目的 探讨广州市公职人员中眼睑黄色瘤(XP)患病情况与生化检验指标异常的相关性。方法 从2018年来广州市干部和人才健康管理中心体检的公职人员中选取1 090例,其中筛选患XP人员545例,作为病例组,依性别、年龄分层随机抽取的未患XP的人员作为对照组,测定空腹血糖、血脂、甲状腺功能等生化指标,采用回顾性病例对照研究的方式,比较两组相关指标水平。P<0.05为差异有统计学意义。结果 XP的患病率为0.94%(男性为0.89%,女性为1.01%)。男性和女性的XP患病率比较差异无统计学意义(χ2=2.142,P=0.143)。两组间体质量、舒张压、血脂等多项指标上的差异具有统计学意义(P<0.05)。高体质量(OR=1.021,95%CI:1.004~1.038,P=0.017)、高舒张压(OR=1.019,95%CI:1.004~1.035,P=0.011)、低高密度脂蛋白(OR=6.127,95%CI:2.568~14.619,P<0.001)、高低密度脂蛋白(OR=2.084,95%CI:1.456~2.981,P<0.001)是患病的危险因素。结论 广州市公职人员中XP的患病率男性和女性接近;高体质量、高舒张压、高密度脂蛋白水平降低、低密度脂蛋白水平升高是患XP的危险因素。
Objective To investigate the correlation between xanthelasma palpebrarum(XP)and abnormal biochemical indices in healthy individuals in Guangzhou,China.Methods A retrospective case-control study was conducted,selecting 1 090 individuals from a total of 58 053 who underwent health examinations at the Guangzhou Cadre and Talent Health Management Centre in 2018.The case group consisted of 545 individuals diagnosed with XP,while the control group included age- and sex-matched individuals without XP,randomly selected from the same database.Biochemical indices analyzed included fasting blood glucose,blood lipids,liver and kidney function,thyroid indicators,body weight,and blood pressure.Statistical significance was set at P<0.05.Results The prevalence of XP was 0.94%(0.89% in men and 1.01% in women).No significant difference was observed in the prevalence of XP between men and women(χ2=2.142,P=0.143).Similarly,no significant differences were observed in thyroid-stimulating hormone(P=0.937),free triiodothyronine(P=0.216),free thyroxin(P=0.206),or fasting blood glucose levels(P=0.668)between the case and control groups.However,significant differences were noted in body weight,diastolic blood pressure,blood lipid levels,and liver and renal biochemical indicators between the two groups(P<0.05).Specifically,higher body weight(OR=1.021,95%CI:1.004–1.038,P=0.017),higher diastolic blood pressure(OR=1.019,95%CI:1.004–1.035,P=0.011),lower high-density lipoprotein(OR=6.127,95%CI:2.568–14.619,P<0.001),and higher low-density lipoprotein(OR=2.084,95%CI:1.456–2.981,P<0.001)were identified as risk factors for XP.Conclusions The prevalence of XP did not differ between males and females.However,high body weight,high diastolic blood pressure,low high-density lipoprotein,and high low-density lipoprotein are risk factors for XP.
