Fulminant hepatitis: a clinical review of 11 years

24 cases of fulminant hepatitis (FH) hospitalized in the Clínica de Doenças Infecciosas e Parasitárias do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo during the period from January 1976 to December 1986 were reviewed from their clinical, epidemiological and laboratorial aspects. 88% of the patients died; 20 patients (83%) presented hemorrhages and, of these, 19 died. Bacterial infections occurred in 14 patients (58%) all of whom died. Ascitis was noted in 3 cases; cerebral edema was present in 16 cases. Maximal ALT levels for each patient during hospitalization ranged widely from 81 to 4,460 UI/l. Thirteen patients presented high creatinine levels (54%). Prothrombin time activity ranged from 2.1% to 67%. Fever was present in 20 cases (83%). Encephalopathy occurred within the first 2 weeks of illness in 72% of the cases. In 7 cases other illnesses were present. The etiology could not be determined in 13 cases. In 3 cases it was due to yellow fever and 6 cases were caused by viruses other than yellow fever. In one case the cause was drug usage and in another case, possibly alcohol. The authors believe that the clinical definition of FH requires further discussion before it is established. In this study FH is a young person's disease. The mortality found was similar to that by other authors. Factors that contributed to death were: hemorrhages and bacterial infection. Factors that worsened the prognosis of hepatitis were: associated illnesses and surgical procedure. The levels of ALT during hospitalization did not correlate well with the severity of the hepatitis. The authors believe that yellow fever should be considered a cause of FH where the clinical picture meets the criteria for such, although its mechanisms of encephalopathy remain obscure. The clinical details of the 3 cases of yellow fever are presented.Vinte e quatro casos de hepatite fulminante (HF), internados na Clínica de Doenças Infecciosas e Parasitárias do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo durante o período de janeiro de 1976 a dezembro de 1986, foram revistos para a obtenção de dados clínicos, epidemiológicos e laboratoriais. 88% dos pacientes morreram. Vinte (83%) dos pacientes apresentaram hemorragias, dentre os quais 19 morreram (95%). Infecções bacterianas secundárias ocorreram em 14 pacientes (58%) todos os quais faleceram. Ascite foi notada em 3 casos e edema cerebral em 16 casos. Os valores máximos de ALT obtidos para cada paciente durante a internação variaram de 81 a 4.460 UI/l. Treze pacientes tiveram elevação de creatinina (54%). A atividade do tempo de protrombina variou de 2,1% a 67%. A febre esteve presente em 20 casos (83%). A encefalopatia surgiu durante as 2 primeiras semanas de doenças em 72% dos casos. Em 7 casos havia doenças associadas à hepatite. A etiologia não pode ser determinada em 13 casos; 3 casos foram por febre amarela; e 6 casos por outros vírus. Em 1 caso a causa foi drogas e em um caso, possivelmente, foi álcool. Os autores acreditam que a definição de HF merece discussão antes de ser totalmente aceita. Neste estudo, a HF foi uma doença que acometeu principalmente jovens. A letalidade encontrada foi semelhante a de outros estudos. Fatores que contribuíram para o óbito foram hemorragias e infecções bacterianas secundárias. Fatores de piora do prognóstico da hepatite foram a presença de outras doenças associadas e de procedimento cirúrgico. Os níveis de ALT durante a internação não refletiram a gravidade da hepatite. Os autores acreditam que a febre amarela deve ser considerada um agente etiológico de HF quando o seu quadro clínico seja compatível com tal, embora os mecanismos fisiopatológicos da encefalopatia sejam ainda obscuros. Os dados clínicos dos 3 casos de febre amarela são apresentados à parte

The minimal inhibitory concentration for sulbactam was not associated with the outcome of infections caused by carbapenem-resistant Acinetobacter sp. treated with ampicillin/sulbactam

