Pub Date : 2024-12-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3204-13
Amani M Alnimr, Mohammad A Alsharari, Fatemah M Alabkari, Fatemah A Alsalem, Bashayer M AlShehail, Mashael Alhajri, Qasim S AlKhaleefah, Marwan J Alwazzeh
Leprosy, a chronic infectious disease caused by Mycobacterium leprae complex, remains a significant global health concern despite being curable with multidrug therapy. Delayed diagnosis is common, particularly in non-endemic regions or when presenting with atypical symptoms. This can lead to missed opportunities for early intervention, potential disabilities, and increased transmission. Misdiagnosis is often compounded by leprosy's ability to mimic other conditions, as illustrated in this case report. We present a 43-year-old Filipino woman residing in Eastern Saudi Arabia, who presented to a dermatology clinic with a four-year history of recurrent skin rashes and a one-year history of painful, itchy nodules on her shins. She denied any systemic symptoms, recent travel, or known tuberculosis (TB) contact. Physical examination revealed multiple erythematous nodules on her shins with hyperpigmentation, but no lymphadenopathy or other skin lesions. Initial laboratory tests, including blood counts, liver and kidney function, inflammatory markers, and HIV screening, were normal. Chest X-ray was unremarkable. The patient's clinical presentation and laboratory results led to a provisional diagnosis of extrapulmonary TB, and she was started on anti-TB treatment. However, her condition did not improve after several months of treatment. A skin biopsy was performed, and histopathological examination revealed granulomatous inflammation with acid-fast bacilli, raising suspicion for leprosy. Subsequent culture of the skin biopsy unexpectedly yielded Mycobacterium leprae, confirming the diagnosis of lepromatous leprosy. The case study highlights the diagnostic challenges associated with leprosy, especially in non-endemic regions. The patient's atypical presentation, lack of systemic symptoms, and the unexpected growth of M. leprae in cell-free culture media contributed to the initial misdiagnosis and delayed treatment. Early suspicion, prompt skin biopsy, and appropriate culture techniques are crucial for accurate diagnosis and timely initiation of effective therapy to prevent disability and transmission. This case also underscores the importance of considering leprosy as a differential diagnosis in patients presenting with atypical skin lesions, even in non-endemic areas. Continued awareness and education among healthcare providers are essential to improve early recognition and management of this treatable disease.
{"title":"Leprosy with subsequent type 2 reaction masquerading as cutaneous tuberculosis: a case report and diagnostic pitfalls in a non-endemic area.","authors":"Amani M Alnimr, Mohammad A Alsharari, Fatemah M Alabkari, Fatemah A Alsalem, Bashayer M AlShehail, Mashael Alhajri, Qasim S AlKhaleefah, Marwan J Alwazzeh","doi":"10.53854/liim-3204-13","DOIUrl":"10.53854/liim-3204-13","url":null,"abstract":"<p><p>Leprosy, a chronic infectious disease caused by <i>Mycobacterium leprae</i> complex, remains a significant global health concern despite being curable with multidrug therapy. Delayed diagnosis is common, particularly in non-endemic regions or when presenting with atypical symptoms. This can lead to missed opportunities for early intervention, potential disabilities, and increased transmission. Misdiagnosis is often compounded by leprosy's ability to mimic other conditions, as illustrated in this case report. We present a 43-year-old Filipino woman residing in Eastern Saudi Arabia, who presented to a dermatology clinic with a four-year history of recurrent skin rashes and a one-year history of painful, itchy nodules on her shins. She denied any systemic symptoms, recent travel, or known tuberculosis (TB) contact. Physical examination revealed multiple erythematous nodules on her shins with hyperpigmentation, but no lymphadenopathy or other skin lesions. Initial laboratory tests, including blood counts, liver and kidney