支撑固定法手术.结果 均采用双支架在胸腔镜辅助下顺利完成Nuss手术.术后住院5～10天,平均(7.48±1.95)天;随访4个月到5年.术中发生出血2例,支架滑动移位和间断疼痛2个月各1例,均治愈.结论 胸腔镜辅助双支架矫正大面积、不对称漏斗胸的Nuss手术对青少年是一种安全、有效的方法.

Abstract：

Objective To investigate the indication, feasibility and technique of minimally invasive nuss procedure with thoracoscope by using double braces in the treatment of wide-scope pectus excavatum repairing in adolescence. Methods 31 patients including 24 boys and 7 girls, suffered from pectus excavtum were corrected by nuss procedure under thoracoscope.The average age was (15.32 ± 3.89)years (ranged, 14 years and 18 years). All cases were moderate to severe degree according to Hallar index with depression scope of 4 ribs or more. A couple of braces of two-point or multipoint fixation for thoracoscopic-assisted nuss procedure were used. Results The procedure was successfully completed under thoracoscopy in all patients. Double braces were utilized in 27 cases, double are bars were required in 4 cases, and multipoint fixations were in 6 patients. The postoperative hospital stay was 5-11 days [average, ( 7.48 ± 1.95 ) days]. The duration of following up was one month to three years. The perioperative complications included intraoperative hemorrhage in 2 patients, bar invertion with displacement in 1, and interrupted pain for two months in 1. All patients recovered after expectant treatment. Conclusion Nuss procedure with double braces for the correction of a large area of asymmetric pectus excavatum under thoracoscopy is safe and effective technique for adolescence.     

鸡胸的微创外科治疗

Objective Minimally invasive technique was used in the treatment of pectus carinatum. Indication, techni-cal details and perioperative complication are discussed in this paper. Methods From March 2008 to January 2009, 6 patients with pectus carinatum underwent minimal invasive operation by using the principle of Nuss procedure in which pressure applied through a curved steel bar that was placed subcutaneously anterior to the sternum, via lateral thoracic incisions. Preoperative CT scan were performed and Hailer index was used as operative indication. Results The average age of patients was (13.6 ± 1.94) years (range, 10 - 16 years). They were all males. The mean operation time was (104.17 ± 15.63) minutes. The av-erage blood loss was (5.17±2.56) ml. The mean hospital stay was (5.67±0.82) days. Postoperative follow-up was 1 -11 months. Displacement of the stablizer was the only complication that was corrected by further fixation procedure. COnClusion The minimally invasive technique for the treatment of peetus earinatum is safe and effective with minimal complications. It can be selected as an alternative techniques and the appropriate age for this procedure is 10-16 years.     

腹腔镜辅助改良Soave术治疗成人先天性巨结肠症

Objective To evaluate the clinical value of laparoscopy-assisted modified Soave procedure for Hirschsprung disease in adults.Methods Twenty-eight patients with a preoperative diagnosis of Hirschsprung disease underwent laparoscopy-assisted modified Soave procedure between March 2005 and December 2009.Clinical data were retrospectively analyzed.Results There were no conversions to open surgery.The mean operative time was (165±12) minutes (range:135-185 minutes).Estimated blood loss ranged from 50 to 250 ml,and no patients required intraoperative blood transfusion.Postoperative pathologic examination showed Hirschsprung diseases in 19 patients and Hirschsprung allied diseases in 9.Only two patients developed rectal cuff infection and three mild seepage.Other patients had no postoperative complications.The mean hospital stay was (17.5±1.0)days.No fecal incontinence or recurrent constipation occurred during follow-up.Conclusion Laparoscopyassisted modified Soave procedure is safe and effective for Hirschsprung disease.     

Does needle calibre affect pain and complication rates in patients undergoing transperineal prostate biopsy？ A prospective,randomized trial

