Superior laryngeal nerve block for treatment of throat pain and cough following laryngeal herpes zoster:A case report

BACKGROUND Herpes zoster is caused by reactivation of latent varicella-zoster virus infection within the sensory nerve ganglion of the spinal or cranial nerves.Laryngeal herpes zoster is rare and involves superior laryngeal nerve,which leads to several complications such as throat pain,and cough.CASE SUMMARY Patient concerns:A 52-year old woman presented with a 70 d history of throat pain and a 67 d history of non-productive cough.Three days after onset of pain,she was diagnosed with laryngeal herpes zoster.Flexible nasolaryngoscopy revealed multiple white ulcerated lesions on the left hemi epiglottis and the left supraglottic area.She was prescribed with 750 mg famciclovir a day for 7 d,and 150 mg pregabalin,100 mg tramadol and 10 mg nortriptyline a day for 67 d.However,despite of these medications,she complained of pain and persistent cough.Therefore,superior laryngeal nerve block under ultrasound guidance was performed.Three days after the intervention,the throat pain and cough disappeared.The patient remained symptom-free at 3 mo follow-up.CONCLUSION A superior laryngeal nerve block can be an effective option for treatment of pain and cough following laryngeal herpes zoster.

Efficacy ofβ2-adrenergic receptor agonist combined with corticosteroid in the treatment of children with cough variant asthma

BACKGROUND Cough variant asthma(CVA)is one of the most common respiratory diseases in children,which has a serious impact on the quality of life and daily activities of children.For severe CVA,immunomodulatory drugs are needed.AIM To evaluate the efficacy of salmeterol combined with budesonide in the treatment of pediatric CVA.METHODS 130 children with CVA from January 2020 to December 2022 were prospectively selected and randomly divided into an observation group(salmeterol combined with budesonide)and a control group(budesonide combined with a placebo).Compare the clinical efficacy of two groups before and after intervention.The evaluation parameters include cough frequency score,nocturnal cough arousal,and lung function indicators.Serum inflammatory markers,immune function markers and airway anatomical indicators were also measured.RESULTS After the intervention,the total effective rate of the observation group was significantly higher than that of the control group,and the cough frequency score and the night cough wake rate of the observation group were lower than that of the control group,with a statistically significant difference.In addition,the changes of lung function indicators,serum markers and immune function markers in the observation group were better than those in the control group.CONCLUSION The clinical efficacy of salmeterol combined with Budesonide in the treatment of CVA is better than that of Budesonide alone.

SRC:Superior Robustness of COVID-19 Detection from Noisy Cough Data Using GFCC

This research is focused on a highly effective and untapped feature called gammatone frequency cepstral coefficients(GFCC)for the detection of COVID-19 by using the nature-inspired meta-heuristic algorithm of deer hunting optimization and artificial neural network(DHO-ANN).The noisy crowdsourced cough datasets were collected from the public domain.This research work claimed that the GFCC yielded better results in terms of COVID-19 detection as compared to the widely used Mel-frequency cepstral coefficient in noisy crowdsourced speech corpora.The proposed algorithm's performance for detecting COVID-19 disease is rigorously validated using statistical measures,F1 score,confusion matrix,specificity,and sensitivity parameters.Besides,it is found that the proposed algorithm using GFCC performs well in terms of detecting the COVID-19 disease from the noisy crowdsourced cough dataset,COUGHVID.Moreover,the proposed algorithm and undertaken feature parameters have improved the detection of COVID-19 by 5%compared to the existing methods.

A systemaic review and meta-analysis of traditional Chinese medicine in the treatment of chronic cough