OBJECTIVE: The objective of this study was to evaluate whether the outcomes of carbapenem-resistant Acinetobacter infections treated with ampicillin/sulbactam were associated with the in vitro susceptibility profiles. METHODS: Twenty-two infections were treated with ampicillin/sulbactam. The median treatment duration was 14 days (range: 3-19 days), and the median daily dose was 9 g (range: 1.5-12 g). The median time between Acinetobacter isolation and treatment was 4 days (range: 0-11 days). RESULTS: The sulbactam minimal inhibitory concentration (MIC) ranged from 2.0 to 32.0 mg/L, and the MIC was not associated with patient outcome, as 4 of 5 (80%) patients with a resistant infection (MIC≥16), 5 of 10 (50%) patients with intermediate isolates (MIC of 8) and only 1 of 7 (14%) patients with susceptible isolates (MIC ≤4) survived hospitalization. CONCLUSION: These findings highlight the need to improve the correlation between in vitro susceptibility tests and clinical outcome

Electricity from solar cells powers the comfort cooling in Staben

Staben is a building in Uppsala Science Park owned by Vasakronan. During 2013, Staben was renovated and a new air conditioning system was installed. The main components of the air conditioning system are three circulation pumps which require electricity. It is desired by Vasakronan to supply this electric power in a way that is environmentally friendly. Therefore, the possibilities of operating the cooling system of Staben using solar power have been examined in this study. To determine an appropriate size of the solar-cell facility, simulations and calculations were performed. The simulations were based on factors such as outside temperature, insolation and the electric power consumption of Staben. In addition to the simulation, an analysis of insolation and outside temperature was performed to validate the correlation between those two factors. The results of the simulations were validated through calculations and use of PVGIS, a computer program specialized in calculating electric production of solar cells. According to the simulations an appropriate size of the solar-cell facility to operate the cooling system would be 3 kW rated power. This way, no electric power is sold to the grid. The investment of a 3 kW solar-cell facility will cost approximately 70 000 SEK, which results in a pay-back time between 10 and 15 years.Uppsala Science Park ägs och förvaltas av fastighetsbolaget Vasakronan. 2013 renoverades kontorslokalen Staben och har sedan dess komfortkyla. Kylsystemet drivs idag med elkraft från elnätet, men i denna studie har möjligheten att driva systemet med solceller utretts eftersom detta ger Staben ett egenförsörjande och ett miljövänligt kylsystem. Även kostnad och återbetalningstid undersöktes för att ge en bild av hur rimligt det vore att driva komfortkylan med en solcellsanläggning. För att undersöka hur stor märkeffekt som behövs för att täcka driftbehovet hos kylsystemet utfördes simuleringar. Simuleringarna baserades på utomhustemperatur, solinstrålning och Stabens elkraftförbrukning. Vidare undersöktes data för solinstrålning och utomhustemperatur för att kvantifiera ett samband dessa förmodades ha. Simuleringens resultat validerades med hjälp av beräkningar och PVGIS, ett program som räknar ut energiproduktionen från solcellsanläggningar. Enligt simuleringarna behövde solcellsanläggningen ha en installerad effekt på 3 kW för att täcka kylsystemets elförbrukning på årsbasis. Eftersom kylsystemet även är i drift nattetid och solcellerna endast producerade elkraft dagtid fanns inga ekonomiskt lämpliga möjligheter att täcka kylssytemets effektbehov med enbart elkraft från solceller. Valideringsberäkningen baserad på PVGIS gav att den installerade effekten blev 3,8 kW. Grundinvesteringen för solcellsanläggningen beräknades till 70 000 SEK för en 3 kW-anläggning. Med en sådan storlek på anläggningen uppstod inget överskott av elkraft, vilket innebär att all elkraft förbrukas i Staben. Återbetalningstiden blev mellan 10 och 15 år beroende på huruvida bidrag för solceller erhölls samt hur elpriset utvecklas i framtiden

Concentrations of S100B and neurofilament light chain in blood as biomarkers for checkpoint inhibitor–induced CNS inflammation