Transperineal prostate biopsy is a procedure that can be used to obtain histological samples from the prostate. To improve both the quality of the biopsy core samples and prostate cancer detection, we are currently performing a prospective, randomized trial comparing prostate biopsy samples obtained using an 18 G-needle to those obtained using a 16 G-needle. The aim of this preliminary study was to evaluate pain and complication rates in both groups in order to assess whether performing a prostate biopsy with a larger calibre needle is a feasible procedure. One hundred and eighty-seven patients undergoing transperineal prostate biopsy were prospectively evaluated and divided into two groups. The first group （94 patients, Group A） received a transperineal prostate biopsy using a 16 G-needle and the second group （93 patients, Group B） underwent transperineal prostate biopsy with an 18 G-needle. Anaesthesia was obtained with a single perineal injection at the prostatic apex in all subjects. A visual analogue scale （VAS） and facial expression scale （FES） were used to assess pain during multiple steps of the procedure in each group. A detailed questionnaire was used to obtain information about drug use because it could potentially influence the pain and complications that patients experienced. Two weeks after the procedure, early and late complications were evaluated. Statistical analysis was carried out using non-parametric tests. Prostate Specific Antigen （PSA） and drug use were similar at baseline between the two groups. Pain during prostate biopsy, which was measured with both the VAS and FES instruments, did not differ significantly between the 18- and 16 G-needle groups, and no significant differences were found in early or late complication rates between the groups. Transperineal prostate biopsy with a 16 G-needle is a feasible Further studies with larger patient populations are required to prostate cancer detection rates. procedure in terms of pain and complication rates. assess whether or not this procedure can improve     

Implications of the presence of an aberrant right hepatic artery in patients undergoing pancreaticoduodenectomy

AIM:To analyze the differences in outcomes and the clinical impact following pancreatoduodenectomy(PD)in patients with and without aberrant right hepatic artery(aRHA).METHODS:All patients undergoing PD between January 2008 and December 2012 were divided into two groups,one with aRHA and the other without.These groups were compared to identify differences in the intraoperative variables,the oncological clearance and the postoperative morbidity,mortality and hospital stay.RESULTS:A total of 225 patients underwent PD,of which 43(19.1%)patients were found to have eitheraccessory or replaced right hepatic arteries(aRHA group).The aRHA was preserved in 79%of the patients.There was no significant difference in the intraoperative blood loss but operative time was prolonged,reflecting the complexity of the procedure[420±44(240-540)min vs 480±45(300-600)min,P0.05)].There were no differences in the incidence of postoperative complications(pancreatic leak,pancreatic fistula,delayed gastric emptying and mortality)and hospital stay.Oncological clearance in the form of positive resection margins[13(7.1%)vs 3(6.9%)]and lymph node yield were also similar in the two groups.CONCLUSION:An aRHA is found in approximately one fifth of patients undergoing PD.Preservation is technically possible in most patients and can increase the operative complexity but does not negatively affect the safety or oncological outcomes of the procedure.     

Supreme喉罩用于腹腔镜手术患者气道管理的效果

Objective To assess the efficacy of laryngeal mask airway Supreme (LMA Supreme) used in patients undergoing laparoscopic surgery. Methods One hundred and twenty ASA I or Ⅱ patients of both sexes aged 35-60 yr weighing 48-85 kg undergoing elective laparoscopic surgery were randomized to 2 groups ( n = 60 each): LMA Supreme group (group S) and tracheal intubation group (group T). Mallampati test was performed before operation in both groups. The patients were classified as I - Ⅲ . In group S the LMA Supreme was inserted after induction of anesthesia with sufentanil 0.2 fig/kg, propofol 2-3 mg/kg and vecuronium 0.1 mg/kg. A gastric tube was inserted through the drain tube of the LMA Supreme. In group T the patients were intubated under direct laryngoscopy. The success rate, LMA placement/intubation time, success rate of gastric tube placement, airway seal pressure, SpO2, PETCO2 , peak airway pressure and complications (hypoxemia, nausea and vomiting, choking hoarseness, sore throat and regurgitation of gastric contents) were recorded. The duration of surgery, anesthesia time, extubation time and emergence time were also recorded. Results There was no significant difference in the success rate between the two groups. The placement and removal time and recovery time were significantly shorter in group S than in group T. The airway seal pressure was (25 ±4) cm H2O in group S. SpO2, PETCO2 and peak pressure were within normal range in both groups. The incidence of postoperative hypoxemia, choking and sore throat were significantly lower in group S than in group T. Conclusion LMA Supreme can provide adequate ventilation during operation with less complications and can be used effectively for laparoscopic surgery.     

