Medscape CME Activity
Medscape, LLC is pleased to provide online continuing medical education (CME) for selected journal articles, allowing clinicians the opportunity to earn CME credit. In support of improving patient care, these activities have been planned and implemented by Medscape, LLC and Emerging Infectious Diseases. Medscape, LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
CME credit is available for one year after publication.
Active CME Articles
Expires 5/19/2024
Babesiosis is a globally distributed parasitic infection caused by intraerythrocytic protozoa. The full spectrum of neurologic symptoms, the underlying neuropathophysiology, and neurologic risk factors are poorly understood. Our study sought to describe the type and frequency of neurologic complications of babesiosis in a group of hospitalized patients and assess risk factors that might predispose patients to neurologic complications. We reviewed medical records of adult patients who were admitted to Yale-New Haven Hospital, New Haven, Connecticut, USA, during January 2011–October 2021 with laboratory-confirmed babesiosis. More than half of the 163 patients experienced >1 neurologic symptoms during their hospital admissions. The most frequent symptoms were headache, confusion/delirium, and impaired consciousness. Neurologic symptoms were associated with high-grade parasitemia, renal failure, and history of diabetes mellitus. Clinicians working in endemic areas should recognize the range of symptoms associated with babesiosis, including neurologic.
EID | Locke S, O’Bryan J, Zubair AS, Rethana M, Moffarah A, Krause PJ, et al. Neurologic Complications of Babesiosis, United States, 2011–2021. Emerg Infect Dis. 2023;29(6):1128-1135. https://doi.org/10.3201/eid2906.221890 |
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AMA | Locke S, O’Bryan J, Zubair AS, et al. Neurologic Complications of Babesiosis, United States, 2011–2021. Emerging Infectious Diseases. 2023;29(6):1128-1135. doi:10.3201/eid2906.221890. |
APA | Locke, S., O’Bryan, J., Zubair, A. S., Rethana, M., Moffarah, A., Krause, P. J....Farhadian, S. F. (2023). Neurologic Complications of Babesiosis, United States, 2011–2021. Emerging Infectious Diseases, 29(6), 1128-1135. https://doi.org/10.3201/eid2906.221890. |
Expires 5/18/2024
Tularemia is a zoonotic infection caused by Francisella tularensis. Its most typical manifestations in humans are ulceroglandular and glandular; infections in prosthetic joints are rare. We report 3 cases of F. tularensis subspecies holarctica–related prosthetic joint infection that occurred in France during 2016–2019. We also reviewed relevant literature and found only 5 other cases of Francisella-related prosthetic joint infections worldwide, which we summarized. Among those 8 patients, clinical symptoms appeared 7 days to 19 years after the joint placement and were nonspecific to tularemia. Although positive cultures are typically obtained in only 10% of tularemia cases, strains grew in all 8 of the patients. F. tularensis was initially identified in 2 patients by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry; molecular methods were used for 6 patients. Surgical treatment in conjunction with long-term antimicrobial treatment resulted in favorable outcomes; no relapses were seen after 6 months of follow-up.
EID | Ponderand L, Guimard T, Lazaro E, Dupuy H, Peuchant O, Roch N, et al. Case Studies and Literature Review of Francisella tularensis–Related Prosthetic Joint Infection. Emerg Infect Dis. 2023;29(6):1117-1126. https://doi.org/10.3201/eid2906.221395 |
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AMA | Ponderand L, Guimard T, Lazaro E, et al. Case Studies and Literature Review of Francisella tularensis–Related Prosthetic Joint Infection. Emerging Infectious Diseases. 2023;29(6):1117-1126. doi:10.3201/eid2906.221395. |
APA | Ponderand, L., Guimard, T., Lazaro, E., Dupuy, H., Peuchant, O., Roch, N....Caspar, Y. (2023). Case Studies and Literature Review of Francisella tularensis–Related Prosthetic Joint Infection. Emerging Infectious Diseases, 29(6), 1117-1126. https://doi.org/10.3201/eid2906.221395. |
Expires 4/14/2024
Clindamycin and β-lactam antibiotics have been mainstays for treating invasive group A Streptococcus (iGAS) infection, yet such regimens might be limited for strains displaying MLSB phenotypes. We investigated 76 iGAS isolates from 66 patients in West Virginia, USA, during 2020–2021. We performed emm typing using Centers for Disease Control and Prevention guidelines and assessed resistance both genotypically and phenotypically. Median patient age was 42 (range 23–86) years. We found 76% of isolates were simultaneously resistant to erythromycin and clindamycin, including all emm92 and emm11 isolates. Macrolide resistance was conferred by the plasmid-borne ermT gene in all emm92 isolates and by chromosomally encoded ermA, ermB, and a single mefA in other emm types. Macrolide-resistant iGAS isolates were typically resistant to tetracycline and aminoglycosides. Vulnerability to infection was associated with socioeconomic status. Our results show a predominance of macrolide-resistant isolates and a shift in emm type distribution compared with historical reports.