Background: Cancer treatment with immune checkpoint inhibition (ICI) can cause immune-related adverse events in the central nervous system (CNS irAE). There are no blood biomarkers to detect CNS irAE. We investigated if concentrations of S100-calcium-binding protein B (S100B) and neurofilament light chain (NfL) in blood can be used as biomarkers for CNS irAE and assessed the incidence of CNS irAE in a cohort of ICI-treated patients. // Methods: In this single-centre, retrospective cohort study, we examined medical records and laboratory data of 197 consecutive patients treated with combined CTLA-4 and PD-1 inhibition (ipilimumab; ipi + nivolumab; nivo) for metastatic melanoma or renal cell carcinoma. CNS irAE was diagnosed using established criteria. Concentrations of S100B and NfL in blood were measured in patients with CNS irAE and in 84 patients without CNS irAE. // Findings: Nine of 197 patients (4.6%) fulfilled criteria for CNS irAE. S100B and NfL in blood increased during CNS inflammation and normalized during immunosuppression. CNS irAE was detected with a sensitivity of 100% (S100B) and 79% (NfL) and a specificity of 89% (S100B) and 74% (NfL). Patients with CNS irAE had simultaneous increased concentration of C-reactive protein (CRP) (9/9) and alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) in blood (8/9). // Interpretation: Analysis of S100B, NfL and CRP in blood facilitates the diagnosis of CNS irAE. CNS irAE may be more common than previously reported. There may be shared immune mechanisms between CNS and hepatitis irAE. // Funding: Supported by funding from the Swedish Cancer Foundation, the ALF-agreement, and Jubileumsklinikens Cancerfond

Using antimicrobial drugs: questions and answers

Para indicar o uso de antimicrobianos é necessário ter à mente várias informações sobre as drogas, tais como espectro de atividade da droga, dados de farmacocinética e farmacodinâmica, como distribuição tecidual, plasmática e excreção, efeitos adversos e é necessário ter várias informações sobre o quadro clínico do paciente e o tipo de infecção e seu agente etiológico, tais como sítio de infecção e sensibilidade antimicrobiana. Não é possível abarcar todos estes aspectos em um artigo e optamos por abordar os princípios gerais do tratamento antimicrobiano por meio de perguntas e respostas. O objetivo é prover os conceitos básicos do uso de antimicrobianos. Apresentamos as principais classes de antimicrobianos e o seu espectro de ação, conceitos como infecção, colonização e contaminação, interpretação de culturas, indicações e duração de tratamento, vias de administração, associação de drogas, critérios de resposta ao tratamento, e profilaxia antimicrobiana.In order to use antimicrobials well it is necessary to have information about the different drugs available, spectrum of activity, pharmacodynamic and pharmacokinetic data such as tissue distribution, excretion and plasma, adverse effects. It is also necessary to have information about the type and site of infection, its causative agent and antimicrobial susceptibility. We could not cover all these aspects in one article and we chose to approach the general principles of antimicrobial treatment using questions and answers. Our goal is to provide the basics for the use of antimicrobials. We present the main classes of antimicrobials and their spectrum, concepts such as infection, colonization and contamination, interpretation of cultures, indications and treatment duration, route of administration, drug combination, criteria to evaluate response to treatment, and antimicrobial prophylaxis

Variantes de Smqnr de isolados clínicos de Stenotrophomonas maltophilia no Brasil

SUMMARY Stenotrophomonas maltophilia contains a novel chromosomally-encoded qnr gene named Smqnr that contributes to low intrinsic resistance to quinolone. We described Smqnr in 13 clinical isolates of S. maltophilia from two Brazilian hospitals, over a 2-year period. The strains were identified by API 20 NE (bioMérieux, France). Susceptibility by microdilution method to trimetroprim/sulfamethoxazole, ciprofloxacin, levofloxacin, minocycline, ceftazidime, chloramphenicol and ticarcillin/clavulanate was performed according to CLSI. PCR detection of Smqnr gene was carried out. The sequence of Smqnr was compared with those deposited in GenBank. Pulsed-field gel electrophoresis (PFGE) of all strains was performed. Thirteen Smqnr positives isolates were sequenced and three novel variants of Smqnr were identified. All 13 Smqnr isolates had distinguishable patterns by PFGE. This is the first report of Smqnr in S. maltophilia isolated in Brazil.RESUMO S. maltophilia contem um novo gene qnr cromossômico denominado Smqnr que contribui para baixa resistência intrínseca a quinolonas. Descrevemos Smqnr em 13 isolados clínicos de S. maltophilia de dois hospitais brasileiros, ao longo do período de dois anos. Os isolados foram identificados pela API 20 NE (bioMérieux, França). Susceptibilidade pelo método de microdiluição dos seguintes antibióticos trimetroprim/sulfametoxazol, ciprofloxacina, levofloxacina, minociclina, ceftazidima, cloranfenicol e ticarcilina/clavulanato foi realizada segundo o CLSI. Detecção do gene de Smqnr foi realizada por PCR. A sequência de Smqnr foi comparada com aquelas depositadas no GenBank. Foi realizada eletroforese em gel de campo pulsado (PFGE) de todos os isolados. Treze isolados contendo Smqnr foram sequenciados e identificados três variantes do gene Smqnr. Todos os 13 isolados de Smqnr apresentaram diferentes padrões por PFGE. Este é o primeiro relato de Smqnr em isolados de S. maltophilia no Brasil

