Study on the clinical effect and safety of Kangfuxin liquid combined with microneedling in the treatment of facial skin photoaging

Background and Objectives:Microneedling has been introduced as a new technique to address the growing concern of facial skin photoaging.Kangfuxin liquid has been found to promote the process of skin wound repair,including reducing inflammatory response,improving immunity and enhancing antioxidant levels.In this prospective randomized double-blinded study,we wanted to explore the clinical efficacy and safety of Kangfuxin liquid combined with microneedling in treating facial skin photoaging.Methods:57 patients with facial skin photoaging were randomly divided into two groups.The treatment group(28 cases)received microneedle therapy with Kangfuxin liquid,while the control group(29 cases)received microneedle therapy with physiological saline.The treatment interval was 4 weeks,and a total of 3 treatments were performed.Compare the VISIA scores of facial photoaging features such as wrinkles,texture,pores,spots and ultraviolet pigmentation between two groups of patients before and after treatment,Global Score for Photoaging,satisfaction evaluation,and record the occurrence of adverse reactions.Results:After treatment,the treatment group showed more significant improvement in wrinkles,texture,pores,spots and ultraviolet pigmentation,and the Global Score for Photoaging was better than the control group(P<0.05).The satisfaction rate with improving skin in the treatment group was 85.71%,which was higher than 75.86%in the control group(P<0.05).Both groups did not experience adverse reactions such as skin infection,pigmentation or hypopigmentation,scar formation,or worsening of melasma.Conclusion:Kangfuxin liquid combined with microneedling therapy has a good improvement effect on facial skin photoaging,with a low incidence of adverse reactions and high patient satisfaction.It is worthy of clinical promotion.

Effects of Kangfuxin Solution (康复新液) Combined with Low-level Laser on Cytokines and Immune Function in Patients with Radiation-induced Oral Mucositis

Objective:To investigate the effect of Kangfuxin Solution(康复新液)combined with low-level laser therapy(LLLT)on cytokines and immune function in patients with radiation-induced oral mucositis.Methods:There were 84 nasopharyngeal carcinoma patients with oral mucositis after intensity-modulated radiation therapy(IMRT)were randomly divided into the control group(CG)and the observation group(OG),with 42 cases in each group.The CG was given LLLT,and the OG was treated with Kangfuxin Solution in addition to LLLT for 10 consecutive days.The healing time of oral mucosa,mucositis grading,oral pain scores,cytokines(interleukin-6,interleukin-1βand tumor necrosis factor-α)and T lymphocyte subsets were compared between the 2 groups before and after treatment.Results:The healing time of oral mucosa in the OG was(6.8±1.4)d,which was significantly shorter than(8.6±1.9)d in the CG(t=4.943,P<0.01).After treatment,the grading of oral mucositis in the OG was better than that in the CG,with a statistically significant difference(Z=2.942,P<0.05).The oral pain scores of the OG was lower than that in the CG at different time points after treatment,and the difference was statistically significant(t=8.207,11.017,P<0.01).After treatment,the levels of IL-6,IL-1βand TNF-αin peripheral blood of the OG were significantly lower than those in the CG(t=5.217,2.775,4.053,P<0.01).There were statistically significant differences in CD4+,CD8+and CD4+/CD8+between the OG and the CG after treatment(t=5.692,6.093,3.658,P<0.01).Conclusion:Kangfuxin Solution combined with LLLT can significantly shorten the healing time of oral mucosal,reduce the grading of oral mucositis,relieve oral pain,reduce inflammatory response and improve the immune function of patients.

Clinical observation and experimental study on Kangfuxin fluid in treating indwelling needle-related phlebitis

