pain response

疼痛反应
  • 文章类型: Journal Article
    背景和目的:尽管肾细胞癌(RCC)的靶向治疗取得了迅速的进展,骨转移仍然是一个显著增加发病率和降低患者生活质量的主要问题.已知常规分割放疗(CF-RT)是骨转移的重要局部治疗选择;然而,肾癌骨转移传统上被认为对CF-RT有抗性.我们旨在研究CF-RT对RCC症状性骨转移的有效性,并确定与靶向治疗时代治疗结果相关的预测因素。材料和方法:在2011年1月至2023年12月之间,对50例接受CF-RT姑息治疗的RCC症状性骨转移患者中的73个病灶进行了评估。41例患者中的62个病变被纳入本研究。在CF-RT期间使用靶向治疗治疗45个病变(72.6%)。最常见的辐射剂量分级是10个部分中的30个灰色(Gy)(50%)和13个部分中的39个Gy(16.1%)。结果:62个病灶中有51个(82.3%)疼痛缓解,12个月局部控制率(LC)为61.2%。值得注意的是,72.6%的疗程结合靶向治疗。接受靶向治疗的患者的12个月LC率为74.8%,未接受靶向治疗的患者仅为10.9%(p<0.001)。有利的东部肿瘤协作组表现状态(p=0.026)和疼痛反应(p<0.001)是改善LC的独立预测因子。辐射剂量递增改善了对辐射敏感的患者的LC。在多个疗程的患者中证实了一致的治疗反应。结论:CF-RT结合靶向治疗可增强疼痛缓解和LC。对初始治疗反应良好的患者通常对随后的CF-RT表现出一致的反应,以引起其他疼痛的骨病变。因此,CF-RT可以是靶向治疗的极好的补充局部治疗方式。
    Background and Objectives: Despite rapid advances in targeted therapies for renal cell carcinoma (RCC), bone metastases remain a major problem that significantly increases morbidity and reduces patients\' quality of life. Conventional fractionated radiotherapy (CF-RT) is known to be an important local treatment option for bone metastases; however, bone metastases from RCC have traditionally been considered resistant to CF-RT. We aimed to investigate the effectiveness of CF-RT for symptomatic bone metastasis from RCC and identify the predictive factors associated with treatment outcomes in the targeted therapy era. Materials and Methods: Between January 2011 and December 2023, a total of 73 lesions in 50 patients treated with a palliative course of CF-RT for symptomatic bone metastasis from RCC were evaluated, and 62 lesions in 41 patients were included in this study. Forty-five lesions (72.6%) were treated using targeted therapy during CF-RT. The most common radiation dose fractionations were 30 gray (Gy) in 10 fractions (50%) and 39 Gy in 13 fractions (16.1%). Results: Pain relief was experienced in 51 of 62 lesions (82.3%), and the 12-month local control (LC) rate was 61.2%. Notably, 72.6% of the treatment course in this study was combined with targeted therapy. The 12-month LC rate was 74.8% in patients who received targeted therapy and only 10.9% in patients without targeted therapy (p < 0.001). Favorable Eastern Cooperative Oncology Group performance status (p = 0.026) and pain response (p < 0.001) were independent predictors of improved LC. Radiation dose escalation improved the LC in radiosensitive patients. A consistent treatment response was confirmed in patients with multiple treatment courses. Conclusions: CF-RT enhances pain relief and LC when combined with targeted therapy. Patients who responded well to initial treatment generally showed consistent responses to subsequent CF-RT for additional painful bone lesions. CF-RT could therefore be an excellent complementary local treatment modality for targeted therapy.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    在许多随机对照试验中已经证实了单次8-Gy放疗对疼痛性骨转移的有效性。然而,很少有报道描述单级分8-Gy放疗治疗骨转移以外的疼痛性肿瘤的有效性.我们进行了一项回顾性分析,以评估疼痛性非骨转移肿瘤对单次8-Gy放疗的疼痛反应。我们纳入了在2017年1月至2022年12月期间接受过此类肿瘤单次8-Gy放疗的患者,不包括脑转移患者。血液肿瘤和接受再照射的患者。疼痛反应评估基于医疗记录中记录的最佳反应,并由两名放射肿瘤学家进行。共有36名符合条件的患者被纳入本研究。照射部位包括8例患者的原发病灶,八个淋巴结转移,七个肌肉转移,四个胸膜播散,皮肤/皮下转移4个和其他5个部位。对24例患者放疗后的疼痛反应进行了评估。可评估患者的疼痛反应率为88%;24例患者中有21例出现反应。疼痛反应的中位评估日期为放疗后37天(范围:8-156天)。对四名患者(11%)进行了重新照射。单次8Gy放疗似乎是疼痛性非骨转移肿瘤的有希望的治疗选择,值得进一步研究。
