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 探讨桑白皮汤加减辅助常规西药治疗痰热郁肺型保留比率的肺功能减损(PRISm)患者的治疗效果,并分析其对中医证候积分、肺功能、气道阻力、免疫功能的影响。方法 选取2024年6月~2025年6月于本院诊治的88例PRISm患者为研究对象,按照随机数字表法将其分为对照组(常规西药治疗)、研究组(桑白皮汤加减联合常规西药治疗),各44例。比较两组临床疗效、不良反应及治疗前后中医证候积分、慢阻肺评估测试(CAT)量表、改良版英国医学研究委员会呼吸困难问卷(mMRC)、吸入支气管扩张剂后检测肺功能、肺弥散功能[一氧化碳弥散量占预计值百分比(DLCO%pred)、残气量/肺总量(RV/TLC)]、气道阻力[抗阻指数(R5-20)、共振频率(Fres)、呼吸总阻抗(Zrs)]、炎症指标[白细胞介素-6(IL-6)、可溶性细胞间黏附分子-1(sICAM-1)、单核细胞趋化蛋白-1(MCP-1)、嗜酸性粒细胞(EOS)、肿瘤坏死因子-α(TNF-α)]、气道重塑[基质金属蛋白酶-2(MMP-2)、缺氧诱导因子-1α(HIF-1α)、转化生长因子-β1(TGF-β1)、碱性成纤维细胞生长因子(bFGF)]、T淋巴细胞亚群水平。结果 研究组总有效率高于对照组(P<0.05);治疗后,与对照组比较,研究组中医证候积分、CAT评分、mMRC评分级RV/TLC降低,FEV1、FEV1/FVC、FEV1%pred、VC%pred、DLCO%pred升高(P<0.05);治疗后,与对照组比较,研究组R5-20、Fres、Zrs降低(P<0.05);治疗后,与对照组比较,研究组血清IL-6、sICAM-1、MCP-1、EOS、TNF-α及MMP-2、HIF-1α、TGF-β1、bFGF水平降低(P<0.05);治疗后,与对照组比较,研究组CD3+、CD4+、CD4+/CD8+水平升高(P<0.05);两组不良反应比较无明显差异(P>0.05)。结论 桑白皮汤加减辅助常规西药治疗PRISm患者的疗效显著,可改善临床症状、肺功能,提高生活质量,降低气道阻力,并可减轻炎症反应,缓解气道重塑,增强机体免疫功能,且具有一定安全性。
目的 分析布地格福吸入、无创正压通气(NIPPV)联合治疗慢性阻塞性肺疾病急性加重(AECOPD)合并呼吸衰竭的效果。方法 本研究采用回顾性对照研究。选取2024-06—2025-05我院96例AECOPD合并呼吸衰竭者,根据治疗方案不同分组,每组48例。对照组接受NIPPV治疗,研究组接布地格福吸入、NIPPV联合治疗,持续治疗1周。观察并对比两组疗效、病情程度、血气指标[动脉血二氧化碳分压(PaCO2)、动脉血氧分压(PaO2)]、肺功能[最大呼气压(MEP)、一秒率(FEV1/FVC)]、炎性因子指标[C反应蛋白(CRP)、白介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)]、氧化应激指标[超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、过氧化脂质(LPO)]及不良反应。结果 研究组治疗有效率为91.67%(44/48),高于对照组75.00%(36/48)(P<0.05);治疗1周后与对照组相比,研究组mMRC分值、CAT分值均较低(P<0.05);治疗1周后,与对照组相比,研究组MEP、FEV1/FVC、PaO2较高,PaCO2较低(P<0.05);治疗1周后与对照组相比,研究组CRP、TNF-α、IL-6较低(P<0.05);治疗1周后与对照组相比,研究组SOD、GSH-Px较高,LPO较低(P<0.05);两组不良反应无明显差异(P>0.05)。结论 布地格福吸入、NIPPV联合治疗AECOPD合并呼吸衰竭,可明显减轻症状,改善血气指标与肺功能,抑制炎症反应,调节氧化应激,且保障安全性。
目的 探讨慢性阻塞性肺疾病急性加重期血嗜酸性粒细胞(EOS)、血清白细胞介素-5(IL-5)水平与第一秒用力呼气容积(FEV1)、第一秒用力呼气容积与用力肺活量的比值(FEV1/FVC)、用力肺活量(FVC)的相关性。方法 纳入2023年3月—2024年3月于佛山市顺德区第五人民医院住院的73例慢性阻塞性肺疾病急性加重期患者,以2%作为外周血EOS比例(EOS%)截断值分为两组,研究组(EOS%≥2%)34例,对照组(EOS%<2%)39例,收集两组患者的一般临床资料、实验室检查结果、肺功能检查结果(FEV1、FVC、FEV1/FVC),比较组间差异,分析指标间的相关性。结果 对照组与实验组患者EOS%分别为0.5(0.1,0.9)%、5.15(2.60,10.05)%,两组患者EOS%差异有统计学意义(P<0.05)。对照组与实验组患者IL-5水平分别为0.98(0.56,1.78)ng/L、3.6(1.73,6.77)ng/L,两组IL-5水平差异有统计学意义(P<0.05)。对照组FEV1(L)、FVC(L)、FEV1/FVC水平分别为1.32(1.18,1.58)、2.07(1.92,2.62)、0.62(0.57,0.67);实验组分别为1.24(1.00,1.52)、2.22(1.94,2.56)、0.58(0.47,0.67),两组FEV1、FVC、FEV1/FVC水平差异均无统计学意义(P>0.05)。Spearman等级相关检验结果显示,EOS%与IL-5水平呈正相关(rs=0.870,P<0.001);按组别进行分层后结果显示,对照组、试验组EOS%与IL-5水平均呈正相关(rs=0.820,P<0.001;rs=0.938,P<0.001)。EOS%、IL-5水平与FEV1、FEV1/FVC呈负相关(P<0.05),与FVC不相关(rs=0.039,P>0.05)。对照组EOS%、IL-5水平与FEV1、FEV1/FVC、FVC不相关(P>0.05);实验组EOS%、IL-5水平与FEV1、FEV1/FVC呈负相关(P<0.05),与FVC不相关(P>0.05)。结论 慢性阻塞性肺疾病急性加重期血EOS%与血清IL-5水平呈正相关,外周血EOS%≥2%时血EOS%、血清IL-5与FEV1、FEV1/FVC呈负相关,与FVC无关。
