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Effect of Desmopressin on Bleeding After Heart Surgeries: A Narrative Review. 去氨加压素对心脏手术后出血的影响:综述。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-133894
Alireza Jahangirifard, Seyed Bashir Mirtajani, Firoozeh Madadi

Desmopressin is an analog of the antidiuretic hormone (vasopressin), which causes anticoagulant activity by increasing plasma factor 8. The use of desmopressin dates back to 1977, when this hormone was used to prevent bleeding during tooth extraction and surgery in patients with hemophilia A and von Willebrand disease. After that, this hormone was expanded to prevent bleeding in congenital defects and conditions such as chronic kidney and liver failure. Also, this hormone is used to prevent bleeding in major surgeries such as heart surgery, where the patient loses much blood and needs a blood transfusion. Considering the importance of desmopressin in bleeding control, the present study was conducted to investigate the possible effect of this hormone in heart surgery.

去氨加压素是抗利尿激素(抗利尿素)的类似物,通过增加血浆因子8引起抗凝血活性。去氨加压素的使用可以追溯到1977年,当时这种激素被用于预防血友病A和血管性血友病患者拔牙和手术期间出血。在那之后,这种激素被扩展到预防先天性缺陷和慢性肾衰竭和肝功能衰竭等疾病的出血。此外,这种激素在心脏手术等大手术中用于防止出血,在这些手术中,患者失血过多,需要输血。考虑到去氨加压素在出血控制中的重要性,本研究旨在探讨该激素在心脏手术中的可能作用。
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引用次数: 0
Renal Colic Pain Management by Tamsulosin with Morphine Versus Morphine in Adults: A Randomized Clinical Trial. 坦索罗辛联合吗啡与吗啡治疗成人肾绞痛:一项随机临床试验
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-134627
Morteza Talebi Doluee, Aida Shams, Maliheh Keshvari Shirvan, Maliheh DadgarMoghadam, Sayyed Majid Sadrzadeh, Elnaz VafadarMoradi

Background: Acute renal colic is one of the most painful situations in patients' life. The best management modality for pain alleviation is of paramount importance.

Objectives: This study aimed to evaluate the effect of intravenously administered morphine and oral tamsulosin compared to the independent use of morphine in patients with renal colic.

Methods: This double-blind clinical trial was conducted on 200 patients aged 18 to 55 years with renal colic referred to the tertiary level referral hospital. The patients were randomly assigned to two groups, A and B. The subjects in group A were treated with intravenously administered morphine and oral tamsulosin hydrochloride capsules, while group B received morphine and control. The patients' pain intensity was evaluated using a visual analog scale.

Results: The mean age of the patients was 35.34 ± 8.32, and 72% were males. Before the study, the mean pain intensity was higher in the tamsulosin group (8.67 ± 1.53) than in the control group (7.85 ± 2.05; P = 0.003). After four and six hours, the mean pain intensity was significantly lower in the tamsulosin group (P = 0.028 and P = 0.008, respectively). According to the results, the pain intensity was significantly reduced six hours after the treatment compared to the pre-therapy phase (P < 0.001).

Conclusions: Given the significant effect of tamsulosin on pain alleviation in patients with renal colic, this medicine can be used as a complementary treatment to manage the pain in these patients and reduce the administration of narcotics.

背景:急性肾绞痛是患者一生中最痛苦的情况之一。减轻疼痛的最佳管理方式是至关重要的。目的:本研究旨在评价静脉注射吗啡和口服坦索罗辛与独立使用吗啡在肾绞痛患者中的效果。方法:对200例18 ~ 55岁的三级转诊医院肾绞痛患者进行双盲临床试验。将患者随机分为A、B两组,A组给予静脉注射吗啡和口服盐酸坦索罗辛胶囊,B组给予吗啡和对照组。采用视觉模拟量表评估患者的疼痛强度。结果:患者平均年龄为35.34±8.32岁,男性占72%。研究前,坦索罗辛组患者平均疼痛强度(8.67±1.53)高于对照组(7.85±2.05);P = 0.003)。治疗4、6小时后,坦索罗辛组平均疼痛强度明显降低(P = 0.028、P = 0.008)。结果显示,与治疗前相比,治疗后6小时疼痛强度显著降低(P < 0.001)。结论:坦索罗辛对肾绞痛患者的疼痛有明显的缓解作用,可作为肾绞痛患者疼痛的辅助治疗,减少麻醉药物的使用。
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引用次数: 0
Comparing Effects of Rhythmic Breathing and Lidocaine Spray on Pain Intensity During Needle Insertion Into Arteriovenous Fistula in Hemodialysis Patients: A Randomized Controlled Trial. 比较节奏呼吸和利多卡因喷雾对血液透析患者动静脉瘘穿刺疼痛强度的影响:一项随机对照试验。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-126384
Houman Sadeghpour Marvi, Tahereh Baloochi Beydokhti, Moosa Sajjadi, Behruz Khaleghimanesh

Background: Hemodialysis patients suffer from pain caused by needle insertion into the fistula site. Non-pharmacological methods may be associated with acceptable effects.