EID | Powell LM, Choi S, Chipman CE, Grund ME, LaSala P, Lukomski S. Emergence of Erythromycin-Resistant Invasive Group A Streptococcus, West Virginia, USA, 2020–2021. Emerg Infect Dis. 2023;29(5):897-907. https://doi.org/10.3201/eid2905.221421 |
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AMA | Powell LM, Choi S, Chipman CE, et al. Emergence of Erythromycin-Resistant Invasive Group A Streptococcus, West Virginia, USA, 2020–2021. Emerging Infectious Diseases. 2023;29(5):897-907. doi:10.3201/eid2905.221421. |
APA | Powell, L. M., Choi, S., Chipman, C. E., Grund, M. E., LaSala, P., & Lukomski, S. (2023). Emergence of Erythromycin-Resistant Invasive Group A Streptococcus, West Virginia, USA, 2020–2021. Emerging Infectious Diseases, 29(5), 897-907. https://doi.org/10.3201/eid2905.221421. |
Expires 4/13/2024
Recurrent Clostridioides difficile infection (RCDI) causes an increased burden on the healthcare system. We calculated RCDI incidence and identified factors associated with RCDI cases in New Haven County, Connecticut, USA, during 2015–2020 by using data from population-based laboratory surveillance. A subset of C. difficile cases had complete chart reviews conducted for RCDI and potentially associated variables. RCDI was defined as a positive C. difficile specimen occurring 2–8 weeks after incident C. difficile infection. We compared cases with and without RCDI by using multiple regression. RCDI occurred in 12.0% of 4,301 chart-reviewed C. difficile cases, showing a U-shaped time trend with a sharp increase in 2020, mostly because of an increase in hospital-onset cases. Malignancy (odds ratio 1.51 [95% CI 1.11–2.07]) and antecedent nitrofurantoin use (odds ratio 2.37 [95% CI 1.23–4.58]) were medical risk factors for RCDI. The 2020 increase may reflect the impact of the COVID-19 pandemic.
EID | Okafor CM, Clogher P, Olson D, Niccolai L, Hadler J. Trends in and Risk Factors for Recurrent Clostridioides difficile Infection, New Haven County, Connecticut, USA, 2015–2020. Emerg Infect Dis. 2023;29(5):877-887. https://doi.org/10.3201/eid2905.221294 |
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AMA | Okafor CM, Clogher P, Olson D, et al. Trends in and Risk Factors for Recurrent Clostridioides difficile Infection, New Haven County, Connecticut, USA, 2015–2020. Emerging Infectious Diseases. 2023;29(5):877-887. doi:10.3201/eid2905.221294. |
APA | Okafor, C. M., Clogher, P., Olson, D., Niccolai, L., & Hadler, J. (2023). Trends in and Risk Factors for Recurrent Clostridioides difficile Infection, New Haven County, Connecticut, USA, 2015–2020. Emerging Infectious Diseases, 29(5), 877-887. https://doi.org/10.3201/eid2905.221294. |
Expires 3/22/2024
During the SARS-CoV-2 pandemic, few cases of Nocardia spp. co-infection have been reported during or after a COVID-19 infection. Nocardia spp. are gram-positive aerobic actinomycetes that stain partially acid-fast, can infect immunocompromised patients, and may cause disseminated disease. We report the case of a 52-year-old immunocompromised man who had Nocardia pseudobrasiliensis pneumonia develop after a SARS-CoV-2 infection. We also summarize the literature for nocardiosis and SARS-CoV-2 co-infections. Nocardia spp. infection should remain a part of the differential diagnosis for pneumonia in immunocompromised hosts, regardless of other co-infections. Sulfonamide/carbapenem combinations are used as empiric therapy for nocardiosis; species identification and susceptibility testing are required to select the optimal treatment for each patient.
EID | Stamos D, Barajas-Ochoa A, Raybould JE. Nocardia pseudobrasiliensis Co-infection in SARS-CoV-2 Patients. Emerg Infect Dis. 2023;29(4):696-700. https://doi.org/10.3201/eid2904.221439 |
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AMA | Stamos D, Barajas-Ochoa A, Raybould JE. Nocardia pseudobrasiliensis Co-infection in SARS-CoV-2 Patients. Emerging Infectious Diseases. 2023;29(4):696-700. doi:10.3201/eid2904.221439. |
APA | Stamos, D., Barajas-Ochoa, A., & Raybould, J. E. (2023). Nocardia pseudobrasiliensis Co-infection in SARS-CoV-2 Patients. Emerging Infectious Diseases, 29(4), 696-700. https://doi.org/10.3201/eid2904.221439. |
Expires 3/16/2024
New Zealand (Aotearoa) experienced a Neisseria meningitidis serogroup B epidemic during 1991–2006, and incidence remains twice that of other high-income countries. We reviewed clinical, laboratory, and immunization data for children <15 years of age with laboratory-confirmed invasive meningococcal disease in Auckland, New Zealand, during January 1, 2004–December 31, 2020. Of 319 cases in 318 children, 4.1% died, and 23.6% with follow-up data experienced sequelae. Children of Māori and Pacific ethnicity and those living in the most deprived areas were overrepresented. Eighty-one percent were positive for N. meningitidis serogroup B, 8.6% for serogroup W, 6.3% for serogroup C, and 3.7% for serogroup Y. Seventy-nine percent had bacteremia, and 63.9% had meningitis. In New Zealand, Māori and Pacific children are disproportionately affected by this preventable disease. N. meningitidis serogroup B vaccine should be included in the New Zealand National Immunization Schedule to address this persistent health inequity.
