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Vacuum-assisted laparostomy with staged peritoneal lavage in management of secondary postoperative diffuse peritonitis: a prospective comparative non-randomised clinical trial 真空辅助剖腹造口联合分阶段腹腔灌洗治疗继发性术后弥漫性腹膜炎:一项前瞻性比较非随机临床试验
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-62-76
I. Uvarov, D. Sichinava, A. Manuilov
Background. Secondary postoperative diffuse peritonitis (SPDP) associates with a high incidence of abdominal sepsis and 35–92% mortality rate. An optimal surgical doctrine in this complication in lacking to date.Objectives. An efficacy assessment of vacuum-assisted laparostomy (VAL) with staged lavage relative to relaparotomy on demand (RD) in SPDP patients.Methods. Patient enrolment and analyses were conducted within period 01.11.2017-31.12.2020, totalling for 141 SPDP patients, 77 (54.6%) males and 64 (45.4%) females aged 64.5 (5972.7) years. Cohort I patients (n = 52) had post-abdominal-lavage VAL using Suprasorb® SNP (SNP-1 and SNP-2) equipment and consumables (Lohmann & Rauscher GmbH, Austria). Staged lavage was performed 48-72 h apart. Cohort II (n = 78) had a standard RD  technique. Cohort III (n = 11) treatment included RD-to-VAL transition. The endpoint was the inpatient treatment outcome, a favourable completion or death. The additional estimated criteria were complications rate and severity (in ACCORDION-modified Clavien-Dindo classification), sepsis rate, C-reactive protein level, abdominal index dynamics, patient’s intensive-care and total-hospital lengths of stay.Results. Cohort I included 157 staged-lavage VALs, cohort II — 107 RDs, cohort III — 49 operations. The mortality rate was 3/52 (5.8%), 24/78 (30.8%) and 7/11 (63.6%) in cohorts I, II and III (respectively, p < 0.001). No difference was observed in the length of hospital stay, with a shorter intensive care stay after final abdominal closure in cohort I. Clavien — Dindo grade 3a complications were observed for 25.0% of cohort I, 60.3 and 45.5% — of cohorts II and III (respectively, p < 0.01); grade 3b complications were 0 (0%), 24.4 and 100% in cohorts I, II and III (respectively, p < 0.001; all 11 patients were reoperated). Multiple organ failure (grade 4b) was reported in 5.8, 30.8 and 63.6% of cohorts I, II and III (respectively, p < 0.001). By end of treatment, sepsis had resolved in 9/11 (81.8%) patients in cohort I, 5/24 (20.8%) and 1/6 (16.7%) — in cohorts II and III (respectively, p = 0.002).Conclusion. Programmed staged-lavage VAL is an optimal surgical treatment tactics in SPDP. Relative to RD, VAL provides a more effective management of local and systemic abdominal sepsis, lower mortality, fewer and less sever complications, shorter intensive care stays after abdominal closure.
背景。继发性术后弥漫性腹膜炎(SPDP)与腹部败血症的高发病率和35-92%的死亡率相关。目前尚缺乏治疗该并发症的最佳手术原则。相对于按需剖腹切开术(RD),真空辅助剖腹切开术(VAL)联合分阶段灌洗在SPDP患者中的疗效评价。患者入组和分析于2017年11月1日至2020年12月31日进行,共141例SPDP患者,其中男性77例(54.6%),女性64例(45.4%),年龄64.5(5972.7)岁。队列1患者(n = 52)使用Suprasorb®SNP (SNP-1和SNP-2)设备和耗材(Lohmann & Rauscher GmbH,奥地利)进行洗腹后VAL。分阶段灌洗,间隔48 ~ 72 h。队列II (n = 78)采用标准RD技术。队列III (n = 11)治疗包括RD-to-VAL转换。终点是住院治疗结果,有利的完成或死亡。其他评估标准包括并发症发生率和严重程度(ACCORDION-modified Clavien-Dindo分类)、败血症率、c反应蛋白水平、腹部指数动态、患者的重症监护和总住院时间。队列1包括157例分期洗胃VALs,队列2 - 107例rd,队列3 - 49例手术。I、II和III组的死亡率分别为3/52(5.8%)、24/78(30.8%)和7/11 (63.6%)(p < 0.001)。住院时间差异无统计学意义,队列I患者最终关闭腹部后的重症监护时间较短,队列I患者Clavien - Dindo 3a级并发症发生率为25.0%,队列II和队列III患者分别为60.3%和45.5% (p < 0.01);I、II和III组3b级并发症发生率分别为0(0%)、24.4%和100% (p < 0.001);11例患者均再次手术)。多器官功能衰竭(4b级)在队列I、II和III中分别占5.8、30.8%和63.6% (p < 0.001)。治疗结束时,队列I中9/11(81.8%)患者脓毒症消退,队列II和队列III中5/24(20.8%)和1/6(16.7%)患者脓毒症消退(p = 0.002)。程序分期灌洗VAL是SPDP的最佳手术治疗策略。与RD相比,VAL提供了更有效的局部和全身性腹部脓毒症的治疗,死亡率更低,并发症越来越少,腹部关闭后重症监护时间更短。
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引用次数: 3