    The effectiveness of single-fraction 8-Gy radiotherapy for painful bone metastases has been verified in numerous randomized controlled trials. However, few reports have described the effectiveness of single-fraction 8-Gy radiotherapy in painful tumors other than bone metastases. We conducted a retrospective analysis to evaluate the pain response to single-fraction 8-Gy radiotherapy in painful non-bone-metastasis tumors. We included patients who had received single-fraction 8-Gy radiotherapy for such tumors between January 2017 and December 2022, excluding those with brain metastases, hematological tumors and those who received re-irradiation. Pain response assessment was based on the best responses documented in the medical records and conducted by two radiation oncologists. A total of 36 eligible patients were included in this study. The irradiation sites included primary lesions in eight patients, lymph node metastases in eight, muscle metastases in seven, pleural dissemination in four, skin/subcutaneous metastases in four and other sites in five. Pain response was assessed in 24 patients after radiotherapy. Pain response rate was 88% in evaluable patients; 21 of the 24 patients experienced response. The median assessment date for pain response was 37 days (range: 8-156 days) after radiotherapy. Re-irradiation was performed in four patients (11%). Single-fraction 8-Gy radiotherapy seemed to be a promising treatment option for painful non-bone-metastasis tumors and warrants further investigation.
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  • 文章类型: Journal Article
    尽管它具有普遍性;感知,应对,回应,治疗方案,疼痛的整体体验在不同程度上受到生物心理社会因素的影响。疼痛感知,表达式,和控制是社会成员之间逐渐学习的行为,并且是特定于文化的。越来越多地报道了种族相关文化(民族文化)对更广泛背景下疼痛体验的影响。然而,来自一个国家不同种族文化群体的证据,特别是基于手术患者,是有限的。因此,作为旨在评估手术疼痛管理的民族文化决定因素的更广泛项目的定性研究工作,这项研究探讨了不同种族文化的患者和家庭对表达手术疾病相关疼痛的看法.
    本研究遵循主观主义-解释主义的哲学假设作为基础研究范式。我们有目的地在埃塞俄比亚三所民族地区的医院中选择了11名患者进行深入访谈,并选择了12名患者的家庭成员进行焦点小组讨论。在现象学框架中,采用专题分析。
    民族文化背景根据发现疼痛和被忽视的文化影响的紧急主题影响个人如何表达和应对疼痛,在文化背景下的痛苦表现力,疼痛表现力的刻板印象,和勇敢通过坚忍的反应。与鼓励疼痛表现的民族文化相比,在国内文化重视对疼痛的坚忍反应的地方,疼痛感觉通常是隐藏的。
    由于一个国家的民族文化多样性,个人可以以不同的方式表达和应对痛苦。研究人员和临床医生应考虑文化背景,同时在具有民族文化多样性的国家的手术患者中应用流行的一刀切的疼痛评估工具。
    UNASSIGNED: Despite its universal nature; perception, coping, responses, treatment options, and overall experiences of pain are influenced by biopsychosocial factors to various extents. Pain perception, expression, and control are progressively learned behaviors among members of a society and are culture-specific. Effects of ethnicity-related culture (ethnoculture) on pain experience in a broader context have increasingly been reported. However, evidence from ethnoculturally diverse groups of a nation, particularly based on surgical patients, is limited. Therefore, as a qualitative research effort of a broader project aimed at assessing ethnocultural determinants of surgical pain management, this study explored the perception of ethnoculturally diverse patients and families about expressing surgical disease-related pain.