Objective: To systematically evaluate the safety and efficacy of traditional Chinese medicine (TCM) in the treatment of chronic cough. Methods: Databases CNKI, WanFang Data, VIP, CBM, PubMed, Web of Science, Cochrane Library from inception to February 2021 were electronically searched by two researchers, to collect randomized controlled trials (RCTs) of traditional Chinese medicine in the treatment of chronic cough, UACS/PNDS, CVA, EB, AC, GERD and other types of cough. Revman 5.3 software was used to analyze and summarize the collected literature, and the methodological quality of the included studies was evaluated by the bias risk assessment scale of Cochrance Collaboration Network. Results: A total of 26 articles involving 2 820 patients, with 1 420 in the experimental group and 1 400 in the control group were included. The results of meta-analysis showed that compared to the control group which was treated with western medicine alone, TCM significantly improved the clinical effective rate [RR=1.20, 95% CI(1.16,1.25), P<0.000 01], alleviated cough syndrome score [SMD=-0.83, 95% CI(-1.21,-0.44)], and enhenced the score of quality of life [MD=-2.18, 95%CI(1.63,2.74), P<0.000 01];at the same time, the experimental group was better than the control group in improving lung function and reducing the time of cough relief. In terms of safety, a total of 24 patients in 5 literatures had adverse reactions, but the symptoms were mild and could be relieved quickly. In addition, there was no significant difference in adverse reactions between the control group and the experimental group, showing good safety. Conclusion: TCM treatment can significantly improve the cure rate of cough, reduce cough score, improve systemic symptoms, relieve psychological anxiety, improve lung function, and improve cough symptoms rapidly, with good safety.

Experimental study on the regulation effect of Qiaoqin Qingfei agent on cough variant asthma based on airway neurogenic inflammation

Objective:To investigate the mechanism of regulation of airway neurogenic inflammation by Qiaoqin Qingfei agent in rats with cough variant asthma(CVA).Methods:48 SD rats were randomly divided into blank group,model group,montelukast sodium group(1.05 mg/kg)and high,medium and low dose groups(26,13,6.5 g/kg),with 8 rats in each group.The rat CVA model was established by the method of ovalbumin(OVA)combined with aluminum hydroxide(Al(OH)3)sensitization and repeated stimulation.From the second day of sensitization,the rat CVA model was given by gavage for 28 days.The pathological changes of lung tissue were observed under microscope by HE staining.The content changes of nerve growth factor(NGF)and substance P(SP)in alveolar lavage fluid(BALF)were determined by double-antibody sandwich ABC-ELISA,and the protein expression levels of NGF and SP in lung tissue were detected by immunohistochemistry.Results:Pathological findings showed significant inflammatory manifestations in the model group,and the inflammatory infiltration in the high-dose,medium-dose and low-dose groups of Qiaoqin Qingfei agent and montelukast sodium groups were alleviated to varying degrees.Compared with blank group,the protein expression levels of NGF and SP in lung tissue of model group were significantly increased(P<0.01).Compared with model group,the protein expression levels of NGF and SP in lung tissue and the contents of NGF and SP in alveolar lavage fluid in high-dose,medium-dose and low-dose groups and montelukast sodium group were significantly decreased(P<0.05).Conclusion:Qiaoqin Qingfei agent may reduce airway inflammation and relieve cough variant asthma by regulating the protein expression levels of NGF and SP in airway neurogenic inflammation.

丙泊酚复合低剂量艾司氯胺酮应用于无痛超声支气管镜检查的效果

目的:评估丙泊酚复合低剂量艾司氯胺酮应用于无痛超声支气管镜(EBUS)检查的效果。方法:纳入2022年4月至8月在郑州大学第一附属医院行无痛EBUS检查的96例患者(年龄18~65岁,BMI 18.5~28.0 kg/m^(2),ASAⅡ或Ⅲ级),随机分为艾司氯胺酮组和对照组,每组48例。对照组麻醉诱导方案为丙泊酚1.5 mg/kg+阿芬太尼30μg/kg+米库氯铵0.15 mg/kg,艾司氯胺酮组在此基础上加用艾司氯胺酮0.25 mg/kg;术中根据患者反应持续泵注瑞芬太尼0.25~4.00μg/(kg·min)和丙泊酚4~6 mg/(kg·h)。记录苏醒期呛咳程度和发生率,记录麻醉前、麻醉诱导后、超声支气管镜进入声门时、穿刺时和苏醒即刻的平均动脉压和心率,记录检查时间、苏醒时间、拔管时间及不良反应发生情况。结果:艾司氯胺酮组苏醒期呛咳程度及发生率均低于对照组(P<0.05);艾司氯胺酮组平均动脉压和心率波动幅度均小于对照组(P<0.05);艾司氯胺酮组低血压、心动过缓发生率低于对照组(P<0.05);两组检查时间、苏醒时间、拔管时间及不良反应发生率(包括心动过速、头晕、躁动、视力模糊)比较,差异均无统计学意义(P>0.05)。结论:丙泊酚复合低剂量艾司氯胺酮能降低无痛EBUS检查苏醒期呛咳的发生,且血流动力学更稳定。