Objective To explore the correlation among blood eosinophil levels,serum interleukin-5(IL-5)levels,and forced expiratory volume in one second(FEV1),the ratio of forced expiratory volume in one second to forced vital capacity(FEV1/FVC),and forced vital capacity(FVC)during the acute exacerbation of chronic obstructive pulmonary disease(AECOPD).Methods From March 2023 to March 2024,73 patients hospitalized for AECOPD at Shunde District Fifth People’s Hospital of Foshan City were included,and divided into two groups based on a cutoff value of 2% for peripheral blood eosinophil(EOS%).The experimental group(EOS%≥2%)included 34 patients,while the control group(EOS%<2%)included 39 patients.General clinical data,laboratory test results,and pulmonary function test results(FEV1,FVC,FEV1/FVC)were collected from both groups.Results The median quartiles of EOS% for the control group and experimental group were 0.5(0.10.9)% and 5.15(2.60,10.05)%,respectively.There was a statistically significant difference between the EOS% of two groups(P<0.05).The median quartiles of IL-5 levels for the control group and experimental group were 0.98(0.56,1.78)ng/L and 3.6(1.73,6.77)ng/L,respectively.There was also a statistically significant difference in IL-5 levels between the two groups(P<0.05).For the control group,the median quartiles of FEV1,FVC,and FEV1/FVC were 1.32(1.18,1.58),2.07(1.92,2.62)and 0.62(0.57,0.67),respectively.For the experimental group,they were 1.24(1.00,1.52),2.22(1.94,2.56)and 0.58(0.47,0.67)respectively.There was no statistically significant difference between the two groups in FEV1,FVC and FEV1/FVC levels(P<0.05).Spearman rank correlation analysis showed a positive correlation between EOS% and IL-5 level (rs=0.870,P<0.001).Stratified by group,both the control and experimental groups showed a positive correlation between EOS% and IL-5 level (rs=0.820,P<0.001;rs=0.938,P<0.001).There was a negative correlation between EOS%,IL-5 level,and FEV1,FEV1/FVC(P<0.05),but no correlation with FVC(P>0.05).In the control group,there was no correlation between EOS%,IL-5 level,and FEV1,FEV1/FVC,or FVC(P>0.05).In the experimental group,there was a negative correlation between EOS%,IL-5 level,and FEV1,FEV1/FVC(P<0.05),but no correlation with FVC(P>0.05).Conclusions During AECOPD,blood EOS% is positivelycorrelated with serum IL-5 levels.When peripheral blood eosinophils are ≥2%,blood EOS%,serum IL-5,and FEV1,FEV1/FVC are negatively correlated,while there is no correlation with FVC.