Current state of prevalence and dynamics of alcohol-associated narcopathology: a retrospective study 酒精相关的麻醉性病理的流行现状和动态:一项回顾性研究
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-14-31
S. Alekseenko, S. V. Gubarev, D. A. Lyubchenko, A. Redko
Background. The population prevalence of alcohol abuse-associated drug-related diseases bears high social impact. This indicator holds special value both as a potential indirect estimator of the quality of life, availability and efficiency of drug addiction treatment, a well as parameter for qualitative prognostic models of social and economic development. The burden of alcohol-associated drug diseases is typically ambiguous in prevalence estimation, both across Russian Federation and worldwide.Objectives. A study of the alcohol abuse-associated drug-related morbidity prevalence in Krasnodar Krai for period 2000–2020.Methods. A retrospective descriptive study included legal-paper data of the “Information on Drug-Related Disorders” federal statistics survey (Form 11) of Krasnodar Krai, years 2000-2020, describing the re-registration rate of alcohol use-associated drug disorders. The inclusion criterion was an established drug-related disease among all age cohorts. The main study indicators were regional prevalence values of alcoholic psychosis, alcohol dependence syndrome and harmful alcohol use relative to gender, area and age.Results. Prevalence trends in alcohol use-related drug pathology were more favourable in Krasnodar Krai over Southern Federal District and country-wide. The decline rate among males was significantly higher (22.1-fold) vs. the female population (3.0-fold). The prevalence of alcohol use-related drug pathology remained higher in urban vs. rural areas, with higher rural vs. urban decline rates. Over the entire study period, the 40–59 years-age population was leading by the incidence of overall alcohol use-related drug pathology and, separately, of alcoholic psychosis and alcohol dependence syndrome. Highest harmful alcohol use values were registered for 20–39-year population.Conclusion. The revealed dynamics of legal-registered alcoholic drug pathology prevalence has a multifactorial origin. The changes are conditioned by improvement in the narcological aid institutional regulation within the state guarantee programme, federal and regional preventive measures, current progress in drug therapy, regional demography, as well as underreporting of alcohol-associated drug diseases due to a missing strict vertical statistic registration at the level of any-type medical institutions.
背景与酗酒相关的毒品相关疾病的人口流行率具有高度的社会影响。该指标作为生活质量、戒毒治疗的可用性和有效性的潜在间接估计指标,以及社会和经济发展定性预测模型的参数,具有特殊价值。在俄罗斯联邦和世界范围内,酒精相关药物疾病的负担在流行率估计中通常是模糊的。目标。2000-2020年克拉斯诺达尔边疆区与酒精滥用相关的药物相关发病率研究。方法。一项回顾性描述性研究包括2000-2020年Krasnodar边疆区“药物相关疾病信息”联邦统计调查(表11)的法律论文数据,描述了与酒精使用相关的药物疾病的重新登记率。纳入标准是在所有年龄组中确定的与药物有关的疾病。主要研究指标是酒精性精神病、酒精依赖综合征和有害饮酒的区域流行值与性别、地区和年龄的关系。后果克拉斯诺达尔边疆区与南联邦区和全国相比,酒精使用相关药物病理学的流行趋势更为有利。男性的下降率(22.1倍)明显高于女性(3.0倍)。城市与农村地区的酒精使用相关药物病理学患病率仍然较高,农村与城市的下降率更高。在整个研究期间,40-59岁的人群在总体酒精使用相关药物病理学的发病率以及酒精性精神病和酒精依赖综合征的发病率中处于领先地位。20-39岁人群的有害酒精使用值最高。结论所揭示的合法登记的酒精性药物病理学患病率的动态有多因素的原因。这些变化的条件是国家保障计划内的药物援助机构监管的改进、联邦和地区预防措施、药物治疗的当前进展、地区人口统计,以及由于任何类型的医疗机构缺乏严格的垂直统计登记而导致的酒精相关药物疾病报告不足。
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引用次数: 1
Impact of bispectral index monitoring on critical incidents rate in high-risk patients: a randomised controlled trial 双谱指数监测对高危患者危重事件发生率的影响:一项随机对照试验
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-48-61
N. Trembach