Objectives: The present study aimed to compare the effects of two interventions on pain intensity during needle insertion into the arteriovenous fistula in hemodialysis patients.

Methods: This self-controlled, single-blind clinical trial was conducted on 54 hemodialysis subjects with arteriovenous fistula in Mashhad in 2021. In this regard, the patients were selected according to the inclusion criteria and randomly assigned to two groups (lidocaine spray and rhythmic breathing). In each group, pain intensity was assessed based on the visual analogue scale (VAS) before the intervention, followed by measuring the post-intervention pain intensity during three consecutive hemodialysis sessions every other day. Regarding the lidocaine spray group, two puffs of 10% lidocaine spray (20 mg) were sprayed on the needle insertion site five minutes before cannulation. However, the patients in another group took a long deep breath through the nose with three numbers, held their breath in the lungs for three numbers, and slowly exhaled through the mouth with three numbers two minutes before cannulation. The data were analyzed using SPSS software version 20, and Mann-Whitney U, Wilcoxon, chi-squared, and paired t-tests were run. In this study, P < 0.05 was considered significant.

Results: The results represented a significant decrease in the pain severity scores of both rhythmic breathing (P = 0.023) and lidocaine spray (P < 0.001) groups after the intervention. Moreover, a more significant difference was observed between pre-and post-intervention pain intensity scores in the group treated with lidocaine spray (1.16 ± 1.56) compared to the other group (0.508 ± 1.25).

Conclusions: The lidocaine spray group had a larger difference in the pre-and post-intervention pain intensity scores than the rhythmic group; however, the difference was not significant. The rhythmic breathing can be used by nurses as a non-pharmacological method with low complications in hemodialysis departments because of declining pain.

背景:血液透析患者常因针头插入瘘管部位引起疼痛。非药物方法可能与可接受的效果相关联。目的:本研究旨在比较两种干预措施对血液透析患者动静脉瘘插入过程中疼痛强度的影响。方法:于2021年在马什哈德对54例血液透析动静脉瘘患者进行自我对照、单盲临床试验。根据纳入标准选择患者,随机分为两组(利多卡因喷雾组和节律呼吸组)。在每组中,干预前根据视觉模拟量表(VAS)评估疼痛强度,随后每隔一天测量干预后连续三次血液透析期间的疼痛强度。利多卡因喷雾组在插管前5分钟,将10%利多卡因喷雾剂(20mg)喷于插针部位2次。而另一组患者则在插管前两分钟,用鼻子长时间深呼吸,用肺憋气,用三个数字,然后用嘴慢慢呼出。采用SPSS软件第20版对数据进行分析,采用Mann-Whitney U、Wilcoxon、卡方、配对t检验。在本研究中,P < 0.05为显著性。结果:干预后节律性呼吸组(P = 0.023)和利多卡因喷雾组(P < 0.001)疼痛严重程度评分均显著降低。此外,利多卡因喷雾组干预前后疼痛强度评分(1.16±1.56)比另一组(0.508±1.25)差异更显著。结论:利多卡因喷雾组干预前后疼痛强度评分差异大于节奏组;然而,差异并不显著。有节奏呼吸法可作为一种并发症低的非药物治疗方法,在血液透析科室因疼痛减轻而被护士采用。
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引用次数: 0
Effect of Intraoperative Lung Recruitment and Transversus Abdominis Plane Block in Laparoscopic Bariatric Surgery on Postoperative Lung Functions: A Randomized Controlled Study. 腹腔镜减肥手术中术中肺补充和经腹平面阻滞对术后肺功能的影响:一项随机对照研究。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-128440
Aboseif Aboseif, Ahmed Bedewy, Magdy Nafei, Raafat Hammad, Salwa Amin

Background: Morbid obesity may cause a restrictive condition. General anesthesia (GA) and supine posture both decrease lung capacity and functional residual capacity (FRC), altering the ventilation/perfusion ratio and raising the pulmonary shunt.

Objectives: To evaluate the impact of recruitment maneuver (RM) and transversus abdominis plane (TAP) block performed during laparoscopic bariatric surgery on spirometry, oxygenation, opioid requirements, and pain score assessed after surgery.

Methods: This pilot prospective randomized controlled study included 80 patients scheduled for elective laparoscopic bariatric surgeries (e.g., laparoscopic sleeve gastrectomy and laparoscopic gastric bypass) under GA. Patients were divided into four equal groups. All patients received a standardized postoperative analgesia regimen. Group I (control group), group II received TAP block after intubation and before surgical incision, group III received RM after intubation and after pneumoperitoneal insufflation, and group IV received RM after intubation and after pneumoperitoneal exsufflation and TAP block after intubation and before surgical incision.

Results: Forced vital capacity (FVC) and forced expiratory volume (FEV1) were significantly higher after group IV operation than in other groups. Intraoperative PaO2 and PaO2/FiO2 were significantly higher in groups III and IV compared to other groups. The numerical rating scale (NRS) at 1, 2, 4, 6, and 12h was significantly decreased in groups II and IV compared to other groups. Morphine consumption was significantly lower in groups II and IV compared to other groups.