目的 探讨支气管镜灌洗用于儿童重症肺部感染合并肺实变的治疗效果及对CT特征、肺功能的影响。方法 选取2022年5月—2024年5月铜仁市人民医院收治的100例重症肺部感染合并肺实变患儿开展前瞻性研究,应用随机数表法分为对照组和观察组,每组各50例。对照组患儿采取常规治疗,观察组则采取常规治疗加支气管镜灌洗治疗。对比其临床疗效,治疗前后炎症因子、CT特征及肺功能变化。结果 观察组治疗总有效率高于对照组(P<0.05);治疗后观察组患儿白细胞计数(10.36±2.52)×109/L、白细胞介素-6(20.57±5.05)ng/L、C反应蛋白(13.12±2.64)mg/L、降钙素原(101.62±12.16)pg/L均低于对照组白细胞计数(13.25±3.32)×109/L、白细胞介素-6(31.69±4.11)ng/L、C反应蛋白(16.16±4.44)mg/L、降钙素原(113.46±18.11)pg/L(P<0.05);治疗后两组患儿胸腔积液、支气管壁增厚、空气支气管征、肺部实变、磨玻璃影等相关CT影像特征占比下降,且观察组低于对照组(P<0.05);治疗后两组患儿呼气流量峰值水平均升高,观察组(90.67±18.45)L/s高于对照组(81.27±17.69)L/s,用力肺活量水平均更高,观察组(3.33±0.68)L高于对照组(2.68±0.25)L(P<0.05)。结论 针对儿童重症肺部感染合并肺实变,在常规治疗基础上增加支气管镜灌洗可提升临床疗效,减轻机体炎症反应,改善胸部CT各种表现及肺功能。
Objective To explore the therapeutic effects of bronchoalveolar lavage in children with severe pulmonary infection complicated by lung consolidation and its impact on CT features and pulmonary function.Methods A prospective study was conducted on 100 children with severe pulmonary infection complicated with pulmonary consolidation in a hospital from May 2022 to May 2024.They were randomly divided into observation group and control group using a random number table method,50 cases in each group.The control group of children received routine treatment,and the observation group received conventional treatment plus bronchoalveolar lavage.Clinical efficacy,inflammatory factors,CT features,and alterations in pulmonary function before and after therapy were compared.Results The total effective rate of the observation group was higher than that of the control group(P<0.05).After treatment,the white blood cell count(10.36±2.52)×109/L,interleukin-6(20.57±5.05)ng/L,C-reactive protein(13.12±2.64)mg/L,and procalcitonin(101.62±12.16)pg/L in the observation group were all lower than those in the control group(13.25±3.32)×109/L,interleukin-6(31.69±4.11)ng/L,C-reactive protein(16.16±4.44)mg/L,and procalcitonin(113.46±18.11)pg/L(P<0.05).After treatment,the proportion of CT imaging features such as pleural effusion,bronchial wall thickening,air bronchogram sign,lung consolidation,ground glass opacities,decreased in both groups of children,and the observation group was lower than the control group(P<0.05).After treatment,the peak levels of expiratory flow in both groups of children increased,with the observation group(90.67±18.45)L/s higher than the control group(81.27±17.69)L/s.The forced vital capacity levels were also higher,with the observation group(3.33±0.68)L higher than the control group(2.68±0.25)L(P<0.05).Conclusions Adding bronchoalveolar lavage to routine treatment for children with severe pulmonary infection complicated with pulmonary consolidation can improve their clinical efficacy,alleviate inflammatory reactions,and improve various chest CT manifestations and lung function.
