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1.
Mundo saúde (Impr.) ; 47: e14502022, 2023.
Article in English, Portuguese | LILACS-Express | LILACS | ID: biblio-1510501

ABSTRACT

Cerca de um terço dos pacientes com COVID-19 em unidades de terapia intensiva (UTI) apresentam injúria renal aguda (IRA) dialítica. Poucos estudos têm avaliado a sobrevida de pacientes com IRA em UTI exclusivamente pública. O objetivo do estudo foi avaliar a sobrevida intra-hospitalar em 90 dias de pacientes com e sem IRA dialítica internados com COVID-19 grave. Trata-se de uma coorte histórica de um hospital geral em Joinville, Santa Catarina/Brasil. Foram incluídos todos os pacientes admitidos na UTI entre março e dezembro de 2020 com diagnóstico confirmado de COVID-19. Definiu-se IRA como a presença de alteração de função renal aguda com necessidade de hemodiálise. Utilizou-se modelo multivariado por regressão de Cox para avaliar a sobrevida de pacientes com e sem IRA dialítica. Os resultados do estudo demonstraram que dos 187 pacientes incluídos (55,5% homens) com média de idade de 62,8±13,6 anos, 37,4% apresentaram IRA dialítica. Pacientes com IRA dialítica usaram mais drogas vasoativas, tinham maior gravidade na admissão e maior mortalidade (84,3% vs. 63,2%; p=0,002) em relação àqueles sem IRA. O risco de morte nos pacientes com IRA foi maior (RR bruto= 1,60; IC 95% 1,13-2,26; p= 0,007). Após ajustes para idade, sexo, comorbidades e gravidade clínica, a presença de IRA dialítica se manteve associada a uma frequência maior de mortalidade em 90 dias (RR= 1,49; IC 95% 1,03-2.15; p=0,032). A sobrevida de pacientes com COVID-19 grave e IRA dialítica na amostra estudada foi menor em relação a UTIs privadas no Brasil, o que sugere desigualdades no sistema público.


About one third of patients with COVID-19 in intensive care units (ICU) have acute kidney injury (AKI) requiring dialysis. Few studies have evaluated the survival ratel of patients with AKI in exclusively public ICUs. The aim of this study was to evaluate the 90-day in-hospital survival of patients with and without AKI requiring dialysis hospitalized with severe COVID-19. This is a historical cohort of a general hospital in Joinville, Santa Catarina/Brazil. All patients admitted to the ICU between March and December of 2020 with a confirmed diagnosis of COVID-19 were included. AKI was defined by the presence of acute renal function alteration requiring hemodialysis. A multivariate Cox regression model was used to assess the survival of patients with and without AKI requiring dialysis. The results of the study showed that, of the 187 patients included (55.5% men) with a mean age of 62.8±13.6 years, 37.4% had AKI requiring dialysis. Patients with AKI requiring dialysis used more vasoactive drugs, had greater severity on admission and higher mortality rate (84.3% vs. 63.2%; p=0.002) compared to those without AKI. The risk of death in patients with AKI was higher (crude RR= 1.60; 95% CI 1.13-2.26; p= 0.007). After adjustments for age, sex, comorbidities and clinical severity, the presence of AKI requiring dialysis remained associated with a higher frequency of 90-day mortality (RR= 1.49; 95% CI 1.03-2.15; p=0.032). The survival of patients with severe COVID-19 and AKI requiring dialysis in the studied sample was lower compared to private ICUs in Brazil, which suggests inequalities in the public system.