function, inflammatory markers, and HIV screening, were normal. Chest X-ray was unremarkable. The patient's clinical presentation and laboratory results led to a provisional diagnosis of extrapulmonary TB, and she was started on anti-TB treatment. However, her condition did not improve after several months of treatment. A skin biopsy was performed, and histopathological examination revealed granulomatous inflammation with acid-fast bacilli, raising suspicion for leprosy. Subsequent culture of the skin biopsy unexpectedly yielded <i>Mycobacterium leprae</i>, confirming the diagnosis of lepromatous leprosy. The case study highlights the diagnostic challenges associated with leprosy, especially in non-endemic regions. The patient's atypical presentation, lack of systemic symptoms, and the unexpected growth of <i>M. leprae</i> in cell-free culture media contributed to the initial misdiagnosis and delayed treatment. Early suspicion, prompt skin biopsy, and appropriate culture techniques are crucial for accurate diagnosis and timely initiation of effective therapy to prevent disability and transmission. This case also underscores the importance of considering leprosy as a differential diagnosis in patients presenting with atypical skin lesions, even in non-endemic areas. Continued awareness and education among healthcare providers are essential to improve early recognition and management of this treatable disease.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 4","pages":"538-543"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11627496/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808592","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}
Pub Date : 2024-12-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3204-11
Monica Pagnoncelli, Marco Arosio, Alessandro Genovesi, Gavino Napolitano, Claudio Farina
Latent Tuberculosis Infection (LTBI) is a state of persistent immune response to Mycobacterium tuberculosis complex antigens without clinical, radiological and microbiological signs of active disease. Effective diagnosis and preventive treatment of LTBI are crucial for tuberculosis (TB) control, especially in high-risk groups. Currently, two main tests are used for LTBI diagnosis: the Tuberculin Skin Test (TST) and the Interferon-Gamma Release Assays (IGRA), including the QuantiFERON-TB Gold Plus (QFT-Plus) and the T-SPOT.TB. Our study evaluated the performance of the T-SPOT.TB test in patients with indeterminate QFT-Plus results, using data from the Clinical Microbiology and Virology Laboratory (M&V) of Papa Giovanni XXIII Hospital in Bergamo, Italy. Blood samples from patients tested for LTBI with QFT-Plus from January 1, 2017 to May 15, 2024 were analyzed. The QFT-Plus is the most widely used test in routine diagnostics for LTBI screening due to the availability of automated systems. Out of 20,995 samples tested with QFT-Plus, 576 (2.7%) gave indeterminate results. In all cases of indeterminate QFT-Plus results, M&V recommends performing the T-SPOT.TB test. However, of the 576 patients who obtained an indeterminate outcome, only 137 (23.8%) followed the indication. The T-SPOT.TB provided a definitive result in 87.6% of the cases, resolving 120 (80 negative and 40 positive) of 137 indeterminate QFT-Plus outcomes. Specifically, 78 of 92 cases, equal to 84.8%, were settled when the T-SPOT. TB test was performed within 30 days of the QFT-Plus. The T-SPOT.TB test has shown potential effectiveness in addressing indeterminate QFT-Plus results (84.8% resolution), indicating its possible role as a complementary diagnostic tool for LTBI. The proposed algorithm for LTBI screening is based on national and international guidelines recommending the use of the TST and/or an IGRA test for individuals at risk. However, it particularly emphasizes the use of QFT-Plus, due to its practicality and rapid execution, while recommending the addition of the T-SPOT.TB within 30 days in cases of indeterminate QFT-Plus results. Nevertheless, the conclusions should be regarded as preliminary and require confirmation through larger or controlled studies.
