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COVID-19 and breastfeeding: can SARS-CoV-2 be spread through lactation? COVID-19和母乳喂养:SARS-CoV-2会通过哺乳传播吗?
Pub Date : 2021-06-30 eCollection Date: 2021-04-01 DOI: 10.15190/d.2021.11
Radu Marian Florea, Camelia Madalina Sultana

SARS-CoV-2 is a new betacoronavirus that was first reported in the Hubei province, China, in December 2019. The virus is likely transmitted through air droplets. However, there are reported cases where SARS-CoV-2-RNA was found in other samples, such as blood or stool. Nonetheless, there is limited information concerning the presence of viral RNA in pregnancy-related samples, specifically breast milk. However unlikely, there is still uncertainty regarding the possibility of vertical transmission from mother to infant through breastfeeding. This review aims to synthetize the literature written so far on this topic. Despite not being extensively researched, vertical transmission through breast milk seems unlikely. Case series showed that milk samples from mothers with COVID-19 were almost entirely negative. So far, there have been only 9 recorded cases of viral shedding in milk samples, uncertain however of the viability of the particles. Furthermore, WHO and UNICEF strongly encourage commencing breastfeeding after parturition, underlining the benefits of lactation. Moreover, some studies have proven the existence of IgG and IgA anti-SARS-CoV-2-antibodies in the maternal milk that could possibly play an important part in the neonate's protection against the virus. Vertical transmission through lactation seems unlikely, most studies pointing towards the safety of breastfeeding. However, further larger-scale studies need to be performed in order to clarify a yet uncertain matter.

SARS-CoV-2是一种新型冠状病毒,于2019年12月在中国湖北省首次报道。这种病毒很可能通过飞沫传播。然而,也有报道称,在血液或粪便等其他样本中发现了sars - cov -2 rna。尽管如此,关于病毒RNA在妊娠相关样本中存在的信息有限,特别是母乳。无论可能性有多大,通过母乳喂养从母亲向婴儿垂直传播的可能性仍然存在不确定性。这篇综述旨在综合迄今为止关于这一主题的文献。尽管没有广泛的研究,但通过母乳垂直传播似乎不太可能。病例系列显示,感染COVID-19的母亲的牛奶样本几乎完全呈阴性。到目前为止,在牛奶样本中只有9例病毒脱落的记录,但不确定这些颗粒的生存能力。此外,世卫组织和儿童基金会强烈鼓励在分娩后开始母乳喂养,强调哺乳的好处。此外,一些研究已经证明,母乳中存在IgG和IgA抗sars - cov -2抗体,这可能在新生儿抵御病毒方面发挥重要作用。通过哺乳的垂直传播似乎不太可能,大多数研究都指出母乳喂养的安全性。然而,需要进行更大规模的研究,以澄清一个尚不确定的问题。
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引用次数: 1
Increased QRS duration and dispersion are associated with mechanical dyssynchrony in patients with permanent right ventricular apical pacing. 永久性右心室心尖起搏患者QRS持续时间和离散度增加与机械非同步化有关。
Pub Date : 2021-06-26 eCollection Date: 2021-04-01 DOI: 10.15190/d.2021.7
Elibet Chávez-González, Arian Nodarse-Concepción, Ionuț Donoiu, Fernando Rodríguez-González, Raimundo Carmona Puerta, Juan Miguel Cruz Elizundia, Gustavo Padrón Peña, Ailed Elena Rodríguez-Jiménez

Background: Permanent right ventricular apical pacing may have negative effects on ventricular function and contribute to development of heart failure. We aimed to assess intra- and interventricular mechanical dyssynchrony in patients with permanent right ventricular apical pacing, and to establish electrocardiographic markers of dyssynchrony.