Background. The likelihood of intraoperative critical incidents depends largely on reflex control of the cardiorespiratory system that is often susceptible to chronic pathology. The reflex suppression may link to the depth of anaesthesia, making the latter monitoring particularly important at higher hypotension risks and their patient predisposition.Objectives. A study of the effect of bispectral index anaesthesia monitoring on critical incidents (CIs) rate in high-risk abdominal surgery patients.Methods. A randomised controlled trial enrolled 80 high-risk and 80 low-risk patients. Each cohort randomly allocated patients between subcohorts (by 40 people): 1 — anaesthesia rendered to maintain a 40–60 bispectral index (treatment cohort), 2 — by clinical values and anaesthetic level control in exhaled gas (control cohort), intraoperative control of anaesthetic requirement, bispectral index and critical incidents.Results. A critical incidents rate analysis in high-risk patients showed a lower rate in the bispectral index anaesthesia control cohort. Total 127 critical incidents were registered in 53 patients. The analysis revealed fewer CIs for objective sedation depth monitoring, 45% patients of treatment cohort vs. 87.5% in control. Significantly fewer (by half) patients exhibited hypotension in the treatment cohort, with lower (4-fold) rates of arrhythmia, bradycardia and general respiratory CIs. Anaesthetic doses and bispectral indices at anaesthesia stages were significantly lower in the treatment cohort as well.Conclusion. Objective anaesthesia depth monitoring in high-risk patients reduces the rates of haemodynamic incidents during anaesthesia maintenance and respiratory incidents at arousal due to prevention of excessive anaesthetic depth.
背景。术中发生危重事件的可能性很大程度上取决于心肺系统的反射控制,而心肺系统往往易受慢性病理的影响。反射抑制可能与麻醉深度有关,这使得后一种监测在低血压风险和患者倾向较高的情况下尤为重要。双谱指数麻醉监测对腹部外科高危患者危重事件发生率的影响。一项随机对照试验招募了80名高风险和80名低风险患者。每个队列随机分配患者至亚队列(每组40人):1 -麻醉给予维持40 - 60双谱指数(治疗组),2 -通过临床值和呼出气体麻醉水平控制(对照组),术中麻醉需求控制,双谱指数和危重事件。高危患者的严重事件发生率分析显示,双谱指数麻醉对照组的发生率较低。53例患者共发生127例危重事件。分析显示,客观镇静深度监测的ci较少,治疗组为45%,对照组为87.5%。在治疗队列中,出现低血压的患者明显减少(一半),心律失常、心动过缓和一般呼吸CIs的发生率较低(4倍)。治疗组麻醉阶段的麻醉剂量和双谱指数均明显低于对照组。对高危患者进行客观麻醉深度监测,可防止麻醉深度过深,从而降低麻醉维持期间的血流动力学事件发生率和唤醒时的呼吸事件发生率。
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引用次数: 0
Study of novel 1,4-dihydropyridine derivatives as prospective anti-inflammatory remedies: a randomised controlled trial 新型1,4-二氢吡啶衍生物作为前瞻性抗炎药物的研究:一项随机对照试验
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-77-95
E. Bibik, D. Krivokolysko, G. A. Batishcheva, A. Samokish, Y. Venidiktova, A. Myazina, A. Pankov, K. Frolov, V. Dotsenko, S. Krivokolysko
Background. Over the past decades, scientific community is motivated on finding new anti-inflammatory agents with a safe and high-effective profile to manage pathology.Objectives. A study of the anti-inflammatory action of novel compounds, 1,4-dihydropyridine derivatives, in a classical formalin-induced paw oedema test in white rats.Methods. Originally synthesised 1,4-dihydropyridine derivatives were preliminarily subjected to virtual screening using the SwissTargetPrediction toolkit. White laboratory rats (130 animals) were divided into a control (formalin oedema) and intact group, 4 comparison (meloxicam, sodium metamizole, sodium diclofenac and indomethacin) and 7 experiment groups by the number of 1,4-dihydropyridine derivatives studied. The samples anti-inflammatory efficacy was evaluated in acute formalin-induced paw oedema model simulated by right hind limb subplantar injection of 0.1 mL 2% formalin. The studied substances were administered intragastrically at 5 mg/kg 1.5 h prior to oedema induction. Oncometry was assessed quantitatively by limb circumference. Animals were managed in compliance with GOST 33044–2014 “Principles of Good Laboratory Practice” at all experiment steps. Experimental data were analysed statistically to describe quantitative variability with variance σ2, mean limb girth a and standard deviation σ. Data homogeneity and reliability were estimated by variation coefficient V and the Wilcoxon T(W) criterion.Results. As the most anti-inflammatory effective, partially hydrogenated mar-040 pyridines (ethyl 