Conclusions: TAP block combined with RM had better postoperative pulmonary function tests. Intraoperative oxygenation was higher in RM.

背景:病态肥胖可引起限制性疾病。全麻(GA)和仰卧位均降低肺活量和功能残气量(FRC),改变通气/灌注比,增加肺分流。目的:评估腹腔镜减肥手术中进行的复吸操作(RM)和经腹平面(TAP)阻滞对肺量测定、氧合、阿片类药物需求和术后疼痛评分的影响。方法:本前瞻性前瞻性随机对照研究纳入80例计划在GA下进行选择性腹腔镜减肥手术(如腹腔镜袖胃切除术和腹腔镜胃旁路术)的患者。患者被分为四组。所有患者均接受标准化的术后镇痛方案。I组(对照组)、II组插管后及手术切口前给予TAP阻滞,III组插管后及气腹充气后给予RM, IV组插管后及气腹排气后给予RM,插管后及手术切口前给予TAP阻滞。结果:IV组术后用力肺活量(FVC)和用力呼气量(FEV1)明显高于其他各组。III、IV组术中PaO2、PaO2/FiO2明显高于其他组。在1、2、4、6和12h时,II和IV组的数值评定量表(NRS)较其他组显著降低。与其他组相比,II组和IV组吗啡用量明显降低。结论:TAP阻滞联合RM术后肺功能检查效果较好。RM组术中氧合较高。
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引用次数: 0
The Effect of Preoperative Combined with Intravenous Lidocaine and Ketamine vs. Intravenous Ketamine on Pediatric Patients Undergoing Upper Gastrointestinal Endoscopy. 术前联合静脉注射利多卡因和氯胺酮与静脉注射氯胺酮对小儿上消化道内镜检查的影响。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-130991
Amir Shafa, Reza Abediny, Hamidreza Shetabi, Sedighe Shahhosseini

Background: Ketamine is widely used in pediatric sedation. New studies have recommended combination therapy to reduce the side effects of ketamine.

Objectives: This study investigated the effect of adding intravenous (IV) lidocaine to ketamine on hemodynamic parameters, endoscopist satisfaction, and recovery time of children undergoing gastrointestinal endoscopy.

Methods: This triple-blind, randomized, controlled clinical trial was conducted in Isfahan, Iran (2021). One hundred twenty children between the ages of 1 and 6 were enrolled. Patients were divided into 2 groups. The intervention group received 1.0 mg/kg of IV lidocaine and 1.0 mg/kg of IV ketamine, and the placebo group received 1.0 mg/kg of IV ketamine and placebo 2 minutes before entering the endoscopic room. Patients in both groups were sedated with 1.0 mg/kg of propofol, 0.1 mg/kg of midazolam, and 2.0 ug/kg of fentanyl for the procedure. The pulse rate, mean arterial pressure (MAP), respiratory rate, and oxygen saturation were recorded 1 minute before injection and every 5 minutes afterward.

Results: The mean (SD) ages of the intervention and control groups were 3.4 (1.5) and 3.4 (1.7), respectively. The mean difference in hemodynamic parameters between the 2 groups was insignificant during the investigation (P > 0.05). Furthermore, no significant differences were found regarding endoscopist satisfaction scores and length of recovery room stay (P > 0.05).

Conclusions: Adding low-dose IV lidocaine to ketamine for pediatric sedation does not significantly affect the hemodynamic status, endoscopist satisfaction, and recovery time.