潜伏结核感染(LTBI)是一种对结核分枝杆菌复合抗原持续免疫应答的状态,没有活动性疾病的临床、放射学和微生物学征象。有效的诊断和预防性治疗对结核病(TB)控制至关重要,特别是在高危人群中。目前,用于LTBI诊断的两种主要检测方法是结核菌素皮肤试验(TST)和干扰素γ释放试验(IGRA),包括QuantiFERON-TB Gold Plus (QFT-Plus)和T-SPOT.TB。我们的研究评估了T-SPOT的性能。使用意大利贝加莫Papa Giovanni XXIII医院临床微生物学和病毒学实验室(M&V)的数据,对QFT-Plus结果不确定的患者进行结核病检测。对2017年1月1日至2024年5月15日使用QFT-Plus检测LTBI患者的血液样本进行分析。由于自动化系统的可用性,QFT-Plus是LTBI筛查常规诊断中使用最广泛的测试。在使用QFT-Plus检测的20,995个样本中,576个(2.7%)给出了不确定的结果。在所有不确定QFT-Plus结果的情况下,M&V建议执行T-SPOT。结核病测试。然而,在576例预后不确定的患者中,只有137例(23.8%)遵循了适应症。T-SPOT。TB在87.6%的病例中提供了明确的结果,解决了137个不确定的QFT-Plus结果中的120个(80个阴性和40个阳性)。其中,92起案件中有78起,占84.8%。在QFT-Plus后30天内进行TB检测。T-SPOT。TB检测在解决不确定的QFT-Plus结果方面显示出潜在的有效性(分辨率为84.8%),表明其可能作为LTBI的补充诊断工具。拟议的LTBI筛查算法基于国家和国际指南,建议对有风险的个体使用TST和/或IGRA测试。然而,它特别强调使用QFT-Plus,由于其实用性和快速执行,同时建议增加T-SPOT。在QFT-Plus结果不确定的情况下,30天内结核。然而,这些结论应被视为初步的,需要通过更大规模或对照研究来证实。
{"title":"Performance of the T-SPOT.TB test in patients with indeterminate QuantiFERON-TB Gold Plus results: proposal for an algorithm for the diagnosis of Latent Tuberculosis Infection.","authors":"Monica Pagnoncelli, Marco Arosio, Alessandro Genovesi, Gavino Napolitano, Claudio Farina","doi":"10.53854/liim-3204-11","DOIUrl":"10.53854/liim-3204-11","url":null,"abstract":"<p><p>Latent Tuberculosis Infection (LTBI) is a state of persistent immune response to <i>Mycobacterium tuberculosis</i> complex antigens without clinical, radiological and microbiological signs of active disease. Effective diagnosis and preventive treatment of LTBI are crucial for tuberculosis (TB) control, especially in high-risk groups. Currently, two main tests are used for LTBI diagnosis: the Tuberculin Skin Test (TST) and the Interferon-Gamma Release Assays (IGRA), including the QuantiFERON-TB Gold Plus (QFT-Plus) and the T-SPOT.TB. Our study evaluated the performance of the T-SPOT.TB test in patients with indeterminate QFT-Plus results, using data from the Clinical Microbiology and Virology Laboratory (M&V) of Papa Giovanni XXIII Hospital in Bergamo, Italy. Blood samples from patients tested for LTBI with QFT-Plus from January 1, 2017 to May 15, 2024 were analyzed. The QFT-Plus is the most widely used test in routine diagnostics for LTBI screening due to the availability of automated systems. Out of 20,995 samples tested with QFT-Plus, 576 (2.7%) gave indeterminate results. In all cases of indeterminate QFT-Plus results, M&V recommends performing the T-SPOT.TB test. However, of the 576 patients who obtained an indeterminate outcome, only 137 (23.8%) followed the indication. The T-SPOT.TB provided a definitive result in 87.6% of the cases, resolving 120 (80 negative and 40 positive) of 137 indeterminate QFT-Plus outcomes. Specifically, 78 of 92 cases, equal to 84.8%, were settled when the T-SPOT. TB test was performed within 30 days of the QFT-Plus. The T-SPOT.TB test has shown potential effectiveness in addressing indeterminate QFT-Plus results (84.8% resolution), indicating its possible role as a complementary diagnostic tool for LTBI. The proposed algorithm for LTBI screening is based on national and international guidelines recommending the use of the TST and/or an IGRA test for individuals at risk. However, it particularly emphasizes the use of QFT-Plus, due to its practicality and rapid execution, while recommending the addition of the T-SPOT.TB within 30 days in cases of indeterminate QFT-Plus results. Nevertheless, the conclusions should be regarded as preliminary and require confirmation through larger or controlled studies.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 4","pages":"525-531"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11627487/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808937","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}
Pub Date : 2024-12-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3204-3
Shriyansh Srivastava, Shivang Dhoundiyal, Sachin Kumar, Awaneet Kaur, Mahalaqua Nazli Khatib, Shilpa Gaidhane, Quazi Syed Zahiruddin, Aroop Mohanty, Andres F Henao-Martinez, Martin Krsak, Alfonso J Rodriguez-Morales, Juan J Montenegro-Idrogo, D Katterine Bonilla-Aldana, Ranjit Sah
