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Urolithiasis Management in Resource-Limited Settings: A Multicentric Retrospective Study in the Democratic Republic of Congo 资源有限环境下尿石症的管理:刚果民主共和国的一项多中心回顾性研究
Pub Date : 2023-03-05 DOI: 10.23958/ijirms/vol08-i03/1630
PABLO DIANGIENDA, Dieudonné Molamba Moningo, Alain Ngoma, Mathieu Nkumu Loposso, Michel Daudon
Introduction: Despite the increasing use of minimally invasive surgery techniques in the management of urolithiasis worldwide, resource-limited countries are still experiencing various challenges. This study aims to analyze different therapeutic modalities used in the treatment of urolithiasis in the Democratic Republic of Congo. Methods: After Institutional Review Board approval, records of 194 patients who presented with documented urolithiasis in 13 hospitals across 4 provinces from January 2010 through September 2019 were retrospectively analyzed. The different layers of stones were analyzed by infrared spectrophotometry. Results: Urolithiasis was symptomatic in 52.6% (n=194) of patients. Overall, 86.1% (i.e. 167 out of 194) of stones were removed by surgery, 9.8% spontaneously resolved; 3.1% were extracted after ureteroscopy and 1% of patients had undergone extracorporeal shock wave lithotripsy. Lumbotomy was the most used route (45.2% of cases) in conventional surgery. Conclusion: Most patients in this study were treated by conventional surgery. These results suggest the need to increase the use of minimally invasive surgery.
导语:尽管世界范围内微创手术技术在尿石症治疗中的应用越来越多,但资源有限的国家仍然面临着各种挑战。本研究旨在分析刚果民主共和国治疗尿石症的不同治疗方式。方法:经机构审查委员会批准,回顾性分析2010年1月至2019年9月期间4个省13家医院194例尿石症患者的记录。采用红外分光光度法对不同层数的宝石进行了分析。结果:尿石症患者中有症状者占52.6% (n=194)。总体而言,86.1%(即194例中的167例)结石通过手术切除,9.8%自发溶解;3.1%的患者在输尿管镜检查后取出,1%的患者接受体外冲击波碎石术。腰切开术是常规手术中使用最多的方法(45.2%)。结论:本组患者多数采用常规手术治疗。这些结果提示需要增加微创手术的使用。
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引用次数: 0
Evidence For Cannabidiol Modulation of Serotonergic Transmission in a Model of Osteoarthritis via in vivo PET Imaging and Behavioral Assessment. 大麻二酚通过体内PET成像和行为评估调节骨关节炎模型中5-羟色胺能传递的证据。
Pub Date : 2022-06-01 Epub Date: 2022-06-03 DOI: 10.23958/ijirms/vol07-i06/1418
Yu-Shin Ding, Jiacheng Wang, Vinay Kumar, James Ciaccio, Sami Dakhel, Cathy Tan, Jonathan Kim, Sabrina Lee, Hilla Katz-Lichtenstein, Zakia Gironda, Orin Mishkit, Jakub Mroz, Raul Jackson, Grace Yoon, Begona Gamallo-Lana, Molly Klores, Adam Mar

Background: Preclinical studies indicate that cannabidiol (CBD), the primary nonaddictive component of cannabis, has a wide range of reported pharmacological effects such as analgesic and anxiolytic actions; however, the exact mechanisms of action for these effects have not been examined in chronic osteoarthritis (OA). Similar to other chronic pain syndromes, OA pain can have a significant affective component characterized by mood changes. Serotonin (5-HT) is a neurotransmitter implicated in pain, depression, and anxiety. Pain is often in comorbidity with mood and anxiety disorders in patients with OA. Since primary actions of CBD are analgesic and anxiolytic, in this first in vivo positron emission tomography (PET) imaging study, we investigate the interaction of CBD with serotonin 5-HT1A receptor via a combination of in vivo neuroimaging and behavioral studies in a well-validated OA animal model.