Objective To investigate the therapeutic effect of Kangfuxin Fluid on indwelling needle-related phlebitis by observation of clinical samples and pharmacological study.Methods Eighty-five patients with indwelling needle-related phlebitis in the neurosurgery department of a Grade A hospital in Shanxi Province from June 2019 to November 2021 were randomly divided into the study group(43 cases)and the vehicle group(42 cases).Patients in the study group were treated with KFX,and patients in the control group were treated with hydrocolloid dressing.The time for symptoms(such as redness and pain)to disappear was recorded.The effect of tissue repair was evaluated by the fin crosscutting model and the anti-inflammatory effect was evaluated by the inflammatory models.Q-PCR assay was used to detect the mRNA expression levels of IL-6 and TNF-αin LPS-stimulated zebrafish.The effect on promoting angiogenesis was evaluated by the inter-segmental blood vascular defect model of zebrafish.Results The curative effect of the study group was better than the control group.The pain resolution time and the swelling resolution time in the study group were(1.67±0.90)d and(2.25±0.92)d,respectively,shorter than those in the control group(P<0.05).KFX can improve the ISV index,increase the regeneration length of the fin,inhibit the migration of neutrophils in three inflammatory models and reduce the mRNA expression levels of IL-6 and TNF-αin LPS-stimulated zebrafish.Conclusion KFX exerts great clinical efficacy in the treatment of indwelling needle-induced phlebitis which may be associated with inflammation inhibition,angiogenesis promotion,and tissue repair.

Effect of Kangfuxin solution on inflammatory, immune, oxidative indexes and vascular factors in patients with ulcerative colitis

Objective:To explore the effect of Kangfuxin solution on inflammatory, immune, oxidative indexes and vascular factorsin patients with ulcerative colitis.Methods: 172 cases of ulcerative colitis from August 2015 to February 2017 were selected and divided into control group (n=86) and observation group (n=86) according to random principle, the control group was treated with Mesalazin Enteric-coated Tablets, and the observation group was treated with enema by infusion of rectal drip on the basis of the control group, and the levels of the two groups of inflammatory factors, immune indexes, oxidation indexes and vascular factors were compared.Results: After treatment, the total effective rate of the observation group (88.37%) was significantly higher than that of the control group (73.26%) (P<0.05);the two groups of CRP and TNF-α were significantly lower than those before treatment (P<0.05), and the observation group was significantly lower than that of the control group (P<0.05);the two groups of CD4+, CD4+/CD8+ and SOD increased significantly compared with those before treatment (P<0.05), while CD8+, MDA and LOP were significantly lower than those before treatment (P<0.05), and the CD4+, CD4+/CD8+ and SOD in the observation group were significantly higher than those in the control group (P<0.05), while CD8+, MDA and LOP were significantly lower than those in the control group (P<0.05);The levels of VEGF and PDGF in both groups were significantly higher than those before treatment (P<0.05), and the levels of VEGF and PDG in observation group were significantly higher than those in control group (P<0.05).Conclusions:The combined treatment of Kangfuxin Liquid and mesalazine can significantly improve the clinical efficacy of the patients. The mechanism of its action is related to reducing the inflammatory response and enhancing the immune, antioxidant functionsand vascular factors. It is worthy of further study in clinical.

Kangfuxin Fluid on the Treatment of Ulcerative Colitis with Retention Enema： a Systematic Review

目的：系统评价康复新液在保留灌肠治疗溃疡性结肠炎中的作用.方法：计算机检索中国期刊全文数据库、维普期刊资源整合平台、万方数据库、PubMed、Medline、Cochranelibrary、Embase数据库;并手工检索纳入文献的参考文献.检索时间为建库至2017年.对检索到的随机对照试验进行了系统的回顾,用RevMan5.3软件进行meta分析.结果：共纳入18篇随机对照试验,1417例患者,其中试验组731例,对照组686例.Meta分析显示,康复新液联合保留灌肠治疗溃疡性结肠炎的疗效显著优于对照治疗（RR=1.2295%CI：[1.16,1.27],Z=8.14,p〈0.00001）,康复新液治疗后生活质量评分显著提高（MD=11.12,95%CI[7.00,15.23],Z=5.30,p〈0.00001）.结论：康复新液联合保留灌肠治疗溃疡性结肠炎能提高患者的生活质量,值得临床推广.同时,有必要对溃疡性结肠炎的治疗效果进行深入的研究并进行高质量的随机对照试验.

Analysis and monitoring of drug therapy in a patient with peptic ulcer complicated by infection:A case report

BACKGROUND The role of primary-level medical pharmacists in medical institutions in China is limited;therefore,it is necessary to explore the role of pharmacists in the process of drug treatment.CASE SUMMARY A Chinese pharmacist participated in the complete treatment of a patient with a duodenal ulcer.The rationale for drug treatment was evaluated,and adjustments were made to the antacid and anti-infective regimen,as well as the dose and frequency of administration.Body temperature,routine blood examination,and adverse drug reactions were strictly monitored.During treatment,the pharmacist recommended anti-infective therapy with ampicillin-sulbactam,which effectively controlled the infection.Additionally,the pharmacist suggested changing famotidine to lansoprazole for acid suppression and gastroprotective treatment,combined with Chinese patent medicine such as Kangfuxin Liquid.This is the first case report of a pharmacist in primary-level medical institutions adjusting drug use for patients with duodenal ulcer and pulmonary infection.CONCLUSION A pharmacist participated in the treatment process,provided individualized medication adjustment,and achieved good clinical results.