Methods: 84 patients (46:38 male:female) who required permanent pacing were studied. Pacing was done from right ventricular apex in all patients. We measured QRS duration and dispersion on standard 12-lead ECG. Intra- and interventricular mechanical dyssynchrony and left ventricular ejection fraction were assessed by transthoracic echocardiography. Patients were followed-up for 24 months.  Results: Six months after implantation, QRS duration increased from 128.02 ms to 132.40 ms, p≤0.05. At 24 months, QRS dispersion increased from 43.26 ms to 46.13 ms, p≤0.05. Intra- and interventricular dyssynchrony increased and left ventricular ejection fraction decreased during follow-up. A QRS dispersion of 47 ms predicted left ventricular dysfunction and long-term electromechanical dyssynchrony with a sensitivity of 80% and a specificity of 76%.  Conclusion: In patients with permanent right ventricular apical pacing there is an increased duration and dispersion of QRS related to dyssynchrony and decreased left ventricular ejection fraction. This study shows that QRS dispersion could be a better predictive variable than QRS duration for identifying left ventricular ejection fraction worsening in patients with permanent right ventricular apical pacing. The electrocardiogram is a simple tool for predicting systolic function worsening in these patients and can be used at the bedside for early diagnosis in the absence of clinical symptoms, allowing adjustments of medical treatment to prevent progression of heart failure and improve the patient's quality of life.

背景:永久性右心室尖起搏可能对心室功能有负面影响,并有助于心力衰竭的发展。我们的目的是评估永久性右心室心尖起搏患者的室内和室间机械非同步化,并建立非同步化的心电图标记。方法:84例需要永久性起搏的患者(男女比例46:38)。所有患者均从右心室心尖起搏。我们在标准12导联心电图上测量QRS持续时间和弥散度。通过经胸超声心动图评估室内外机械非同步化和左心室射血分数。随访24个月。结果:植入后6个月QRS持续时间由128.02 ms增加至132.40 ms, p≤0.05;24个月时,QRS弥散度由43.26 ms增加到46.13 ms, p≤0.05。随访期间,室内和室间非同步化增加,左室射血分数下降。47 ms的QRS离散度预测左心室功能障碍和长期机电不同步,敏感性为80%,特异性为76%。结论:永久性右室心尖起搏患者QRS持续时间和离散度增加与非同步化和左室射血分数降低有关。本研究表明,QRS离散度比QRS持续时间能更好地预测永久性右室起搏患者左室射血分数恶化。心电图是预测这些患者收缩功能恶化的简单工具,可以在没有临床症状的情况下用于床边的早期诊断,允许调整药物治疗以防止心力衰竭的进展并改善患者的生活质量。
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引用次数: 4
Detection of a Recurrent TMEM38B Gene Deletion Associated with Recessive Osteogenesis Imperfecta. 与隐性成骨不全相关的复发性TMEM38B基因缺失的检测。
Pub Date : 2021-03-31 DOI: 10.15190/d.2021.3
Khushnooda Ramzan, Maha Alotaibi, Rozeena Huma, Sibtain Afzal

Osteogenesis imperfecta is a clinically and genetically group of heterogeneous disorders associated with decreased bone density, brittle bones, bone deformity, recurrent fractures, and growth retardation. Osteogenesis imperfecta is commonly associated with mutations of the genes encoding for type I collagen (COL1A1/COL1A2). Mutations in other genes, some associated with type I collagen post-translational processing, have also been identified as the cause of osteogenesis imperfecta. Mutations in the transmembrane protein 38B (TMEM38B) gene have been reported in a rare autosomal recessive form of osteogenesis imperfecta.  TMEM38B encodes TRIC-B - a trimeric intracellular cation channel type B which is essential to modulate intracellular calcium signaling. In this study, we are reporting a case of osteogenesis imperfecta type XIV from a Saudi consanguineous family. Our patient was an eight-month-old child with short limbs, club feet, and lower limb deformities with developmental delay. Radiological findings were consistent with the evidence of osteogenesis imperfecta. There was no evidence of impaired hearing or blue sclera and based on the clinical assessment, we classified our patient as a non-syndromic osteogenesis imperfecta. A pathogenic deletion in the chromosome 9q31.2 region, partially encompassing the TMEM38B gene, was detected using chromosomal microarray analysis. This study expands our knowledge about the rare type of osteogenesis imperfecta in our consanguineous population. Besides, it emphasizes the use of genomic medicine in clinical practices to formulate early interventions to clinically improve the patient's condition.