4-({[5-cyano-6-{[2-(diphenylamino)-2-oxoethyl]thio}-4-(2-furyl)-2-methyl-1,4-dihydropyridin-3-yl]carbonyl}amino) benzoate) were shown 33-fold superior to indomethacin, 26-fold — to sodium diclofenac, 25-fold — to meloxicam and 30-fold — to sodium metamizole; mar-037 pyridines (ethyl 4-[({[3-cyano-5-({[4-(ethoxycarbonyl)phenyl]amino}carbonyl)-4-(2-furyl)-6-methyl-1,4-dihydropyridin-2-yl]thio}acetyl)amino] benzoate) — 17–23-fold superior vs. reference drugs. We also show that mаr-014 (ethyl 4-({[5-cyano-6-({2-[(3,5-dichlorophenyl) amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridin-3-yl]carbonyl}amino)benzoate) and mar033 (ethyl 2-[({[3-cyano-5-({[4-(ethoxycarbonyl)phenyl]amino}carbonyl)-4-(2-furyl)-6-methyl-1,4-dihydropyridin-2-yl]thio}acetyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate) compounds are 2.7-fold more effective vs. reference drugs.Conclusion. The synthesised 1,4-dihydropyridine compounds reveal high efficacy in experimental assays. Selected novel 1,4-dihydropyridine derivatives exhibit a marked anti-inflammatory activity and offer value in future preclinical trials.
背景在过去的几十年里,科学界一直致力于开发新的抗炎药,以安全高效的方式管理病理。目标。新型化合物1,4-二氢吡啶衍生物在经典福尔马林诱导的大鼠爪水肿试验中的抗炎作用研究。方法。使用SwissTargetPrediction工具包对最初合成的1,4-二氢吡啶衍生物进行初步的虚拟筛选。根据所研究的1,4-二氢吡啶衍生物的数量,将白色实验大鼠(130只动物)分为对照组(福尔马林水肿)和完整组、4个对照组(美洛昔康、安乃近钠、双氯芬酸钠和吲哚美辛)和7个实验组。通过右后肢皮下注射0.1mL 2%福尔马林模拟急性福尔马林诱导的足水肿模型,评估样品的抗炎效果。研究物质在水肿诱导前1.5小时以5 mg/kg的剂量灌胃给药。通过肢体周长对肿瘤测量进行定量评估。在所有实验步骤中,动物均按照GOST 33044–2014“良好实验室规范原则”进行管理。对实验数据进行统计分析,以描述方差σ2、平均肢体周长a和标准差σ的定量变异性。通过变异系数V和Wilcoxon T(W)标准估计数据的同质性和可靠性。后果作为最有效的抗炎药,部分氢化的mar-040吡啶(4-({[5-氰基-6-{[2-(二苯基氨基)-2-氧代乙基]硫代}-4-(2-呋喃基)-2-甲基-1,4-二氢吡啶-3-基]羰基}氨基)苯甲酸乙酯)比吲哚美辛高33倍,比双氯芬酸钠高26倍,比美洛昔康高25倍,比安乃近钠高30倍;mar-037吡啶(4-[({[3-氰基-5-({[4-(乙氧基羰基)苯基]氨基}羰基)-4-(2-呋喃基)-6-甲基-1,4-二氢吡啶-2-基]硫代}乙酰基)氨基]苯甲酸乙酯)——比对照药物高17-23倍。我们还表明,mаr-014(4-({[5-氰基-6-({2-[(3,5-二氯苯基)氨基]-2-氧代乙基}硫基)-4-(2-呋喃基)-2-甲基-1,4-二氢吡啶-3-基]羰基}氨基)苯甲酸乙酯)和mar033(2-[({[3-氰基-5-({[4-(乙氧基羰基)苯基]氨基}羰基)-4-(-2-呋喃基)-6-甲基-1,4-四氢吡啶-2-基]硫代}乙酰基)氨基]-4,5,6,7-四氢-1-苯并噻吩-3-羧酸乙酯)化合物的有效性高2.7倍与参考药物相比。结论合成的1,4-二氢吡啶化合物在实验测定中显示出很高的效率。选定的新型1,4-二氢吡啶衍生物具有显著的抗炎活性,在未来的临床前试验中具有价值。
{"title":"Study of novel 1,4-dihydropyridine derivatives as prospective anti-inflammatory remedies: a randomised controlled trial","authors":"E. Bibik, D. Krivokolysko, G. A. Batishcheva, A. Samokish, Y. Venidiktova, A. Myazina, A. Pankov, K. Frolov, V. Dotsenko, S. Krivokolysko","doi":"10.25207/1608-6228-2022-29-1-77-95","DOIUrl":"https://doi.org/10.25207/1608-6228-2022-29-1-77-95","url":null,"abstract":"Background. Over the past decades, scientific community is motivated on finding new anti-inflammatory agents with a safe and high-effective profile to manage pathology.Objectives. A study of the anti-inflammatory action of novel compounds, 1,4-dihydropyridine derivatives, in a classical formalin-induced paw oedema test in white rats.Methods. Originally synthesised 1,4-dihydropyridine derivatives were preliminarily subjected to virtual screening using the SwissTargetPrediction toolkit. White laboratory rats (130 animals) were divided into a control (formalin oedema) and intact group, 4 comparison (meloxicam, sodium metamizole, sodium diclofenac and indomethacin) and 7 experiment groups by the number of 1,4-dihydropyridine derivatives studied. The samples anti-inflammatory efficacy was evaluated in acute formalin-induced paw oedema model simulated by right hind limb subplantar injection of 0.1 mL 2% formalin. The studied substances were administered intragastrically at 5 mg/kg 1.5 h prior to oedema induction. Oncometry was assessed quantitatively by limb circumference. Animals were managed in compliance with GOST 33044–2014 “Principles of Good Laboratory Practice” at all experiment steps. Experimental data were analysed statistically to describe quantitative variability with variance σ2, mean limb girth a and standard