CDC, Centers for Disease Control and Prevention

CDC,疾病控制和预防中心
  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    UNASSIGNED:本报告的目的是在母亲对青霉素过敏时,提高对头孢曲松作为预防先天性梅毒(CS)的替代疗法的认识,尤其是对青霉素脱敏不能进行或不安全时。
    UNASSIGNED:一名梅毒阳性的37岁孕妇对青霉素伴史蒂文斯-约翰逊综合征(SJS)有反应;在传染病诊所就诊时,她的快速血浆反应素(RPR)为1:64。用两个疗程的头孢曲松预防了CS:在第12周每天1gIV10天,然后在第28周每天250mgIM10天,RPR滴度下降了4倍,达到1:16,表明治愈。根据美国儿科学会(AAP)的指南,当母亲在出生时不使用青霉素时,对新生儿进行全面检查。除了体检,血液中的梅毒抗体有检测不到的RPR,腰椎穿刺产生正常的脑脊液(CSF),长骨的X线照相术是正常的。该儿童肌内给药50,000单位/kg的苄星青霉素。在儿科医生的2个月随访中,母亲或新生儿没有过敏或后遗症的担忧。
    UNASSIGNED:本报告的目标是提高对头孢曲松替代青霉素预防CS的认识,并提高相应调整AAP指南的可能性。然而,研究以确定最佳的治疗途径和时机是必要的。
    UNASSIGNED: The purpose of this report is to increase awareness of ceftriaxone as an alternative therapy for the prevention of congenital syphilis (CS) when the mother is allergic to penicillin, especially when desensitization to penicillin cannot be performed or is unsafe.
    UNASSIGNED: A 37-year-old pregnant woman who was syphilis positive reacted to penicillin with Stevens-Johnson syndrome (SJS); her rapid plasma reagin (RPR) was 1:64 at presentation to the infectious disease clinic. CS was prevented with two courses of ceftriaxone: 10 days 1 g IV daily at week 12 followed by 10 days of 250 mg IM daily at week 28 achieved a 4-fold fall in RPR titer to 1:16, indicating cure. Full work-up of the neonate according to the guidelines of the American Academy of Pediatrics (AAP) when penicillin is not used in the mother was conducted at birth. In addition to physical exam, syphilis antibodies in blood had an undetectable RPR, a lumbar puncture produced normal cerebrospinal fluid (CSF), and roentgenography of long bones was normal. The child was administered 50,000 units/kg of benzathine penicillin intramuscularly. There were no concerns for allergy or sequela in the mother or neonate at 2-month follow-up with the pediatrician.
    UNASSIGNED: The goal of this report is to increase awareness of ceftriaxone as an alternative to penicillin in the prevention of CS and to raise the possibility of adjusting AAP guidelines accordingly. However, studies to determine the best route and timing of therapy are necessary.
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  • 文章类型: Case Reports
    孤立的颅神经VI麻痹是未诊断的神经梅毒的罕见初始表现。一名33岁的男性,有一个月的进行性头痛和复视病史。神经系统检查仅显示左侧有孤立的外展麻痹。头颅成像无异常。他的脑脊液检查显示淋巴细胞为主的白细胞增多和蛋白质升高。微生物检查均为阴性。进一步检查显示患者血清快速血浆Reagin和酶免疫分析反应。人类免疫缺陷病毒的酶联免疫吸附试验也呈阳性。然后将他的脑脊液送去快速血浆Reagin以确认神经梅毒的诊断。他完成了14天的静脉注射青霉素,并最终部分治愈了外展麻痹。我们描述了第二例仅表现为孤立的颅神经VI受累的神经梅毒。在进一步审查时,我们的病例是记录的第一例患者患有未确诊的人类免疫缺陷病毒感染.孤立的颅神经炎有各种区别,但有感染原因,尤其是神经梅毒,尽管有明显的良性病史,但仍应在具有已知危险因素的年轻人中考虑。
    An isolated cranial nerve VI palsy is a rare initial manifestation of undiagnosed neurosyphilis. A 33-year-old male presented with a one month history of progressive headache and diplopia. Neurologic examination only revealed an isolated abducens palsy on the left. Cranial imaging was unremarkable. Examination of his cerebrospinal fluid revealed lymphocytic predominant leukocytosis and elevated protein. Microbiologic work-up were all negative. Further work-up revealed the patient to be serum Rapid Plasma Reagin and Enzyme Immunoassay reactive. Enzyme-linked immunosorbent assay for Human Immunodeficiency Virus also tested positive. His cerebrospinal fluid was then sent for Rapid Plasma Reagin to confirm the diagnosis of neurosyphilis. He completed 14 days of intravenous penicillin and was eventually discharged with partial resolution of the abducens palsy. We describe the second case of neurosyphilis presenting only with an isolated cranial nerve VI involvement. On further review, ours was the first case documented on an individual who had an undiagnosed Human Immunodeficiency Virus infection. There are various differentials for an isolated cranial neuritis but infectious causes, particularly neurosyphilis, should be considered among young individuals with known risk factors despite their apparently benign medical history.