目的 探究肺炎支原体(MP)感染大叶性肺炎患儿常规通气、脉冲振荡肺功能特点。方法 将2022年5月—2023年5月广州市妇女儿童医疗中心收治的90例MP感染大叶性肺炎患儿为观察组,通气体检健康儿童50例为对照组,依据病变将累及多肺叶作为观察A组(10例),累及单肺叶作为观察B组(80例)。均接受常规通气与脉冲振荡肺功能测定,观察测定结果,以此为基础,分析肺功能特点。结果 观察组各常规通气肺功能指标测定结果均低于对照组健康儿童,差异有统计学意义(P<0.05)。观察组R5、R20的实测值/预计值高于对照组,X5实测值低于对照组,差异有统计学意义(P<0.05)。气道阻力指标与肺功能呈负相关关系(P<0.05)。观察组两组最大肺活量(VCMAX)、呼气流量峰值(PEF)、用力肺活量(FVC)75%、FVC50%、FVC25%的实测值/预计值差异无统计学意义,观察A组患儿FVC、FEV1的实测值/预计值低于观察B组患儿,差异有统计学意义(P<0.05)。两组患儿脉冲振荡肺功能对比差异无统计学意义(P>0.05)。90例患儿中,常规通气异常患儿12例,患儿治疗前后VCMAX、FVC75%、FVC50%的实测值/预计值差异无统计学意义,患儿治疗前FVC、FEV1、PEF、FVC25%的实测值/预计值均低于治疗后,差异有统计学意义(P<0.05)。结论 常规通气与脉冲振荡相关性良好,气道阻力对VCMAX及FVC具有反向作用,MP感染大叶性肺炎主要表现为小气道通气功能受损,气道阻力升高。
Objective To explore the lung function characteristics of routine ventilation and pulse oscillation in children with lobar pneumonia infected with Mycoplasma pneumoniae(MP).Methods Ninety children with MP infected lobar pneumonia admitted to Guangzhou Women and Children's Medical Center from May 2022 to May 2023 were selected as the observation group,and 50 healthy children undergoing ventilation examination were selected as the control group.Based on the lesion,cases with multi lobar involvement were selected as the observation group A(10 cases),cases with single lobar involvement were selected as the observation group B(80 cases).All patients underwent routine ventilation and pulse oscillation received pulmonary function measurement,and the measurement results were observed.Based on this,the characteristics of lung function were analyzed.Results The results of routine ventilation lung function indicators in the observation group were lower than those in the control group,and the difference was statistically significant(P<0.05).The measured/expected values of R5 and R20 in the observation group were higher than those in the control group,while the measured values of X5 were lower than those in the control group,with statistical significance(P<0.05).There is a negative correlation between airway resistance indicators and lung function(P<0.05).The measured/predicted values of vital capacity max(VCMAX),peak expiratory flow(PEF),forced vital capacity(FVC)75%,FVC50%,and FVC25% in the observation group were not with statistically significant difference.The measured/predicted values of FVC and FEV1 in the observation group A were lower than those in the observation group B,and the difference was statistically significant(P<0.05).There was no statistically significant difference in pulmonary function between the two groups of pediatric patients with pulse oscillation(P>0.05).Among the 90 patients,12 had abnormal conventional ventilation.The measured/predicted values of VCMAX,FVC75%,and FVC50% before and after treatment were not significantly different.The measured/predicted values of FVC,FEV1,PEF,and FVC25% before treatment were lower than those after treatment,and the difference was statistically significant(P<0.05).Conclusions There is good correlation between conventional ventilation and pulse oscillation.Airway resistance has a reverse effect on VCMAX and FVC.MP infected lobar pneumonia is mainly characterized by impaired small airway ventilation function and increased airway resistance.