Effect of glycyrrhetinic acid on Th1/Th2 balance in cough variant asthma mice

Objective:To evaluate the therapeutic effect of Glycyrrhetinic Acid on cough variant asthma(CVA)mice and to investigate the possible mechanism in reducing lung inflammation.Methods:48 young female Balb/c mice were divided into Control,CVA,Prednisone Acetate,Glycyrrhetinic Acid high-dose,Glycyrrhetinic Acid middle-dose and Glycyrrhetinic Acid lowdose groups randomly,with 8 mice in each group.The CVA mice model was established by ovalbumin(OVA)sensitization and OVA challenge,the animal asthma behavior was observed after drug administration,and the index of the lung of mice were recorded.The level of OVAsIgE in the bronchoalveolar lavage fluid(BALF)was tested by ELISA.The pathological changes of the lung tissue were observed by Hematoxylin and Eosin(H&E)staining.The protein expressions of T-bet,IFN-γ,Gata3,IL-4 and IL-13 in the lung tissue were determined by Western blot.Results:Compared with the CVA group,the index of lung of mice,the OVA-sIgE level in BALF and expression levels of Th2-related factor in the lung tissue of mice in Prednisone Acetate and Glycyrrhetinic Acid groups were significantly decreased(P<0.05 or P<0.01),the infiltration of inflammatory cells in the lung tissue was reduced,while expressions of Th1-related factor in the lung tissue was significantly increased(P<0.05 or P<0.01).Conclusion:Glycyrrhetinic acid has therapeutic effect on CVA mice,the underlying mechanism of Glycyrrhetinic acid alleviating lung impairment and airway inflammation may be associated with mediating the Th1/Th2 imbalance in the lung tissue.

孟鲁司特钠单用、布地奈德/福莫特罗单用及两者联用治疗对儿童咳嗽变异型哮喘的疗效比较

目的本研究旨在比较孟鲁司特钠(Mon)单用、布地奈德/福莫特罗(BF)单用及两者联用治疗儿童咳嗽变异型哮喘(CVA)的疗效。方法选取2021年6月至2023年6月北京市海淀医院诊治的CVA患儿为研究对象。根据治疗方案,将CVA患儿分为Mon组、BF组和联合组。观察治疗8周后的治疗总有效率(TER)、不良反应发生率(TAER)、咳嗽症状评分[日间咳嗽症状评分(DCSS)和夜间咳嗽症状评分(NCSS)]、免疫功能[肿瘤坏死因子-α(TNF-α)、白细胞介素-4(IL-4)和免疫球蛋白E(IgE)]、肺功能[第1秒用力呼出气体容量(FEV_(1))、肺活量(FVC)和呼气峰值流速(PEF)]和血清嗜酸性粒细胞计数(EOS)。结果共选取180例CVA患儿,Mon组62例,BF组60例,联合组58例。治疗后,3组TER、TAER、DCSS、NCSS、血清TNF-α、血清IL-4和血清IgE水平差异无统计学意义(P>0.05)。联合组患儿FEV_(1)、FVC和PEF显著高于Mon组和BF组(P<0.05),EOS显著低于Mon组和BF组(P<0.05);而Mon组和BF组FEV1、FVC、PEF和EOS学差异无统计学意义(P>0.05)。结论Mon或BF可有效改善CVA患儿咳嗽症状和免疫功能,其镇咳作用和抗炎作用同Mon和BF联用相似。此外,Mon和BF联用可进一步改善CVA患儿肺功能,减少血清EOS水平。

名中医杨毅从“以平为期”理论探讨中医治疗肺癌思路

总结杨毅教授治疗肺癌的临床思路,临证时注重外感祛邪宣肺为要,因势利导。内伤调理脏腑为主,以平为安,辨证施治,匠心独运,验效颇丰。现择取杨师验案进行分析,为治疗肺癌拓宽思路,提高临床疗效。