Yellow fever poses a substantial global health concern as one of the re-emerging diseases with pandemic potential in a scenario of the worldwide distribution of some vectors (such as Aedes aegypti); in the context of climatic change, an unclear knowledge about the immune behaviour of the virus, between other determinants. This review details the historical foundations, intricate evolution of geographical spread, and transmission mechanisms of the disease to understand the behaviour of outbreaks over time in a multifactorial context that could be difficult to understand. This article approaches to epidemiological, pathophysiological, immunological, social determinants, and climatic crisis by understanding possible control mechanisms and anticipating potential future epidemics. This article explores the evidence of yellow fever virus (YFV) pathogenesis and its complex interactions with the immune response in the host, the vector, and in the context of immunisation. These discussions contribute to a more comprehensive understanding of the disease's progression. Despite the global presence of the vector and other factors that could facilitate an epidemic spread, yellow fever outbreaks have remained confined to specific endemic areas. This limited distribution is not entirely understood. However, it may be influenced by the complex immune interactions between the virus, the vector, and the host, preventing its spread to other regions.
{"title":"Yellow Fever: Global Impact, Epidemiology, Pathogenesis, and Integrated Prevention Approaches.","authors":"Shriyansh Srivastava, Shivang Dhoundiyal, Sachin Kumar, Awaneet Kaur, Mahalaqua Nazli Khatib, Shilpa Gaidhane, Quazi Syed Zahiruddin, Aroop Mohanty, Andres F Henao-Martinez, Martin Krsak, Alfonso J Rodriguez-Morales, Juan J Montenegro-Idrogo, D Katterine Bonilla-Aldana, Ranjit Sah","doi":"10.53854/liim-3204-3","DOIUrl":"10.53854/liim-3204-3","url":null,"abstract":"<p><p>Yellow fever poses a substantial global health concern as one of the re-emerging diseases with pandemic potential in a scenario of the worldwide distribution of some vectors (such as <i>Aedes aegypti</i>); in the context of climatic change, an unclear knowledge about the immune behaviour of the virus, between other determinants. This review details the historical foundations, intricate evolution of geographical spread, and transmission mechanisms of the disease to understand the behaviour of outbreaks over time in a multifactorial context that could be difficult to understand. This article approaches to epidemiological, pathophysiological, immunological, social determinants, and climatic crisis by understanding possible control mechanisms and anticipating potential future epidemics. This article explores the evidence of yellow fever virus (YFV) pathogenesis and its complex interactions with the immune response in the host, the vector, and in the context of immunisation. These discussions contribute to a more comprehensive understanding of the disease's progression. Despite the global presence of the vector and other factors that could facilitate an epidemic spread, yellow fever outbreaks have remained confined to specific endemic areas. This limited distribution is not entirely understood. However, it may be influenced by the complex immune interactions between the virus, the vector, and the host, preventing its spread to other regions.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 4","pages":"434-450"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11627485/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808945","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}
Pasteurella multocida is a Gram-negative coccobacillus that is a part of normal oral flora of animals, especially cats and dogs. It is the most common causative agent for soft tissue infections following a bite or scratch from domestic pets. Prosthetic Joint Infections (PJIs) due to Pasteurella multocida are rarely but increasingly reported. Since 1992, only a few cases of PJIs caused by P. multocida have been described. Herein we present a case of a 67-year-old immunocompetent elderly female who developed total hip arthroplasty infection due to P. multocida and was treated successfully with left hip washout, pseudo-tumor removal, and intravenous antibiotics and a review of the literature on prosthetic joint infections caused by P. multocida since 1992.