目的 探讨福莫特罗联合格隆溴铵对慢性阻塞性肺疾病急性加重期(AECOPD)患者的疗效。方法 选择2021年1月—2023年6月廉江市人民医院收治的97例AECOPD患者进行研究,在双方知情基础上,通过单双号抽签方式分组,抽取单号纳入对照组(n=48,予以福莫特罗治疗),抽取双号纳入观察组(n=48,予以福莫特罗联合格隆溴铵治疗),对比两组肺功能指标、血气指标、症状改善情况及出现的不良反应。结果 治疗后两组的肺功能指标均高于治疗前,而观察组各指标高于对照组(P<0.05);治疗后两组PaO2高于治疗前,PaCO2低于治疗前,且观察组上述血气指标与对照组比较差异有统计学意义(P<0.05);治疗后两组的CAT及SGRQ评分均低于治疗前,其中观察组评分低于对照组(P<0.05);观察组(8.33%)与对照组(12.24%)不良反应率比较,差异不显著(P>0.05)。结论 采用福莫特罗联合格隆溴铵治疗AECOPD患者,有助于改善患者肺功能,使其血气指标得到改善,还可有效缓解其呼吸道症状,且安全性得到保障。
Objective To explore the curative effect of formoterol combined with glycopyrronium bromide on patients with acute exacerbation of chronic obstructive pulmonary disease(AECOPD). Methods The research cut-off period was from January 2021 to June 2023.A total of 97 patients with AECOPD were selected from Lianjiang People's Hospital for research.On the basis of mutual knowledge,they were divided into groups by odd and even numbers.The odd numbers were drawn into the control group(n=48,treated with formoterol)and the odd numbers were drawn into the observation group(n=48,treated with formoterol+glycopyrronium bromide),the pulmonary function index,blood gas index,symptom improvement and adverse reactions were compared between the two groups. Results After treatment,the lung function indexes of the two groups were higher than those before treatment,while the indexes of the observation group were higher than those of the control group(P<0.05).PaO2 was higher and PaCO2 was lower in the two groups after treatment,and the blood gas indexes in the observation group were different from those in the control group(P<0.05).The scores of COPD assessment test and St. George's Respiratory Questionaire in the two groups after treatment were lower than those before treatment,while the scores in the observation group were lower than those in the control group(P<0.05);There was no significant difference between the observation group(8.33%)and the control group(12.24%)(P>0.05). Conclusions The choice of formoterol and qualified ammonium bromide for AECOPD is helpful to improve the lung function,blood gas index and respiratory symptoms,And the security is guaranteed.