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  • 文章类型: Case Reports
    电子香烟是通过加热含有多种化学物质的流体来产生气溶胶的设备,比如尼古丁,添加剂,和调味品。它们是为了帮助戒烟而开发的,并被推广为社会可接受的,更健康,比传统香烟便宜。据报道,与电子烟使用相关的多种肺部疾病,它们的范围从轻度肺炎病例到可能需要插管和机械通气的危及生命的肺部疾病。大多数并发症是由于在电子烟中产生的气溶胶中产生各种未知和潜在有害的化学物质。这些疾病统称为电子烟/蒸发相关肺损伤(EVALI)。电子香烟作为传统香烟的更安全的替代品销售,年轻吸烟者的使用率最高。鉴于电子烟的使用及其肺部并发症的显著流行,EVALI应被认为是肺部疾病和电子烟病史患者广泛鉴别诊断的潜在病因。在这里,我们介绍了一例隐源性机化性肺炎,胸部C.T.显示一名有电子烟病史的患者的疯狂铺路模式.
    E-cigarettes are devices that generate an aerosol by heating a fluid containing multiple chemicals, such as nicotine, additives, and flavorings. They were developed to aid in smoking cessation and were promoted as socially acceptable, healthier, cheaper than conventional cigarettes. Multiple lung disorders related to e-cigarette use are reported, and they range from mild cases of pneumonitis to life-threatening lung disorders that may require intubation and mechanical ventilation. Most of the complications are due to the generation of various unknown and potentially harmful chemicals within the aerosol generated in the e-cigarette. These disorders are known collectively as e-cigarette/Vaping-associated lung injury (EVALI). E-cigarettes are marketed as safer alternatives to traditional cigarettes, with the highest rates of use are noted in young smokers. Given the significant prevalence of e-cigarettes use and their pulmonary complications, EVALI should be considered a potential etiology in the broad differential diagnosis of patients with pulmonary disease and a history of vaping. Herein, we present a case of cryptogenic organizing pneumonia with a chest C.T. showing a crazy-paving pattern in a patient with a history of vaping.
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  • 文章类型: Case Reports
    连体双胞胎是一种罕见的先天性异常,其特征是某些解剖结构的融合。冠状病毒-19(COVID-19)是一种新出现的传染性呼吸道疾病,影响全球,并可能导致儿童急性呼吸窘迫(ARDS)。COVID-19重建了医疗保健系统,包括外科护理和决策。
    在这里,我们描述了一个手术分离2.5个月大的脐眼连体双胞胎,其中一人(婴儿A)出现COVID-19相关的呼吸窘迫,以及在准备和执行复杂外科手术过程中面临的挑战。
    婴儿A接受了抗病毒治疗,氧气补充,和ICU的通风,而婴儿B保持稳定,并确认SARS-CoV-2阴性。在婴儿A变得临床稳定后进行分离手术。完成了缺陷闭合和重建。在一周的随访中,婴儿A死于肺部感染,而婴儿B在一年后仍然很好。
    手术分离的复杂性需要多学科团队的精心计划。大流行时期连体双胞胎的手术分离在文献中报道不多,需要更多的报告来提供进一步的见解。
    UNASSIGNED: Conjoined twin is a rare congenital anomaly characterized by a fusion of certain anatomical structures. Coronavirus-19 (COVID-19) is a new emerging infectious respiratory disease affecting worldwide and potentially leads to acute respiratory distress (ARDS) in children. COVID-19 has reconstructed the healthcare system, including surgical care and decision-making.
    UNASSIGNED: Herein we describe a surgical separation of 2.5 months old omphalopagus conjoined twins, with one of them (Baby A) presenting COVID-19-associated respiratory distress, as well as the challenges faced during the preparation and the execution of the complex surgical procedure.
    UNASSIGNED: Baby A underwent antiviral therapy, oxygen supplementation, and ventilation in the ICU, while baby B remained stable and confirmed negative for SARS-CoV-2. The separation surgery was conducted after baby A had become clinically stable. Defect closure and reconstruction were accomplished. At one week follow-up, Baby A died of lung infection, while baby B remained well after one year.
    UNASSIGNED: The complexity of surgical separation requires careful planning by a multidisciplinary team. Surgical separation of conjoined twins during the pandemic era has not been reported much in the literature, more reports are required to provide further insight.