    UNASSIGNED: This study follows subjectivist-interpretivist philosophical assumptions as an underpinning research paradigm. We purposively selected 11 patients for in-depth interviews and 12 patients\' family members for focus group discussions in three hospitals of ethnic-based regions of Ethiopia. In the phenomenological frame, thematic analysis was employed.
    UNASSIGNED: Ethnocultural background influences how individuals express and respond to pain according to emergent themes of finding- Pain and overlooked cultural influence, Pain expressiveness in cultural context, Stereotypes of pain expressiveness, and Bravehood through stoic response. Pain feelings are commonly hidden where the domestic culture values stoic response to pain compared to ethnoculture where pain expressiveness is encouraged.
    UNASSIGNED: Individuals can express and respond to pain differently due to ethnocultural diversity within a nation. Researchers and clinicians should consider cultural context while applying the prevailing one-size-fits-all pain assessment tools among surgical patients of a nation with ethnocultural diversity.
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  • 文章类型: Randomized Controlled Trial
    背景:膀胱测压对于评估膀胱功能至关重要。然而,儿童可能会对导尿的身体疼痛或焦虑以及对陌生环境的恐惧做出负面反应。膀胱测压过程中的这些疼痛反应可能会干扰膀胱测压过程,并难以解释膀胱测压结果。在这方面,国际儿童连续性协会建议在抱着婴儿时进行膀胱测压作为一种有效的非药物疼痛管理方法,但是没有足够的证据支持这一点。
    目的:本研究旨在分析父母在膀胱测压期间对减轻儿童疼痛的影响。
    方法:这是一项随机对照前后试验设计的实验研究。总共招募了64名6-18个月的参与者。在膀胱测压期间,实验组的参与者被放在父母的膝盖上,并抱在父母的怀里。对照组的参与者被放在检查台上。在手术过程中,两组父母都被允许以各种方式触摸他们的孩子,除了抱着他们,如果他们愿意,可以使用安抚奶嘴。行为(面部,腿,活动,哭泣,在三个时间点(立即,3,以及插入尿道导管后10分钟)。
    结果:比较两组,在实验组中,导尿管插入后3分钟(t=-2.165,p=0.034)和10分钟(t=-3.155,p=0.002)的行为疼痛反应比导尿管插入后立即降低。此外,氧饱和度增加更多(t=2.021,p=0.048),实验组插入导尿管后10min心率比3min下降更多(t=-2.033,p=0.047)。
    结论:这项研究表明,父母抱抱可以减轻儿童膀胱测压过程中的疼痛反应。需要进一步的研究来确认在膀胱测压期间父母持有的适用性和有用性。
    BACKGROUND: Cystometry is essential for evaluating bladder function. However, children may react negatively to the physical pain of urethral catheterization or anxiety and fear of an unfamiliar environment. These pain responses during the cystometry procedure may interfere with the cystometry procedure and make it difficult to interpret the cystometry result. In this regard, the International Children\'s Continence Society has advised performing cystometry while holding infants as an effective nonpharmacological pain management method, but there is insufficient evidence to support this.
    OBJECTIVE: This study aimed to analyze the effect of parental holding on reducing pain in children during cystometry.
    METHODS: This was an experimental study in a randomized controlled pre-post test design. A total of 64 participants aged 6-18 months were recruited. During cystometry, the participants in the experimental group were placed on the parent\'s laps and held in the parents\' arms. The participants in the control group were laid down on the examination table. During the procedure, both groups of parents were allowed to touch their children in all ways except holding them and to use the pacifier if they wished. The behavioral (face, leg, activity, cry, consolability scale) and physiological (oxygen saturation and heart rate) pain responses were measured at three-time points (immediately, 3, and 10 min after urethral catheter insertion).