EID | Burton C, Best E, Broom M, Heffernan H, Briggs S, Webb R. Pediatric Invasive Meningococcal Disease, Auckland, New Zealand (Aotearoa), 2004–2020. Emerg Infect Dis. 2023;29(4):686-695. https://doi.org/10.3201/eid2904.221397 |
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AMA | Burton C, Best E, Broom M, et al. Pediatric Invasive Meningococcal Disease, Auckland, New Zealand (Aotearoa), 2004–2020. Emerging Infectious Diseases. 2023;29(4):686-695. doi:10.3201/eid2904.221397. |
APA | Burton, C., Best, E., Broom, M., Heffernan, H., Briggs, S., & Webb, R. (2023). Pediatric Invasive Meningococcal Disease, Auckland, New Zealand (Aotearoa), 2004–2020. Emerging Infectious Diseases, 29(4), 686-695. https://doi.org/10.3201/eid2904.221397. |
Expires 2/23/2024
Molecular methods can enable rapid identification of Bartonella spp. infections, which are difficult to diagnose by using culture or serology. We analyzed clinical test results of PCR that targeted bacterial 16S rRNA hypervariable V1–V2 regions only or in parallel with PCR of Bartonella-specific ribC gene. We identified 430 clinical specimens infected with Bartonella spp. from 420 patients in the United States. Median patient age was 37 (range 1–79) years; 62% were male. We identified B. henselae in 77%, B. quintana in 13%, B. clarridgeiae in 1%, B. vinsonii in 1%, and B. washoensis in 1% of specimens. B. quintana was detected in 83% of cardiac specimens; B. henselae was detected in 34% of lymph node specimens. We detected novel or uncommon Bartonella spp. in 9 patients. Molecular diagnostic testing can identify Bartonella spp. infections, including uncommon and undescribed species, and might be particularly useful for patients who have culture-negative endocarditis or lymphadenitis.
EID | McCormick DW, Rassoulian-Barrett SL, Hoogestraat DR, Salipante SJ, SenGupta D, Dietrich EA, et al. Bartonella spp. Infections Identified by Molecular Methods, United States. Emerg Infect Dis. 2023;29(3):467-476. https://doi.org/10.3201/eid2903.221223 |
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AMA | McCormick DW, Rassoulian-Barrett SL, Hoogestraat DR, et al. Bartonella spp. Infections Identified by Molecular Methods, United States. Emerging Infectious Diseases. 2023;29(3):467-476. doi:10.3201/eid2903.221223. |
APA | McCormick, D. W., Rassoulian-Barrett, S. L., Hoogestraat, D. R., Salipante, S. J., SenGupta, D., Dietrich, E. A....Lieberman, J. A. (2023). Bartonella spp. Infections Identified by Molecular Methods, United States. Emerging Infectious Diseases, 29(3), 467-476. https://doi.org/10.3201/eid2903.221223. |
Expires 1/23/2024
Crimean-Congo hemorrhagic fever (CCHF) is a viral infectious disease for which distribution of the main vector, Hyalomma spp. ticks, is expanding. We analyzed all 10 cases of CCHF diagnosed in Spain during 2013–2021; case-patient median age was 56.5 years, and 7 were men. We identified CCHF virus genotypes III and V. Six case-patients acquired the infection in urban areas. Sixty percent of patients were infected in summer and 40% in spring. Two patients met criteria for hemophagocytic syndrome. Seven patients survived. The epidemiologic pattern of CCHF in Spain is based on occasional cases with an elevated mortality rate. Genotype III and, to a less extent also genotype V, CCHF circulates in humans in a common geographic area in Spain. Those data suggest that the expansion pathways are complex and may change over time. Physicians should remain alert to the possibility of new CCHF cases.
EID | Lorenzo Juanes H, Carbonell C, Sendra B, López-Bernus A, Bahamonde A, Orfao A, et al. Crimean-Congo Hemorrhagic Fever, Spain, 2013–2021. Emerg Infect Dis. 2023;29(2):252-259. https://doi.org/10.3201/eid2902.220677 |
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AMA | Lorenzo Juanes H, Carbonell C, Sendra B, et al. Crimean-Congo Hemorrhagic Fever, Spain, 2013–2021. Emerging Infectious Diseases. 2023;29(2):252-259. doi:10.3201/eid2902.220677. |
APA | Lorenzo Juanes, H., Carbonell, C., Sendra, B., López-Bernus, A., Bahamonde, A., Orfao, A....Belhassen-García, M. (2023). Crimean-Congo Hemorrhagic Fever, Spain, 2013–2021. Emerging Infectious Diseases, 29(2), 252-259. https://doi.org/10.3201/eid2902.220677. |
Expires 1/20/2024
Infant botulism (IB) is an intestinal toxemia that manifests as descending paralysis, constipation, and, in some cases, respiratory failure. Laboratory-confirmed IB cases are rare, and recent data in Israel are lacking. We conducted a national multicenter retrospective study of laboratory-confirmed IB cases reported in Israel during 2007–2021. A total of 8 cases were reported during the study period. During 2019–2021, incidence may have increased because of a cluster of 5 cases. Infant median age for diagnosis was 6.5 months, older than previously reported (3 months). Most cases occurred during March–July. Honey consumption was reported in 1 case, and possible environmental risk factors (living nearby rural or construction areas, dust exposure, and having a father who works as a farmer) were reported in 6 cases. Although IB is rare, its incidence in Israel may have increased over recent years, and its epidemiology and risk factors differ from cases reported previously in Israel.