背景:氯胺酮广泛应用于小儿镇静。新的研究建议联合治疗来减少氯胺酮的副作用。目的:探讨氯胺酮加静脉利多卡因对儿童胃肠内镜血流动力学参数、内镜医师满意度及恢复时间的影响。方法:该三盲、随机、对照临床试验于2021年在伊朗伊斯法罕进行。120名年龄在1到6岁之间的儿童参加了这项研究。患者分为两组。干预组给予1.0 mg/kg静脉注射利多卡因和1.0 mg/kg静脉注射氯胺酮,安慰剂组在进入内镜室前2分钟给予1.0 mg/kg静脉注射氯胺酮和安慰剂。两组患者均使用1.0 mg/kg异丙酚、0.1 mg/kg咪达唑仑和2.0 ug/kg芬太尼镇静。注射前1分钟和注射后每5分钟记录一次脉搏率、平均动脉压(MAP)、呼吸率和血氧饱和度。结果:干预组和对照组的平均(SD)年龄分别为3.4(1.5)岁和3.4(1.7)岁。两组患者血流动力学参数的平均差异无统计学意义(P > 0.05)。两组在内镜医师满意度评分和恢复室住院时间方面差异无统计学意义(P > 0.05)。结论:在小儿镇静氯胺酮的基础上添加小剂量静脉利多卡因对血流动力学状态、内镜医师满意度和恢复时间无显著影响。
{"title":"The Effect of Preoperative Combined with Intravenous Lidocaine and Ketamine vs. Intravenous Ketamine on Pediatric Patients Undergoing Upper Gastrointestinal Endoscopy.","authors":"Amir Shafa,&nbsp;Reza Abediny,&nbsp;Hamidreza Shetabi,&nbsp;Sedighe Shahhosseini","doi":"10.5812/aapm-130991","DOIUrl":"https://doi.org/10.5812/aapm-130991","url":null,"abstract":"<p><strong>Background: </strong>Ketamine is widely used in pediatric sedation. New studies have recommended combination therapy to reduce the side effects of ketamine.</p><p><strong>Objectives: </strong>This study investigated the effect of adding intravenous (IV) lidocaine to ketamine on hemodynamic parameters, endoscopist satisfaction, and recovery time of children undergoing gastrointestinal endoscopy.</p><p><strong>Methods: </strong>This triple-blind, randomized, controlled clinical trial was conducted in Isfahan, Iran (2021). One hundred twenty children between the ages of 1 and 6 were enrolled. Patients were divided into 2 groups. The intervention group received 1.0 mg/kg of IV lidocaine and 1.0 mg/kg of IV ketamine, and the placebo group received 1.0 mg/kg of IV ketamine and placebo 2 minutes before entering the endoscopic room. Patients in both groups were sedated with 1.0 mg/kg of propofol, 0.1 mg/kg of midazolam, and 2.0 ug/kg of fentanyl for the procedure. The pulse rate, mean arterial pressure (MAP), respiratory rate, and oxygen saturation were recorded 1 minute before injection and every 5 minutes afterward.</p><p><strong>Results: </strong>The mean (SD) ages of the intervention and control groups were 3.4 (1.5) and 3.4 (1.7), respectively. The mean difference in hemodynamic parameters between the 2 groups was insignificant during the investigation (P > 0.05). Furthermore, no significant differences were found regarding endoscopist satisfaction scores and length of recovery room stay (P > 0.05).</p><p><strong>Conclusions: </strong>Adding low-dose IV lidocaine to ketamine for pediatric sedation does not significantly affect the hemodynamic status, endoscopist satisfaction, and recovery time.</p>","PeriodicalId":7841,"journal":{"name":"Anesthesiology and Pain Medicine","volume":"13 2","pages":"e130991"},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/73/84/aapm-13-2-130991.PMC10461382.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10175898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of the Effect of Intercostobrachial Nerve Block with and Without Ultrasound Guidance on Tourniquet Pain After Axillary Block of Brachial Plexus: A Randomized Clinical Trial. 超声引导下肋间臂神经阻滞对臂丛腋窝阻滞后止血带疼痛的疗效比较:随机临床试验。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-134819
Seyed Alireza Seyed Siamdoust, Behrooz Zaman, Samad Noorizad, Mahzad Alimian, Mona Barekati

Background: A tourniquet is used to control bleeding in the surgical field. Because part of the inner arm is innervated by the intercostobrachial nerve (ICBN), a tourniquet can cause intolerable pain.

Objectives: The present study aimed to compare the effect of ICBN block with and without ultrasound (US) guidance on tourniquet pain after axillary block.

Methods: This study was performed on 60 patients who were candidates for surgery. The patients were divided into 3 groups: the control group (n = 22), the traditional ICBN (TICBN) blockade group (n = 19), and the US-guided ICBN blockade group (n = 19). After the intervention, the duration of the onset and intensity of pain was recorded for all patients according to the Numeric Rating Scale (NRS). Data analysis was performed using SPSS.

Results: No significant differences were observed in demographic variables between the 3 groups (P > 0.05). The pain intensity in the TICBN blockade (P = 0.001) and US-guided ICBN blockade (P = 0.001) groups was significantly less than in the control group. The mean duration of pain onset was significantly higher in the TICBN blockade (P = 0.021) and US-guided ICBN blockade (P = 0.013) groups than in the control group. No significant difference was observed in the mean of pain intensity (P = 0.48) and the mean duration of pain onset (P = 0.44) between the US-guided ICBN blockade and TICBN blockade groups.

Conclusions: The pain caused by a tourniquet can be managed by ICBN block during hand and forearm surgery. It is recommended to use US guidance for more success and safety.