Supreme喉罩用于腹腔镜手术患者气道管理的效果

Objective To assess the efficacy of laryngeal mask airway Supreme (LMA Supreme) used in patients undergoing laparoscopic surgery. Methods One hundred and twenty ASA I or Ⅱ patients of both sexes aged 35-60 yr weighing 48-85 kg undergoing elective laparoscopic surgery were randomized to 2 groups ( n = 60 each): LMA Supreme group (group S) and tracheal intubation group (group T). Mallampati test was performed before operation in both groups. The patients were classified as I - Ⅲ . In group S the LMA Supreme was inserted after induction of anesthesia with sufentanil 0.2 fig/kg, propofol 2-3 mg/kg and vecuronium 0.1 mg/kg. A gastric tube was inserted through the drain tube of the LMA Supreme. In group T the patients were intubated under direct laryngoscopy. The success rate, LMA placement/intubation time, success rate of gastric tube placement, airway seal pressure, SpO2, PETCO2 , peak airway pressure and complications (hypoxemia, nausea and vomiting, choking hoarseness, sore throat and regurgitation of gastric contents) were recorded. The duration of surgery, anesthesia time, extubation time and emergence time were also recorded. Results There was no significant difference in the success rate between the two groups. The placement and removal time and recovery time were significantly shorter in group S than in group T. The airway seal pressure was (25 ±4) cm H2O in group S. SpO2, PETCO2 and peak pressure were within normal range in both groups. The incidence of postoperative hypoxemia, choking and sore throat were significantly lower in group S than in group T. Conclusion LMA Supreme can provide adequate ventilation during operation with less complications and can be used effectively for laparoscopic surgery.     

Laparoscopic approach in complicated diverticular disease

AIM: To analyze the results of laparoscopic colectomy in complicated diverticular disease.METHODS: This was a retrospective cohort study conducted at an academic teaching hospital. Data were collected from a database established earlier, which comprise of all patients who underwent laparoscopic colectomy for diverticular disease between 2000 and 2013. The series was divided into two groups that were compared: Patients with complicated disease(abscess, perforation, fistula, or stenosis)(G1) and patients undergoing surgery for recurrent diverticulitis(G2). Recurrent diverticulitis was defined as two or more episodes of diverticulitis regardless of patient age. Data regarding patient demographics, comorbidities, prior abdominal operations, history of acute diverticulitis, classification of acute diverticulitis at index admission and intra and postoperative variables were extracted. Univariate analysis was performed in both groups.RESULTS: Two hundred and sixty patients were included: 28%(72 patients) belonged to G1 and 72%(188 patients) to G2. The mean age was 57(27-89) years. The average number of episodes of diverticulitis before surgery was 2.1(r 0-10); 43 patients had no previous inflammatory pathology. There were significant differences between the two groups with respect to conversion rate and hospital stay(G1 18% vs G2 3.2%, P = 0.001; G1: 4.7 d vs G2 3.3 d, P < 0.001). The anastomotic dehiscence rate was 2.3%, with no statistical difference between the groups(G1 2.7% vs G2 2.1%, P = 0.5). There were no differences in demographic data(body mass index, American Society of Anesthesiology and previous abdominal surgery), operative time and intraoperative and postoperative complications between the groups. The mortality rate was 0.38%(1 patient), represented by a death secondary to septic shock in G2.CONCLUSION: The results support that the laparoscopic approach in any kind of complicated diverticular disease can be performed with low morbidity and acceptable conversion rates when compared with patients undergoing laparoscopic surgery for recurrent diverticulitis.     

Obese patients have similar short-term outcomes to nonobese in laparoscopic colorectal surgery

AIM: To determine whether obese patients undergoing laparoscopic surgery within an enhanced recovery program had worse short-term outcomes.METHODS: A prospective study of consecutive patients undergoing laparoscopic colorectal resection was carried out between 2008 and 2011 in a single institution. Patients were divided in groups based on body mass index(BMI). Short-term outcomes including operative data, length of stay, complications and readmission rates were recorded and compared between the groups. Continuous data were analysed using t-test or oneway Analysis of Variance. χ2 test was used to compare categorical data.RESULTS: Two hundred and fifty four patients were included over the study period. The majority of individuals(41.7%) recruited were of a healthy weight(BMI 25), whilst 50 patients were classified as obese(19.6%). Patients were matched in terms of the presence of comorbidities and previous abdominal surgery. Obese patients were found to have a statistically significant difference in The American Society of Anesthesiologists grade. Length of surgery and intra-operative blood loss were no different according to BMI.CONCLUSION: Obesity(BMI 25) does not lead to worse short-term outcomes in laparoscopic colorectal surgery and therefore such patients should not be precluded from laparoscopic surgery.     