成骨不全症是一种临床和遗传异质性疾病,与骨密度降低、骨脆、骨畸形、复发性骨折和生长迟缓有关。成骨不全通常与编码I型胶原蛋白(COL1A1/COL1A2)的基因突变有关。其他基因的突变,一些与I型胶原翻译后加工有关,也被确定为成骨不全的原因。据报道,跨膜蛋白38B (TMEM38B)基因突变是一种罕见的常染色体隐性成骨不全症。TMEM38B编码tricc -B -一种三聚体细胞内阳离子通道B型,对调节细胞内钙信号传导至关重要。在这项研究中,我们报告了一例来自沙特近亲家庭的成骨不完全性XIV型。我们的病人是一个8个月大的婴儿,四肢短,足内翻,下肢畸形,发育迟缓。影像学表现与成骨不全的证据一致。没有证据表明听力受损或蓝色巩膜,根据临床评估,我们将患者分类为非综合征性成骨不全。染色体微阵列分析检测到染色体9q31.2区域的致病性缺失,部分包含TMEM38B基因。本研究扩大了我们对近亲人群中罕见的成骨不全类型的认识。强调基因组医学在临床实践中的应用,制定早期干预措施,在临床上改善患者的病情。
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引用次数: 3
Anaesthesia for Awake Fiberoptic Intubation: Ultrasound-Guided Airway Nerve Block versus Ultrasonic Nebulisation with Lignocaine. 清醒纤维插管的麻醉:超声引导的气道神经阻滞与利多卡因超声雾化。
Pub Date : 2021-03-31 DOI: 10.15190/d.2021.4
Jharana Mohanta, Ajit Kumar, Ashutosh Kaushal, Praveen Talawar, Priyanka Gupta, Gaurav Jain
Background: In anticipated difficult airway, awake fiberoptic guided intubation should be the ideal plan of management. It requires sufficient upper airway anesthesia for patient’s comfort and cooperation. We compared the efficacy of ultrasound guided airway nerve blocks and ultrasonic nebulisation with lignocaine for airway anesthesia before performing awake fibreoptic guided intubation. Methods: This prospective, randomised study included sixty consenting adult patients of both genders (American Society of Anesthesiologists' physical status 1–3) with anticipated difficult airway undergoing surgery. Ultrasound guided airway nerve blocks group received ultrasound-guided bilateral superior laryngeal (1 ml of 2% lignocaine) and transtracheal recurrent laryngeal (2 ml of 2% lignocaine) airway nerve blocks and ultrasonic nebulisation with lignocaine group received ultrasonic nebulisation of 4 ml of lignocaine 4%. The primary outcome was to compare the time required to intubate, whereas the secondary outcomes were to compare cough reflex and gag reflex, hemodynamic changes, number of attempts required, and comfort score during awake fibreoptic guided intubation in both the groups. Results: The time taken for intubation was significantly lower in the ultrasound guided airway nerve blocks group 69.27±21.85 s than ultrasonic nebulisation with lignocaine group 92.43 ± 42.90 s (p = 0.015). Hemodynamic variables changed during the procedure but the values were comparable in both groups. There were no statistical differences in cough and gag reflexes, number of attempts, and comfort score in both groups. Conclusions: This study shows that significant lesser time required for performing awake fiberoptic intubation when patient received ultrasound guided airway nerve block in comparison to ultrasonic nebulisation for airway anaesthesia.
背景:在预期气道困难的情况下,清醒纤维引导插管是理想的治疗方案。需要充足的上呼吸道麻醉,以保证患者的舒适和配合。我们比较了超声引导下气道神经阻滞和超声雾化加利多卡因气道麻醉在清醒纤维引导插管前的疗效。方法:这项前瞻性随机研究包括60名同意接受手术气道困难的成年患者(美国麻醉医师协会生理状态1-3)。超声引导下气管神经阻滞组行双侧上喉(2%利多卡因1ml)和经气管返喉(2%利多卡因2ml)气管神经阻滞和超声雾化,利多卡因组行4%利多卡因4ml超声雾化。主要结果是比较插管所需的时间,而次要结果是比较两组清醒纤维引导插管时咳嗽反射和呕吐反射、血流动力学变化、所需尝试次数和舒适度评分。结果:超声引导下气道神经阻滞组插管时间(69.27±21.85 s)明显低于超声雾化加利多卡因组(92.43±42.90 s) (p = 0.015)。血流动力学变量在手术过程中发生了变化,但两组的数值具有可比性。两组在咳嗽和呕吐反射、尝试次数和舒适评分方面无统计学差异。结论:本研究表明,与超声雾化气道麻醉相比,超声引导气道神经阻滞患者在清醒状态下进行纤维插管所需的时间明显更少。
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引用次数: 8
High mortality co-infections of COVID-19 patients: mucormycosis and other fungal infections. COVID-19 患者的高死亡率合并感染:粘孢子菌病和其他真菌感染。
Pub Date : 2021-03-31 DOI: 10.15190/d.2021.5
Kinal Bhatt, Arjola Agolli, Mehrie H Patel, Radhika Garimella, Madhuri Devi, Efrain Garcia, Harshad Amin, Carlos Domingue, Roberto Guerra Del Castillo, Marcos Sanchez-Gonzalez