背景:止血带用于控制手术野出血。由于手臂内侧部分受肋臂间神经(ICBN)支配,止血带会引起无法忍受的疼痛。目的:本研究旨在比较超声引导下和不引导下ICBN阻滞对腋窝阻滞后止血带疼痛的影响。方法:本研究对60例手术候选者进行研究。将患者分为3组:对照组(n = 22)、传统ICBN (TICBN)阻断组(n = 19)和美国引导ICBN阻断组(n = 19)。干预后,根据数字评定量表(NRS)记录所有患者的疼痛发作时间和疼痛强度。数据分析采用SPSS软件。结果:3组患者人口学指标比较,差异均无统计学意义(P > 0.05)。TICBN阻断组(P = 0.001)和us引导ICBN阻断组(P = 0.001)疼痛强度明显小于对照组。与对照组相比,TICBN阻断组(P = 0.021)和us引导ICBN阻断组(P = 0.013)的平均疼痛持续时间显著增加。美国引导的ICBN阻断组和TICBN阻断组的平均疼痛强度(P = 0.48)和平均疼痛持续时间(P = 0.44)无显著差异。结论:在手部和前臂手术中,止血带引起的疼痛可以通过ICBN阻滞来控制。建议使用美国指南,以获得更大的成功和安全性。
{"title":"Comparison of the Effect of Intercostobrachial Nerve Block with and Without Ultrasound Guidance on Tourniquet Pain After Axillary Block of Brachial Plexus: A Randomized Clinical Trial.","authors":"Seyed Alireza Seyed Siamdoust,&nbsp;Behrooz Zaman,&nbsp;Samad Noorizad,&nbsp;Mahzad Alimian,&nbsp;Mona Barekati","doi":"10.5812/aapm-134819","DOIUrl":"https://doi.org/10.5812/aapm-134819","url":null,"abstract":"<p><strong>Background: </strong>A tourniquet is used to control bleeding in the surgical field. Because part of the inner arm is innervated by the intercostobrachial nerve (ICBN), a tourniquet can cause intolerable pain.</p><p><strong>Objectives: </strong>The present study aimed to compare the effect of ICBN block with and without ultrasound (US) guidance on tourniquet pain after axillary block.</p><p><strong>Methods: </strong>This study was performed on 60 patients who were candidates for surgery. The patients were divided into 3 groups: the control group (n = 22), the traditional ICBN (TICBN) blockade group (n = 19), and the US-guided ICBN blockade group (n = 19). After the intervention, the duration of the onset and intensity of pain was recorded for all patients according to the Numeric Rating Scale (NRS). Data analysis was performed using SPSS.</p><p><strong>Results: </strong>No significant differences were observed in demographic variables between the 3 groups (P > 0.05). The pain intensity in the TICBN blockade (P = 0.001) and US-guided ICBN blockade (P = 0.001) groups was significantly less than in the control group. The mean duration of pain onset was significantly higher in the TICBN blockade (P = 0.021) and US-guided ICBN blockade (P = 0.013) groups than in the control group. No significant difference was observed in the mean of pain intensity (P = 0.48) and the mean duration of pain onset (P = 0.44) between the US-guided ICBN blockade and TICBN blockade groups.</p><p><strong>Conclusions: </strong>The pain caused by a tourniquet can be managed by ICBN block during hand and forearm surgery. It is recommended to use US guidance for more success and safety.</p>","PeriodicalId":7841,"journal":{"name":"Anesthesiology and Pain Medicine","volume":"13 2","pages":"e134819"},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/06/c2/aapm-13-2-134819.PMC10439685.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10040821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Spinal Versus General Anesthesia for Spine Surgery During the COVID-19 Pandemic: A Case Series. COVID-19大流行期间脊柱手术的脊柱麻醉与全身麻醉:病例系列
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-134783
Seyed Abdolhadi Daneshi, Mohsen Nabiuni, Morteza Taheri, Reza Pour Roustaei Ardekani

Background: Hospitals are one of the primary resources for disease transmission, so many guidelines were published, and neurosurgeons were advised to postpone elective spine surgeries during the COVID-19 pandemic.

Objectives: To avoid pulmonary complications and reduce the risk of spreading the virus and contracting the disease during the COVID-19 era, we operated a group of our patients under spinal anesthesia rather than general anesthesia.

Methods: We retrospectively analyzed all patients who underwent discectomy surgery for lumbar spinal disc herniation under SA between September 2020 and 2021.

Results: Sixty-four patients diagnosed with lumbar disc herniation underwent lumbar discectomy with SA. All patients except three were male. The mean age was 44.52 ± 7.95 years (28 to 64 years). The mean procedure time for SA was 10 minutes. The duration of the surgery was 40 to 90 minutes per each level of disc herniation. The mean blood loss was 350 cc (200 to 600 cc). The most common involved level was L4/L5 intervertebral disc (n = 40 patients; 63.5%). The mean recovery time was 20 minutes. Only three patients requested more analgesics for relief of their pain postoperatively. All patients with discectomy were discharged a day after surgery, and in the case of fusion, two days after surgery. All the patients were followed up for six months, showing no recurrence symptoms, good pain relief, satisfaction with the surgery, and no bad memory of the surgery.

Conclusions: Spinal anesthesia is a good alternative or even the main anesthesia route for patients with lumbar disc herniation. More studies are needed to elucidate the best candidate for SA in patients with lumbar pathology.