{"title":"<i>Pasteurella multocida</i> prosthetic joint infection. A case report and review of the literature.","authors":"Maria Lagadinou, Panagiotis Antzoulas, Georgios Eleftherakis, Christodoulos Chatzigrigoriadis, Marina Amerali, Christos Michailides, Petros Zampakis, Leonidia Leonidou, Markos Marangos","doi":"10.53854/liim-3204-12","DOIUrl":"10.53854/liim-3204-12","url":null,"abstract":"<p><p><i>Pasteurella multocida</i> is a Gram-negative coccobacillus that is a part of normal oral flora of animals, especially cats and dogs. It is the most common causative agent for soft tissue infections following a bite or scratch from domestic pets. Prosthetic Joint Infections (PJIs) due to <i>Pasteurella multocida</i> are rarely but increasingly reported. Since 1992, only a few cases of PJIs caused by <i>P. multocida</i> have been described. Herein we present a case of a 67-year-old immunocompetent elderly female who developed total hip arthroplasty infection due to <i>P. multocida</i> and was treated successfully with left hip washout, pseudo-tumor removal, and intravenous antibiotics and a review of the literature on prosthetic joint infections caused by <i>P. multocida</i> since 1992.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 4","pages":"532-537"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11627493/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142809055","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}
Pub Date : 2024-12-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3204-2
Stefano Di Bella, Stella Babich, Roberto Luzzati, Rosario Alessandro Cavasio, Barbara Massa, Neva Braccialarghe, Verena Zerbato, Marco Iannetta
Crimean-Congo haemorrhagic fever (CCHF) is an emerging severe tick-borne illness. The expanding habitat of Hyalomma ticks, coupled with migratory birds harbouring CCHF-infected ticks, contributes to an increasing number of potential hosts. The seroprevalence of anti-CCHF virus antibodies in livestock is approximately one-quarter, with a noticeable upward trend in recent years. The management of CCHF patients predominantly relies on supportive therapy, although a potential arsenal of antivirals, convalescent and hyperimmune plasma, monoclonal antibodies, and vaccines exists, both currently and in the future. This review aims to critically examine the current therapeutic approaches to managing CCHF, highlighting both the potential and limitations of existing treatments, and identifying future directions for improving patient outcomes.
{"title":"Crimean-Congo haemorrhagic fever (CCHF): present and future therapeutic armamentarium.","authors":"Stefano Di Bella, Stella Babich, Roberto Luzzati, Rosario Alessandro Cavasio, Barbara Massa, Neva Braccialarghe, Verena Zerbato, Marco Iannetta","doi":"10.53854/liim-3204-2","DOIUrl":"10.53854/liim-3204-2","url":null,"abstract":"<p><p>Crimean-Congo haemorrhagic fever (CCHF) is an emerging severe tick-borne illness. The expanding habitat of <i>Hyalomma</i> ticks, coupled with migratory birds harbouring CCHF-infected ticks, contributes to an increasing number of potential hosts. The seroprevalence of anti-CCHF virus antibodies in livestock is approximately one-quarter, with a noticeable upward trend in recent years. The management of CCHF patients predominantly relies on supportive therapy, although a potential arsenal of antivirals, convalescent and hyperimmune plasma, monoclonal antibodies, and vaccines exists, both currently and in the future. This review aims to critically examine the current therapeutic approaches to managing CCHF, highlighting both the potential and limitations of existing treatments, and identifying future directions for improving patient outcomes.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 4","pages":"421-433"},"PeriodicalIF":0.0,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11627488/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142808386","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}
Pub Date : 2024-09-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3203-12
Raimondo Maria Pavarin, Lorenzo Badia, Sebastiano Nisi, Claudia Iormetti, Fabio Caputo
Our aim was to estimate the prevalence of HCV in a highly vulnerable population of substance users living with social difficulties and marginality who came into contact with the mobile harm reduction service in the city of Bologna (Northern Italy). Testing was offered in a van (mobile unit) by using a point-of-care HCV antibody test. For the HCV RNA test, the Xpert HCV Viral Load Fingerstick Test was used. Participants with a detectable HCV RNA were accompanied within two weeks to the Infectious Diseases Department Sant' Orsola Hospital Bologna to start HCV treatment. With regard to the main study findings, 54% reported having never been HCV tested before; a prevalence of HCV RNA of 6% among all participants and 22% among those injecting drugs was found; among the HCV RNA positive participants, 80% were accompanied to treatment. Our study suggests that mobile harm reduction services, in networks with healthcare facilities, are able to offer a continuous HCV screening service and linkage to care for people with drug use living in socially marginalized conditions.