Severe COVID-19 disease is associated with an increase in pro-inflammatory markers, such as IL-1, IL-6, and tumor necrosis alpha, less CD4 interferon-gamma expression, and fewer CD4 and CD8 cells, which increase the susceptibility to bacterial and fungal infections. One such opportunistic fungal infection is mucormycosis. Initially, it was debated whether a person taking immunosuppressants, such as corticosteroids, and monoclonal antibodies will be at higher risk for COVID-19 or whether the immunosuppresive state would cause a more severe COVID-19 disease. However, immunosuppressants are currently continued unless the patients are at greater risk of severe COVID-19 infection or are on high-dose corticosteroids therapy. As understood so far, COVID-19 infection may induce significant and persistent lymphopenia, which in turn increases the risk of opportunistic infections. It is also noted that 85% of the COVID-19 patients' laboratory findings showed lymphopenia. This means that patients with severe COVID-19 have markedly lower absolute number of T lymphocytes, CD4+T and CD8+ T cells and, since the lymphocytes play a major role in maintaining the immune homeostasis, the patients with COVID-19 are highly susceptible to fungal co-infections. This report is intended to raise awareness of the importance of early detection and treatment of mucormycosis and other fungal diseases, such as candidiasis, SARS-CoV-2-associated pulmonary aspergillosis, pneumocystis pneumonia and cryptococcal disease, in COVID-19 patients, to reduce the risk of mortality.