deviation σ. Data homogeneity and reliability were estimated by variation coefficient V and the Wilcoxon T(W) criterion.Results. As the most anti-inflammatory effective, partially hydrogenated mar-040 pyridines (ethyl 4-({[5-cyano-6-{[2-(diphenylamino)-2-oxoethyl]thio}-4-(2-furyl)-2-methyl-1,4-dihydropyridin-3-yl]carbonyl}amino) benzoate) were shown 33-fold superior to indomethacin, 26-fold — to sodium diclofenac, 25-fold — to meloxicam and 30-fold — to sodium metamizole; mar-037 pyridines (ethyl 4-[({[3-cyano-5-({[4-(ethoxycarbonyl)phenyl]amino}carbonyl)-4-(2-furyl)-6-methyl-1,4-dihydropyridin-2-yl]thio}acetyl)amino] benzoate) — 17–23-fold superior vs. reference drugs. We also show that mаr-014 (ethyl 4-({[5-cyano-6-({2-[(3,5-dichlorophenyl) amino]-2-oxoethyl}thio)-4-(2-furyl)-2-methyl-1,4-dihydropyridin-3-yl]carbonyl}amino)benzoate) and mar033 (ethyl 2-[({[3-cyano-5-({[4-(ethoxycarbonyl)phenyl]amino}carbonyl)-4-(2-furyl)-6-methyl-1,4-dihydropyridin-2-yl]thio}acetyl)amino]-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate) compounds are 2.7-fold more effective vs. reference drugs.Conclusion. The synthesised 1,4-dihydropyridine compounds reveal high efficacy in experimental assays. Selected novel 1,4-dihydropyridine derivatives exhibit a marked anti-inflammatory activity and offer value in future preclinical trials.","PeriodicalId":33483,"journal":{"name":"Kubanskii nauchnyi meditsinskii vestnik","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46624160","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ultrasonic diagnosis of cosmetic injectable-induced neuropathy: Clinical cases 美容注射性神经病变的超声诊断:临床病例
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-108-118
I. Bondarenko
Background. Facial nerve injury, filler-induced compression or soft tissue infiltrations are among the neuropathic complications of aesthetic injection procedures. The prospects of ultrasound imaging in neuropathy diagnosis are understudied. National and foreign literature does not describe facial soft tissues ultrasound in patients with cosmetic injectable-induced clinical neuropathy.Clinical Cases Description. Two clinical cases are presented of high resolution ultrasound (HRU)-empowered verification of injectable cosmetic procedures-induced neuropathy. Ultrasound imaging was proved necessary for differential neuropathic causes diagnosis via the clinical assessment of facial soft tissues, filler and thread depth, as well as topography relative to blood vessels and nerves. In the first case, threads were visualised at a 4.6 and 5.8 mm depth from epidermis, which can coincide in location with large facial nerve branches usually running along vessels in deeper subcutaneous fat. Vessels were not detected in immediate proximity to threads along the entire trajectory from implantation to fixation sites by colour Doppler imaging (CDI). The ultrasound pattern corresponded to dermal and soft tissue infiltration. In the second case, ultrasound was applied to differentially diagnose a iatrogenic cause of neuropathy, considering a 3-year-past history of filler injection at temporal muscle projection. A filler bolus was revealed adjacent to a vessel in subaponeurotic fat of right temporal region, with infiltrative signs of perifocal oedema around a piece of hyaluronic acid. Temporal soft tissue of the opposite facial half remained unchanged. According to HRU evidence, neuropathy developed due to nerve compression by facial soft tissue infiltrative distortions after thread implantation in the first case and by filler directly in the second. The HRU examination facilitated a correct diagnosis and choice of patient management.Conclusion. Ultrasonography is indicated in patients with cosmetic procedures-induced neuropathy for differential diagnosis of complication causes and current therapy monitoring.