康复新液联合PPI治疗反流性食管炎的疗效及安全性Meta分析

目的纳入系统评价康复新液联合质子泵抑制剂(Proton pump inhibitor,PPI)治疗反流性食管炎(Reflux esophagitis,RE)相较于单独使用PPI的疗效和安全性评价。方法以康复新液、反流性食管炎、反流性食道炎、KangFuXin、reflux esophagitis等为检索词在CNKI、WanFang Data、VIP、Embase、Web of Science、PubMed和The Cochrane Library数据库检索康复新液联合PPI治疗RE的随机对照研究,采用RevMan 5.4软件进行Meta分析。结果共纳入25项研究,统计分析结果显示康复新液联合PPI治疗RE较单独PPI治疗能显著提高临床有效率(95%CI:1.15,1.24)、胃镜下有效率(95%CI:1.14,1.22),血清胃泌素(95%CI:1.15,2.03)和胃动素的分泌(95%CI:0.96,1.39),降低复发率(95%CI:0.20,0.61),且不会增高不良反应发生率(95%CI:0.33~0.79),此外,不同PPI种类以及患者年龄高低对临床有效率无显著影响,而不同内镜下诊断标准对内镜下有效率也无显著影响。结论康复新液联合PPI治疗RE较单独PPI治疗能取得更好的疗效且减少疾病复发,并不会额外造成不良反应的发生。

止痛如神汤加减方联合康复新液灌肠治疗气滞血瘀型混合痔术后肛门疼痛的临床效果

目的:观察止痛如神汤加减方联合康复新液灌肠治疗气滞血瘀型混合痔术后肛门疼痛的临床效果。方法:选择2021年1月—2022年12月在崇州市人民医院收治的100例混合痔患者,按照随机数字表法分为A组、B组、C组三组。A组30例,予常规西医治疗;B组35例,在A组基础上予康复新液灌肠治疗;C组35例,在B组基础上,予止痛如神汤加减方治疗。三组术后1 d、7 d均评价创面水肿、创面肉芽组织生长情况,通过数字疼痛评分法(NRS)评价肛门疼痛情况,记录三组患者肛门水肿消退时间、创面分泌物消失时间、创面愈合时间,检测三组肿瘤坏死因子α(TNF-α)、表皮生长因子(EGF)、β-内啡肽(β-EP)、白细胞介素-22(IL-22)、纤维连接蛋白(FN)、血管内皮生长因子(VEGF)水平,术前、术后1个月测量患者直肠肛管抑制反射阈值、肛管静息压、肛管高压带长度。结果:C组创面水肿、NRS评分较A组、B组低(P<0.05),创面肉芽组织生长评分较A组、B组高(P<0.05);C组创面分泌物消失时间、肛门水肿消退时间、创面愈合时间较A组、B组短(P<0.05);C组直肠肛管抑制反射阈值、肛管静息压较A组、B组高(P<0.05),C组肛管高压带长度较A组、B组短(P<0.05);C组TNF-α、IL-22水平较A组、B组低(P<0.05),C组β-EP、EGF、FN、VEGF水平较A组、B组高(P<0.05)。结论:止痛如神汤加减方联合康复新液灌肠可抑制炎症因子水平,调节疼痛介质及EGF、FN、VEGF指标,缓解肛门疼痛,促进创面愈合,提升肛门功能。