目的 观察慢性阻塞性肺疾病急性加重期(AECOPD)患者应用基于Caprini量表评估的干预模式联合充气加压泵(IPC)预防静脉血栓(VTE)的效果。方法 选取河南省人民医院在2023年11月—2024年11月收入的82例AECOPD患者作为研究对象,经随机数表法分为对照组41例予以VTE常规干预,观察组41例在对照组的基础上接受基于Caprini量表评估的干预模式联合IPC预防。比较两组AECOPD患者肢体情况及深静脉血栓(VTE)发生情况、凝血指标及股静脉血流速度。结果 观察组肢体肿胀率、肢体疼痛率及VTE发生率均低于对照组(P<0.05)。干预前,两组AECOPD患者凝血酶时间(TT)、凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、D-二聚体水平比较差异无统计学意义(P>0.05);干预后,两组患者TT、PT、APTT、D-二聚体水平均降低,观察组较低(P<0.05)。干预前,两组AECOPD患者平均流速、血流峰速及阻力指数比较差异无统计学意义(P>0.05);干预后,两组患者平均流速、血流峰速均升高,观察组高于对照组(P<0.05);阻力指数均降低,观察组低于对照组(P<0.05)。结论 AECOPD患者应用基于Caprini量表评估的干预模式联合IPC能有效降低肢体肿胀率、肢体疼痛率及VTE发生率,改善凝血指标与股静脉血流速。
Objective To observe the effect of a Caprini score?based intervention model combined with intermittent pneumatic compression(IPC)in preventing venous thromboembolism(VTE)in patients with acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Methods A total of 82 AECOPD patients admitted to Henan Provincial People’s Hospital from November 2023 to November 2024 were selected as subjects and randomly divided into a control group(41 cases)and an observation group(41 cases)using a random number table.The control group received routine VTE prevention,while the observation group received the Caprini score?based intervention combined with IPC in addition to the routine care.The extremity conditions,occurrence of VTE,coagulation parameters,and femoral venous blood flow velocity were compared between the two groups.Results The rates of extremity swelling,extremity pain,and VTE incidence in the observation group were lower than those in the control group(P<0.05).Before the intervention,there were no statistically significant differences in thrombin time(TT),prothrombin time(PT),activated partial thromboplastin time(APTT),or D?dimer levels between the two groups(P>0.05).After the intervention,TT,PT,APTT,and D?dimer levels decreased in both groups,with lower values in the observation group(P<0.05).Before the intervention,there were no statistically significant differences in mean flow velocity,peak flow velocity,or resistance index between the two groups(P>0.05).After the intervention,mean flow velocity and peak flow velocity increased in both groups,with higher values in the observation group(P<0.05),while the resistance index decreased,with a lower value in the observation group(P<0.05).Conclusions The application of a Caprini score?based intervention model combined with IPC in AECOPD patients can effectively reduce the rates of extremity swelling,extremity pain,and VTE incidence,and improve coagulation parameters and femoral venous blood flow velocity.
目的 合并肺纤维化的慢性阻塞性肺疾病(COPD)是COPD的特殊亚型,患者兼具气流受限与肺组织纤维化病理特征,临床症状更严重、肺功能下降更快,且现有单一治疗方案难以同时改善气流受限与纤维化进展,预后较差。基于此,本研究旨在分析尼达尼布联合格隆溴铵治疗合并肺纤维化的COPD患者的效果及对肺功能的影响,为优化临床治疗方案提供依据。方法 选取2022年3月—2024年12月收治的96例合并肺纤维化的COPD患者,采用前瞻性随机对照研究设计,应用随机数字表法分为试验组与对照组。所有患者均采取常规治疗,对照组48例采取尼达尼布治疗,试验组采取尼达尼布联合格隆溴铵治疗。两组均治疗24周后,比较治疗前后症状评分、肺功能、纤维化指标、炎症指标,并分析两组治疗安全性。结果 治疗后,两组CAT评分、mMRC评分及VAS降低(P<0.05);且与对照组比较,试验组CAT评分、mMRC评分及咳嗽VAS评分较低(P<0.05)。治疗后,两组FVC、FEV1、DLCO及FEV1/FVC比值均较治疗前改善(P<0.05);且与对照组比较,试验组FVC、FEV1、DLCO及FEV1/FVC比值较优(P<0.05)。治疗后,两组血清KL-6、SP-D水平及CT纤维化评分均降低(P<0.05);且与对照组比较,试验组血清KL-6、SP-D水平及CT纤维化评分较低(P<0.05)。治疗后,两组血清IL-6、TNF-α及TGF-β1水平降低(P<0.05);且与对照组比较,试验组血清IL-6、TNF-α及TGF-β1水平较低(P<0.05)。试验组总不良反应发生率为8.33%(4/48),对照组为10.42%(5/48),两组比较差异无统计学意义(P>0.05)。结论 尼达尼布联合格隆溴铵治疗合并肺纤维化的COPD效果良好,可减轻患者临床症状,改善肺功能与肺纤维化,降低机体炎症反应,安全性较高。