背景面部神经损伤、填充物引起的压迫或软组织浸润是美容注射程序的神经性并发症。超声成像在神经病变诊断中的前景研究不足。国内外文献均未描述美容注射诱导的临床神经病变患者的面部软组织超声检查。临床病例描述。两例临床病例是高分辨率超声(HRU)授权验证注射美容程序诱导的神经病变。通过对面部软组织、填充物和螺纹深度以及与血管和神经相关的地形图的临床评估,证明超声成像对于鉴别神经性病因诊断是必要的。在第一种情况下,在距离表皮4.6毫米和5.8毫米的深度处可以看到线,这可以与通常沿着较深皮下脂肪中的血管运行的大型面神经分支在位置上重合。通过彩色多普勒成像(CDI),在从植入到固定部位的整个轨迹上,没有检测到紧邻螺纹的血管。超声模式对应于真皮和软组织的过滤。在第二种情况下,考虑到颞肌投影处注射填充剂的3年历史,应用超声来区别诊断神经病变的医源性原因。在右侧颞区的亚蛋白尿脂肪血管附近发现了一个小药丸,透明质酸片周围有局灶性水肿的浸润迹象。对面面部的颞侧软组织保持不变。根据HRU的证据,第一种情况下,神经病变是由于植入线后面部软组织的渗透性变形压迫神经而发生的,第二种情况下则是直接由填充物压迫神经。HRU检查有助于正确诊断和选择患者管理。结论超声检查适用于美容手术诱导的神经病变患者,用于并发症原因的鉴别诊断和当前治疗监测。
{"title":"Ultrasonic diagnosis of cosmetic injectable-induced neuropathy: Clinical cases","authors":"I. Bondarenko","doi":"10.25207/1608-6228-2022-29-1-108-118","DOIUrl":"https://doi.org/10.25207/1608-6228-2022-29-1-108-118","url":null,"abstract":"Background. Facial nerve injury, filler-induced compression or soft tissue infiltrations are among the neuropathic complications of aesthetic injection procedures. The prospects of ultrasound imaging in neuropathy diagnosis are understudied. National and foreign literature does not describe facial soft tissues ultrasound in patients with cosmetic injectable-induced clinical neuropathy.Clinical Cases Description. Two clinical cases are presented of high resolution ultrasound (HRU)-empowered verification of injectable cosmetic procedures-induced neuropathy. Ultrasound imaging was proved necessary for differential neuropathic causes diagnosis via the clinical assessment of facial soft tissues, filler and thread depth, as well as topography relative to blood vessels and nerves. In the first case, threads were visualised at a 4.6 and 5.8 mm depth from epidermis, which can coincide in location with large facial nerve branches usually running along vessels in deeper subcutaneous fat. Vessels were not detected in immediate proximity to threads along the entire trajectory from implantation to fixation sites by colour Doppler imaging (CDI). The ultrasound pattern corresponded to dermal and soft tissue infiltration. In the second case, ultrasound was applied to differentially diagnose a iatrogenic cause of neuropathy, considering a 3-year-past history of filler injection at temporal muscle projection. A filler bolus was revealed adjacent to a vessel in subaponeurotic fat of right temporal region, with infiltrative signs of perifocal oedema around a piece of hyaluronic acid. Temporal soft tissue of the opposite facial half remained unchanged. According to HRU evidence, neuropathy developed due to nerve compression by facial soft tissue infiltrative distortions after thread implantation in the first case and by filler directly in the second. The HRU examination facilitated a correct diagnosis and choice of patient management.Conclusion. Ultrasonography is indicated in patients with cosmetic procedures-induced neuropathy for differential diagnosis of complication causes and current therapy monitoring.","PeriodicalId":33483,"journal":{"name":"Kubanskii nauchnyi meditsinskii vestnik","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47173262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mucopolysaccharidosis type IVA in children: Clinical cases 儿童IVA型粘多糖病:临床病例
Pub Date : 2022-01-25 DOI: 10.25207/1608-6228-2022-29-1-119-131
A. Burlutskaya, N. Savel'eva, G. V. Naumenko