清凉汤含漱联合康复新液喷剂防治鼻咽癌放射性口腔炎的临床研究

目的:观察予以鼻咽癌(NPC)并发放射性口腔炎病人清凉汤含漱联合康复新液喷剂治疗的临床效果。方法:选取2022年6月—2023年8月医院收治的60例NPC并发放射性口腔炎病人(均初次接受根治性放射治疗、治疗前口腔黏膜完整)为研究对象,按照随机数字表法分为对照组、观察组,每组30例。对照组采取生理盐水含漱治疗;观察组给予清凉汤含漱联合康复新液喷剂治疗。比较两组病人放射性口腔炎发生时间、C反应蛋白(CRP)水平、中医证候积分、治疗效果及口腔炎分级。结果:观察组病人放射性口腔炎发生时间长于对照组(P<0.05);治疗后观察组病人CRP水平、中医证候积分均低于对照组;观察组病人总有效率为90.00%,高于对照组的63.33%(P<0.05);观察组病人口腔炎分级程度轻于对照组(P<0.05)。结论:予以NPC并发放射性口腔炎病人清凉汤含漱+康复新液喷剂治疗可延缓放射性口腔炎发生时间,改善病人临床症状,减轻机体炎症水平,获得良好防治效果。

康复新治疗牙周炎的机制研究

目的通过研究康复新对牙周组织相关细胞增殖的影响及康复新在细胞炎症反应模型中的抗炎作用,从促进牙周组织再生和抗炎2个方面探讨康复新治疗牙周炎的相关机制。方法(1)采用淋巴细胞增殖检测法(MTS法)检测不同浓度康复新对人牙周膜成纤维细胞(hPDLFs)、人牙龈上皮细胞(hGECs)、人单核巨噬细胞(THP-1)和小鼠胚胎成骨细胞(MC3T3-E1)活性的影响;(2)通过细菌脂多糖(LPS)刺激小鼠巨噬细胞RAW264.7建立细胞炎症模型,采用实时定量聚合酶链反应(qRT-PCR)法检测康复新对细胞白细胞介素-1β(IL-1β)、IL-10、一氧化氮合酶(NOS)和基质金属蛋白酶-13(MMP-13)mRNA表达水平的影响。结果(1)与对照组比较:0.1000、0.0500、0.0250、0.0125 mg/mL的康复新组在24 h和48 h时间点均可刺激hPDLFs、THP-1和MC3T3-E1增殖(P<0.01),且促增殖作用具有浓度依赖性;(2)在炎症细胞模型中,与对照组比较,0.0500 mg/mL和0.0125 mg/mL的康复新组IL-1β和IL-10 mRNA表达水平比较,差异均无统计学意义(P>0.05),NOS和MMP-13 mRNA表达水平降低,差异有统计学意义(P<0.05)。结论康复新在一定浓度范围内能促进hPDLFs、hGECs、THP-1和MC3T3-E1增殖;康复新可抑制LPS诱导的RAW264.7细胞炎症反应,其抗炎机制可能是降低NOS和MMP-13 mRNA表达水平。康复新可能是通过促进牙周组织再生和抗感染治疗牙周炎。

拔毒生肌散联合康复新液对单纯性肛瘘术后创面愈合的临床观察

目的:观察拔毒生肌散联合康复新液对单纯性肛瘘术后创面愈合的治疗效果。方法:选取60例单纯性肛瘘患者按随机数字表法分成对照组和试验组,每组30例。对照组术后予以复方芩柏颗粒剂溶液熏洗坐浴,拔毒生肌散换药,试验组在对照组基础上用拔毒生肌散联合康复新液换药,观察各组患者临床疗效、创面肉芽生长评分、创面分泌物评分、创面愈合率、创面愈合时间、术后疼痛评分等。结果:两组比较,试验组的临床疗效、创面愈合率更高,创面肉芽生长评分、创面分泌物评分、术后疼痛评分更低,创面愈合时间更短,差异均有统计学意义(P<0.05)。结论:拔毒生肌散联合康复新液对单纯性肛瘘术后创面的促愈效果肯定,可有效改善患者体验。