Cutaneous Naganishia albida (Cryptococcus albidus) infection: a case report and literature review

Naganishia albida (Cryptococcus albidus) is considered saprophytic fungi, and is rarely reported as a human pathogen. Cutaneous infections caused by non-neoformans cryptococcus are rare. We describe a case of an immunocompetent older male with cutaneous cryptococcosis caused by Naganishia albida following skin trauma, and conduct a literature review in PubMed, Lilacs, and Embase. Only six previous similar reports were found. The seven cases (including ours) were widely distributed geographically (Brazil, the US, the UK, Hungary, South Korea, and Iran), all males, and their ages varied, ranging from 14 to 86 years. Four individuals had underlying skin diseases (Sezary Syndrome, psoriasis, and skin rash without etiology) plus potentially immunosuppressive underlying conditions (diabetes mellitus, kidney transplantation, and the use of etanercept, adalimumab, and methylprednisolone). Cutaneous presentation was polymorphic, with lesions characterized as warts, ulcers, plaques, and even macules. Two patients presented disseminated disease. Serum cryptococcal antigen was negative in six patients, and diagnosis was made by fungal culture in all. There is a lack of data on optimal antifungal treatment and outcomes

Prevalence of methicillin-resistant Staphylococcus aureus colonization in individuals from the community in the city of Sao Paulo, Brazil

Staphylococcus aureus (SA) is a commensal habitant of nasal cavities and skin. Colonization by community-acquired methicillin-resistant SA (CA-MRSA) is associated with infections in patients who have not been recently hospitalized. The aim of this study is to determine the prevalence of MRSA colonization in an outpatient population, currently unknown in Brazil. Three-hundred patients or caregivers from two teaching hospitals were included. A questionnaire was applied and nasal swabs were obtained from patients. Swabs were inoculated in brain heart infusion (BHI) with 2.5% NaCl and seeded in mannitol. Suspicious colonies were subjected to MALDI-TOF MS Microflex™ identification. Antimicrobial susceptibility test for oxacillin was performed for SA-positive samples by microdilution. Polymerase chain-reactions for detection of mecA and coA genes were performed for resistant samples. Data about MRSA carriers were compared with non-carriers. There were 127 S. aureus isolates, confirmed by MALDI-TOF. Only seven (2.3%) were MRSA and positive for mecA and coA genes. Factors associated with MRSA carriage were African ethnicity, skin diseases or antibiotic use. The majority of them were from Dermatology clinics. Prevalence of MRSA colonization in individuals from the community was low in our study (2.3%). This finding raises the hypothesis of inter-household transmission of SA, although we did not find any association between MRSA-colonization and the shared use of personal objects. Given the low prevalence of MRSA carriers observed, empirical antimicrobial coverage for MRSA in community-acquired infections should be not necessary

Prevalence of methicillin-resistant Staphylococcus aureus colonization in individuals from the community in the city of Sao Paulo, Brazil