背景:医院是疾病传播的主要资源之一,因此发布了许多指南,并建议神经外科医生在COVID-19大流行期间推迟选择性脊柱手术。目的:为避免新冠肺炎时期肺部并发症的发生,降低病毒传播和感染的风险,我们选择了一组患者在脊髓麻醉下进行手术,而不是全身麻醉。方法:我们回顾性分析了2020年9月至2021年9月在SA下接受腰椎间盘切除术治疗腰椎间盘突出症的所有患者。结果:64例诊断为腰椎间盘突出症的患者行腰椎间盘切除术。除3例患者外,其余均为男性。平均年龄44.52±7.95岁(28 ~ 64岁)。SA的平均手术时间为10分钟。每个椎间盘突出程度的手术时间为40 - 90分钟。平均失血量为350毫升(200至600毫升)。最常见的受累水平是L4/L5椎间盘(n = 40例;63.5%)。平均恢复时间为20分钟。只有3例患者要求更多的镇痛药以缓解术后疼痛。所有椎间盘切除术患者术后1天出院,融合术患者术后2天出院。所有患者随访6个月,无复发症状,疼痛缓解良好,手术满意,手术记忆无不良。结论:腰麻是治疗腰椎间盘突出症的一种很好的替代麻醉途径,甚至是主要麻醉途径。需要更多的研究来阐明腰椎病变患者的最佳SA候选方案。
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引用次数: 0
Comparison of Dextrose Prolotherapy and Triamcinolone Intraarticular Injection on Pain and Function in Patients with Knee Osteoarthritis - A Randomized Clinical Trial. 葡萄糖前体治疗和曲安奈德关节内注射对膝关节骨性关节炎患者疼痛和功能的影响——一项随机临床试验。
Q2 Medicine Pub Date : 2023-04-01 DOI: 10.5812/aapm-134415
Masume Bayat, Fateme Hojjati, Najmeh Sadat Boland Nazar, Mohsen Modabberi, Maryam Sadat Rahimi

Background: The present study was performed to assess the therapeutic effects of combined intra and extraarticular dextrose prolotherapy on knee osteoarthritis and its comparison with intra- articular triamcinolone injection.

Methods: In this study, 50 patients suffering from knee osteoarthritis were allocated into two groups as a double-blind randomized clinical trial. The first group received one session of dextrose prolotherapy as one intra-articular injection of 10cc dextrose 16% and periarticular intradermal injections of dextrose 12% at 4 points around the knee (2.5 cc at each point). The second group underwent therapy with one intra-articular injection of triamcinolone (40 mg).

Results: Compared to pretreatment, both interventions caused significant improvement in pain (evaluated by VAS) and WOMAC (all its components) in 1 and 3 months postintervention (all with P-value < 0.005). In the first month, pain reduction was significantly better in corticosteroid group (P-Value 0.002 and 0.048 respectively). In third month post intervention, improvements in VAS and WOMAC components were significantly greater in prolotherapy group.

Conclusions: Both methods of corticosteroid and dextrose prolotherapy (combined intra and extraarticular technique) are effective on pain and function of patients with knee osteoarthritis. Compared to corticosteroid, prolotherapy method was associated with less pain reduction in short- term, but its effects were more persistent and in midterm examinations (3 months), it was more effective than corticosteroid.