    RESULTS: Comparing the two groups, in the experimental group, the behavioral pain response at 3 min after urethral catheter insertion (t = -2.165, p = 0.034) and 10 min after (t = -3.155, p = 0.002) was decreased compared with that immediately after urethral catheter insertion. In addition, oxygen saturation increased more (t = 2.021, p = 0.048), and the heart rate decreased more (t = -2.033, p = 0.047) at 10 min than at 3 min after urethral catheter insertion in the experimental group.
    CONCLUSIONS: This study revealed that parental holding could reduce pain responses during cystometry in children. Further research is required to confirm the applicability and usefulness of parental holding during cystometry.
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  • 文章类型: Journal Article
    目的:在新生儿重症监护病房中,早产儿会经历许多痛苦的手术。本研究旨在评估示波血压(BP)测量对早产儿疼痛反应的影响。
    方法:这项前瞻性研究在III级新生儿重症监护病房进行了4个月。如果没有全身性疾病,则包括胎龄<34周和月经后年龄<36周的早产新生儿。在右臂上进行BP测量。早产儿疼痛谱修订(PIPP-R)评分被评估前三次,during,和10分钟后的BP测量。
    结果:在5个月期间,100名早产儿(53名男婴)纳入研究。婴儿的平均出生体重和胎龄为1148(IQR:1015-1300)g和28(IQR:27-30)周,分别。34%的新生儿PIPP-R评分≥7。PIPP-R评分在BP测量期间增加,之后降低。
    结论:我们的结果表明,作为一种非侵入性监测工具,示波法血压测量通常被认为可以在月经后<36周龄的早产儿中产生轻度疼痛。
    OBJECTIVE: Preterm neonates are exposed to many painful procedures in neonatal intensive care units. This study aims to evaluate the effect of oscillometric blood pressure (BP) measurement on pain response in preterm infants.
    METHODS: This prospective study was performed over 4 months in a level III neonatal intensive care unit. Premature neonates whose gestational age was <34 weeks and postmenstrual age <36 weeks were included if they had no systemic diseases. BP measurement was performed on the right arm. The Premature Infant Pain Profile-Revised (PIPP-R) scores were evaluated three times before, during, and 10 min after BP measurement.
    RESULTS: During the 5-month period, 100 preterm neonates (53 male infants) were included in the study. Median birth weight and gestational age of the infants were 1148 (IQR: 1015-1300) g and 28 (IQR: 27-30) weeks, respectively. PIPP-R scores were found to be ≥7 in 34% of neonates. PIPP-R scores increased during BP measurement and decreased after.
    CONCLUSIONS: Our results demonstrated that oscillometric BP measurement which is generally accepted as a non-invasive tool for monitoring can produce mild pain in premature neonates of postmenstrual age <36 weeks.