EID | Goldberg B, Danino D, Levinsky Y, Levy I, Straussberg R, Dabaja-Younis H, et al. Infant Botulism, Israel, 2007–2021. Emerg Infect Dis. 2023;29(2):235-241. https://doi.org/10.3201/eid2902.220991 |
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AMA | Goldberg B, Danino D, Levinsky Y, et al. Infant Botulism, Israel, 2007–2021. Emerging Infectious Diseases. 2023;29(2):235-241. doi:10.3201/eid2902.220991. |
APA | Goldberg, B., Danino, D., Levinsky, Y., Levy, I., Straussberg, R., Dabaja-Younis, H....Scheuerman, O. (2023). Infant Botulism, Israel, 2007–2021. Emerging Infectious Diseases, 29(2), 235-241. https://doi.org/10.3201/eid2902.220991. |
Expires 12/21/2023
The emergence of SARS-CoV-2 and the worldwide COVID-19 pandemic triggered considerable attention to the emergence and evolution of novel human pathogens. Bourbon virus (BRBV) was first discovered in 2014 in Bourbon County, Kansas, USA. Since its initial discovery, several cases of BRBV infection in humans have been identified in Kansas, Oklahoma, and Missouri. BRBV is classified within the Thogotovirus genus; these negative-strand RNA viruses appear to be transmitted by ticks, and much of their biology remains unknown. In this review, we describe the emergence, virology, geographic range and ecology, and human disease caused by BRBV and discuss potential treatments for active BRBV infections. This virus and other emerging viral pathogens remain key public health concerns and require continued surveillance and study to mitigate human exposure and disease.
EID | Roe MK, Huffman ER, Batista YS, Papadeas GG, Kastelitz SR, Restivo AM, et al. Comprehensive Review of Emergence and Virology of Tickborne Bourbon Virus in the United States. Emerg Infect Dis. 2023;29(1):1-7. https://doi.org/10.3201/eid2901.212295 |
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AMA | Roe MK, Huffman ER, Batista YS, et al. Comprehensive Review of Emergence and Virology of Tickborne Bourbon Virus in the United States. Emerging Infectious Diseases. 2023;29(1):1-7. doi:10.3201/eid2901.212295. |
APA | Roe, M. K., Huffman, E. R., Batista, Y. S., Papadeas, G. G., Kastelitz, S. R., Restivo, A. M....Stobart, C. C. (2023). Comprehensive Review of Emergence and Virology of Tickborne Bourbon Virus in the United States. Emerging Infectious Diseases, 29(1), 1-7. https://doi.org/10.3201/eid2901.212295. |
Expires 12/19/2023
We performed a case–control study across 25 hospitals in India for the period of January–June 2021 to evaluate the reasons for an COVID-19–associated mucormycosis (CAM) outbreak. We investigated whether COVID-19 treatment practices (glucocorticoids, zinc, tocilizumab, and others) were associated with CAM. We included 1,733 cases of CAM and 3,911 age-matched COVID-19 controls. We found cumulative glucocorticoid dose (odds ratio [OR] 1.006, 95% CI 1.004–1.007) and zinc supplementation (OR 2.76, 95% CI 2.24–3.40), along with elevated C-reactive protein (OR 1.004, 95% CI 1.002–1.006), host factors (renal transplantation [OR 7.58, 95% CI 3.31–17.40], diabetes mellitus [OR 6.72, 95% CI 5.45–8.28], diabetic ketoacidosis during COVID-19 [OR 4.41, 95% CI 2.03–9.60]), and rural residence (OR 2.88, 95% CI 2.12–3.79), significantly associated with CAM. Mortality rate at 12 weeks was 32.2% (473/1,471). We emphasize the judicious use of COVID-19 therapies and optimal glycemic control to prevent CAM.