Methods: The first aim of this study was to evaluate the target involvement, including the evaluation of modulation by acute administration of CBD, or a specific target antagonist/agonist intervention, in control animals. The brain 5-HT1A activity/availability was assessed via in vivo dynamic PET imaging (up to 60 min) using a selective 5-HT1A radioligand ([18F]MeFWAY). Tracer bindings of 17 ROIs were evaluated based on averaged SUVR values over the last 10 min using CB as the reference region. We subsequently examined the neurochemical and behavioral alterations in OA animals (induction with monosodium iodoacetate (MIA) injection), as compared to control animals, via neuroimaging and behavioral assessment. Further, we examined the effects of repeated low-dose CBD treatment on mechanical allodynia (von Frey tests) and anxiety-like (light/dark box tests, L/D), depressive-like (forced swim tests, FST) behaviors in OA animals, as compared to after vehicle treatment.

Results: The tracer binding was significantly reduced in control animals after an acute dose of CBD administered intravenously (1.0 mg/kg, i.v.), as compared to that for baseline. This binding specificity to 5-HT1A was further confirmed by a similar reduction of tracer binding when a specific 5-HT1A antagonist WAY1006235 was used (0.3 mg/kg, i.v.). Mice subjected to the MIA-induced OA for 13-20 days showed a decreased 5-HT1A tracer binding (25% to 41%), consistent with the notion that 5-HT1A plays a role in the modulation of pain in OA. Repeated treatment with CBD administered subcutaneously (5 mg/kg/day, s.c., for 16 days after OA induction) increased 5-HT1A tracer binding, while no significant improvement was observed after vehicle. A trend of increased anxiety or depressive-like behavior in the light/dark box or forced swim tests after OA induction, and a decrease in those behaviors after repeated low-dose C

背景:临床前研究表明,大麻的主要非附加成分大麻二酚(CBD)具有广泛的药理作用,如镇痛和抗焦虑作用;然而,这些作用的确切机制尚未在慢性骨关节炎(OA)中得到检验。与其他慢性疼痛综合征类似,OA疼痛可能具有以情绪变化为特征的重要情感成分。血清素(5-HT)是一种与疼痛、抑郁和焦虑有关的神经递质。OA患者的疼痛通常与情绪和焦虑障碍共病。由于CBD的主要作用是镇痛和抗焦虑,在这项首次体内正电子发射断层扫描(PET)成像研究中,我们在一个经过充分验证的OA动物模型中,通过体内神经成像和行为研究的结合,研究了CBD与5-羟色胺5-HT1A受体的相互作用。方法:本研究的第一个目的是评估靶点参与,包括评估对照动物急性给予CBD或特异性靶点拮抗剂/激动剂干预的调节作用。使用选择性5-HT1A放射性配体([18F]MeFWAY)通过体内动态PET成像(长达60分钟)评估大脑5-HT1A活性/可用性。使用CB作为参考区域,基于过去10分钟内的平均SUVR值来评估17个ROI的示踪剂结合。随后,我们通过神经成像和行为评估,与对照动物相比,检查了OA动物的神经化学和行为变化(碘乙酸单钠(MIA)注射诱导)。此外,与载体治疗后相比,我们研究了重复低剂量CBD治疗对OA动物机械性异常性疼痛(von Frey测试)和焦虑样(光/暗箱测试,L/D)、抑郁样(强迫游泳测试,FST)行为的影响。结果:与基线相比,静脉注射急性剂量CBD(1.0 mg/kg,i.v.)后,对照动物的示踪剂结合显著降低。当使用特异性5-HT1A拮抗剂WAY1006235(0.3 mg/kg,i.v.)时,示踪剂结合的类似减少进一步证实了这种对5-HT1A的结合特异性。接受MIA诱导的OA 13-20天的小鼠显示出5-HT1A示踪剂结合的减少(25%至41%),这与5-HT1A在调节OA疼痛中起作用的概念一致。用皮下施用的CBD重复治疗(OA诱导后5 mg/kg/天,皮下注射,持续16天)增加了5-HT1A示踪剂结合,而在载体后没有观察到显著改善。OA诱导后,在光/暗箱或强迫游泳测试中焦虑或抑郁样行为增加的趋势,以及重复低剂量CBD治疗后这些行为的减少,与CBD通过5HT1A受体激活的抗焦虑作用一致。似乎存在性别差异:女性在基线时对疼痛刺激的反应较弱,而对CBD治疗更敏感。结论:首次在OA动物模型中进行体内PET成像研究,为CBD与5-羟色胺5-HT1A受体的相互作用提供了证据。需要进行更多药理学干预的行为研究来支持靶点参与,以进一步证实这些关键发现。
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引用次数: 0
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International journal of innovative research in medical science
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