{"title":"HCV testing and linkage to care for hepatitis C virus infection for marginalized drug user populations attending a harm reduction service in Bologna, Italy.","authors":"Raimondo Maria Pavarin, Lorenzo Badia, Sebastiano Nisi, Claudia Iormetti, Fabio Caputo","doi":"10.53854/liim-3203-12","DOIUrl":"https://doi.org/10.53854/liim-3203-12","url":null,"abstract":"<p><p>Our aim was to estimate the prevalence of HCV in a highly vulnerable population of substance users living with social difficulties and marginality who came into contact with the mobile harm reduction service in the city of Bologna (Northern Italy). Testing was offered in a van (mobile unit) by using a point-of-care HCV antibody test. For the HCV RNA test, the Xpert HCV Viral Load Fingerstick Test was used. Participants with a detectable HCV RNA were accompanied within two weeks to the Infectious Diseases Department Sant' Orsola Hospital Bologna to start HCV treatment. With regard to the main study findings, 54% reported having never been HCV tested before; a prevalence of HCV RNA of 6% among all participants and 22% among those injecting drugs was found; among the HCV RNA positive participants, 80% were accompanied to treatment. Our study suggests that mobile harm reduction services, in networks with healthcare facilities, are able to offer a continuous HCV screening service and linkage to care for people with drug use living in socially marginalized conditions.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 3","pages":"373-380"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11392550/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305666","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}
Pub Date : 2024-09-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3203-14
Gregory Tsoucalas
Crete, strategically situated at the crossroads of three continents, was historically embroiled in incessant conflicts between colonisers and Greek revolutionaries, as well as recurrent battles against disease. In 1918, the island faced a novel adversary: influenza. In response, the state, local authorities, and medical professionals on the island mounted a formidable defence. Hospitals, health centres, and the military all contributed to the effort. Essential provisions of medicine and food were distributed to support the populations in areas most inflicted. The Heraklion-based newspaper Nea Ephimeris played a crucial role in documenting these events. Through its articles, reports, interviews, and reviews of the influenza situation, it disseminated vital information that helped the public understand both preventive measures and the necessary actions to combat the spread of the virus. This study examines the coverage by Nea Ephimeris from January 1918 to January 1919, assessing how the newspaper informed, supported, and uplifted the urban and rural populations of Crete. The data collected reconstruct the events of that period and demonstrate how historical pandemics offer lessons that can prepare health professionals for future challenges.