EID | Muthu V, Agarwal R, Rudramurthy S, Thangaraju D, Shevkani M, Patel AK, et al. Multicenter Case–Control Study of COVID-19–Associated Mucormycosis Outbreak, India. Emerg Infect Dis. 2023;29(1):8-19. https://doi.org/10.3201/eid2901.220926 |
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AMA | Muthu V, Agarwal R, Rudramurthy S, et al. Multicenter Case–Control Study of COVID-19–Associated Mucormycosis Outbreak, India. Emerging Infectious Diseases. 2023;29(1):8-19. doi:10.3201/eid2901.220926. |
APA | Muthu, V., Agarwal, R., Rudramurthy, S., Thangaraju, D., Shevkani, M., Patel, A. K....Chakrabarti, A. (2023). Multicenter Case–Control Study of COVID-19–Associated Mucormycosis Outbreak, India. Emerging Infectious Diseases, 29(1), 8-19. https://doi.org/10.3201/eid2901.220926. |
Expires 11/18/2023
Noncholera vibriosis is a rare, opportunistic bacterial infection caused by Vibrio spp. other than V. cholerae O1/O139 and diagnosed mainly during the hot summer months in patients after seaside activities. Detailed knowledge of circulating pathogenic strains and heterogeneities in infection outcomes and disease dynamics may help in patient management. We conducted a multicenter case-series study documenting Vibrio infections in 67 patients from 8 hospitals in the Bay of Biscay, France, over a 19-year period. Infections were mainly caused by V. alginolyticus (34%), V. parahaemolyticus (30%), non-O1/O139 V. cholerae (15%), and V. vulnificus (10%). Drug-susceptibility testing revealed intermediate and resistant strains to penicillins and first-generation cephalosporins. The acute infections (e.g., those involving digestive disorder, cellulitis, osteitis, pneumonia, and endocarditis) led to a life-threatening event (septic shock), amputation, or death in 36% of patients. Physicians may need to add vibriosis to their list of infections to assess in patients with associated risk factors.
EID | Hoefler F, Pouget-Abadie X, Roncato-Saberan M, Lemarié R, Takoudju E, Raffi F, et al. Clinical and Epidemiologic Characteristics and Therapeutic Management of Patients with Vibrio Infections, Bay of Biscay, France, 2001–2019. Emerg Infect Dis. 2022;28(12):2367-2373. https://doi.org/10.3201/eid2812.220748 |
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AMA | Hoefler F, Pouget-Abadie X, Roncato-Saberan M, et al. Clinical and Epidemiologic Characteristics and Therapeutic Management of Patients with Vibrio Infections, Bay of Biscay, France, 2001–2019. Emerging Infectious Diseases. 2022;28(12):2367-2373. doi:10.3201/eid2812.220748. |
APA | Hoefler, F., Pouget-Abadie, X., Roncato-Saberan, M., Lemarié, R., Takoudju, E., Raffi, F....Allix-Béguec, C. (2022). Clinical and Epidemiologic Characteristics and Therapeutic Management of Patients with Vibrio Infections, Bay of Biscay, France, 2001–2019. Emerging Infectious Diseases, 28(12), 2367-2373. https://doi.org/10.3201/eid2812.220748. |
Expires 11/17/2023
Acinetobacter baumannii is a nosocomial pathogen associated with severe illness and death. Glucocorticoid aerosol is a common inhalation therapy in patients receiving invasive mechanical ventilation. We conducted a prospective cohort study to analyze the association between glucocorticoid aerosol therapy and A. baumannii isolation from ventilator patients in China. Of 497 enrolled patients, 262 (52.7%) received glucocorticoid aerosol, and A. baumannii was isolated from 159 (32.0%). Glucocorticoid aerosol therapy was an independent risk factor for A. baumannii isolation (hazard ratio 1.5, 95% CI 1.02–2.28; p = 0.038). Patients receiving glucocorticoid aerosol had a higher cumulative hazard for A. baumannii isolation and analysis showed that glucocorticoid aerosol therapy increased A. baumannii isolation in most subpopulations. Glucocorticoid aerosol was not a direct risk factor for 30-day mortality, but A. baumannii isolation was independently associated with 30-day mortality in ventilator patients. Physicians should consider potential A. baumannii infection when prescribing glucocorticoid aerosol therapy.
EID | Zhang W, Yin M, Li W, Xu N, Lu H, Qin W, et al. Acinetobacter baumannii among Patients Receiving Glucocorticoid Aerosol Therapy during Invasive Mechanical Ventilation, China. Emerg Infect Dis. 2022;28(12):2404. https://doi.org/10.3201/eid2812.220347 |
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AMA | Zhang W, Yin M, Li W, et al. Acinetobacter baumannii among Patients Receiving Glucocorticoid Aerosol Therapy during Invasive Mechanical Ventilation, China. Emerging Infectious Diseases. 2022;28(12):2404. doi:10.3201/eid2812.220347. |
APA | Zhang, W., Yin, M., Li, W., Xu, N., Lu, H., Qin, W....Wang, H. (2022). Acinetobacter baumannii among Patients Receiving Glucocorticoid Aerosol Therapy during Invasive Mechanical Ventilation, China. Emerging Infectious Diseases, 28(12), 2404. https://doi.org/10.3201/eid2812.220347. |
Expires 10/19/2023
We investigated the proportion and characteristics of severe Corynebacterium striatum pneumonia in South Korea during 2014–2019. As part of an ongoing observational study of severe pneumonia among adult patients, we identified 27 severe C. striatum pneumonia cases. Most (70.4%) cases were hospital-acquired, and 51.9% of patients were immunocompromised. C. striatum cases among patients with severe hospital-acquired pneumonia (HAP) increased from 1.0% (2/200) during 2014–2015 to 5.4% (10/185) during 2018–2019, but methicillin-resistant Staphylococcus aureus (MRSA) infections among severe HAP cases decreased from 12.0% to 2.7% during the same timeframe. During 2018–2019, C. striatum was responsible for 13.3% of severe HAP cases from which bacterial pathogens were identified. The 90-day mortality rates were similarly high in the C. striatum and MRSA groups. C. striatum was a major cause of severe HAP and had high mortality rates. This pathogen is emerging as a possible cause for severe pneumonia, especially among immunocompromised patients.