目的 探讨乙酰半胱氨酸泡腾片联合布地格福气雾剂治疗慢性阻塞性肺疾病疗效及对患者肺功能的影响。方法 以2020年4月—2022月4月在本院诊治的84例慢性阻塞性肺疾病患者作为研究对象,根据1∶1简单分配原则把患者分为联合组与对照组各42例。对照组行传统治疗,联合组在对照组治疗的基础上,再给予乙酰半胱氨酸泡腾片联合布地格福气雾剂治疗,联合组与对照组都治疗观察4周。检测患者的疗效、肺功能与血清超敏C反应蛋白(hs-CRP)与降钙素原(PCT)含量变化情况。结果 联合组治疗后的总有效率与对照组相比有提高(P<0.05)。治疗后,联合组与对照组的第一秒用力呼气容积占用力肺活量百分比(FEV1/FVC)、第一秒用力呼气容积占预计值百分比(FEV1%)更高(P<0.05),且联合组与对照组对比有提高(P<0.05)。联合组治疗后的疾病影响、活动能力、症状部分等SGRQ生活质量评分与对照组相比降低(P<0.05)。联合组与对照组治疗后的血清 hs-CRP与 PCT含量低于治疗前(P<0.05),联合组与对照组相比也降低(P<0.05)。结论 乙酰半胱氨酸泡腾片联合布地格福气雾剂治疗慢性阻塞性肺疾病能有效抑制hs-CRP、PCT的表达,能促进改善患者的肺功能,提高治疗效果与生活质量。
Objective To investigate the efficacy of acetylcysteine effervescent tablets combined with budigraf aerosol in the treatment of chronic obstructive pulmonary disease(COPD)and its effect on the pulmonary function of patients.Methods From April 2020 to April 2022,a total of 84 patients with COPD diagnosed and treated in our hospital were selected as the research objects,and the patients were divided into the combination group and the control group with 42 cases in each group,according to the 1∶1 simple allocation principle.The control group were given traditional treatment,and the combination group were given acetylcysteine effervescent tablets combined with budigraf aerosol additionally.Both the combined group and the control group were observed for 4 weeks.The efficacy of patients,lung function and serum hypersensitive C-reactive protein(hs-CRP)and procalcitonin(PCT)levels were detected.Results The total effective rates after treatment in the combination group were higher than the control group(P<0.05).After treatment,The forced expiratory volume in 1 second/forced vital capacity(FEV1/FVC),FEV1% value of the two groups were higher(P<0.05),and the combination group had greater improvement(P<0.05).The SGRQ quality of life scores,such as disease impact,activity ability,and symptom in the combination group were lower(P<0.05).After treatment,the serum high-sensitivity C-reactive protein(hs-CRP)and procalcitonin(PCT)levels in the two groups were significantly lower(P<0.05),and the combined group decreased more(P<0.05).Conclusions Acetylcysteine effervescent tablets combined with budigraf aerosol in the treatment of COPD can effectively inhibit the expression of hs-CRP,PCT,promote the improvement of lung function,improve the treatment effect and quality of life.
目的 探讨苏黄止咳胶囊联合多索茶碱对慢性持续期支气管哮喘的疗效及对肺功能、呼出气一氧化氮(FeNO)的影响。方法 选择2020年3月—2022年3月70例慢性持续期支气管哮喘患者,随机分为2组各35例,对照组仅予以多索茶碱治疗,研究组在对照组基础上加服苏黄止咳胶囊治疗。治疗3个月,采用哮喘控制测试(ACT)对患者进行评估,记录哮喘急性加重、急救药物使用情况及急诊入院情况,测定肺功能和呼出FeNO。结果 2组治疗1月的ACT评分比较无统计学意义(P>0.05),治疗2、3个月时研究组的ACT评分高于对照组(P<0.05)。研究组哮喘急性加重次数、急救药物使用次数均少于对照组(P<0.05),而2组急诊入院次数比较差异无统计学意义(P>0.05)。与基线值相比,2组治疗3个月时的肺功能指标无改变(P>0.05)且组间比较差异亦无统计学意义(P>0.05);2组治疗3个月时的FeNO无改变(P>0.05),而研究组的FeNO低于对照组(P<0.05)。结论 苏黄止咳胶囊联合多索茶碱治疗慢性持续期支气管哮喘可降低FeNO,提高哮喘控制水平。
Objective To investigate the effect of Suhuang Zhike capsule combined with doxofylline on chronic persistent bronchial asthma, pulmonary function and exhaled nitric oxide(FeNO).Methods Seventy patients with chronic persistent bronchial asthma from March 2020 to March 2022 were randomly divided into two groups, 35 cases in each group.The control group was only treated with doxofylline, and the study group was treated with Suhuang Zhike capsule additionally.After 3 months of treatment, the patients were evaluated by asthma control test(ACT), the acute exacerbation of asthma was recorded, and the