Background. Mucopolysaccharidosis type IVA (Morquio syndrome) is a rare genetic lysosomal storage disease. Due to rarity, the syndrome is typically diagnosed at a later stage of gross affections of musculoskeletal and central nervous systems, leading to disability and a markedly reduced quality of life. A replacement therapy is nowadays available with recombinant human N-acetylgalactosamine-6-sulfatase (elosulfase alfa) enzyme.Clinical cases description. Two siblings, 10-yo male and 8-yo female, were admitted with complaints of growth retardation, deformity of the spine, thorax and joints, impaired hearing and visual acuity, poor tolerance to exercise. In the boy’s medical history, first manifestations appeared in the first year of life and progressed gradually; the patient was being observed as spondylodysplastic. Mental development was unaffected. The diagnosis was confirmed only by age of 7 at the National Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation. Genotyping revealed two SNP mutations in gene GALNS (g.88909227C>A and g.88884454G>A in heterozygous state), and enzymatic assays — a severely reduced N-acetylgalactosamin-6-sulfatase activity. A routine elosulfase alfa replacement therapy has been received since 8-year age.The younger sister had neonatal cardiomegaly; congenital carditis and cardiomyopathy not excluded. Musculoskeletal affections developed by age of 3–4 years. By age of 5 and simultaneously with brother, the same GALNS mutations and severely impaired N-acetylgalactosamine-6-sulfatase activity were detected. A replacement therapy has been routinely received since 6-year age. The therapy triggered positive dynamics of restoring activity and muscle strength in both children, as well as significantly abating the musculoskeletal affection progress.Conclusion. The clinical cases of Morquio syndrome presented demonstrate its long-term and complex diagnosis. A replacement therapy is nowadays available, which warrants an earliest disease detection to halt progression and improve the patient’s life quality and expectancy.
背景粘多糖病IVA型(Morquio综合征)是一种罕见的遗传性溶酶体贮积病。由于罕见,该综合征通常在肌肉骨骼和中枢神经系统严重受损的后期诊断,导致残疾和生活质量显著降低。目前,重组人N-乙酰氨基半乳糖-6-硫酸酯酶(elosulfse alfa)酶可用于替代疗法。临床病例描述。两个兄弟姐妹,10岁男性和8岁女性,因生长迟缓、脊椎、胸部和关节畸形、听力和视力受损、运动耐受性差而入院。在男孩的病史中,最初的表现出现在出生的第一年,并逐渐发展;患者被观察为脊椎发育异常。心理发展没有受到影响。俄罗斯联邦卫生部国家儿童健康医学研究中心联邦国立自治机构仅在7岁时确诊。基因分型显示GALNS基因中有两个SNP突变(g.88909227C>A和g.88884454G>A处于杂合状态),酶分析显示N-乙酰氨基半乳糖-6-硫酸酯酶活性严重降低。从8岁起,就接受了常规的艾洛磺胺酶-阿尔法替代疗法。妹妹患有新生儿心脏肥大;先天性心肌炎和心肌病不排除。肌肉骨骼情感在3-4岁时发展起来。在5岁时,与兄弟同时检测到相同的GALNS突变和严重受损的N-乙酰氨基半乳糖-6-硫酸酯酶活性。从6岁起就开始常规接受替代疗法。该疗法引发了两名儿童恢复活动和肌肉力量的积极动力,并显著减轻了肌肉骨骼疾病的进展。结论Morquio综合征的临床病例显示出其长期而复杂的诊断。如今,一种替代疗法已经问世,它保证了尽早发现疾病,以阻止病情发展,提高患者的生活质量和预期寿命。
{"title":"Mucopolysaccharidosis type IVA in children: Clinical cases","authors":"A. Burlutskaya, N. Savel'eva, G. V. Naumenko","doi":"10.25207/1608-6228-2022-29-1-119-131","DOIUrl":"https://doi.org/10.25207/1608-6228-2022-29-1-119-131","url":null,"abstract":"Background. Mucopolysaccharidosis type IVA (Morquio syndrome) is a rare genetic lysosomal storage disease. Due to rarity, the syndrome is typically diagnosed at a later stage of gross affections of musculoskeletal and central nervous systems, leading to disability and a markedly reduced quality of life. A replacement therapy is nowadays available with recombinant human N-acetylgalactosamine-6-sulfatase (elosulfase alfa) enzyme.Clinical cases description. Two siblings, 10-yo male and 8-yo female, were admitted with complaints of growth retardation, deformity of the spine, thorax and joints, impaired hearing and visual acuity, poor tolerance to exercise. In the boy’s medical history, first manifestations appeared in the first year of life and progressed gradually; the patient was being observed as spondylodysplastic. Mental development was unaffected. The diagnosis was confirmed only by age of 7 at the National Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation. Genotyping revealed two SNP mutations in gene GALNS (g.88909227C>A and g.88884454G>A in heterozygous state), and enzymatic assays — a severely reduced N-acetylgalactosamin-6-sulfatase activity. A routine elosulfase alfa replacement therapy has been received since 8-year age.The younger sister had neonatal cardiomegaly; congenital carditis and cardiomyopathy not excluded. Musculoskeletal affections developed by age of 3–4 years. By age of 5 and simultaneously with brother, the same GALNS mutations and severely impaired N-acetylgalactosamine-6-sulfatase activity were detected. A replacement therapy has been routinely received since 6-year age. The therapy triggered positive dynamics of restoring activity and muscle strength in both children, as well as significantly abating the musculoskeletal affection progress.Conclusion. The clinical cases of Morquio syndrome presented demonstrate its long-term and complex diagnosis. A replacement therapy is nowadays available, which warrants an earliest disease detection to halt progression and improve the patient’s life quality and expectancy.","PeriodicalId":33483,"journal":{"name":"Kubanskii nauchnyi meditsinskii vestnik","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47909611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integrated approach to radiodiagnosis of follicular thyroid neoplasia: a retrospective cohort trial 甲状腺滤泡性肿瘤放射诊断的综合方法:回顾性队列试验
Pub Date : 2021-12-06 DOI: 10.25207/1608-6228-2021-28-6-42-58
L. Timofeeva, Y. Aleksandrov, M. A. Yusova, T. N. Aleshina
{"title":"Integrated approach to radiodiagnosis of follicular thyroid neoplasia: a retrospective cohort trial","authors":"L. Timofeeva, Y. Aleksandrov, M. A. Yusova, T. N. Aleshina","doi":"10.25207/1608-6228-2021-28-6-42-58","DOIUrl":"https://doi.org/10.25207/1608-6228-2021-28-6-42-58","url":null,"abstract":"","PeriodicalId":33483,"journal":{"name":"Kubanskii nauchnyi meditsinskii vestnik","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47685912","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Oropharyngeal microbiota profi ling in chronic tonsillitis patients receiving polyvalent pyobacteriophage: A non-randomised experimental clinical trial 接受多价化脓性噬菌体治疗的慢性扁桃体炎患者口咽微生物群的形成:一项非随机实验性临床试验
Pub Date : 2021-12-06 DOI: 10.25207/1608-6228-2021-28-6-29-41
Y. V. Misyurina, M. V. Gadeliya
{"title":"Oropharyngeal microbiota profi ling in chronic tonsillitis patients receiving polyvalent pyobacteriophage: A non-randomised experimental clinical trial","authors":"Y. V. Misyurina, M. V. Gadeliya","doi":"10.25207/1608-6228-2021-28-6-29-41","DOIUrl":"https://doi.org/10.25207/1608-6228-2021-28-6-29-41","url":null,"abstract":"","PeriodicalId":33483,"journal":{"name":"Kubanskii nauchnyi meditsinskii vestnik","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46316278","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
New outreach of ultrasound in aesthetic medicine: a systematic review 超声在美容医学中的新拓展:系统综述
Pub Date : 2021-12-06 DOI: 10.25207/1608-6228-2021-28-6-73-89
I. Bondarenko
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引用次数: 1
Prospects in non-invasive diagnosis of bronchial asthma-related gastroesophageal reflux disease: a single-stage open uncontrolled non-randomised observational study 支气管哮喘相关胃食管反流疾病无创诊断的前景:一项单阶段开放非对照非随机观察性研究
Pub Date : 2021-12-06 DOI: 10.25207/1608-6228-2021-28-6-14-28
E. V. Gorban, E. S. Kameneva, V. Gorban
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引用次数: 1
期刊
Kubanskii nauchnyi meditsinskii vestnik
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