严重的 COVID-19 疾病与促炎标志物(如 IL-1、IL-6 和肿瘤坏死α)的增加、CD4 干扰素-γ 表达的减少以及 CD4 和 CD8 细胞的减少有关,这增加了对细菌和真菌感染的易感性。粘孢子菌病就是其中一种机会性真菌感染。最初,人们对服用皮质类固醇等免疫抑制剂和单克隆抗体的人是否会有更高的 COVID-19 风险,或者免疫抑制状态是否会导致更严重的 COVID-19 疾病进行了争论。不过,除非患者感染严重 COVID-19 的风险更高,或正在接受大剂量皮质类固醇治疗,否则目前都会继续使用免疫抑制剂。据目前了解,COVID-19 感染可能会诱发严重和持续的淋巴细胞减少症,进而增加机会性感染的风险。我们还注意到,85% 的 COVID-19 患者的实验室检查结果显示存在淋巴细胞减少症。这意味着重症 COVID-19 患者的 T 淋巴细胞、CD4+T 和 CD8+ T 细胞的绝对数量明显降低,而淋巴细胞在维持免疫平衡方面发挥着重要作用,因此 COVID-19 患者极易合并真菌感染。本报告旨在提高 COVID-19 患者对早期发现和治疗粘孢子菌病及其他真菌疾病(如念珠菌病、SARS-CoV-2 相关肺曲霉菌病、肺孢子菌肺炎和隐球菌病)重要性的认识,以降低死亡风险。
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引用次数: 0
First COVID-19 Vaccines Receiving the US FDA and EMA Emergency Use Authorization. 首批获得美国FDA和EMA紧急使用授权的COVID-19疫苗
Pub Date : 2021-03-05 DOI: 10.15190/d.2021.1
Andra Fortner, David Schumacher

On December 31, 2019, the Wuhan Municipal Health Commission reported an increase in the incidence of pneumonia from an unknown cause. Shortly after, SARS-CoV-19 was identified as the responsible coronavirus for the heavy progress of the disease, which can manifest itself distinctively in different individuals. Coronavirus Disease 2019 (COVID-19) triggered a pandemic because of its high contagiousness before COVID-19 associated symptoms actually appear. In response to the rapid and continuous spread of the virus around the globe governments have mobilized their forces to restrict contact and thus avoid further infection and invested significant resources in treatment and prevention strategies to tackle COVID-19. As a result, US FDA and EMA have granted emergency use authorization for two mRNA-based vaccines, namely the vaccines developed by BioNTech/Pfizer and Moderna, for use in the USA and Europe. Due to the existing critical situation, the stages of vaccine development and testing have probably never been gone through so fast as at present. Here, we are briefly commenting on these two vaccines with their benefits, advantages and limitations.

2019年12月31日,武汉市卫生健康委通报,不明原因肺炎病例有所增加。不久之后,SARS-CoV-19被确定为导致该疾病严重进展的冠状病毒,这种病毒在不同的个体中表现出不同的特征。2019冠状病毒病(COVID-19)在出现相关症状之前就因其高传染性引发了大流行。为应对该病毒在全球范围内的快速和持续传播,各国政府已动员其力量限制接触,从而避免进一步感染,并在治疗和预防战略上投入了大量资源,以应对COVID-19。因此,美国FDA和EMA已经批准了两种基于mrna的疫苗的紧急使用授权,即BioNTech/辉瑞和Moderna开发的疫苗,用于美国和欧洲。由于目前的严峻形势,疫苗开发和试验的阶段可能从未像目前这样迅速完成。在这里,我们简要地评论一下这两种疫苗的优点、优点和局限性。
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引用次数: 32
Transdiaphragmatic Intercostal Hernia-An Unusual Hepatic Injury After a Car Accident: A Case Report and Review of the Literature. 经膈肋间疝:一例车祸后罕见的肝损伤病例报告及文献复习。
Pub Date : 2021-03-04 DOI: 10.15190/d.2021.2
Orestis Ioannidis, Chrysovalantis Mariorakis, Anastasia Malliora, Panagiotis Christidis, Lydia Loutzidou, Ioannis Mantzoros, Manousos George Pramateftakis, Efstathios Kotidis, Nikolaos Ouzounidis, Vasilis Foutsitzis, Stamatios Aggelopoulos