EID | Lee Y, Huh J, Hong S, Jung J, Kim M, Chong Y, et al. Severe Pneumonia Caused by Corynebacterium striatum in Adults, Seoul, South Korea, 2014–2019. Emerg Infect Dis. 2022;28(11):2147-2154. https://doi.org/10.3201/eid2811.220273 |
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AMA | Lee Y, Huh J, Hong S, et al. Severe Pneumonia Caused by Corynebacterium striatum in Adults, Seoul, South Korea, 2014–2019. Emerging Infectious Diseases. 2022;28(11):2147-2154. doi:10.3201/eid2811.220273. |
APA | Lee, Y., Huh, J., Hong, S., Jung, J., Kim, M., Chong, Y....Choi, S. (2022). Severe Pneumonia Caused by Corynebacterium striatum in Adults, Seoul, South Korea, 2014–2019. Emerging Infectious Diseases, 28(11), 2147-2154. https://doi.org/10.3201/eid2811.220273. |
Expires 10/18/2023
A multispecies outbreak of Nocardia occurred among heart transplant recipients (HTR), but not lung transplant recipients (LTR), in Sydney, New South Wales, Australia, during 2018–2019. We performed a retrospective review of 23 HTR and LTR who had Nocardia spp. infections during June 2015–March 2021, compared risk factors for Nocardia infection, and evaluated climate conditions before, during, and after the period of the 2018–2019 outbreak. Compared with LTR, HTR had a shorter median time from transplant to Nocardia diagnosis, higher prevalence of diabetes, greater use of induction immunosuppression with basiliximab, and increased rates of cellular rejection before Nocardia diagnosis. During the outbreak, Sydney experienced the lowest monthly precipitation and driest surface levels compared with time periods directly before and after the outbreak. Increased immunosuppression of HTR compared with LTR, coupled with extreme weather conditions during 2018–2019, may explain this outbreak of Nocardia infections in HTR.
EID | Li J, Lau C, Anderson N, Burrows F, Mirdad F, Carlos L, et al. Multispecies Outbreak of Nocardia Infections in Heart Transplant Recipients and Association with Climate Conditions, Australia. Emerg Infect Dis. 2022;28(11):2155-2164. https://doi.org/10.3201/eid2811.220262 |
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AMA | Li J, Lau C, Anderson N, et al. Multispecies Outbreak of Nocardia Infections in Heart Transplant Recipients and Association with Climate Conditions, Australia. Emerging Infectious Diseases. 2022;28(11):2155-2164. doi:10.3201/eid2811.220262. |
APA | Li, J., Lau, C., Anderson, N., Burrows, F., Mirdad, F., Carlos, L....Dharan, N. J. (2022). Multispecies Outbreak of Nocardia Infections in Heart Transplant Recipients and Association with Climate Conditions, Australia. Emerging Infectious Diseases, 28(11), 2155-2164. https://doi.org/10.3201/eid2811.220262. |
Expires 9/21/2023
Fungal infections cause substantial rates of illness and death. Interest in the association between demographic factors and fungal infections is increasing. We analyzed 2019 US hospital discharge data to assess factors associated with fungal infection diagnosis, including race and ethnicity and socioeconomic status. We found male patients were 1.5–3.5 times more likely to have invasive fungal infections diagnosed than were female patients. Compared with hospitalizations of non-Hispanic White patients, Black, Hispanic, and Native American patients had 1.4–5.9 times the rates of cryptococcosis, pneumocystosis, and coccidioidomycosis. Hospitalizations associated with lower-income areas had increased rates of all fungal infections, except aspergillosis. Compared with younger patients, fungal infection diagnosis rates, particularly for candidiasis, were elevated among persons >65 years of age. Our findings suggest that differences in fungal infection diagnostic rates are associated with demographic and socioeconomic factors and highlight an ongoing need for increased physician evaluation of risk for fungal infections.
EID | Rayens E, Rayens M, Norris KA. Demographic and Socioeconomic Factors Associated with Fungal Infection Risk, United States, 2019. Emerg Infect Dis. 2022;28(10):1955-1969. https://doi.org/10.3201/eid2810.220391 |
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AMA | Rayens E, Rayens M, Norris KA. Demographic and Socioeconomic Factors Associated with Fungal Infection Risk, United States, 2019. Emerging Infectious Diseases. 2022;28(10):1955-1969. doi:10.3201/eid2810.220391. |
APA | Rayens, E., Rayens, M., & Norris, K. A. (2022). Demographic and Socioeconomic Factors Associated with Fungal Infection Risk, United States, 2019. Emerging Infectious Diseases, 28(10), 1955-1969. https://doi.org/10.3201/eid2810.220391. |
Expires 9/15/2023
Tick-borne encephalitis (TBE) is a viral infection of the central nervous system that occurs in many parts of Europe and Asia. Humans mainly acquire TBE through tick bites, but TBE occasionally is contracted through consuming unpasteurized milk products from viremic livestock. We describe cases of TBE acquired through alimentary transmission in Europe during the past 4 decades. We conducted a systematic review and meta-analysis of 410 foodborne TBE cases, mostly from a region in central and eastern Europe. Most cases were reported during the warmer months (April–August) and were associated with ingesting unpasteurized dairy products from goats. The median incubation period was short, 3.5 days, and neuroinvasive disease was common (38.9%). The clinical attack rate was 14% (95% CI 12%–16%), and we noted major heterogeneity. Vaccination programs and public awareness campaigns could reduce the number of persons affected by this potentially severe disease.