阻塞性黄疸术前经皮肝穿刺胆管引流对围手术期的影响

【Abstract】〓Objective〓To summarize the experience in treatment of the obstructive jaundice by preoperative percutaneous puncture of liver bile duct drainage. Methods〓Eight-six patients with obstructive jaundice were included and divided into two groups according to the operation procedure, 44 cases were given preoperative percutaneous transhepatic cholangial drainage(observation group) and then,.underwent internal or external drainage or radical operation,.42 cases were served as control group without preoperative percutaneous transhepatic cholangial drainage..Intraoperative blood loss, operative time,..hospital stay and complications were compared between two groups. The preoperative and postoperative liver function tests,such as total bilirubin(TB),.serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) were evaluated and compared in two groups. Results〓The operation time,.blood loss,.length of hospital stay and complication rates between observation group were lower than that in control group (P<0.05). The levels of TB, ALT, AST in 14 days after operation reduced in two groups, but were significantly decreased in observation group,.as compared to control group (P<0.05). Conclusion〓For patients with obstructive jaundice, preoperative percutaneous transhepatic cholangial drainage would shorten the length of hospital stay,.reduce complications occurrence,.and improve liver function.     

非胸腔镜下Nuss矫正术治疗漏斗胸

目的 探讨非胸腔镜下微创Nuss术矫正漏斗胸的安全性、有效性和治疗经验.方法 2007年10月至2009年5月,手术治疗48例漏斗胸病儿中男28例,女20例;年龄4～13岁,平均(6.5± 2.1)岁.术前CT示胸廓指数3.76±0.54;其中26例行非胸腔镜下微创Nuss术(非胸腔镜组),22例行胸腔镜辅助下Nuss术(胸腔镜组).结果 两组均顺利完成手术,术中均无死亡、大出血及胸腔脏器损伤等严重并发症发生.非胸腔镜下Nuss组无气胸,血胸等并发症,无需放置胸腔闭式引流管.其手术时间、术后入院时间与胸腔镜组比较,差异有统计学意义(P<0.05).非胸腔镜下Nuss组手术时间24～38 min,平均(25.4±2.6)min;住院3～6天,平均(4.5±1.1)天;术中出血量5～10 ml.胸腔镜组手术时间40～60 min,平均(53.5±3.4)min,住院5～8天,平均(7.0±2.2)天;出血量10～15 ml.两组病儿术后均获随访,随访时间至少3个月,平均10.4个月,均无漏斗胸复发.非胸腔镜手术组1例术后2月出现肋骨矫形板移位,再次手术重新放置肋骨矫形板.结论 非胸腔镜下Nuss术矫正漏斗胸是安全有效的,与胸腔镜辅助下Nuss术相比创伤更小,恢复更快.     

Nuss手术矫治复发性和胸部手术后继发性漏斗胸

目的 总结Nuss手术矫治复发性和胸部手术后继发性漏斗胸经验.方法 2004年6月至2011年9月18例复发性或胸部手术后继发性漏斗胸Nuss手术者中男12例,女6例;年龄3.1 ～14.8岁,平均(8.8±4.0)岁;体重11 ～55kg,平均(30.2±14.8)kg.10例为开放式漏斗胸矫治术后复发病例,8例为其他胸部手术后继发性漏斗胸.16例畸形为对称性,2例为非对称性.CT检查Haller指数5.4±3.4.手术均在胸腔镜辅助下完成.结果 全组均成功实施手术.所有患儿均置入1根钢板.17例置入右侧固定片,1例置入双侧固定片.16例矫形效果为优良,2例良好.矫形效果与初次Nuss手术相比,早期优良及良好率差异无统计学意义(P＞0.05).术后胸腔引流管放置1～4天.1例钢板移位于术后5个月行Nuss修正,重新固定移位之钢板.1例心脏穿孔出血,术中紧急行扩大胸骨正中切口,直视下修补心脏破口,术后复查超声心动图,心脏功能正常,无神经系统并发症.1例术后当天气胸合并皮下气肿,1例术后3天胸腔积液,此2例均行胸腔闭式引流后治愈.12例钢板拆除,钢板滞留24～45个月,拆除者10例保持优良,2例良好,无复发病例.结论 Nuss手术矫治复发性和胸部手术后继发性漏斗胸效果良好.     