基于网络药理学探讨紫苏子—杏仁药对治疗咳嗽变异性哮喘的作用机制

目的 基于网络药理学探讨紫苏子—杏仁药对治疗咳嗽变异性哮喘(CVA)的潜在分子作用靶点及机制。方法 采用中药系统药理学数据库和分析平台(TCMSP)数据库对紫苏子—杏仁药对的有效活性成分进行筛选,并采用SwissTargetPrediction网站进行靶点预测。采用GeneCards数据库检索CVA相关靶点,借助Venny 2.1.0获取交集靶点,对交集靶点分别运用Cytoscape 3.9.1软件和STRING数据库构建主要活性成分—潜在治疗靶基因网络图和PPI蛋白互作网络,并筛选出关键有效活性成分和核心靶蛋白,通过DAVID数据库对交集靶点进行GO功能及KEGG通路的富集分析。结果 筛选出紫苏子—杏仁药对有效成分19个,与CVA相关靶点224个,核心靶点为AKT1、IL-6、TP53、SRC、MAPK3、EGFR、JUN、PTGS2、HSP90AA1、ESR1。GO功能富集分析显示分子功能165个、细胞组分79个、生物过程630个。KEGG通路富集分析显示得到信号通路155条,主要涉及cAMP信号通路、PI3K-Akt信号通路、癌症通路、化学致癌—受体激活通路、神经活性配体—受体相互作用等。结论 紫苏子—杏仁药对可通过多成分、多靶点、多通路的协同作用抗CVA。

调和五脏辨治咳嗽浅析

咳嗽既是一种独立疾病,又是一种临床常见病症,可见于多种其他疾病,若咳嗽反复发作、迁延不愈会严重影响人们的工作和生活。本课题组基于“五脏六腑皆令人咳”理论,在临证实践过程中,审病因以分外感内伤,析主症以辨寒热虚实,参兼症以定五脏六腑,尤善于剖析五脏致咳病机,辨析咳嗽脏腑病位,注重调和脏腑功能,明析痰液性质,重视宣降肺气,恢复肺之宣肃而达到治疗咳嗽的目的。文章总结了本课题组调和五脏辨治咳嗽的经验成果。

小儿咳嗽变异性哮喘标准治疗后停药1年复发的影响因素及其交互效应

目的研究咳嗽变异性哮喘(CVA)患儿标准治疗后停药一年复发的影响因素及其交互效应。方法回顾性分析2018年1月-2020年1月玉林市红十字会医院收治的167例CVA患儿的临床资料,所有患儿均接受吸入性糖皮质激素(ICS)规范治疗(疗程≥6个月),停药后随访观察≥2年,按照患儿2年的随访结果,将CVA标准治疗后停药1年复发的98例患儿纳为CVA复发组,69例未复发纳为CVA未复发组,进行对照研究,分析CVA复发影响因素及其交互效应。结果单因素分析得出两组患儿反复呼吸道感染病史、变应性鼻炎、过敏性皮炎及停药时呼出气一氧化氮(FeNO)比较,差异有统计学意义(P<0.05)。多因素分析得出,有反复呼吸道感染病史(OR=4.543,P=0.001)、有变应性鼻炎(OR=7.146,P<0.001)、FeNO>20.00 ppb(OR=3.770,P=0.001)为CVA标准治疗后停药一年复发独立危险因素。反复呼吸道感染病史与变应性鼻炎、反复呼吸道感染病史与FeNO、变应性鼻炎与FeNO的交互作用指数S分别为2.152、1.527、1.397。结论有反复呼吸道感染、变应性鼻炎和FeNO>20.00ppb均是影响CVA标准治疗后停药1年复发的影响因素,且两两因素间有正向交互作用。