Transdiaphragmatic intercostal hernia, in which the abdominal contents of the hernia protrude through the diaphragm and the thoracic wall defect. is a very rare type of hernia with only a few cases having been reported in the literature. That type of hernia is usually manifested in male patients after trauma, penetrating or blunt. It is frequently presented with a palpable thoracic mass and pain. The indicated treatment is surgery. We present the case of a 60-year-old female admitted to the hospital after a car accident and suffered multiple rib fractures (6th, 7th, 8th right ribs / 7th, 8th, 9th left ribs), as well as flail thorax, hemothorax bilaterally, left subcutaneous emphysema and swelling of soft tissues of the right lateral thoracoabdominal wall. CT scan revealed herniation of hepatic parenchyma and intestinal loops into the thorax. The patient was treated surgically, and his postoperative course was uneventful. We also review the relevant literature concerning this transdiaphragmatic, intercostal hernia and identify 42 cases. Transdiaphragmatic intercostal hernia is a rare condition, usually manifested in male patients after trauma, penetrating or blunt. It is frequently presented with a palpable thoracic mass and pain. The indicated treatment is surgery.

膈间疝是一种非常罕见的疝气类型,文献中仅报道过几例。这种疝气通常发生在男性患者身上,多见于穿透性或钝性外伤后。这种疝气通常表现为可触及的胸腔肿块和疼痛。治疗方法是手术。本病例为一名 60 岁女性,因车祸入院,多发性肋骨骨折(右侧第 6、7、8 肋骨/左侧第 7、8、9 肋骨),同时伴有胸廓外翻、双侧血气胸、左侧皮下气肿和右侧胸腹壁软组织肿胀。CT 扫描显示肝实质和肠襻疝入胸腔。患者接受了手术治疗,术后恢复顺利。我们还回顾了有关这种经膈肋间疝的相关文献,并确定了 42 个病例。横膈肋间疝是一种罕见的疾病,通常表现为男性患者在穿透性或钝性外伤后出现。它通常表现为可触及的胸部肿块和疼痛。治疗方法是手术。
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引用次数: 0
Drug Repurposing for Prevention and Treatment of COVID-19: A Clinical Landscape. 预防和治疗 COVID-19 的药物再利用:临床前景。
Pub Date : 2020-12-16 DOI: 10.15190/d.2020.18
Md Shahadat Hossain, Ithmam Hami, Md Sad Salabi Sawrav, Md Fazley Rabbi, Otun Saha, Newaz Mohammed Bahadur, Md Mizanur Rahaman

SARS-CoV-2, the novel coronavirus strain responsible for the current pandemic of COVID-19, has rendered the entire humanity suffering. Several months have passed since the pandemic has struck. However, the world is still looking for an effective treatment plan to battle the viral infection. The first vaccine just received emergency approval in December 2020 for use in USA and UK. These are excellent news, however, the worldwide distribution of such vaccine, the possibility of virus mutation and the lack of data regarding the long-term effects of such vaccines are a significant concern. In addition, although remdesivir was recently approved by the FDA to be used as a clinical drug against COVID-19, it hasn't stood out yet as a proven form of therapeutics. Such inability to produce a novel therapy has caused enough inconveniences for the affected people worldwide. Repurposing the already available drugs to fight against the virus seems to be a reasonable option amidst such uncertainty. Given the vast collection of potential treatment candidates to be explored against COVID-19, there is a decent chance that a success in this regard will serve the intermediary purpose of clinically treating the infection until a COVID-19 vaccine is widely distributed worldwide and will be able to treat COVID-19 patients that do not adequately respond to vaccines. Such treatments may prove very useful in future coronavirus outbreaks too. Proper research into these repurposing treatments may yield a certain insight into the field of novel treatment production as well. This review study accumulates a relevant set of information about drugs and vaccines against COVID-19, in terms of their repurposing properties and the specific phases of clinical trials they are undergoing across the world.  A potential timeline is also suggested to estimate when an effective result can be expected from the ongoing clinical trials for a better anticipation of the drug landscape. This study will hopefully help accelerate investment of resources into development and discovery of drugs and vaccines against the infection.