2.
Arq. ciências saúde UNIPAR ; 27(7): 3632-3642, 2023.
Article in English | LILACS-Express | LILACS | ID: biblio-1442989

ABSTRACT

SARS-COV-2 is transmitted among human beings by saliva droplets that come in direct contact with the oral cavity, nose, and eyes. Since the mouth is one of the anatomical sites primarily contaminated, oral manifestations have also been reported beyond the serious consequences inherent to progressive respiratory failure. This study aimed to identify oral manifestations possibly related to the infection by COVID-19 in hospitalized patients. A prospective study was carried out with patients diagnosed with COVID-19 in the period between March and June 2021, admitted to the Moderate COVID-19 Care Unit of the Hans Dieter Schmidt Regional Hospital, by applying a form and performing a clinical exam of the oral cavity. Out of all patients (n=45), 33.3% reported both olfactory (anosmia) and taste dysfunction (dysgeusia), with an average duration of 5.9 ±3.0 days. Regarding other oral manifestations evaluated, two patients reported dry and burning mouth and one patient reported a change in taste associated with plaque-like changes in the tongue. No patients presented ulcers or other lesions in the oral cavity. Olfactory and taste dysfunction were symptoms recognized of the novel coronavirus disease (COVID-19). However, the association with other oral manifestations is still controversy. Unfortunately, dentistry professionals are still not part of most teams in the hospital environment, mostly because of the lack of prioritization of dental care. Working with a multidisciplinary team may avoid possible systemic complications due to poor dental care.


Sars-COV-2 é transmitida entre os seres humanos por gotículas de saliva que entram em contato direto com a cavidade oral, nariz e olhos. Uma vez que a boca é um dos sítios anatômicos principalmente contaminados, as manifestações orais também foram relatadas para além das graves consequências inerentes à insuficiência respiratória progressiva. Este estudo teve como objetivo identificar manifestações orais possivelmente relacionadas à infecção por Covid-19 em pacientes hospitalizados. Foi realizado um estudo prospetivo com pacientes diagnosticados com Covid-19 no período entre março e junho de 2021, internados na Unidade de Atendimento Moderado contra a Covid-19 do Hospital Regional Hans Dieter Schmidt, aplicando um formulário e realizando um exame clínico da cavidade oral. De todos os pacientes (n=45), 33,3% relataram disfunção olfativa (anosmia) e gustativa (disgeusia), com duração média de 5,9 ±3,0 dias. Em relação a outras manifestações orais avaliadas, dois pacientes relataram boca seca e ardente e um paciente relatou alteração no paladar associada a alterações semelhantes a placas na língua. Nenhum paciente apresentou úlceras ou outras lesões na cavidade oral. Disfunção olfativa e gustativa foram sintomas reconhecidos do novo coronavírus (Covid-19). No entanto, a associação com outras manifestações orais ainda é controversa. Infelizmente, os profissionais de odontologia ainda não fazem parte da maioria das equipes do ambiente hospitalar, principalmente por causa da falta de priorização dos cuidados odontológicos. Trabalhar com uma equipe multidisciplinar pode evitar possíveis complicações sistêmicas devido a cuidados odontológicos deficientes.


SARS-COV-2 se transmite entre los seres humanos por las gotitas de saliva que entran en contacto directo con la cavidad oral, la nariz y los ojos. Dado que la boca es uno de los sitios anatómicos principalmente contaminados, también se han informado manifestaciones orales más allá de las consecuencias graves inherentes a la insuficiencia respiratoria progresiva. El objetivo de este estudio fue identificar las manifestaciones bucales posiblemente relacionadas con la infección por COVID-19 en pacientes hospitalizados. Se realizó un estudio prospectivo con pacientes diagnosticados de COVID-19 en el periodo comprendido entre marzo y junio de 2021, ingresados en la Unidad de Cuidados Moderados de COVID-19 del Hospital Regional Hans Dieter Schmidt, mediante la aplicación de un formulario y la realización de un examen clínico de la cavidad oral. De todos los pacientes (n=45), el 33,3% notificó tanto disfunción olfativa (anosmia) como gustativa (disgeusia), con una duración media de 5,9 ±3,0 días. En cuanto a las demás manifestaciones orales evaluadas, dos pacientes notificaron sequedad y ardor de boca y un paciente notificó un cambio en el gusto asociado a cambios en la lengua en forma de placa. Ningún paciente presentó úlceras u otras lesiones en la cavidad oral. La disfunción olfativa y gustativa fueron síntomas reconocidos de la nueva enfermedad por coronavirus (COVID-19). Sin embargo, la asociación con otras manifestaciones orales es aún controvertida. Desafortunadamente, los profesionales de la odontología todavía no son parte de la mayoría de los equipos en el entorno hospitalario, principalmente debido a la falta de priorización de la atención odontológica. Trabajar con un equipo multidisciplinario puede evitar posibles complicaciones sistémicas debido a la mala atención dental.