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  • 文章类型: Journal Article
    223Ra,靶向α治疗,已被批准用于治疗具有骨转移的转移性去势抵抗性前列腺癌(mCRPC)的患者。在第三阶段ALSYMPCA研究中,与安慰剂相比,223Ra延长了生存期并改善了生活质量。我们的真实世界研究,PARABO,研究了在临床实践中接受223Ra治疗的mCRPC和有症状骨转移患者的疼痛和骨痛相关生活质量。方法:PARABO是一种前瞻性的,观察,在德国核医学中心进行的非介入性单臂研究(NCT02398526)。主要终点是有临床意义的疼痛反应(简短疼痛清单中最严重疼痛项目评分比基线改善≥2分)。结果:分析包括354例患者,谁接受了6个223Ra注射的中位数(范围,1-6).67%(236/354)接受了5-6次注射,33%(118/354)接受了1-4次注射。在216名基线疼痛评分超过1的患者中,59%(128)在治疗期间有临床意义的疼痛反应。对应率为67%(范围,98/146),5-6次223Ra注射与43%(范围,30/70)进行1-4次注射,60%(范围,60/100)在不超过20个病变的患者中与59%(范围,65/111)在那些有20个以上病变的人中,和65%(范围,69/106)在没有先前或同时使用阿片类药物的患者中,与54%(范围,59/110)在先前或同时使用阿片类药物的人中。治疗期间,简短疼痛清单的平均子量表评分(疼痛严重程度和疼痛干扰)得到改善。结论:223Ra减轻了mCRPC和有症状骨转移患者的疼痛,特别是在接受5-6次注射的患者中。转移性疾病的程度不影响疼痛反应。
    223Ra, a targeted α-therapy, is approved for the treatment of patients with metastatic castration-resistant prostate cancer (mCRPC) who have bone metastases. In the phase 3 ALSYMPCA study, 223Ra prolonged survival and improved quality of life versus placebo. Our real-world study, PARABO, investigated pain and bone pain-related quality of life in patients with mCRPC and symptomatic bone metastases receiving 223Ra in clinical practice. Methods: PARABO was a prospective, observational, noninterventional single-arm study conducted in nuclear medicine centers across Germany (NCT02398526). The primary endpoint was a clinically meaningful pain response (≥2-point improvement from baseline for the worst-pain item score in the Brief Pain Inventory-Short Form). Results: The analysis included 354 patients, who received a median of 6 223Ra injections (range, 1-6). Sixty-seven percent (236/354) received 5-6 injections, and 33% (118/354) received 1-4 injections. Of 216 patients with a baseline worst-pain score of more than 1, 59% (128) had a clinically meaningful pain response during treatment. Corresponding rates were 67% (range, 98/146) with 5-6 223Ra injections versus 43% (range, 30/70) with 1-4 injections, 60% (range, 60/100) in patients with no more than 20 lesions versus 59% (range, 65/111) in those with more than 20 lesions, and 65% (range, 69/106) in patients without prior or concomitant opioid use versus 54% (range, 59/110) in those with prior or concomitant opioid use. Mean subscale scores (pain severity and pain interference) on the Brief Pain Inventory-Short Form improved during treatment. Conclusion: 223Ra reduced pain in patients with mCRPC and symptomatic bone metastases, particularly in patients who received 5-6 injections. The extent of metastatic disease did not impact pain response.
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  • 文章类型: Journal Article
    The aim of this study was to compare the pain responses (as measured by noise and movement) during administration of local anaesthetic and during and after disbudding in goat kids. Eighty, seven- to ten-day-old, Saanen goat kids from one farm were enrolled and randomly assigned to one of four different methods of pain relief. Twenty kids had local anaesthetic (LA) applied at two sites per horn bud (LA group), 20 kids had LA applied to the two locations using a jet injector (JI group) and 20 kids were given a general anaesthetic (GA) using a combination of 0.02 mg/kg medetomidine and 2 mg/kg ketamine followed by a horn bud block applied as per the LA group (GA group). The remaining 20 kids had no treatment other than meloxicam (control group). Although responses between goat kids and at different time periods were variable, in comparison to the control group, GA eliminated the responses associated with injection of lignocaine and the responses during the period of disbudding, and provided a reduction in head scratches and shakes across multiple time periods.
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  • 文章类型: Journal Article
    由于复杂的解剖结构和生物力学,目前对于颈椎转移瘤的标准姑息治疗与高复发风险和并发症相关.立体定向放射治疗(SBRT)可以在最大程度上保护正常器官的同时为肿瘤提供根治性剂量。然而,SBRT治疗颈椎转移瘤的疗效和安全性尚不明确.从我们前瞻性维护的数据库中获得了2006年至2021年期间使用射波刀进行SBRT治疗的71例颈椎转移患者的数据。主要终点是SBRT完成后12周的疼痛反应;次要终点包括局部控制(LC),总生存期(OS),和不良事件。根据脊髓和食道剂量限制,标准风险患者计划接受30Gy(范围21-36),中位分数为3(范围1-3),高危患者接受35Gy(范围24-50),中位分数为5(范围4-5)。中位随访时间为17.07个月(范围3.1-118.9)。SBRT完成12周后,55例基线疼痛患者中有54例(98.2%)达到疼痛反应,46例(83.6%)达到完全疼痛反应。1年和2年的LC率分别为93.1%和90%,分别。1年和2年OS率分别为66.2%和37.4%,分别。8例患者出现1-4级不良事件(6个椎体压缩性骨折[VCF],其中五人在SBRT之前有VCF;和两次偏瘫)。没有观察到5级不良事件。因此,经风险适应的SBRT治疗颈椎转移瘤获得了较高的疼痛控制和LC发生率,且不良事件可接受.