Kangfuxin(Periplaneta americana)Lotion for Adjunctive Treatment of Ulcerative Colitis:A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Objective: The objective of the study is to investigate the effect of Kangfuxin lotion as adjunctive therapy for treating ulcerative colitis(UC) through a systematic review and meta?analysis of randomized controlled trials(RCTs). Materials and Methods: RCTs comparing Kangfuxin lotion with no treatment, placebo, western medications or combination therapy for treatment of UC were included in this study. Two English and three Chinese electronic databases were searched. All searches ended in December 2017. Data and quality assessment carried out respectively. Rev Man 5.2 software(Copenhagen, The Nordic Cochrane Centre, The Cochrane Collaboration, 2014) was used to analyze with effect estimate presented as mean difference(MD), risk ratio(RR) and 95% confidence interval(CI). Results: Fifteen trials with 1050 participants were included in this review. Overall, 13 trials were eligible for meta?analysis. Kangfuxin lotion combined with Mesalazine was better than Mesalazine on clinical cure rate(RR 1.45, 95% CI 1.24–1.70, 7 trials), recurrence rate of UC(RR 0.22, 95% CI 0.07–0.72, 2 trials), or endoscopic mucosal recovery(RR 8.05, 95% CI 2.64–24.57, 2 trials). And Kangfuxin lotion combined with triple live bacteria tablets(Bifidobacterium-Lactobacillus? Streptococcus thermophilus)was superior with regard to symptoms remission rate(RR 5.36, 95% CI 1.73–16.60, 3 trials), endoscopic disease activity score(MD-2.30, 95% CI-2.64–-1.96, 1 trial). There were no reports on the serious adverse events of Kangfuxin lotion. Conclusion: Kangfuxin lotion as adjunctive treatment appears more effective than medications alone on clinical cure rate, recurrence rate, endoscopic mucosal recovery and improvement rate of related symptoms.

部队门诊部采用康复新液联合新癀片治疗早期智齿冠周炎的临床疗效观察

目的对康复新液联合新癀片治疗早期智齿冠周炎的临床疗效进行观察分析,为部队患者冠周炎治疗寻求简便有效的临床治疗方案提供数据支持及理论依据。方法将于某门诊部口腔科就诊的180例智齿冠周炎临床早期患者,按实际就诊顺序根据单双号分为观察组和对照组,比较上述两组治疗方案用药后局部龈瓣水肿、疼痛、溢脓的病情变化及症状控制情况。结果观察组患者的治疗效果明显优于对照组,两组数据对比具有统计学意义(P<0.05)。结论运用康复新液联合新癀片治疗早期冠周炎简便易行,效果显著,可以有效减轻局部水肿,控制炎症,缓解疼痛,值得在基层单位推广。

复方黄柏液涂剂与康复新液促进肛周脓肿术后创面恢复的效果对比

目的探讨复方黄柏液涂剂与康复新液促进肛周脓肿术后创面恢复的效果。方法200例肛周脓肿患者,随机分为观察组和对照组,每组100例。两组均行低位切开高位挂线手术,对照组术后使用康复新液,观察组术后使用复方黄柏液涂剂。比较两组患者临床疗效、各项恢复指标(疼痛缓解时间、水肿减轻时间、腐肉脱落时间、创面愈合时间)、肛周湿疹发生情况以及手术前后肛缘水肿、疼痛评分。结果观察组治疗总有效率97.00%高于对照组的78.00%(P<0.05)。观察组患者术后3、7、14 d的肛缘水肿评分分别为(1.61±0.37)、(1.04±0.29)、(0.62±0.15)分,低于对照组的(2.09±0.40)、(1.76±0.34)、(1.13±0.21)分,视觉模拟评分法(VAS)评分分别为(3.04±1.02)、(2.07±0.78)、(1.56±0.62)分,低于对照组的(4.91±1.15)、(3.46±0.95)、(2.43±0.87)分(P<0.05)。观察组疼痛缓解时间(5.72±1.46)d、水肿减轻时间(4.23±1.37)d、腐肉脱落时间(4.42±0.86)d、创面愈合时间(23.45±5.26)d均短于对照组的(7.84±1.65)、(6.47±1.52)、(6.78±1.17)、(31.38±6.04)d(P<0.05)。观察组肛周湿疹发生率2.00%明显低于对照组的16.00%(P<0.05)。结论复方黄柏液涂剂应用于肛周脓肿术后创面恢复的效果更好,能加快肛缘水肿、疼痛的消退,促进切口愈合,降低肛周湿疹发生率,具有积极的临床意义。

康复新液联合奥美拉唑治疗反流性食管炎患者的疗效分析

目的研讨康复新液联合奥美拉唑治疗反流性食管炎患者的疗效。方法84例反流性食管炎患者,根据随机抽签法分为参照组和实验组,每组42例。参照组采取奥美拉唑治疗,实验组采取康复新液联合奥美拉唑治疗。比较两组的治疗效果、不良反应发生情况。结果实验组的治疗总有效率为95.24%,参照组为78.57%,实验组高于参照组,差异显著(P<0.05)。实验组的不良反应发生率为4.76%(2/42),参照组为19.05%(8/42),实验组低于参照组,差异显著(P<0.05)。结论在反流性食管炎的临床治疗中,选择康复新液及奥美拉唑联合治疗方案,有助于发挥联合治疗机制,为溃疡面彻底愈合提供条件,可降低炎症侵袭,避免疾病复发,临床应用效果显著。