Nuss手术矫治漏斗胸412例

目的 探讨非胸腔镜辅助下Nuss手术治疗漏斗胸的手术方法并总结治疗经验.方法 2005年10月到2011年6月非胸腔镜辅助下Nuss手术治疗漏斗胸412例,其中男329例,女83例.年龄2岁8个月～28岁5个月,平均7岁8个月.其中102例行内固定取出手术.结果 患儿均顺利完成手术,无术中严重并发症发生.手术平均40 min,出血(10±2) ml.结论 非胸腔镜辅助Nuss手术安全可行,并且不用进入胸腔操作,手术创伤更小,耗时更短,微创效果更好.     

Nuss手术矫治复杂漏斗胸95例

目的 总结Nuss手术矫治复杂漏斗胸的经验和方法.方法 2006年8月至2011年7月施行漏斗胸Nuss手术443例,其中Haller指数＞6的极重度漏斗胸、严重不对称漏斗胸、有合并症的漏斗胸、复发性漏斗胸以及需放置多根钢板方能矫形满意者纳入复杂漏斗胸范畴,共95例,依漏斗胸复杂性的不同,分别和综合采用多种改良的Nuss手术技术:多钢板、斜行钢板、双弧形钢板等个性化技术;改进钢丝固定方式;合用截骨术;辅助小切口;不同侧置入胸腔镜;合并症的分期或同期手术等.结果 95例均顺利完成手术,手术(90.13 ±39.12) min,失血量(45.41±19.23) ml,无严重术中并发症,术后并发症13.6％.术后平均住院(7.21±2.87)天,效果良好,优良率92.6％.结论 对复杂的漏斗胸采用改良的Nuss手术,综合运用多种技术能取得较满意的矫形效果.     

后置入胸腔镜辅助Nuss手术矫治漏斗胸

目的 验证非胸腔镜Nuss手术的安全性,探讨后置入胸腔镜辅助治疗漏斗胸的手术方法和治疗经验.方法 2009年9月到2010年10月,191例后胸腔镜辅助下Nuss手术治疗漏斗胸,其中男146例,女45例.年龄2.8 ～20.0岁,平均(6.46±3.66)岁.Haller指数3.2 ～16.8,平均4.68±1.84.所有病例均先行非胸腔镜Nuss手术后再用胸腔镜观察.结果 均顺利完成手术,手术27～50 min,平均( 32.49±2.79) min;出血l～l0ml,平均(2.19±0.87) ml.随访10 ～ 23个月,术后优良率100％,手术并发症13例,占6.81％.支撑架双侧均在胸膜外者18例,占9.42％;右侧在胸膜外者23例,占12.04％;左侧在胸膜外者17例,占8.90％.结论 有经验术者在掌握一定方法的前是下,非胸腔镜Nuss手术也是安全可行的,但后置入胸腔镜辅助Nuss手术治疗漏斗胸更为安全、可靠,能及时发现和处理非胸腔镜Nuss手术造成的损伤.     

漏斗胸患者Nuss手术后慢性疼痛的危险因素

目的探讨漏斗胸微创矫正术(Nuss手术)后慢性疼痛的危险因素。方法回顾性分析2013年1月至2019年9月择期行胸腔镜Nuss手术患者168例,男130例,女38例。收集患者联系方式、人口学资料、术前合并症、漏斗胸严重程度分级、神经阻滞情况、手术时间和术后24 h VAS疼痛评分。电话随访患者或家属完成术后慢性疼痛情况、术后并发症、对日常生活的影响、是否服用镇痛药物的问卷调查。根据问卷调查结果将患者分为两组:慢性疼痛组(P组)和非慢性疼痛组(N组)。采用多因素Logistic回归分析患者Nuss手术后慢性疼痛的独立危险因素。结果有78例(46.4%)发生了不同程度的慢性疼痛。P组年龄、体重明显大于N组,术前合并症比例、漏斗胸严重程度明显高于N组(P<0.001)。P组术后24 h VAS疼痛评分及术后并发症发生率明显高于N组(P<0.001),对日常生活的影响程度明显大于N组(P<0.001)。多因素logistic回归分析显示,漏斗胸严重程度分级(中度OR=3.043,95%CI 1.235~7.498;重度OR=15.856,95%CI 2.765~90.981)、术后有并发症(OR=3.642,95%CI 1.517~8.743)、术后24 h VAS疼痛评分(每增高1分OR=2.716,95%CI 1.600~4.612)是Nuss手术后慢性疼痛的独立危险因素。结论漏斗胸患者Nuss手术后慢性疼痛存在较高的发病率,漏斗胸严重程度、术后并发症和术后24 h VAS疼痛评分是漏斗胸患者Nuss手术后慢性疼痛的预警因素。     