背景:观察关节内、关节外联合葡萄糖前驱治疗膝关节骨性关节炎的疗效,并与关节内注射曲安奈德酮进行比较。方法:本研究将50例膝关节骨性关节炎患者分为两组,采用双盲随机临床试验。第一组接受1次葡萄糖前驱治疗,关节内注射葡萄糖10cc 16%,关节周皮内注射葡萄糖12%,膝关节周围4个点(每个点2.5 cc)。第二组患者关节内注射曲安奈德(40 mg) 1次。结果:与预处理相比,两种干预措施在干预后1个月和3个月的疼痛(以VAS评估)和WOMAC(其所有成分)均有显著改善(p值均< 0.005)。在第一个月,皮质类固醇组疼痛减轻明显更好(p值分别为0.002和0.048)。干预后第3个月,前哨治疗组VAS和WOMAC评分改善明显大于前哨治疗组。结论:糖皮质激素联合葡萄糖前驱治疗(关节内外联合技术)对膝关节骨性关节炎患者的疼痛和功能均有较好的疗效。与皮质类固醇相比,前驱疗法在短期内减轻疼痛的效果较差,但其效果更持久,在中期检查(3个月)中,前驱疗法比皮质类固醇更有效。
{"title":"Comparison of Dextrose Prolotherapy and Triamcinolone Intraarticular Injection on Pain and Function in Patients with Knee Osteoarthritis - A Randomized Clinical Trial.","authors":"Masume Bayat,&nbsp;Fateme Hojjati,&nbsp;Najmeh Sadat Boland Nazar,&nbsp;Mohsen Modabberi,&nbsp;Maryam Sadat Rahimi","doi":"10.5812/aapm-134415","DOIUrl":"https://doi.org/10.5812/aapm-134415","url":null,"abstract":"<p><strong>Background: </strong>The present study was performed to assess the therapeutic effects of combined intra and extraarticular dextrose prolotherapy on knee osteoarthritis and its comparison with intra- articular triamcinolone injection.</p><p><strong>Methods: </strong>In this study, 50 patients suffering from knee osteoarthritis were allocated into two groups as a double-blind randomized clinical trial. The first group received one session of dextrose prolotherapy as one intra-articular injection of 10cc dextrose 16% and periarticular intradermal injections of dextrose 12% at 4 points around the knee (2.5 cc at each point). The second group underwent therapy with one intra-articular injection of triamcinolone (40 mg).</p><p><strong>Results: </strong>Compared to pretreatment, both interventions caused significant improvement in pain (evaluated by VAS) and WOMAC (all its components) in 1 and 3 months postintervention (all with P-value < 0.005). In the first month, pain reduction was significantly better in corticosteroid group (P-Value 0.002 and 0.048 respectively). In third month post intervention, improvements in VAS and WOMAC components were significantly greater in prolotherapy group.</p><p><strong>Conclusions: </strong>Both methods of corticosteroid and dextrose prolotherapy (combined intra and extraarticular technique) are effective on pain and function of patients with knee osteoarthritis. Compared to corticosteroid, prolotherapy method was associated with less pain reduction in short- term, but its effects were more persistent and in midterm examinations (3 months), it was more effective than corticosteroid.</p>","PeriodicalId":7841,"journal":{"name":"Anesthesiology and Pain Medicine","volume":"13 2","pages":"e134415"},"PeriodicalIF":0.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/0a/39/aapm-13-2-134415.PMC10439689.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10047207","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Comparative Study on the Effect of Intrathecal Bupivacaine vs. Ropivacaine on Maternal and Neonatal Outcomes After Cesarean Section: A Systematic Review and Meta-analysis. 鞘内布比卡因与罗哌卡因对剖宫产产妇和新生儿结局影响的比较研究:系统评价和荟萃分析
Q2 Medicine Pub Date : 2023-03-17 eCollection Date: 2023-06-01 DOI: 10.5812/aapm-134732
Molouk Jaafarpour, Aminolah Vasigh, Fatemeh Najafi, Hojat Sayadi, Elham Shafiei

Context: The type of anesthesia in cesarean section can affect the mother and baby. This study aimed to determine the comparative effect of intrathecal hyperbaric bupivacaine vs. hyperbaric ropivacaine on maternal and neonatal outcomes after cesarean section.

Evidence acquisition: PubMed, Web of Science, Embase, Google Scholar, IranDoc, MagIran, and Scopus databases were searched from 1 September 2022 to 1 November 2022. Eighteen clinical trials with 1542 patients were included in the analysis.

Results: There was no statistically significant difference in hypotension, bradycardia, and Apgar score between the 2 groups (P > 0.05). The risk of nausea (relative risk (RR), 1.526; 95% CI, 1.175 - 1.981; P = 0.001) and vomiting (RR, 1.542; 95% CI, 1.048 - 2.268; P = 0.02) caused by bupivacaine was 0.53% and 0.54% higher than that of ropivacaine. The incidence of shivering (RR, 2.24; 95% CI, 1.480 - 3.39; P = 0.00) was 2.24 times higher in the bupivacaine group than in the ropivacaine group. The average onset time of sensory block (standardized mean difference (SMD), -0.550; 95% CI, -1.054 to -0.045; P = 0.032) and motor block (SMD, -0.812; 95% CI, -1.254 to -0.371; P = 0.000) was significantly lower in the bupivacaine group than in the ropivacaine group.

Conclusions: Despite the fact that ropivacaine and bupivacaine are effective in cesarean section, ropivacaine is more favorable because of less hemodynamic changes, less duration of sensory and motor block, and fewer side effects, which are effective in patient recovery.