SARS-CoV-2 是导致目前 COVID-19 大流行的新型冠状病毒株,它使全人类深受其害。大流行已经过去了几个月。然而,全世界仍在寻找有效的治疗方案来对抗病毒感染。第一种疫苗刚刚于 2020 年 12 月获得紧急批准,可在美国和英国使用。这些都是好消息,然而,此类疫苗在全球范围内的分布、病毒变异的可能性以及缺乏有关此类疫苗长期效果的数据,都是令人严重关切的问题。此外,尽管雷米替韦最近获得了美国食品及药物管理局的批准,可用作抗 COVID-19 的临床药物,但它尚未成为一种行之有效的治疗方法。这种无法生产新型疗法的情况给全世界的受感染者带来了诸多不便。在这种不确定的情况下,重新利用现有药物来抗击病毒似乎是一个合理的选择。鉴于COVID-19潜在候选治疗药物种类繁多,在COVID-19疫苗在全球广泛传播之前,这方面的成功很有可能起到临床治疗感染的中介作用,并能治疗对疫苗反应不佳的COVID-19患者。这种治疗方法在未来冠状病毒爆发时也可能非常有用。对这些再利用疗法的适当研究可能会对新型疗法的生产领域产生一定的启示。本综述研究积累了一系列关于针对 COVID-19 的药物和疫苗的相关信息,包括它们的再利用特性以及它们在世界各地正在进行的临床试验的具体阶段。 同时还提出了一个潜在的时间表,以估计正在进行的临床试验何时能取得有效结果,从而更好地预测药物前景。希望这项研究能有助于加快对抗病毒药物和疫苗的开发和发现的资源投入。
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引用次数: 0
Is COVID-19 Fatality Rate Associated with Malaria Endemicity? COVID-19致死率与疟疾流行率有关吗?
Pub Date : 2020-12-11 DOI: 10.15190/d.2020.17
Abdul Rehman Arshad, Imtiaz Bashir, Farhat Ijaz, Nicholas Loh, Suraj Shukla, Ubaid Ur Rehman, Rana Khurram Aftab

COVID-19 (coronavirus disease 2019) is a disease caused by the coronavirus SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2). COVID-19 has yielded many reported complications and unusual observations. In this article, we have reviewed one such observation: an association between malaria endemicity and reduced reported COVID-19 fatality. Malaria-endemic regions have a significantly lower reported COVID-19 fatality rate as compared to regions where malaria is non-endemic. Statistical analyses show that there is a strong negative correlation between the reported SARS-CoV-2 fatality and endemicity of malaria. In this review, we have discussed the potential role of CD-147, and potential malaria-induced immunity and polymorphisms in COVID-19 patients. Noteworthy, the results may also be due to underreported cases or due to the economic, political, and environmental differences between the malaria endemic and non-endemic countries. The study of this potential relationship might be of great help in COVID-19 therapy and prevention.

COVID-19(冠状病毒病2019)是由冠状病毒SARS-CoV-2(严重急性呼吸综合征冠状病毒2)引起的疾病。COVID-19已经产生了许多报道的并发症和不寻常的观察结果。在本文中,我们回顾了其中一个观察结果:疟疾流行与报告的COVID-19死亡率降低之间的关联。与非疟疾流行地区相比,疟疾流行地区报告的COVID-19死亡率要低得多。统计分析表明,报告的SARS-CoV-2病死率与疟疾流行之间存在很强的负相关。在这篇综述中,我们讨论了CD-147的潜在作用,以及在COVID-19患者中潜在的疟疾诱导免疫和多态性。值得注意的是,这一结果也可能是由于少报病例,或由于疟疾流行国家和非流行国家之间的经济、政治和环境差异。研究这种潜在的关系可能对COVID-19的治疗和预防有很大的帮助。
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引用次数: 6
A Novel Metric System to Quantify Antibiotic Consumption in Paediatric Population: A Hospital Based, Biphasic Pilot Study. 一种量化儿科人群抗生素消费的新度量系统:一项基于医院的两期试点研究。
Pub Date : 2020-12-10 DOI: 10.15190/d.2020.16
Shah Newaz Ahmed, Ratinder Jhaj, Ritendra Patidar, Mahendra Dangi, Shikha Malik, Balakrishnan Sadasivam, Shubham Atal

Background: The Anatomical Therapeutic Chemical Classification / Defined Daily Dose (ATC/DDD) system recommended by World Health Organization is accepted worldwide as the standard method of quantification of drug consumption. However, owing to individual variation in body weight, the ATC/DDD system cannot be used for comparison across paediatric population.