Staphylococcus aureus (SA) is a commensal habitant of nasal cavities and skin. Colonization by community-acquired methicillin-resistant SA (CA-MRSA) is associated with infections in patients who have not been recently hospitalized. The aim of this study is to determine the prevalence of MRSA colonization in an outpatient population, currently unknown in Brazil. Three-hundred patients or caregivers from two teaching hospitals were included. A questionnaire was applied and nasal swabs were obtained from patients. Swabs were inoculated in brain heart infusion (BHI) with 2.5% NaCl and seeded in mannitol. Suspicious colonies were subjected to MALDI-TOF MS Microflex™ identification. Antimicrobial susceptibility test for oxacillin was performed for SA-positive samples by microdilution. Polymerase chain-reactions for detection of mecA and coA genes were performed for resistant samples. Data about MRSA carriers were compared with non-carriers. There were 127 S. aureus isolates, confirmed by MALDI-TOF. Only seven (2.3%) were MRSA and positive for mecA and coA genes. Factors associated with MRSA carriage were African ethnicity, skin diseases or antibiotic use. The majority of them were from Dermatology clinics. Prevalence of MRSA colonization in individuals from the community was low in our study (2.3%). This finding raises the hypothesis of inter-household transmission of SA, although we did not find any association between MRSA-colonization and the shared use of personal objects. Given the low prevalence of MRSA carriers observed, empirical antimicrobial coverage for MRSA in community-acquired infections should be not necessary

Diarreia por Clostridium difficile em pacientes hematológicos e transplantados de células tronco hematopoiéticas: fatores de risco da forma grave e morte

Descrevemos a taxa de incidência de diarreia associada a Clostridium difficile (CDAD) em pacientes hematológicos e submetidos a transplante de células-tronco hematopoiéticas (TCTH) internados no HC-FMUSP no período de janeiro de 2007 a junho de 2011 usando dois denominadores 1.000 paciente e 1.000 dias de neutropenia e os fatores de risco associados à forma grave da doença e morte. O método de ELISA (Ridascreen-Biopharm, Germany) de detecção de toxinas A/B foi utilizado para o diagnóstico de C. difficile. Análise multivariada usando regressão logística múltipla foi conduzida para avaliar os potenciais fatores de risco associados com forma grave de CDAD e morte em até 14 dias do diagnóstico. Sessenta e seis episódios foram identificados em 64 pacientes entre 439 pacientes que apresentaram diarreia durante o período do estudo. A taxa de incidência de CDAD variou de 0,78 a 5,45 por 1.000 dias de neutropenia e de 0,65 para 5,45 por 1.000 pacientes-dias. A doença de base mais comum foi leucemia mielóide aguda 30/64(44%), 32/64 (46%) pacientes estavam neutropênicos, 31/64 (45%) foram submetidos à TCTH alogênico, 61/64 (88%) usaram antibióticos previamente e 9/64 (13%) apresentaram forma grave da doença. A maioria dos pacientes (89%) utilizou metronidazol oral no tratamento da CDAD e 19/64 (26%) evoluiram para óbito. Os fatores de risco independentes associados à morte foram forma grave da doença e uso de linezolida.We describe the rate of incidence of Clostridium difficile-associated diarrhea (CDAD) in hematologic and patients undergone stem cell transplant (HSCT) at HC-FMUSP, from January 2007 to June 2011, using two denominators 1,000 patient and 1,000 days of neutropenia and the risk factors associated with the severe form of the disease and death. The ELISA method (Ridascreen-Biopharm, Germany) for the detections of toxins A/B was used to identify C. difficile. A multivariate analysis was performed to evaluate potential factors associated with severe CDAD and death within 14 days after the diagnosis of CDAD, using multiple logistic regression. Sixty-six episodes were identified in 64 patients among 439 patients with diarrhea during the study period. CDA rate of incidence varied from 0.78 to 5.45 per 1,000 days of neutropenia and from 0.65 to 5.45 per 1,000 patient-days. The most common underlying disease was acute myeloid leukemia 30/64 (44%), 32/64 (46%) patients were neutropenic, 31/64 (45%) undergone allogeneic HSCT, 61/64 (88%) had previously used antibiotics and 9/64 (13%) have severe CDAD. Most of the patients (89%) received treatment with oral metronidazole and 19/64 (26%) died. The independent risk factors associated with death were the severe form of CDAD, and use of linezolid