3.
Rev. Soc. Bras. Med. Trop ; 56: e0277, 2023. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1422902

ABSTRACT

ABSTRACT Background: The spread of carbapenemase- and extended-spectrum β-lactamase (ESBL)-producing gram-negative bacilli (GNB) represent a global public health threat that limits therapeutic options for hospitalized patients. This study aimed to evaluate the in-vitro susceptibility of β-lactam-resistant GNB to ceftazidime-avibactam (C/A) and ceftolozane-tazobactam (C/T), and investigate the molecular determinants of resistance. Methods: Overall, 101 clinical isolates of Enterobacterales and Pseudomonas aeruginosa collected from a general hospital in Brazil were analyzed. Susceptibility to the antimicrobial agents was evaluated using an automated method, and the minimum inhibitory concentrations (MIC50/90) of C/A and C/T were determined using Etest®. The β-lactamase-encoding genes were investigated using polymerase chain reaction. Results: High susceptibility to C/A and C/T was observed among ESBL-producing Enterobacterales (100% and 97.3% for CLSI and 83.8% for BRCAST, respectively) and carbapenem-resistant P. aeruginosa (92.3% and 87.2%, respectively). Carbapenemase-producing Klebsiella pneumoniae exhibited high resistance to C/T (80%- CLSI or 100%- BRCAST) but high susceptibility to C/A (93.4%). All carbapenem-resistant K. pneumoniae isolates were susceptible to C/A, whereas only one isolate was susceptible to C/T. Both antimicrobials were inactive against metallo-β-lactamase-producing K. pneumoniae isolates. Resistance genes were concomitantly identified in 44 (44.9%) isolates, with bla CTX-M and bla SHV being the most common. Conclusions: C/A and C/T were active against microorganisms with β-lactam-resistant phenotypes, except when resistance was mediated by metallo-β-lactamases. Most C/A- and C/T-resistant isolates concomitantly carried two or more β-lactamase-encoding genes (62.5% and 77.4%, respectively).

4.
J. bras. nefrol ; 44(4): 482-489, Dec. 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1421905

ABSTRACT

Abstract Introduction: Urgent-start peritoneal dialysis (US-PD) has been proposed as a safe modality of renal replacement therapy (RRT) for end-stage renal disease (ESRD) patients with an indication for emergency dialysis initiation. We aimed to compare the characteristics, 30-day complications, and clinical outcomes of US-PD and planned peritoneal dialysis (Plan-PD) patients over the first year of therapy. Methods: This was a single-center retrospective study that included incident adult patients followed for up to one year. US-PD was considered when incident patients started therapy within 7 days after Tenckhoff catheter implantation. Plan-PD group consisted of patients who started therapy after the breaking period (15 days). Mechanical and infectious complications were compared 30 days from PD initiation. Hospitalization and technique failure during the first 12 months on PD were assessed by Kaplan-Meier curves and the determinants were calculated by Cox regression models. Results: All patients starting PD between October/2016 and November/2019 who fulfilled the inclusion criteria were analyzed. We evaluated 137 patients (70 in the US-PD x 67 Plan-PD). The main complications in the first 30 days were catheter tip migration (7.5% Plan-PD x 4.3% US-PD - p= 0.49) and leakage (4.5% Plan-PD x 5.7% US-PD - p=0.74). Most catheters were placed using the Seldinger technique. The main cause of dropout was death in US-PD patients (15.7%) and transfer to HD in Plan-PD patients (13.4%). The occurrence of complications in the first 30 days was the only risk factor for dropout (OR = 2.9; 95% CI 1.1-7.5, p = 0.03). Hospitalization rates and technique survival were similar in both groups. Conclusion: The lack of significant differences in patients' outcomes between groups reinforces that PD is a safe and applicable dialysis method in patients who need immediate dialysis.