温润辛金方治疗微寒恋肺型咳嗽变异型哮喘的临床疗效研究

目的:观察温润辛金方治疗微寒恋肺型咳嗽变异型哮喘(CVA)的临床疗效及安全性,为CVA的中医临床治疗提供依据和思路。方法:选取2017年6月~2019年12月期间于某院就诊的60例微寒恋肺型CVA患者,根据随机数字表法分为对照组和观察组,每组30例。对照组给予沙美特罗替卡松吸入粉雾剂,观察组给予温润辛金方,两组均治疗6周。观察两组患者的中医证候疗效以及不良反应,比较两组患者治疗前后呼出气一氧化氮(FeNO)及咳嗽症状积分的变化。结果:对照组和观察组分别脱落2例和4例。两组临床治疗总有效率比较无统计学差异(P>0.05)。治疗后,两组咳嗽症状积分、FeNO均较治疗前下降(P<0.05),且观察组咳嗽症状积分低于对照组(P<0.05),但两组FeNO水平比较无统计学差异(P>0.05)。观察组有2例患者在服药期间出现恶心等胃部不适,嘱其改为饭后服药后症状消失;对照组有2例患者出现轻微不良反应,但不影响后续治疗。结论:温润辛金方可有效改善微寒恋肺型CVA患者的临床症状和咳嗽症状积分,临床疗效较佳且安全性良好。

极低剂量右美托咪定对老年患者全身麻醉苏醒期呛咳的影响

目的探讨极低剂量右美托咪定对老年患者颈动脉支架置入术(CAS)全身麻醉苏醒期呛咳的影响。方法选择择期行CAS的无症状单侧重度颈动脉狭窄老年患者111例,男75例,女36例,年龄≥65岁,BMI 18~32 kg/m^(2),ASAⅡ或Ⅲ级。采用随机数字表法将患者分为两组:右美托咪定组(D组,n=55)和对照组(C组,n=56)。D组于麻醉诱导前给予右美托咪定0.2~0.5μg/kg,麻醉诱导后至手术结束前30 min静脉输注极低剂量右美托咪定0.1~0.2μg·kg^(-1)·h^(-1);C组不给予右美托咪定。两组麻醉方案及术中用药方案相同。记录麻醉诱导前15 min(T_(0))、麻醉诱导后5 min(T_(1))、支架置入前5 min(T_(2))、支架置入后5 min(T_(3))、气管拔管后5 min(T_(4))的MAP和HR。记录术中丙泊酚和瑞芬太尼用量、麻醉苏醒期呛咳、躁动、呼吸抑制(SpO_(2)<90%)、拔管时间以及术后穿刺处感染、术后24 h VAS疼痛评分、术后恶心呕吐的发生情况。结果与C组比较,D组T_(1)、T_(2)时MAP明显升高,T_(3)、T_(4)时MAP明显降低,T_(1)、T_(3)、T_(4)时HR明显减慢(P<0.05),术中丙泊酚和瑞芬太尼用量明显减少(P<0.05),麻醉苏醒期呛咳、躁动发生率明显降低(P<0.05)。两组呼吸抑制发生率、拔管时间、术后24 h VAS疼痛评分以及术后恶心呕吐发生率差异无统计学意义,两组均未发生术后穿刺处感染。结论极低剂量右美托咪定可有效维持术中血流动力学稳定性,降低麻醉苏醒期呛咳、躁动发生率,且不增加术后不良反应,提高全身麻醉苏醒质量。

标准化分级药学监护服务在慢性气道疾病住院患者中的多维价值分析

目的 为构建慢性气道疾病住院患者科学、合理的药学服务新模式提供参考。方法 选取2023年10月-2024年3月在河北省人民医院呼吸科住院并接受药学监护(PC)服务的慢性阻塞性肺疾病及哮喘急性加重的患者250例,采用随机数字表法将其分成对照组(125例)和观察组(125例)。对照组患者住院期间全程给予一般药学服务,观察组患者住院期间全程给予标准化分级PC服务。比较不同PC服务模式在患者临床价值指标、人文价值指标及质量管理指标间的差异。结果 在临床价值评价指标中,观察组患者的疾病治疗目标达成率、吸入装置正确使用得分、药品不良反应发生率、解决药物相关问题数量均显著优于对照组(P<0.05)。在人文价值评价指标中,观察组的患者用药依从性得分、药师干预成功率、患者满意度均显著高于对照组(P<0.05)。在质量管理评价指标中,观察组患者的药品费用占比、静脉用药占比、抗菌药物使用率、抗菌药物使用强度均显著优于对照组(P<0.05);观察组药事服务例数也多于对照组,但两组间各项药事服务例数占比的差异无统计学意义(P>0.05)。结论 标准化分级PC服务可帮助药师识别更需要关注和管理的高危患者,提高药师工作效率,提升患者就医体验,是值得推广的新型药学服务模式。