EID | Elbaz M, Gadoth A, Shepshelovich D, Shasha D, Rudoler N, Paran Y. Systematic Review and Meta-analysis of Foodborne Tick-Borne Encephalitis, Europe, 1980–2021. Emerg Infect Dis. 2022;28(10):1945-1954. https://doi.org/10.3201/eid2810.220498 |
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AMA | Elbaz M, Gadoth A, Shepshelovich D, et al. Systematic Review and Meta-analysis of Foodborne Tick-Borne Encephalitis, Europe, 1980–2021. Emerging Infectious Diseases. 2022;28(10):1945-1954. doi:10.3201/eid2810.220498. |
APA | Elbaz, M., Gadoth, A., Shepshelovich, D., Shasha, D., Rudoler, N., & Paran, Y. (2022). Systematic Review and Meta-analysis of Foodborne Tick-Borne Encephalitis, Europe, 1980–2021. Emerging Infectious Diseases, 28(10), 1945-1954. https://doi.org/10.3201/eid2810.220498. |
Expires 8/22/2023
We investigated invasive group A Streptococcus epidemiology in Idaho, USA, during 2008–2019 using surveillance data, medical record review, and emm (M protein gene) typing results. Incidence increased from 1.04 to 4.76 cases/100,000 persons during 2008–2019. emm 1, 12, 28, 11, and 4 were the most common types, and 2 outbreaks were identified. We examined changes in distribution of clinical syndrome, patient demographics, and risk factors by comparing 2008–2013 baseline with 2014–2019 data. Incidence was higher among all age groups during 2014–2019. Streptococcal toxic shock syndrome increased from 0% to 6.4% of cases (p = 0.02). We identified no differences in distribution of demographic or risk factors between periods. Results indicated that invasive group A Streptococcus is increasing among the general population of Idaho. Ongoing surveillance of state-level invasive group A Streptococcus cases could help identify outbreaks, track regional trends in incidence, and monitor circulating emm types.
EID | Dunne EM, Hutton S, Peterson E, Blackstock AJ, Hahn CG, Turner K, et al. Increasing Incidence of Invasive Group A Streptococcus Disease, Idaho, USA, 2008–2019. Emerg Infect Dis. 2022;28(9):1785-1795. https://doi.org/10.3201/eid2809.212129 |
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AMA | Dunne EM, Hutton S, Peterson E, et al. Increasing Incidence of Invasive Group A Streptococcus Disease, Idaho, USA, 2008–2019. Emerging Infectious Diseases. 2022;28(9):1785-1795. doi:10.3201/eid2809.212129. |
APA | Dunne, E. M., Hutton, S., Peterson, E., Blackstock, A. J., Hahn, C. G., Turner, K....Carter, K. K. (2022). Increasing Incidence of Invasive Group A Streptococcus Disease, Idaho, USA, 2008–2019. Emerging Infectious Diseases, 28(9), 1785-1795. https://doi.org/10.3201/eid2809.212129. |
Expires 8/15/2023
Invasive Haemophilus influenzae infection during pregnancy can cause preterm birth and fetal loss, but the mechanism is unclear. We investigated 54 cases of pregnancy-associated invasive H. influenzae disease in 52 unique pregnancies in the Auckland region of New Zealand during October 1, 2008‒September 30, 2018. Intraamniotic infection was identified in 36 (66.7%) of 54 cases. Outcome data were available for 48 pregnancies. Adverse pregnancy outcomes, defined as fetal loss, preterm birth, or the birth of an infant requiring intensive/special care unit admission, occurred in 45 (93.8%) of 48 (pregnancies. Fetal loss occurred in 17 (35.4%) of 48 pregnancies, before 24 weeks’ gestation in 13 cases, and at >24 weeks’ gestation in 4 cases. The overall incidence of pregnancy-associated invasive H. influenzae disease was 19.9 cases/100,000 births, which exceeded the reported incidence of pregnancy-associated listeriosis in New Zealand. We also observed higher rates in younger women and women of Māori ethnicity.