Resumo Introdução: A diálise peritoneal de início urgente (US-PD) foi proposta como modalidade segura de terapia renal substitutiva (TRS) para pacientes com doença renal em estágio 5 (DRC-5) com indicação de início de diálise de emergência. Buscamos comparar características, complicações em 30 dias e desfechos clínicos de pacientes em US-PD e diálise peritoneal planejada (DP-plan) no primeiro ano de terapia. Métodos: Estudo retrospectivo de centro único, que incluiu pacientes adultos incidentes em DP acompanhados por até um ano. Considerou-se US-PD quando os pacientes iniciaram terapia até 7 dias após implante do cateter Tenckhoff. O grupo DP-plan consistiu de pacientes iniciando terapia após período break-in (15 dias). Compararam-se complicações mecânicas e infecciosas 30 dias após o início da DP. Hospitalização e falha da técnica durante os primeiros 12 meses em terapia foram avaliados por curvas Kaplan-Meier e os seus determinantes foram analisados por modelos de regressão de Cox. Resultados: Analisaram-se todos os pacientes iniciando DP entre Outubro/2016-Novembro/2019 que preencheram os critérios de inclusão. Avaliamos 137 pacientes (70 US-PD x 67 DP-plan). As principais complicações nos primeiros 30 dias foram migração da ponta do cateter (7,5% DP-plan x 4,3% US-PD - p= 0,49) e extravasamento (4,5% DP-plan x 5,7% US-PD - p=0,74). A maioria dos cateteres foi implantada pela técnica de Seldinger. A principal causa de saída da terapia foi óbito em pacientes em US-PD (15,7%) e transferência para HD em pacientes em DP-plan (13,4%). A ocorrência de complicações nos primeiros 30 dias foi o único fator de risco para saída da terapia (OR = 2,9; IC 95% 1,1-7,5, p = 0,03). Taxas de hospitalização e sobrevida da técnica foram similares em ambos os grupos. Conclusão: A ausência de diferenças significativas nos desfechos dos pacientes entre os grupos reforça que DP é um método de diálise seguro e aplicável em pacientes que necessitam diálise imediata.

5.
J. Bras. Patol. Med. Lab. (Online) ; 58: e4482022, 2022. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1375689

ABSTRACT

ABSTRACT Introduction In Brazil, 8,000 new cases of childhood cancer are estimated each year, whose causes are still little known, although some have genetically determined factors. Approximately 70% of human cancers have alterations in the TP53 gene, which encodes the protein responsible for inhibiting the disordered growth of cells exposed to injuries. However, the frequency of alterations in the expression of TP53 in childhood cancers in Brazil remains poorly known. Objective To evaluate the expression of TP53 gene in patients with childhood cancer in northeastern of Santa Catarina, Brazil. Materials and Methods: Retrospectively, 282 patients diagnosed with cancer between 2005 and 2015 in Joinville were included. TP53 expression was evaluated by immunohistochemistry using a score based on the intensity and percentage of stained cells. Results The p53 protein was positive in 25.2% of cases, with no difference between sexes. Considering the five main groups of tumors in the sample, the expression was positive in 31.8%, 27.3%, 20%, 17.2% and 5.9% of lymphomas, nephroblastomas, neuroblastomas, tumors of the Central Nervous System and leukemias, respectively. Conclusion The prevalence of TP53 expression was evaluated in different childhood cancers in the northeastern of Santa Catarina. Positivity was higher among lymphomas and lower in leukemias, but with no significant difference among the five most frequent tumors. Further studies that allow correlation with aggressiveness and disease evolution are required.