苏黄止咳胶囊联合盐酸西替利嗪片治疗感冒后咳嗽的效果

目的 探讨苏黄止咳胶囊联合盐酸西替利嗪片治疗感冒后咳嗽的效果。方法 选取2020年10月至2022年2月感冒后咳嗽患者90例,随机数字法分为3组,A组接受苏黄止咳胶囊治疗30例,B组接受盐酸西替利嗪片治疗30例,C组为上述药物联合应用治疗30例,对3组所得不同治疗结局进行分析。结果 3组治疗前咳嗽症状总评分、咳嗽视觉模拟评分、FeNO水平对比,差异无统计学意义(P>0.05);C组治疗后咳嗽总评分、咳嗽视觉模拟评分,优于A、B组(P<0.05);A、B组治疗后咳嗽总评分、咳嗽视觉模拟评分对比,差异无统计学意义(P>0.05);C组治疗后FeNO水平优于A、B组(P<0.05);A、B组治疗后FeNO水平对比,差异无统计学意义(P>0.05);C组治疗有效率,高于A、B组(P<0.05);A、B组治疗有效率差异无统计学意义(P>0.05)。A、B、C组治疗前EV1/FVC较治疗后显著偏低(P<0.05),组间EV1/FVC差异无统计学意义(P>0.05)。结论 感冒后咳嗽患者,使用苏黄止咳胶囊与盐酸西替利嗪片治疗,可有效改善患者临床咳嗽症状,提高治疗有效率,临床价值较为明显。

推拿联合闪罐改善儿童肺炎支原体肺炎后慢性咳嗽临床观察

目的 观察小儿推拿联合闪罐改善儿童肺炎支原体肺炎(MPP)后慢性咳嗽的治疗效果。方法 选取72例MPP后慢性咳嗽患儿,随机分为试验组36例和对照组36例。试验组采用小儿推拿联合闪罐交替进行治疗,对照组予孟鲁司特钠咀嚼片口服。比较2组患儿治疗前后咳嗽视觉模拟(VAS)评分、简易咳嗽程度(CET)评分、临床疗效。结果 治疗后,2组患儿咳嗽VAS评分、CET评分均降低(P<0.05),试验组各评分改善程度优于对照组(P<0.05);试验组总有效率高于对照组(P<0.05)。结论 小儿推拿联合闪罐能够减轻MPP后患儿咳嗽严重程度,实现对患儿气道高反应性的良性调节,降低咳嗽对患儿日常生活及心理的影响,相对单纯口服孟鲁司特钠具备一定优势,值得在临床上进一步推广应用。

加味芎蝎散对咳嗽高敏综合征大鼠神经源性炎症的影响

目的探讨加味芎蝎散对咳嗽高敏综合征大鼠咳嗽及神经源性炎症的影响。方法取雄性SD大鼠36只,随机选取6只作为正常组,剩余大鼠采用密室烟熏法建立咳嗽高敏综合征模型。将造模成功大鼠随机分成5组,每组6只。加味芎蝎散高、中、低剂量组分别给予加味芎蝎散12 g/(kg·d)、6 g/(kg·d)、3 g/(kg·d)灌胃,磷酸可待因组给予磷酸可待因10 mg/(kg·d)灌胃,正常组及模型组给予等量蒸馏水灌胃,均连续灌胃3周。分别在灌胃1周、2周、3周末进行咳嗽反应检测,记录3 min内的咳嗽次数;灌胃3周后,HE染色观察肺组织病理形态,尼氏染色观察大脑皮质神经元尼氏体,免疫组化法检测支气管组织中P物质(SP)、降钙素基因相关肽(CGRP)、瞬态电压感受器阳离子通道(TRPV1)蛋白和大脑皮质中白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)表达情况。结果与正常组比较,模型组大鼠咳嗽次数明显增多(P<0.05);支气管黏膜上皮变性,平滑肌层排列紊乱、增生,管壁大量炎性细胞浸润;神经元细胞形态不规则,尼氏体减少;支气管组织中SP、CGRP、TRPV1蛋白表达积分光密度值和大脑皮质中IL-6、IL-1β表达积分光密度值均明显升高(P均<0.05)。与模型组比较,加味芎蝎散高、中剂量组大鼠咳嗽次数明显减少(P均<0.05),病理变化均有不同程度的减轻,支气管组织中SP、CGRP、TRPV1蛋白表达积分光密度值和大脑皮质中IL-6、IL-1β表达积分光密度值均明显降低(P均<0.05)。结论加味芎蝎散可以明显减轻咳嗽高敏综合征大鼠气道上皮及大脑皮质神经元病变,抑制咳嗽反射,机制可能与抑制神经源性炎症有关。