Objective To analyze the effects of the combination of nintedanib and glycopyrrolate in treating chronic obstructive pulmonary disease(COPD)patients with associated pulmonary fibrosis and its impact on lung function,providing a basis for optimizing clinical treatment strategies.Methods Ninety-six COPD patients with pulmonary fibrosis admitted from March 2022 to December 2024 were selected,and divided into experimental group and control group using a random number table method.Using a prospective randomized controlled study design,all patients received conventional treatment,with 48 cases in the control group receiving treatment with nintedanib and the experimental group receiving treatment with nintedanib combined with glycopyrrolate bromide.After 24 weeks of treatment in both groups,the symptom scores,lung function,fibrosis indicators,and inflammation indicators were compared before and post-treatment,and the drug safety of the two groups was analyzed.Results Post-treatment,CAT score,mMRC score and VAS decreased in both groups(P<0.05).Compared with the control group,CAT score,mMRC score and cough VAS score were lower in the experimental group(P<0.05).Post-treatment,FVC,FEV1,DLCO and FEV1/FVC ratio of both groups improved compared with that before treatment(P<0.05).Compared with the control group,FVC,FEV1,DLCO and FEV1/FVC ratio of the experimental group were better(P<0.05).Post-treatment,serum KL-6,SP-D levels and CT fibrosis scores of both groups decreased(P<0.05).Compared with the control group,serum KL-6,SP-D levels and CT fibrosis scores of the experimental group were lower(P<0.05).Post-treatment,serum IL-6,TNF-α and TGF-β1 levels in both groups decreased(P<0.05).Compared with the control group,serum IL-6,TNF-α and TGF-β1 levels in the experimental group were lower(P<0.05).The incidence of total adverse reactions in the experimental group was 8.33%(4/48),and that in the control group was 10.42%(5/48).There was no difference between the two groups(P>0.05).Conclusions The combination of nintedanib and glycopyrrolate has a significant effect on the treatment of COPD complicated with pulmonary fibrosis,which can alleviate its clinical symptoms,improve lung function and pulmonary fibrosis,reduce the body’s inflammatory response,which is relatively safe.
目的 通过年龄、性别等多方面研究各亚型注意缺陷多动障碍(ADHD)儿童的智力结构分布特征的临床研究,为ADHD的个体化干预提供科学依据。方法 实验组纳入ADHD儿童754例,其中注意缺陷型(ADHD-I)280例(37.13%)、多动-冲动型(ADHD-HI)212例(28.12%)、混合型(ADHD-C)262例(34.75%),按年龄分为三组:低龄组(6~8岁)、中龄组(9~11岁)及高龄组(12~14岁);对照组为正常儿童412例,为同期选择的性别、年龄相匹配的儿童。选择采用韦氏智力评估等方法分别对两组儿童进行评估等,对评估结果进行比较和综合分析。结果 ADHD儿童的智力评估结果低于对照组(P<0.01),且在言语智商方面表现更为明显,在各分测验中以A因子(言语理解)和C因子(记忆/注意集中)为主,而B因子(知觉组织能力)方面则无差异。ADHD-HI型及ADHD-C型的总智商及操作智商均高于ADHD-I型,ADHD-C型言语智商和A因子均高于ADHD-I型(P<0.01),ADHD-HI型的智力水平最高,而ADHD-I型与ADHD-C型的智力水平差异无统计学意义(P>0.05)。各年龄段ADHD儿童的智力发育均受到不同程度的影响,尤其是中龄组儿童及高龄组女童所受影响更明显;低、中龄组儿童的智力发育水平均高于高龄组儿童,提示ADHD儿童的智力损害随年龄增长而加重;同一年龄段ADHD女童的智力损害较男童更为严重。结论 本地区6~14岁ADHD儿童的智力水平较低,以言语智商低下更为明显,ADHD-HI型在3个亚型中智力损害最小,ADHD儿童的智力损害随年龄增长而加重,同一年龄段ADHD女童的智力损害较男童更为严重。