    Owing to the complex anatomical structure and biomechanics, the current standard palliative treatments for cervical spinal metastases are associated with a high risk of recurrence and complications. Stereotactic body radiotherapy (SBRT) can provide radical dose to tumors while protecting normal organs to the maximum extent. However, the efficacy and safety of SBRT for cervical spinal metastases is not well characterized. Data from 71 patients with cervical spine metastases who were treated with SBRT using CyberKnife between 2006 and 2021 were obtained from our prospectively maintained database. Primary endpoint was pain response at 12 weeks following SBRT completion; secondary endpoints included local control (LC), overall survival (OS), and adverse events. Standard-risk patients were planned to receive 30 Gy (range 21-36) with median fractions of 3 (range 1-3) and high-risk patients 35 Gy (range 24-50) with median fractions of 5 (range 4-5) according to the spinal cord and esophagus dose constraints. The median follow-up time was 17.07 months (range 3.1-118.9). After 12 weeks of SBRT completion, 54 (98.2%) of 55 patients with baseline pain achieved pain response and 46 (83.6%) achieved complete pain response. LC rates were 93.1% and 90% at 1 year and 2 year, respectively. The 1-year and 2-year OS rates were 66.2% and 37.4%, respectively. Eight patients experienced grades 1-4 adverse events (six vertebral compression fracture [VCF], five of them had VCF before SBRT; and two hemiparesis). No grade 5 adverse events were observed. Therefore, risk-adapted SBRT for cervical spine metastases achieved high pain control and LC rates with acceptable adverse events.
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  • 文章类型: Journal Article
    探索了麻醉奶山羊孩子角芽周围皮肤的三种选择。将45名<10天大的Saanen山羊孩子随机分为五个治疗组(局部麻醉乳膏(TA),蒸汽冷却液喷雾(VS),喷射注射器(JI)应用的局部麻醉药,控制-没有治疗,但施加了痛苦的刺激(C),假-没有治疗和触摸部位用手指。痛苦的刺激是在角芽周围的皮肤上多次针刺。测量的结果变量是心率运动,在治疗应用和角芽周围疼痛刺激的施用过程中发声。与TA相比,在应用VS期间心率更大。TA和VS似乎对疼痛刺激的反应都没有任何影响。与TA组相比,JI组的孩子表达明显疼痛反应的几率降低了96%,与其他三个治疗组的综合结果相比,在疼痛过程中出现高运动等级的几率降低了83%。
    Three options for anesthetizing the skin around the horn bud of dairy goat kids were explored. Forty-five <10-day-old Saanen goat kids from were randomly split into five treatment groups (topical anesthetic cream (TA), vapocoolant spray (VS), local anesthetic applied by jet injector (JI), control - no treatment but painful stimulus applied (C), sham - no treatment and touching sites with a finger. The painful stimulus was multiple needle pricks on the skin around the horn bud. The outcome variables measured were heart rate movement, and vocalization during treatment application and administration of a painful stimulus around the horn bud. Heart rates were greater during application of a VS compared to TA.Neither the TA nor the VS appeared to have any effect on the response to the painful stimulus. Kids in the JI group had a 96% reduced odds of expressing a marked pain response in comparison to TA group and an 83% reduction in the odds of a high movement grade during a painful procedure in comparison to the combined results of the other three treatment groups.
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