Objective: This study aimed to develop a novel metric system for standard quantification of antibiotic consumption in paediatric population.

Method: The standard unit of drug quantification in adult population is DDD/100 patient days (PD). We conceived a new unit of DDD/1000 kg-days (KD) where KD is the product of the body weight and length of hospital stay of an individual patient. We simulated the quantification and comparison of drugs in a computer model of five virtual paediatric hospitals (H1 to H5, n=100, 200, 100, 100, 100 respectively). We re-applied the metric system on two, real world, hospital-based, time cohorts (TC) (TC18, n=38 and TC19, n=47) of 2 weeks each, in two consecutive years.

Results: The body weights (mean±SD) in H1-H5 were 5.7±3.0, 5.7±2.8, 25.3±8.5, 20.6±11.7 and 19.8±11.4 kg, respectively. The antibiotic consumption in terms of DDD/100 PD and DDD/1000 KD in the five hospitals was 1.26, 1.20, 5.52, 4.41 and 2.00, and 2.24, 2.14, 2.22, 2.17 and 1.06 respectively. In TC18 and TC19, the mean body weight, DDD/100 PD and DDD/1000 KD were 12.24±13.17, 30.93, 20.34 and 19.51±12.28, 11.99, 6.23, respectively.

Conclusion: DDD/1000 kg-days is a potential standard unit for drug quantification in paediatric population independent of weight distribution and size of the study sample. The universal application and comparison across diverse samples can generate useful information for resource allocation, anti-microbial stewardship, disease burden and drug use, and can help in taking policy decisions to improve healthcare delivery in the paediatric population.

背景:世界卫生组织推荐的解剖治疗化学分类/限定日剂量(ATC/DDD)系统是世界范围内公认的药物用量定量标准方法。然而,由于个体体重的差异,ATC/DDD系统不能用于儿科人群的比较。目的:本研究旨在建立一种新的计量体系,用于儿科人群抗生素消费的标准定量。方法:成人用药定量标准单位为DDD/100患者日(PD)。我们设想了一个新的DDD/1000 kg-days (KD)单位,其中KD是个体患者体重和住院时间的乘积。我们在五家虚拟儿科医院(H1至H5, n分别=100、200、100、100、100)的计算机模型中模拟药物的量化和比较。我们连续两年在两个真实世界的、以医院为基础的时间队列(TC) (TC18, n=38和TC19, n=47)中重新应用度量系统,每个队列2周。结果:h1 ~ h5组体重(平均±SD)分别为5.7±3.0、5.7±2.8、25.3±8.5、20.6±11.7、19.8±11.4 kg。5家医院DDD/100 PD和DDD/1000 KD的抗生素用量分别为1.26、1.20、5.52、4.41、2.00和2.24、2.14、2.22、2.17、1.06。TC18和TC19的平均体重、DDD/100 PD和DDD/1000 KD分别为12.24±13.17、30.93、20.34和19.51±12.28、11.99、6.23。结论:DDD/1000 kg-days是独立于研究样本的体重分布和大小的儿科人群药物定量的潜在标准单位。不同样本之间的普遍应用和比较可以为资源分配、抗微生物管理、疾病负担和药物使用产生有用的信息,并有助于制定政策决定,以改善儿科人群的医疗保健服务。
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引用次数: 1
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Discoveries (Craiova, Romania)
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