Early results following the Nuss operation for pectus excavatum--a single-institution experience of 383 patients

The prevalence of pectus excavatum is low but many patients are disabled from this thoracic deformity. The Nuss operation is a well-established surgical correction, however, until recently it has been rarely used in Europe. We have performed the Nuss operation regularly between 2001 and 2006 where a total of 383 patients were operated on for pectus excavatum. The indication for surgery was disabling cosmetic appearance as described by the patient. Patient records were reviewed for retrospective analysis. The median age was 16 years (range 7-43) and 86% were males. A satisfactory peri-operative result was achieved in all but one patient with one pectus bar (81%), two bars (19%) and three bars in one patient. Postoperative complications included bleeding, pleural effusion, seroma and deep infection. Seven patients were reoperated because the bar dislocated. At present the bars have been removed in 73 patients and their final result was excellent in all but one. The Nuss procedure for pectus excavatum can be implemented with excellent early results and few complications. There is a surprisingly high demand for surgical correction of pectus excavatum and the number of referred patients continues to increase as patients learn about the ease of this procedure and its excellent results.     

Modification of the Nuss procedure for pectus excavatum to prevent cardiac perforation

Purpose

In a few patients, cardiac perforation and aortic injury have occurred during the Nuss procedure for pectus excavatum. The article details a modification of this procedure that enables the prevention of fatal complications.

Methods

Our subjects were 22 males and 13 females with pectus excavatum who were aged 8.2 ± 3.7 years. Their Haller's computed tomography index was 5.2 ± 1.5. An introducer is inserted into the pleura between the sternum and thymus instead of the thoracic depression under right thoracoscopic guidance. After the introducer reaches the internal cranial position of the left nipple, the thoracoscope is shifted to the left thoracic cavity. The introducer is subsequently guided to the left highest intercostal space under left thoracoscopic guidance.

Results

A single bar was inserted in 34 patients; 2 bars were required in 1 patient. The operating time was 95 ± 27 minutes and blood loss was 11 ± 6 g. Cardiac perforation did not occur in any patient.

Conclusions

Our modified technique has certain advantages: (1) the introducer does not rub against the pericardium and heart; (2) the tip of the introducer can be observed at all times with a thoracoscope; (3) the anterior mediastinum between the left and right thoracic cavities is very narrow at the cranial level; (4) the introducer can be accurately directed to the left highest intercostal space; and (5) hemostasis and no injury of the bilateral thoracic organs can be confirmed.     

非胸腔镜辅助Nuss手术矫治漏斗胸

目的 探讨非胸腔镜辅助Nuss手术治疗漏斗胸的手术方法和治疗经验.方法 2005年9月到2007年8月对108例漏斗胸患者行非胸腔镜辅助下Nuss手术,男性91例,女性17例;年龄2岁10个月～25岁,平均年龄7岁9个月;胸廓指数3.6～10.1.结果 108例患者均顺利完成手术,无术中严重并发症发生.平均手术时间40 min,平均术中出血量10 ml.术后患者顺利恢复出院.92例获得随访,随访时间2～21个月,矫形效果满意.结论 非胸腔镜辅助Nuss手术安全可行,并且不用进入胸腔操作,手术创伤更小.     

Nuss手术治疗漏斗胸6例报告

目的探讨Nuss手术治疗漏斗胸的安全性及其近期疗效。方法采用Nuss手术矫治漏斗胸6例,均在胸腔镜直视下将矫形钢板经过胸骨凹陷最低点将凹陷的胸骨撑起,使胸骨和前胸壁凸起恢复正常的形状。结果6例均顺利完成手术,无中转开放手术者。平均手术时间48（40-55）min,出血量平均10（5-20）ml。无血（气）胸、皮下气肿、切口感染、心包或心脏损伤等手术并发症。术后平均住院5（4-7）d。均获随访,平均12.3（6-18）个月,优5例,良1例。胸廓外观维持良好,未见矫形板旋转、移位或固定器滑脱等。结论Nuss手术矫治小儿漏斗胸安全有效,具有微创、塑型美观等优点;近期效果满意,远期效果还需进一步观察。