背景:剖宫产的麻醉类型会影响母亲和婴儿。本研究旨在确定鞘内高压布比卡因与高压罗哌卡因对剖宫产术后产妇和新生儿结局的比较效果。证据获取:从2022年9月1日至2022年11月1日检索PubMed、Web of Science、Embase、谷歌Scholar、IranDoc、MagIran和Scopus数据库。18项临床试验1542例患者纳入分析。结果:两组患者低血压、心动过缓、Apgar评分比较,差异无统计学意义(P < 0.05)。恶心风险(相对危险度RR, 1.526);95% ci, 1.175 - 1.981;P = 0.001)和呕吐(RR, 1.542;95% ci, 1.048 - 2.268;P = 0.02)分别比罗哌卡因高0.53%和0.54%。寒战发生率(RR, 2.24;95% ci, 1.480 - 3.39;P = 0.00)比罗哌卡因组高2.24倍。感觉阻滞平均发作时间(标准化平均差(SMD), -0.550;95% CI, -1.054 ~ -0.045;P = 0.032)和电机块(SMD, -0.812;95% CI, -1.254 ~ -0.371;P = 0.000),布比卡因组明显低于罗比卡因组。结论:罗哌卡因与布比卡因在剖宫产术中均有效,但罗哌卡因血流动力学变化小,感觉和运动阻滞持续时间短,副作用少,有利于患者康复。
{"title":"A Comparative Study on the Effect of Intrathecal Bupivacaine vs. Ropivacaine on Maternal and Neonatal Outcomes After Cesarean Section: A Systematic Review and Meta-analysis.","authors":"Molouk Jaafarpour, Aminolah Vasigh, Fatemeh Najafi, Hojat Sayadi, Elham Shafiei","doi":"10.5812/aapm-134732","DOIUrl":"10.5812/aapm-134732","url":null,"abstract":"<p><strong>Context: </strong>The type of anesthesia in cesarean section can affect the mother and baby. This study aimed to determine the comparative effect of intrathecal hyperbaric bupivacaine vs. hyperbaric ropivacaine on maternal and neonatal outcomes after cesarean section.</p><p><strong>Evidence acquisition: </strong>PubMed, Web of Science, Embase, Google Scholar, IranDoc, MagIran, and Scopus databases were searched from 1 September 2022 to 1 November 2022. Eighteen clinical trials with 1542 patients were included in the analysis.</p><p><strong>Results: </strong>There was no statistically significant difference in hypotension, bradycardia, and Apgar score between the 2 groups (P > 0.05). The risk of nausea (relative risk (RR), 1.526; 95% CI, 1.175 - 1.981; P = 0.001) and vomiting (RR, 1.542; 95% CI, 1.048 - 2.268; P = 0.02) caused by bupivacaine was 0.53% and 0.54% higher than that of ropivacaine. The incidence of shivering (RR, 2.24; 95% CI, 1.480 - 3.39; P = 0.00) was 2.24 times higher in the bupivacaine group than in the ropivacaine group. The average onset time of sensory block (standardized mean difference (SMD), -0.550; 95% CI, -1.054 to -0.045; P = 0.032) and motor block (SMD, -0.812; 95% CI, -1.254 to -0.371; P = 0.000) was significantly lower in the bupivacaine group than in the ropivacaine group.</p><p><strong>Conclusions: </strong>Despite the fact that ropivacaine and bupivacaine are effective in cesarean section, ropivacaine is more favorable because of less hemodynamic changes, less duration of sensory and motor block, and fewer side effects, which are effective in patient recovery.</p>","PeriodicalId":7841,"journal":{"name":"Anesthesiology and Pain Medicine","volume":" ","pages":"e134732"},"PeriodicalIF":0.0,"publicationDate":"2023-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664161/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47341392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
General Anesthesia in Schwartz-Jampel Syndrome: A Case Report. 全身麻醉治疗Schwartz-Jampel综合征1例
Q2 Medicine Pub Date : 2023-03-16 eCollection Date: 2023-06-01 DOI: 10.5812/aapm-129305
Pooya Derakhshan, Azadeh Habibi, Saied Amniati

Introduction: Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disease characterized by muscle weakness and stiffness, abnormal bone development, short stature, joint contractures, and facial dysmorphisms. Myopathy, anatomical deformities, and malignant hyperthermia are challenging for anesthesiologists.

Case presentation: This case report describes one case of SJS. The female patient was scheduled for Blepharoplasty in Rasuol Akram General Hospital.

Conclusions: These patients may have difficult intubation and be prone to malignant hyperthermia. We managed this patient by applying Rocuronium, propofol, and C-MAC video laryngoscopy.

简介:Schwartz-Jampel综合征(SJS)是一种罕见的常染色体隐性疾病,其特征是肌肉无力和僵硬、骨骼发育异常、身材矮小、关节挛缩和面部畸形。肌病、解剖畸形和恶性热疗对麻醉师来说是一项挑战。病例介绍:本病例报告描述了一例SJS病例。女患者安排在xxx综合医院进行眼睑整形术。结论:这些患者插管困难,易发生恶性高热。我们通过应用罗库、丙泊酚和C-MAC视频喉镜对该患者进行了治疗。
{"title":"General Anesthesia in Schwartz-Jampel Syndrome: A Case Report.","authors":"Pooya Derakhshan, Azadeh Habibi, Saied Amniati","doi":"10.5812/aapm-129305","DOIUrl":"10.5812/aapm-129305","url":null,"abstract":"<p><strong>Introduction: </strong>Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disease characterized by muscle weakness and stiffness, abnormal bone development, short stature, joint contractures, and facial dysmorphisms. Myopathy, anatomical deformities, and malignant hyperthermia are challenging for anesthesiologists.</p><p><strong>Case presentation: </strong>This case report describes one case of SJS. The female patient was scheduled for Blepharoplasty in Rasuol Akram General Hospital.</p><p><strong>Conclusions: </strong>These patients may have difficult intubation and be prone to malignant hyperthermia. We managed this patient by applying Rocuronium, propofol, and C-MAC video laryngoscopy.</p>","PeriodicalId":7841,"journal":{"name":"Anesthesiology and Pain Medicine","volume":" ","pages":"e129305"},"PeriodicalIF":0.0,"publicationDate":"2023-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664156/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43008574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Anesthesiology and Pain Medicine
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