{"title":"An examination of the influenza pandemic in early 20<sup>th</sup> century in Crete through the lens of the 1918 editions of Nea Ephimeris, a Cretan newspaper.","authors":"Gregory Tsoucalas","doi":"10.53854/liim-3203-14","DOIUrl":"https://doi.org/10.53854/liim-3203-14","url":null,"abstract":"<p><p>Crete, strategically situated at the crossroads of three continents, was historically embroiled in incessant conflicts between colonisers and Greek revolutionaries, as well as recurrent battles against disease. In 1918, the island faced a novel adversary: influenza. In response, the state, local authorities, and medical professionals on the island mounted a formidable defence. Hospitals, health centres, and the military all contributed to the effort. Essential provisions of medicine and food were distributed to support the populations in areas most inflicted. The Heraklion-based newspaper <i>Nea Ephimeris</i> played a crucial role in documenting these events. Through its articles, reports, interviews, and reviews of the influenza situation, it disseminated vital information that helped the public understand both preventive measures and the necessary actions to combat the spread of the virus. This study examines the coverage by <i>Nea Ephimeris</i> from January 1918 to January 1919, assessing how the newspaper informed, supported, and uplifted the urban and rural populations of Crete. The data collected reconstruct the events of that period and demonstrate how historical pandemics offer lessons that can prepare health professionals for future challenges.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 3","pages":"392-402"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11392547/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305651","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}
In the summer of 1630, Milan experienced the most devastating plague epidemic in its history. In this study, addressed to investigate the earliest phases of the epidemic in the autumn of 1629, a set of unpublished and only partially known primary sources produced by the city's Officium Sanitatis was consulted and compared for the first time. Including those of two foreigners who died in the Lazzaretto, it was possible to ascertain a total of 39 cases of plague occurred in Milan between 9 October 1629 and the first weeks of 1630, of which 29 (74.4%) ended in death. Seven deaths presumably occurred at home were not recorded in the Liber Mortuorum, in which at least three other deaths caused by plague were deliberately attributed to a different cause. In particular, the case of the Vicario di Provisione in charge, Alfonso Visconti, probably the first death from plague occurred in Milan that year, was deliberately concealed for political reasons. Nevertheless, the spread of the disease remained limited in autumn 1629 and it was probably stopped until the following spring more by climatic factors than by the interventions of public health officials.
{"title":"Unveiling Milan's hidden cases of plague occurred in autumn 1629, before the great 1630 epidemic.","authors":"Riccardo Nodari, Luca Fois, Ester Luconi, Folco Vaglienti, Francesco Comandatore, Massimo Galli","doi":"10.53854/liim-3203-15","DOIUrl":"https://doi.org/10.53854/liim-3203-15","url":null,"abstract":"<p><p>In the summer of 1630, Milan experienced the most devastating plague epidemic in its history. In this study, addressed to investigate the earliest phases of the epidemic in the autumn of 1629, a set of unpublished and only partially known primary sources produced by the city's <i>Officium Sanitatis</i> was consulted and compared for the first time. Including those of two foreigners who died in the Lazzaretto, it was possible to ascertain a total of 39 cases of plague occurred in Milan between 9 October 1629 and the first weeks of 1630, of which 29 (74.4%) ended in death. Seven deaths presumably occurred at home were not recorded in the <i>Liber Mortuorum</i>, in which at least three other deaths caused by plague were deliberately attributed to a different cause. In particular, the case of the <i>Vicario di Provisione</i> in charge, Alfonso Visconti, probably the first death from plague occurred in Milan that year, was deliberately concealed for political reasons. Nevertheless, the spread of the disease remained limited in autumn 1629 and it was probably stopped until the following spring more by climatic factors than by the interventions of public health officials.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 3","pages":"403-412"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11392551/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305672","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}
Pub Date : 2024-09-01eCollection Date: 2024-01-01DOI: 10.53854/liim-3203-7
Vishakh C Keri, Ankesh Gupta, Sarita Mohapatra, Manish Soneja, Arti Kapil, Immaculata Xess, Naveet Wig, Bimal Kumar Das
Objective: MALDI-TOF-MS facilitates the identification of microorganisms from positive cultures in a timely and accurate manner. It eliminates the necessity for the application of biochemicals and operates on the principle of proteomics. It decreases the time required to report culture results. Prompt detection and notification of the pathogen, prior to the disclosure of antimicrobial susceptibilities, could potentially shorten the duration until the initial antibiotic adjustment is necessary, thereby influencing patients' clinical prognoses.