培菲康联合美沙拉嗪及康复新液治疗溃疡性结肠炎的效果研究

目的探讨双歧杆菌三联活菌胶囊(商品名:培菲康)联合美沙拉嗪及康复新液治疗溃疡性结肠炎的临床效果。方法89例接受药物治疗的溃疡性结肠炎患者,按随机数字表法分成对照组(40例)及研究组(49例)。对照组应用美沙拉嗪+康复新液治疗,研究组在对照组基础上联合应用培菲康治疗。对比两组治疗效果、症状消退时间、不良反应发生率、免疫功能指标(CD^(3+)、CD^(4+)/CD^(8+))水平、血清炎性因子指标[C反应蛋白(CRP)、降钙素原(PCT)、肿瘤坏死因子-α(TNF-α)]水平、症状评分、生活质量评分。结果研究组总有效率97.96%高于对照组的82.50%(P<0.05)。研究组腹泻消退时间、腹痛消退时间、便血消退时间分别为(3.29±0.81)、(4.12±0.76)、(4.37±0.89)d,均短于对照组的(4.32±0.97)、(5.30±0.93)、(5.64±1.02)d(P<0.05)。两组不良反应发生率对比,差异不明显(P>0.05)。治疗后,两组CD^(3+)、CD^(4+)/CD^(8+)与治疗前相比均显著增高,且研究组CD^(3+)(45.39±2.87)%、CD^(4+)/CD^(8+)(2.10±0.48)均高于对照组的(41.18±2.91)%、(1.52±0.39)(P<0.05)。治疗后,两组CRP、PCT、TNF-α对比于治疗前均明显降低,且研究组CRP(5.89±1.06)mg/L、PCT(0.46±0.15)ng/ml、TNF-α(10.83±2.07)μg/L均低于对照组的(7.02±1.27)mg/L、(0.69±0.23)ng/ml、(13.49±2.46)μg/L(P<0.05)。治疗后,两组腹泻、腹痛、便血评分相比于治疗前均明显降低,且研究组腹泻、腹痛、便血评分分别为(1.17±0.39)、(1.06±0.31)、(1.16±0.40)分,均低于对照组的(1.58±0.43)、(1.52±0.48)、(1.61±0.45)分(P<0.05)。治疗后,两组生理、心理、环境、社会关系评分较治疗前均显著增高,且研究组生理、心理、环境、社会关系评分分别为(89.75±6.48)、(89.07±6.02)、(90.14±6.15)、(89.96±6.27)分,高于对照组的(82.93±6.85)、(82.40±6.13)、(83.27±6.30)、(83.14±6.54)分(P<0.05)。结论在溃疡性结肠炎患者治疗时,应用美沙拉嗪、康复新液与培菲康联合治疗可增强疗效,起到加快症状缓解、调节免疫功能、减轻炎症反应等作用,有助于改善生活质量,且联合用药后的不良反应未增多,具有良好的安全性。

自拟促愈方与康复新液治疗肛肠术后难愈性创面临床疗效及对ECM的影响

目的探究自拟促愈方与康复新液治疗肛肠术后难愈性创面临床疗效及对细胞外基质(extracellular matrix,ECM)的影响。方法选取商丘市中医院肛肠科2021年4月—2022年6月收治的90例肛肠术后创面难愈患者,按照随机数字表法分为对照组与治疗组,各45例,对照组采用康复新液治疗,治疗组采用自拟促愈方治疗,比较3个疗程后两组治疗总有效率、创面愈合及住院时间、创面疼痛程度[视觉模拟评分法(visual analogue scale,VAS)]ECM含量。结果治疗组总有效率82.22%(37/45),显著高于对照组62.22%(28/45)(P<0.05)。治疗组的创面愈合及住院时间明显短于对照组(P<0.05)。治疗后,两组VAS评分均明显下降(P<0.05),且治疗组VAS评分明显低于对照组(P<0.05),治疗组患者疼痛减轻明显优于对照组;治疗14 d后,两组ECM含量明显增多(P<0.05),且治疗组明显高于对照组(P<0.05)。结论自拟促愈方较康复新液治疗肛肠术后难愈性创面的临床疗效较好。可明显缓解患者临床病症、减轻患者痛苦。