布地奈德雾化吸入治疗肺炎支原体感染后咳嗽的效果分析

目的:分析布地奈德雾化吸入治疗肺炎支原体感染后咳嗽的效果。方法:选取2022年5月—2023年5月武警山西总队医院收治的肺炎支原体感染后咳嗽患者90例作为研究对象,采用抽签法随机分为试验组和对照组,每组45例。对照组给予常规止咳治疗,试验组在对照组基础上应用布地奈德粉吸入剂雾化吸入治疗。比较两组咳嗽症状积分、治疗效果、肺功能指标。结果:治疗前,两组咳嗽症状积分无显著差异(P>0.05);治疗后,两组咳嗽症状积分降低,且试验组低于对照组(P<0.05)。试验组治疗总有效率高于对照组(P=0.044)。治疗前,两组肺功能指标无显著差异(P>0.05);治疗后,两组第1秒用力呼气容积、用力肺活量、第1秒用力呼气容积/用力肺活量、呼气峰值流量升高,且试验组高于对照组(P<0.05)。结论:布地奈德雾化吸入治疗肺炎支原体感染后咳嗽的效果显著,可减轻患者咳嗽症状,改善肺功能。

咳嗽变异性哮喘患儿血清25(OH)D_(3)、IL-6水平变化与T淋巴细胞免疫平衡的关系及预测预后的价值分析

目的分析咳嗽变异性哮喘(CVA)患儿血清25-羟维生素D_(3)[25(OH)D_(3)]、白介素-6(IL-6)水平变化与T淋巴细胞免疫平衡的关系及预测预后的价值。方法选取98例CVA患儿作为研究组,49例健康儿童作为对照组。比较两组一般资料、血清25(OH)D_(3)、IL-6水平、T淋巴细胞免疫平衡指标,分析研究组血清25(OH)D_(3)、IL-6水平与免疫平衡指标的相关性,比较治疗4周后不同预后患儿治疗前后血清25(OH)D_(3)、IL-6水平及变化值(以△表示治疗前后变化值的绝对值),分析△25(OH)D_(3)、△IL-6与预后的相关性及治疗前血清25(OH)D_(3)、IL-6预测预后的价值。结果研究组血清25(OH)D_(3)水平、外周血CD4^(+)T淋巴细胞百分比低于对照组,血清IL-6水平高于对照组(P<0.05);研究组血清25(OH)D_(3)水平与外周血CD4^(+)T淋巴细胞百分比呈正相关,血清IL-6水平与外周血CD4^(+)T淋巴细胞百分比呈负相关(P<0.05);预后不良患儿治疗前、治疗后血清25(OH)D_(3)水平低于预后良好患儿,IL-6水平高于预后良好患儿,△IL-6小于预后良好患儿(P<0.05);研究组△IL-6与预后呈正相关(P<0.05);治疗前血清25(OH)D_(3)、IL-6单独预测CVA患儿预后不良的曲线下面积(AUC)分别为0.784、0.764,与单独预测比较,联合预测的AUC(0.926)明显增大,NRI、IDI均>0(P<0.05)。结论CVA患儿血清25(OH)D_(3)、IL-6水平变化与T淋巴细胞免疫平衡失调有关,且各指标联合在预测患儿预后方面具有良好应用价值。