Objective To investigate the distribution characteristics of intellectual structure in children with different subtypes of attention deficit hyperactivity disorder(ADHD)by age and gender,providing scientific basis for individualized treatment and intervention of ADHD.Methods The experimental group consisted of 754 children with ADHD,including 280 cases(37.13%)of inattentive type(ADHD-I),212 cases(28.12%)of hyperactivity impulsive type(ADHD-HI),and 262 cases(34.75%)of combined type(ADHD-C).They were divided into three groups by age:young group(6-8 years old),middle group(9-11 years old),and older group(12-14 years old).The control group consisted of 412 normal children with matched sex and age recruited during the same period and had similar sex ratio.The specific methods of Wechsler Intelligence Scale were mainly applied to evaluate normal children and children with ADHD,and the evaluation results were subjected to multidimensional analysis and comparison.Results The intelligence assessment results of ADHD children were significantly lower than those of the control group(P<0.01),with a more pronounced performance in verbal intelligence.In various sub tests,factors A(verbal comprehension)and C(memory and attention concentration)were the main factors,while there was no difference in factor B(perceptual organization ability).The ADHD-HI and ADHD-C types had higher total intelligence and operational intelligence than the ADHD-I type,and the ADHD-C type had higher verbal intelligence and factor A than the ADHD-I type(P<0.01).The intelligence level of the ADHD-HI type is the highest,while there is no statistically significant difference in intelligence level between the ADHD-I type and the ADHD-C type.The intellectual development of children in different age groups was affected to varying degrees,especially in the middle and older groups of girls.This study found that the intellectual development of children in the young and middle group was higher than that of children in the older group,indicating that the intellectual development of ADHD children will be increasingly damaged with age.At the same time,it was also found that ADHD girls in the same age group had more severe intellectual development impairment than boys.Conclusions The intelligence level of children with ADHD aged 6-14 in this region is relatively low,with verbal intelligence quotient being more pronounced.ADHD-HI has the smallest intellectual impairment among the three subtypes,and the intellectual development of ADHD children becomes more severe with age.ADHD girls in the same age group have more severe intellectual development impairment than boys.
目的 分析药品集中带量采购(集采)政策下医院药品供应保障实况,提出优化政策及保障的对策建议。方法 通过提取重庆市渝北区人民医院2023年1月—2024年12月集采药品供应采购数据,描述性统计分析集采药品供应情况。结果 采购的416个中标药品中,69个在购销合同期内短缺,短缺率16.59%。短缺原因与企业生产能力、季节性需求波动相关,季节性强,以慢性病药和抗感染药为主。结论 建议建立监测平台、完善报告制度、制定应急预案、评估供货能力,保障供应。
Objective To analyzes the current situation of hospital drug supply guarantee under the policy of centralized and volume-based procurement(hereinafter referred to as “central procurement”),and proposes optimization strategies and suggestions for the policy and guarantee.Methods By extracting the procurement data of drugs supplied through centralized procurement at Yubei District People’s Hospital in Chongqing from January 2023 to December 2024,descriptive statistical analysis of the drug supply situation through centralized procurement was conducted.Results Among the 416 selected drugs purchased,69 were in short supply during the contract period,with a shortage rate of 16.59%.The reasons for the shortage were related to the production capacity of the enterprise,seasonal demand fluctuations,strong seasonality,and mainly chronic diseases and anti-infective.Conclusions It is suggested to build a monitoring platform,improve the reporting system,formulate emergency plans,and evaluate the supply capacity to ensure supply.