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  • 文章类型: Case Reports
    描述了两名接受梅毒治疗的婴儿,这些婴儿在第一次产前检查时筛查为阴性,但在分娩时没有重新筛查。首先提出了经典,但无法识别,先天性梅毒的特征。在第二种情况下,可能的早期母体梅毒在分娩后不久使用密螺旋体先行反向筛查算法被诊断出来.虽然孩子的体格检查是正常的,母亲快速血浆反应素(RPR)阴性,该患儿接受梅毒治疗,因为母体证实的密螺旋体测试显示近期血清转换。鉴于先天性梅毒的再次出现,我们的报告旨在证明对风险增加的妇女进行重新筛查的重要性,并提高对新生儿梅毒疾病常见表现的认识。对于风险增加的女性来说,建议在妊娠晚期早期和在梅毒流行率高的社区和人群中再次进行梅毒检测。
    Two infants treated for syphilis born to at risk mothers who screened negative at their first prenatal visit but were not rescreened at delivery are described. The first presented with classic, but unrecognized, features of congenital syphilis. In the second case, possible early maternal syphilis was diagnosed soon after delivery using the treponemal first reverse-screening algorithm. Although the child\'s physical exam was normal and the maternal rapid plasma reagin (RPR) negative, the child was treated for syphilis because maternal confirmatory treponemal tests suggested recent seroconversion. Given the re-emergence of congenital syphilis, our report aims to demonstrate the importance of rescreening women at increased risk and improve awareness of common manifestations of the syphilis disease in the newborn. For women at increased risk, repeat syphilis testing early in the third trimester and again at delivery in communities and populations with a high prevalence of syphilis is recommended.
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  • 文章类型: Case Reports
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  • 文章类型: Journal Article
    背景:阿片类药物使用障碍(OUD)的特征是阿片类药物使用的问题模式导致临床上显著的损害或痛苦。阿片类激动剂治疗是OUD管理的组成部分,和丁丙诺啡经常用于OUD治疗,因为有强有力的临床疗效证据。然而,丁丙诺啡代谢的个体间遗传差异可能导致不同的治疗反应,导致一些患者治疗不足,复发风险增加。临床药物基因组学研究遗传遗传变异对药物反应的影响。我们的目标是证明药物遗传学测试对OUD管理结果的影响。
    方法:我们分析了一名患者,该患者报告每日剂量为24mg丁丙诺啡时出现不适,这是药房福利经理规定的每日最高限额。定期进行尿液筛查,以检测是否存在未经授权的物质,药物遗传学检测用于确定用于OUD管理的丁丙诺啡的合适剂量。
    结果:每天服用24毫克丁丙诺啡时,患者因使用未经授权的药物多次复发.药物遗传学测试显示,患者表现出细胞色素P4503A4超快速代谢表型,需要高于推荐剂量的丁丙诺啡(32mg)以进行适当的OUD管理。与标准给药相比,患者表现出基于药物遗传学的剂量推荐的复发次数减少。
    结论:作为临床决策支持的药物基因组学检测有助于OUD管理的个性化。关键利益相关者的合作对于将药物遗传学测试作为OUD管理中的护理标准至关重要。
    BACKGROUND: Opioid use disorder (OUD) is characterized by a problematic pattern of opioid use leading to clinically-significant impairment or distress. Opioid agonist treatment is an integral component of OUD management, and buprenorphine is often utilized in OUD management due to strong clinical evidence for efficacy. However, interindividual genetic differences in buprenorphine metabolism may result in variable treatment response, leaving some patients undertreated and at increased risk for relapse. Clinical pharmacogenomics studies the effect that inherited genetic variations have on drug response. Our objective is to demonstrate the impact of pharmacogenetic testing on OUD management outcomes.
    METHODS: We analyzed a patient who reported discomfort at daily buprenorphine dose of 24 mg, which was a mandated daily maximum by the pharmacy benefits manager. Regular urine screenings were conducted to detect the presence of unauthorized substances, and pharmacogenetic testing was used to determine the appropriate dose of buprenorphine for OUD management.
    RESULTS: At the 24 mg buprenorphine daily dose, the patient had multiple relapses with unauthorized substances. Pharmacogenetic testing revealed that the patient exhibited a cytochrome P450 3A4 ultrarapid metabolizer phenotype, which necessitated a higher than recommended daily dose of buprenorphine (32 mg) for adequate OUD management. The patient exhibited a reduction in the number of relapses on the pharmacogenetic-based dose recommendation compared to standard dosing.
    CONCLUSIONS: Pharmacogenomic testing as clinical decision support helped to individualize OUD management. Collaboration by key stakeholders is essential to establishing pharmacogenetic testing as standard of care in OUD management.
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