肛周脓肿术后应用生肌止痛方联合康复新液临床观察

目的:观察肛周脓肿术后应用生肌止痛方联合康复新液的临床效果。方法:90例分为两组各45例。两组术后均用康复新液治疗,联合组加用生肌止痛方坐浴。结果:联合组显效率高于对照组(P<0.05)。治疗14d后联合组创面分泌物、创面肉芽生长情况、疼痛评分均低于对照组,创面愈合时间短于对照组(P<0.05)。治疗14d后联合组IL-1β、TNF-α水平低于对照组而EGF高于对照组(P<0.05)。治疗14d后联合组CD4^(+)、CD4^(+)/CD8^(+)、CD3^(+)水平高于对照组(P<0.05)。治疗14d后联合组肛管最大收缩压、肛管静息压低于对照组(P<0.05)。结论:肛周脓肿术后用生肌止痛方联合康复新液可减轻炎症、痛感,提高机体免疫力,改善肛门功能,促进康复。

康复新液联合雷尼替丁对复发性口腔溃疡患者血清免疫指标及炎性因子的影响

目的 探讨康复新液联合雷尼替丁对复发性口腔溃疡患者血清免疫指标及炎性因子的影响。方法 选取2021年2月至2022年11月我院收治的82例复发性口腔溃疡患者,随机分为两组各41例。对照组采用雷尼替丁治疗,观察组在此基础上采用康复新液治疗。两组均持续治疗7 d。对比两组患者的血清免疫指标、炎性因子水平和生活质量。结果 治疗后,观察组的CD3^(+)、 CD4^(+)、 CD4^(+)/CD8^(+)及SF-36评分均高于对照组,CRP、 IL-2、 TNF-α水平均低于对照组(P <0.05)。结论 康复新液联合雷尼替丁治疗复发性口腔溃疡,能够降低患者炎性因子水平,提高其免疫能力和生活质量。

人参白茅根汤联合康复新液对肛瘘术后切口愈合效果及对血清TNF-α、IL-1β和IL-6水平的影响

目的探讨人参白茅根汤联合康复新液对肛瘘术后切口愈合的效果及对血清肿瘤坏死因子(tumor necrosis factor-α,TNF-α)、白细胞介素-1β(interleukin-1β,IL-1β)和白细胞介素-6(interleukin-6,IL-6)水平影响。方法选取南充市中心医院收治的肛瘘患者124例,患者均行肛瘘切开挂线术,随机分为对照组(64例,康复新液)和观察组(60例,人参白茅根汤联合康复新液),两组持续治疗10 d,对比两组临床疗效、创面愈合时间和创面面积、临床症状评分、血清TNF-α、IL-6和IL-1β水平及血清成纤维细胞生长因子-1(fibroblast growth factor-1,FGF-1)、血管内皮细胞生长因子(vascular endothelial growth factor,VEGF)及创面表皮生长因子(wound epidermal growth factor,EGF)浓度水平的改变情况。结果观察组总有效率更高(P<0.05);观察组创面愈合时间和术后7 d和10 d创面面积治疗后较对照组更低(P<0.05),而两组术后2 d的创面面积比较差异无统计学意义(P>0.05);两组临床症状的评分治疗前比较差异无统计学意义(P>0.05);术后疼痛、创面分泌物的评分以及创缘水肿的评分方面,两组治疗后均下降明显(P<0.05);且观察组的下降程度更为明显(P<0.05);治疗前两组血清内的IL-6、TNF-α和IL-1β浓度水平比较差异无统计学意义(P>0.05);而两组治疗后血清内的IL-6、TNF-α浓度水平下降明显,而血清内的IL-1β浓度水平升高(P<0.05);且观察组下降更为明显(P<0.05);两组治疗前血清内的FGF-1、VEGF和EGF浓度水平比较差异无统计学意义(P>0.05);治疗后两组血清FGF-1、VEGF和EGF水平显著升高(P<0.05);且观察组上升更为明显(P<0.05)。结论术后肛瘘病人实施康复新液结合人参白茅根汤治疗具有较好的疗效,可改善血清TNF-α、IL-1β和IL-6水平。