目的:评估血细胞分离机单采制备自体富血小板血浆(PRP)治疗雄激素性脱发(AGA)的疗效及安全性。方法:纳入31例AGA患者,采用单采技术制备血小板浓度803~1669×10?/L的自体PRP,激活后行头皮注射治疗3次(间隔1个月)。于基线(T1)及每次治疗后1、2、3个月(T2~T4)评估毛发密度与不良反应。结果:患者均为男性。毛发密度由T1的(111.77±12.00)根/cm2升至T4的(133.74±16.34)根/cm2(均P<0.001)。医师评估有效率80.6%,患者满意率74.2%。主要不良反应为注射部位出血、肿痛及灼热感,均自行缓解;1例出现额部及眼睑明显水肿,5 d后消退。结论:单采自体PRP治疗AGA疗效确切且安全。规范控制PRP制备质量及血小板浓度有助于优化疗效。
Objective: To evaluate the clinical efficacy and safety of autologous platelet-rich plasma (PRP) prepared via apheresis using a blood cell separator for the treatment of androgenetic alopecia (AGA). Methods: A total of 31 patients with AGA who completed the study were enrolled. Autologous PRP with a platelet concentration of 803-1669×10?/L was prepared using apheresis technology. After activation, the PRP was administered via intralesional scalp injections for a total of 3 sessions at 1-month intervals. Hair density changes and adverse reactions were evaluated at baseline (T1) and at 1, 2, and 3 months after the initial treatment (T2-T4). Results: All included patients were male. Hair density significantly increased from (111.77±12.00) hairs/cm2 at baseline to (133.74±16.34) hairs/cm2 at T4 (all P<0.001). The clinician-evaluated effective rate was 80.6%, and the patient satisfaction rate was 74.2%. The primary adverse reactions included hemorrhage, swelling, burning sensation, and transient pain at the injection site, all of which resolved spontaneously. Notably, 1 patient developed marked edema in the forehead and eyelids, which subsided spontaneously after approximately 5 days. Conclusion: Autologous PRP prepared via apheresis is effective and safe for the treatment of AGA. Standardized quality control of PRP preparation and platelet concentration may contribute to further optimizing the therapeutic outcomes.
肛周脓肿术后防瘘是临床的关注点,本文基于“治未病”思想,提出覆盖肛周脓肿术后防瘘全周期的防治策略,包括未病调体质、调摄饮食、优化手术、加强创面管理降低风险,既发截断病势、辨证防治并发症及局部干预防蔓延,康复期整体调养与随访促愈防复,为中医药在肛周脓肿术后防瘘的临床实践应用方面提供参考。
Prevention of fistula formation after perianal abscess surgery is a clinical concern. Based on the concept of "treating disease before it arises," this paper proposes a comprehensive prevention and treatment strategy covering the entire cycle of fistula prevention after perianal abscess surgery, including regulating constitution before disease onset, adjusting diet, optimizing surgery, strengthening wound management to reduce risk, interrupting disease progression after onset, treating complications based on syndrome differentiation, and local intervention to prevent spread. During the rehabilitation period, holistic recuperation and follow-up are emphasized to promote healing and prevent recurrence, providing a reference for the clinical application of traditional Chinese medicine in preventing fistula after perianal abscess surgery.
目的:探讨沙库巴曲缬沙坦钠对慢性心力衰竭(CHF)患者心电稳定性及心脏负荷的改善作用。方法:病例纳入2023年10月~2025年5月收治的102例CHF患者为研究对象,依据就诊时间段及治疗方案不同,将2023年3月~2024年6月沿用缬沙坦+螺内酯+比索洛尔治疗的51例患者列为常规组,将2024年7月~2025年9月采用沙库巴曲缬沙坦+螺内酯+比索洛尔治疗的51例患者列为试验组,比较两组患者的心肌纤维化,心电稳定性,心脏负荷及治疗安全性。所有患者均接受为期半年随访,比较两组患者的预后情况。结果:治疗后,试验组的基质金属蛋白酶-2(MMP-2)、基质金属蛋白酶-9(MMP-9)、半乳糖凝集素-3(Gal-3)、可溶性生长刺激表达基因2蛋白(sST2)均低于常规组(t=5.045,2.889,4.115,4.582;P<0.05)。试验组的校正QT间期(QTc)、QT离散度(QTd)、T波峰-末间期(Tp-e)、室性早搏次数分别为(405.39±40.26)ms、(45.25±5.33)ms、(90.33±5.28)ms、(80.36±5.39)次/24h,均低于常规组[(450.22±42.19)ms、(50.37±6.15)ms、(95.29±6.44)ms、(85.27±6.18)次/24h](t=5.490,4.493,4.253,4.276;P<0.05)。试验组的收缩期肺动脉压(sPAP)、三尖瓣反流峰值速度(TRVmax)、左心室舒张末期内径(LVEDD)、左心室收缩末期内径(LVESD)分别为(20.48±5.26)mmHg、(2.13±0.25)m/s、(45.29±5.62)mm、(30.61±5.33)mm,均低于常规组[(25.35±6.29)mmHg、(3.22±0.47)m/s、(50.45±6.15)mm、(35.49±6.27)mm](t=4.242,14.622,4.423,4.235;P<0.05)。试验组的药物相关副反应发生率与常规组比较,差异无统计学意义(P>0.05)。截至随访结束时,试验组的不良预后发生率9.80%(5/51)低于常规组27.45%(14/51)(x2=5.239;P<0.05)。结论:沙库巴曲缬沙坦钠能延缓CHF患者的心肌纤维化进程并改善心电稳定性,在有效改善心电稳定性并降低不良预后发生风险同时未显著增加治疗风险。