6.
Arq. neuropsiquiatr ; 79(12): 1070-1075, Dec. 2021. tab
Article in English | LILACS | ID: biblio-1355707

ABSTRACT

ABSTRACT Background: Ischemic stroke (IS) is a multifactorial disease that presents high rates of morbimortality in Brazil. Several studies proved that there is a link between the ABO blood group system and the occurrence of thrombotic events. Nonetheless, its association with IS is not well established. Objective: For that reason, the purpose hereof was to investigate the relation between the ABO blood groups and the occurrence of IS in a Brazilian cohort of cerebrovascular diseases. Methods: Five hundred and twenty-nine subjects were included over 12 months, from which 275 presented an IS episode and 254 composed the control group. Blood samples were drawn for direct and reverse serotyping. The control and IS groups were compared regarding the traditional risk factors and the distribution of the ABO blood groups. Results: The IS group presented a higher prevalence of systemic arterial hypertension (SAH), diabetes mellitus, smoking habits, family history, cardiopathy, and sedentary lifestyle in comparison with the control group. The AB blood type prevailed among the patients (5.1 vs. 1.6%; p<0.05) and this group had more SAH cases in comparison with the O type group (92.9 vs. 67.3%; p<0.05). Conclusions: Our results suggest that the occurrence of IS is more frequent among patients of the AB blood type.


RESUMO Antecedentes: O acidente vascular cerebral isquêmico (AVCI) é uma doença multifatorial que apresenta altas taxas de morbimortalidade no Brasil. Vários estudos provaram que existe uma ligação entre o sistema ABO de grupos sanguíneos e a ocorrência de eventos trombóticos. No entanto, sua associação com AVCI não está bem estabelecida. Objetivo: Por essa razão, o objetivo deste trabalho foi investigar a relação entre os grupos sanguíneos ABO e a ocorrência de AVCI em uma coorte brasileira de doenças cerebrovasculares. Métodos: Ao longo de 12 meses foram incluídos 529 indivíduos, dos quais 275 apresentaram um episódio de AVCI e 254 compuseram o grupo controle. Amostras de sangue foram coletadas para sorotipagem direta e reversa. Os grupos controle e AVCI foram comparados em relação aos fatores de risco tradicionais e à distribuição dos grupos sanguíneos ABO. Resultados: O grupo AVCI apresentou maior prevalência de hipertensão arterial sistêmica (HAS), diabetes mellitus, tabagismo, história familiar, cardiopatia e estilo de vida sedentário em comparação ao grupo controle. O tipo sanguíneo AB prevaleceu entre os pacientes (5,1 vs. 1,6%; p<0,05) e apresentou mais casos de HAS em comparação ao tipo O (92,9 vs. 67,3%; p<0,05). Conclusões: Nossos resultados sugerem que a ocorrência de AVCI é mais frequente entre os pacientes do tipo sanguíneo AB.


Subject(s)
Humans , Brain Ischemia/epidemiology , Stroke/etiology , Stroke/epidemiology , Ischemic Stroke , ABO Blood-Group System , Risk Factors
7.
Pesqui. vet. bras ; 40(9): 690-695, Sept. 2020. tab
Article in English | LILACS, VETINDEX | ID: biblio-1143420

ABSTRACT

Plasmid-mediated polymyxin resistance was first described in 2015, in China, in Escherichia coli carrying the mcr-1 (Mobile Colistin Resistance-1) gene. Since then, it has become a major public health challenge worldwide, representing a major threat to human and animal health. In addition, there are still few reports on the prevalence of mcr-1 in Enterobacteriaceae isolated from humans, animals and food. Therefore, the purpose of the study was to investigate the occurrence of the mcr-1 gene in bacterial isolates with phenotypic resistance to polymyxin B obtained from clinical specimens of companion animals. Phenotypic resistance to polymyxin B were determined by broth microdilution and the susceptibility profile to other antimicrobials (amikacin, amoxicillin/clavulanate, ampicillin, ampicillin/sulbactam, aztreonam, cefazolin, cefepime, cefotaxime, cefoxitin, ceftazidime, ceftriaxone, chloramphenicol, ciprofloxacin, doxycycline, ertapenem, gentamicin, imipenem, marbofloxacin, meropenem, phosphomycin, piperacillin/tazobactam, tetracycline, ticarcillin/clavulanate, tobramycin and trimethoprim/sulfamethoxazole) by disc-diffusion agar method. The extraction of bacterial DNA was performed via heat shock followed by spectrophotometric evaluation. To verify the presence of mcr-1, the Polymerase Chain Reaction was employed using specific primers, followed by agarose gel electrophoresis. The positive isolates had the corresponding amplicons sequenced. In this study, there were identified the first isolates of Escherichia coli, Klebsiella spp. and Enterobacter spp. carrying the mcr-1 gene derived from specimens of companion animals in Brazil. Our results suggest the dissemination of resistance to polymyxins in the community and the environment, highlighting the need for surveillance and optimized treatment guidelines.(AU)