Methodology: Fifty patients in the conventional arm and one hundred patients in the interventional arm were compared in a pre and post quasi-experimental study conducted at a tertiary care centre in North India. Patients with positive cultures from medical wards and intensive care units were included. Comparing the time to first antibiotic modification after culture positivity, MALDI-TOF-MS-based identification, and clinical outcomes in both arms was the primary objective. Antibiotic modifications, escalation, and de-escalation were all recorded.
Results: The intervention arm exhibited a substantially shorter median time to first antibiotic modification (2010 mins vs 2905 mins, p=0.002) than the conventional arm. In the interventional group, a total of 44 out of 100 antibiotic modifications were implemented. Of these, 19 (43.3%) were determined solely by the MALDI report, without the anticipation of susceptibility assessments. De-escalation of antibiotics constituted the pre-dominant form of modification (47.4%). The difference between the 27% and 32% mortality rates in the intervention arm and the conventional arm was not statistically significant (p=0.52).
Conclusion: MALDI-TOF-MS facilitates the modification of antibiotics early on. The primary benefit lies in the reduction of superfluous antibiotic usage. Early organism identification and reporting prior to the availability of susceptibility results did not result in any mortality benefit. This strategy, when combined with a strong antimicrobial stewardship programme, can aid in the reduction of antibiotic use.
{"title":"Early organism identification by Matrix Assisted Laser Desorption Ionization Time of Flight Mass Spectrometry (MALDI-TOF-MS) decreases the time to appropriate antibiotic modifications for common bacterial infections.","authors":"Vishakh C Keri, Ankesh Gupta, Sarita Mohapatra, Manish Soneja, Arti Kapil, Immaculata Xess, Naveet Wig, Bimal Kumar Das","doi":"10.53854/liim-3203-7","DOIUrl":"https://doi.org/10.53854/liim-3203-7","url":null,"abstract":"<p><strong>Objective: </strong>MALDI-TOF-MS facilitates the identification of microorganisms from positive cultures in a timely and accurate manner. It eliminates the necessity for the application of biochemicals and operates on the principle of proteomics. It decreases the time required to report culture results. Prompt detection and notification of the pathogen, prior to the disclosure of antimicrobial susceptibilities, could potentially shorten the duration until the initial antibiotic adjustment is necessary, thereby influencing patients' clinical prognoses.</p><p><strong>Methodology: </strong>Fifty patients in the conventional arm and one hundred patients in the interventional arm were compared in a pre and post quasi-experimental study conducted at a tertiary care centre in North India. Patients with positive cultures from medical wards and intensive care units were included. Comparing the time to first antibiotic modification after culture positivity, MALDI-TOF-MS-based identification, and clinical outcomes in both arms was the primary objective. Antibiotic modifications, escalation, and de-escalation were all recorded.</p><p><strong>Results: </strong>The intervention arm exhibited a substantially shorter median time to first antibiotic modification (2010 mins vs 2905 mins, p=0.002) than the conventional arm. In the interventional group, a total of 44 out of 100 antibiotic modifications were implemented. Of these, 19 (43.3%) were determined solely by the MALDI report, without the anticipation of susceptibility assessments. De-escalation of antibiotics constituted the pre-dominant form of modification (47.4%). The difference between the 27% and 32% mortality rates in the intervention arm and the conventional arm was not statistically significant (p=0.52).</p><p><strong>Conclusion: </strong>MALDI-TOF-MS facilitates the modification of antibiotics early on. The primary benefit lies in the reduction of superfluous antibiotic usage. Early organism identification and reporting prior to the availability of susceptibility results did not result in any mortality benefit. This strategy, when combined with a strong antimicrobial stewardship programme, can aid in the reduction of antibiotic use.</p>","PeriodicalId":502111,"journal":{"name":"Le infezioni in medicina","volume":"32 3","pages":"330-339"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11392554/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305662","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}