Objective:To explore the improvement effect of sacubitril valsartan sodium on electrocardiogram stability and cardiac load in patients with CHF.Methods:A total of 102 CHF patients admitted from October 2023 to May 2025 were included in the study. Based on the treatment period and regimen, 51 patients treated with valsartan, spironolactone, and bisoprolol from March 2023 to June 2024 were classified as the conventional group, while 51 patients treated with sacubitril/valsartan, spironolactone, and bisoprolol from July 2024 to September 2025 were designated as the experimental group. The myocardial fibrosis, electrocardiographic stability, cardiac workload, and treatment safety were compared between the two groups. All patients underwent a six-month follow-up to assess their prognosis.Results:After treatment, the levels of MMP-2, MMP-9, Gal-3, and sST2 in the experimental group were lower than the control group (t=5.045,2.889,4.115,4.582; P<0.05). The QTc, QTd, Tp-e, and number of ventricular premature beats in the experimental group were (405.39 ± 40.26) ms, (45.25 ± 5.33) ms, (90.33 ± 5.28) ms, and (80.36 ± 5.39) beats per 24 hours, lower than the control group [(450.22 ± 42.19) ms, (50.37 ± 6.15) ms, (95.29 ± 6.44) ms, and (85.27 ± 6.18) beats per 24 hours] (t=5.490,4.493,4.253,4.276; P<0.05). The sPAP, TRVmax, LVEDD, and LVESD of the experimental group were (20.48 ± 5.26) mmHg, (2.13 ± 0.25) m/s, (45.29 ± 5.62) mm, and (30.61 ± 5.33) mm, lower than the conventional group [(25.35 ± 6.29) mmHg, (3.22 ± 0.47) m/s, (50.45 ± 6.15) mm, and (35.49 ± 6.27) mm] (t=4.242,14.622,4.423,4.235; P<0.05). The incidence of drug-related side effects in the experimental group was not significantly different from that in the control group (P>0.05). As of the end of follow-up, the incidence of poor prognosis in the experimental group was 9.80% (5/51) lower than that in the conventional group 27.45% (14/51) (x2=5.239; P<0.05).Conclusion:Sacubitril valsartan sodium can delay the progression of myocardial fibrosis and improve electrocardiogram stability in CHF patients, effectively improving electrocardiogram stability and reducing the risk of adverse prognosis without significantly increasing treatment risk.
【摘要】目的:探讨器械护士术中分区精细化器械管理对心脏瓣膜置换术(HVR)手术效率及安全性的影响。方法:研究对象包括2024年6月~2026年5月至我院行HVR治疗的110例心脏瓣膜病(VHD)患者,以及同期参与手术的22名器械护士,采用随机数字表法将入组患者及护士分别列为常规组(55例患者、11名护士)、试验组(55例患者、11名护士),常规组内护士术中实施常规器械管理,试验组内护士术中实施分区精细化器械管理。比较两组患者的手术效率、围手术期安全事件,以及两组护士所参与手术的工作效率、术中器械管理情况。结果:在不同器械管理模式下,试验组内患者的主动脉阻断时间、体外循环时间、术中非必要等待时间、手术总耗时均低于常规组(t=8.817,5.730,20.609,9.632;P<0.05)。试验组内患者的围手术期安全事件发生率9.09%(5/55)低于常规组25.45%(14/55)(x2=5.153;P<0.05)。试验组内护士的器械摆台时间、器械传递反应时间、手术中断次数、器械整理时间、器械移交时间均低于常规组(t=3.347,6.505,5.971,3.795,5.838;P<0.05)。试验组内护士的器械管理差错率低于常规组(x2=5.238;P<0.05)。结论:器械护士术中分区精细化器械管理能提高HVR患者的手术效率并降低围手术期安全事件发生风险,对提高器械护士的器械管理质量、预防器械管理差错有积极影响