EID | Hills T, Sharpe C, Wong T, Cutfield T, Lee A, McBride S, et al. Fetal Loss and Preterm Birth Caused by Intraamniotic Haemophilus influenzae Infection, New Zealand. Emerg Infect Dis. 2022;28(9):1747-1754. https://doi.org/10.3201/eid2809.220313 |
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AMA | Hills T, Sharpe C, Wong T, et al. Fetal Loss and Preterm Birth Caused by Intraamniotic Haemophilus influenzae Infection, New Zealand. Emerging Infectious Diseases. 2022;28(9):1747-1754. doi:10.3201/eid2809.220313. |
APA | Hills, T., Sharpe, C., Wong, T., Cutfield, T., Lee, A., McBride, S....Thomas, M. (2022). Fetal Loss and Preterm Birth Caused by Intraamniotic Haemophilus influenzae Infection, New Zealand. Emerging Infectious Diseases, 28(9), 1747-1754. https://doi.org/10.3201/eid2809.220313. |
Expires 7/20/2023
Since Mycoplasma genitalium was identified 40 years ago, much of the epidemiology has been described, diagnostic tests have been developed and approved, and recommended treatment approaches have been identified. However, the natural history remains incompletely understood, and antimicrobial resistance has rapidly increased. This review summarizes evidence published since the US Centers for Disease Control and Prevention 2015 Sexually Transmitted Diseases Treatment Guidelines. Data on sequelae remain insufficient, macrolide resistance is common, and fluoroquinolone resistance is increasing. Potential benefits of testing and treatment include resolving symptoms, interrupting transmission, and preventing sequelae. Potential harms include cost, patient anxiety, and increasing antimicrobial resistance.
EID | Manhart LE, Geisler WM, Bradshaw CS, Jensen JS, Martin DH. Weighing Potential Benefits and Harms of Mycoplasma genitalium Testing and Treatment Approaches. Emerg Infect Dis. 2022;28(8):1-11. https://doi.org/10.3201/eid2808.220094 |
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AMA | Manhart LE, Geisler WM, Bradshaw CS, et al. Weighing Potential Benefits and Harms of Mycoplasma genitalium Testing and Treatment Approaches. Emerging Infectious Diseases. 2022;28(8):1-11. doi:10.3201/eid2808.220094. |
APA | Manhart, L. E., Geisler, W. M., Bradshaw, C. S., Jensen, J. S., & Martin, D. H. (2022). Weighing Potential Benefits and Harms of Mycoplasma genitalium Testing and Treatment Approaches. Emerging Infectious Diseases, 28(8), 1-11. https://doi.org/10.3201/eid2808.220094. |
Expires 6/17/2023
We combined American Community Survey data with age-specific Trypanosoma cruzi prevalence derived from US surveys and World Health Organization reports to yield estimates of Chagas disease in the United States, which we mapped at the local level. In addition, we used blood donor data to estimate the relative prevalence of autochthonous T. cruzi infection. Our estimates indicate that 288,000 infected persons, including 57,000 Chagas cardiomyopathy patients and 43,000 infected reproductive-age women, currently live in the United States; 22–108 congenital infections occur annually. We estimated ≈10,000 prevalent cases of locally acquired T. cruzi infection. Mapping shows marked geographic heterogeneity of T. cruzi prevalence and illness. Reliable demographic and geographic data are key to guiding prevention and management of Chagas disease. Population-based surveys in high prevalence areas could improve the evidence base for future estimates. Knowledge of the demographics and geographic distribution of affected persons may aid practitioners in recognizing Chagas disease.
EID | Irish A, Whitman JD, Clark EH, Marcus R, Bern C. Updated Estimates and Mapping for Prevalence of Chagas Disease among Adults, United States. Emerg Infect Dis. 2022;28(7):1313-1320. https://doi.org/10.3201/eid2807.212221 |
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AMA | Irish A, Whitman JD, Clark EH, et al. Updated Estimates and Mapping for Prevalence of Chagas Disease among Adults, United States. Emerging Infectious Diseases. 2022;28(7):1313-1320. doi:10.3201/eid2807.212221. |
APA | Irish, A., Whitman, J. D., Clark, E. H., Marcus, R., & Bern, C. (2022). Updated Estimates and Mapping for Prevalence of Chagas Disease among Adults, United States. Emerging Infectious Diseases, 28(7), 1313-1320. https://doi.org/10.3201/eid2807.212221. |
Expires 6/16/2023
Serum agglutination test plus exposure history were used to diagnose most cases of human brucellosis in 2 China provinces. After appropriate treatment, 13.3% of acute brucellosis cases progressed to chronic disease; arthritis was an early predictor. Seropositivity can persist after symptoms disappear, which might cause physicians to subjectively extend therapeutic regimens.
EID | Wang H, Liu H, Zhang Q, Lu X, Li D, Zhang H, et al. Natural History of and Dynamic Changes in Clinical Manifestation, Serology, and Treatment of Brucellosis, China. Emerg Infect Dis. 2022;28(7):1460-1465. https://doi.org/10.3201/eid2807.211766 |
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AMA | Wang H, Liu H, Zhang Q, et al. Natural History of and Dynamic Changes in Clinical Manifestation, Serology, and Treatment of Brucellosis, China. Emerging Infectious Diseases. 2022;28(7):1460-1465. doi:10.3201/eid2807.211766. |
APA | Wang, H., Liu, H., Zhang, Q., Lu, X., Li, D., Zhang, H....Zhang, W. (2022). Natural History of and Dynamic Changes in Clinical Manifestation, Serology, and Treatment of Brucellosis, China. Emerging Infectious Diseases, 28(7), 1460-1465. https://doi.org/10.3201/eid2807.211766. |
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