pulmonary function and exhaled FeNO were measured.Results There was no statistical significance in the ACT score of the two groups after one month of treatment(P>0.05).The ACT scores of the study group after two months and three months of treatment were significantly higher than those of the control group(P<0.05).The times of acute exacerbation of asthma and the use of emergency drugs in the study group were less than those in the control group(P<0.05), but there was no significant difference in the number of emergency hospitalizations between the two groups(P>0.05).Compared with the baseline value, there was no significant change in lung function indexes in the two groups after 3 months of treatment(P>0.05).Compared with the baseline value, there was no significant change in FeNO in the two groups after 3 months of treatment(P<0.05), while FeNO in the study group was lower than that in the control group(P<0.05).Conclusions Suhuang Zhike capsule combined with doxofylline in the treatment of chronic persistent bronchial asthma can reduce FeNO and improve the level of asthma control.
目的 探究新斯的明拮抗顺阿曲库铵的时机对患者腹腔镜结直肠癌根治术后肌松残留和早期肺功能的影响。方法 选取于2021年2月—2022年9月在我院行结肠癌根治手术的194例患者为研究对象,以随机数字表法将患者分为空白对照组和试验组,然后结合给予新斯的明治疗时所体现的4个成串刺激(TOF)比值将试验组患者分为试验组A(TOF≤0.1)、试验组B(0.10.8)。对比组间肌松残余情况以及肺功能情况。结果 插管前,试验组A患者TOF比值低于其他组(P<0.01),空白对照组患者TOF比值高于其他组(P<0.01);空白对照组分别与试验组A~E在复苏室接受观察的时间比较,差异无统计学意义(P>0.01);试验组A患者肌松恢复指数低于其他组(P<0.01),空白对照组患者肌松恢复指数高于其他组(P<0.01)。插管前、拔管0.5 h以及拔管24 h时,组间1秒用力呼气容积(FEV1)、用力肺活量(FVC)和FEV1/FVC比较差异无统计学意义(P>0.05)。结论 结直肠癌根治术后给予新斯的明,有助于加快肌松恢复,但不会影响复苏室停留时间与肺功能水平。
Objective To investigate the effect of timing of neostigmine antagonizing cisatracurium on residual muscle relaxation and early lung function in patients underwent laparoscopic radical resection of colorectal cancer.Methods February 2021 to September 2022,194 patients who underwent radical colon cancer surgery in our hospital were selected as the research subjects.The patients were randomly divided into a blank control group and an experimental group using a random number table method.Then,combined with the train-of-four(TOF)ratios observed during neostigmine treatment,the experimental group patients were divided into experimental group A(TOF≤0.1),experimental group B(0.10.8).The residual muscle relaxation and lung function between groups were compared.Results Before intubation,the TOF ratio of patients in experimental group A was lower than that of other groups(P<0.01),while the TOF ratio of patients in the blank control group was higher than that of other groups(P<0.01).There was no significant difference in the observation time between the blank control group and the experimental group A~E in the postanesthesia care unit(P>0.01).The muscle relaxation recovery index of patients in experimental group A was lower than that of other groups(P<0.01),while the muscle relaxation recovery index of patients in the blank control group was higher than that of other groups(P<0.01).There were no significant differences in force expiratory volume in one second(FEV1),forced Vital capacity(FVC)and FEV1/FVC between groups before intubation,0.5 h after extubation and 24 h after extubation(P>0.05).Conclusions Administration of neostigmine after radical surgery for colorectal cancer can accelerate muscle relaxation recovery,but it will not affect the residence time of the postanesthesia care unit and lung function levels.