[Abstract]Objective:To explore the impact of refined intraoperative instrument management by operating room nurses on the efficiency and safety of HVR surgery.Methods:The study subjects included 110 patients with VHD who underwent HVR treatment at our hospital from June 2024 to May 2026, along with 22 instrument nurses who participated in the surgeries synchronously. Using the random number table method, the enrolled patients and nurses were divided into a control group (55 patients, 11 nurses) and an experimental group (55 patients, 11 nurses). Nurses in the conventional group implemented routine instrument management during surgery, while nurses in the experimental group implemented zoned and refined instrument management during surgery. The surgical efficiency, perioperative safety events of the two groups of patients, as well as the work efficiency and intraoperative instrument management of the surgeries participated by the nurses in the two groups were compared.Results:Under different instrument management modes, the aortic occlusion time, extracorporeal circulation time, intraoperative non-essential waiting time, and total surgical time of patients in the experimental group were all lower than the control group (t=8.817,5.730,20.609,9.632; P<0.05). The incidence of perioperative safety events in the experimental group was 9.09% (5/55) lower than that in the control group 25.45% (14/55) (x2=5.153; P<0.05). The instrument placement time, instrument delivery response time, number of surgical interruptions, instrument sorting time, and instrument handover time of nurses in the experimental group were lower than those in the control group (t=3.347,6.505,5.971,3.795,5.838; P<0.05). The error rate of nurses in the experimental group was lower than the control group (x2=5.238; P < 0.05).Conclusion:Refined intraoperative zone-specific instrument management by instrument nurses enhances surgical efficiency for HVR patients and reduces the risk of perioperative safety incidents, thereby positively impacting the quality of instrument care provided by nurses and preventing instrument-related adverse events.
目的 对比三维中等权重压缩感知并行采集序列(3D IW-CS-SENSE)与常规并行采集序列(3D IW-SENSE)在膝关节磁共振成像中的扫描时间、图像质量及诊断效能。方法 前瞻性采集100例膝关节磁共振影像。对比两组三维序列的定量指标、主观评分以及对损伤分级的准确率。结果 IW-CS-SENSE序列扫描时间显著缩短(122.0 ± 28.0 s vs. 221.0 ± 49.0 s,p<0.001)。IW-CS-SENSE序列信噪比、对比噪声比及显示效果评分均低于IW-SENSE序列(p<0.001),但IW-CS-SENSE序列的SENSE伪影评分更优(5.00 ± 0.00 vs. 4.59 ± 0.62,p<0.001)。两序列对半月板、韧带及软骨损伤分级的准确率均无统计学差异(p值分别为0.33,0.58和0.15)。 结论 3D IW-CS-SENSE序列可显著缩短扫描时间和消除SENSE伪影,同时保持与4倍加速3D IW-SENSE序列相当的诊断效能。
Objective To compare the imaging times, image quality, and diagnostic performance of three-dimensional (3D) intermediate-weighted compressed sensing sensitivity encoding (IW-CS-SENSE) sequence with conventional 3D IW-SENSE sequence in knee MR imaging. Methods MR images of one hundred knees were obtained prospectively. The quantitative indices, qualitative scores, and grading accuracies between the two 3D sequences were compared. Results Imaging times of IW-CS-SENSE sequences were significantly reduced (122.0 ± 28.0 s vs. 221.0 ± 49.0 s, p < 0.001). The signal-to-noise ratios, contrast-to-noise ratios, and visualization scores of IW-CS-SENSE sequences were significantly lower than IW-SENSE sequences (p < 0.001), while scores of SENSE artefact for IW-CS-SENSE sequences were superior (5.00 ± 0.00 vs. 4.59 ± 0.62, p < 0.001). The accuracies in grading meniscal, ACL, and cartilage tears were comparable between the two sequences (p = 0.33, p = 0.58 and p = 0.15, respectively). Conclusion 3D IW-CS-SENSE sequences can reduce scanning time significantly and eliminate SENSE artefacts, while maintaining the same diagnostic performance as the 4-fold accelerated 3D IW-SENSE sequences.