A resistência à polimixina mediada por plasmídeo teve sua primeira descrição em 2015, na China, em Escherichia coli portadora do gene mcr-1 (Mobile Colistin Resistance-1) e a partir de então tornou-se um grande desafio para a saúde pública em todo o mundo, constituindo uma grande ameaça à saúde humana e animal. Além disso, ainda existem poucos relatos sobre a prevalência de mcr-1 em Enterobacteriaceae isoladas de humanos, animais e alimentos. Sendo assim, o objetivo do estudo foi investigar a ocorrência do gene mcr-1 em isolados bacterianos com resistência fenotípica à polimixina B, oriundos de materiais clínicos de animais de companhia. A resistência fenotípica à polimixina B foi determinada por microdiluição em caldo e o perfil de sensibilidade aos demais antimicrobianos (amicacina, amoxicilina/clavulanato, ampicilina, ampicilina/sulbactam, aztreonam, cefazolina, cefepime, cefotaxima, cefoxitina, ceftazidima, ceftriaxona, cloranfenicol, ciprofloxacina, doxiciclina, ertapenem, gentamicina, imipinem, marbofloxacino, meropenem, fosfomicina, piperacilina/tazobactam, tetraciclina, ticarcilina/clavulanato, tobramicina sulfametoxazol/trimetoprim) foram determinados pelo método disco difusão. A extração do DNA bacteriano foi realizada via choque térmico, seguido de avaliação espectrofotométrica. Para a verificação da presença do mcr-1 foi utilizada a Reação em Cadeia da Polimerase com emprego de iniciadores específicos, seguida de eletroforese em gel de agarose. Os isolados positivos tiveram os correspondentes amplicons sequenciados. Nesse estudo foram identificados os primeiros isolados de Escherichia coli, Klebsiella spp. e Enterobacter spp. portadores do gene mcr-1 derivados de espécimes de animais de companhia no Brasil. Este estudo sugere a disseminação da resistência às polimixinas na comunidade e no meio ambiente, destacando a necessidade de vigilância e diretrizes otimizadas de tratamento.(AU)


Subject(s)
Animals , Dogs , Polymyxin B , Genes, MDR , Drug Resistance, Bacterial , Enterobacteriaceae , Cats
8.
J. Bras. Patol. Med. Lab. (Online) ; 56: e1552020, 2020. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1090763

ABSTRACT

ABSTRACT Introduction: The cervical cytological examination and the investigation of high-risk human papillomavirus (HPV) deoxyribonucleic acid (DNA) are well-known valuable tools for screening of cervical lesions, since they allow the early diagnosis of cancer and its precursor lesions. Objective: This study aimed to evaluate the ability of high-risk HPV DNA detection by hybrid capture to predict intraepithelial lesions and cancer in patients with initial cervical cytological diagnosis of atypical squamous cells (ASC). Method: Retrospective analysis of histological or cervical cytological results after one-year follow-up from hybrid capture for high-risk HPV DNA research in patients with previous ASC diagnosis. Sensitivity, specificity and positive and negative predictive values of hybrid capture were calculated in relation to the identification of squamous intraepithelial lesions. Results: Among the 163 patients previously diagnosed with ASC and absence of high-risk HPV DNA, nine (5.5%) showed low-grade (LSIL) or high-grade squamous intraepithelial lesion (HSIL) during the follow-up. On the other hand, among the 110 patients presenting ASC and high-risk HPV DNA positivity, 43 (39%) showed cervical lesions within one year. Sensitivity and specificity values and positive and negative predictive values applied to hybrid capture for the identification of squamous intraepithelial lesions were 82.3%, 69.3%, 38.1%, and 94.4%, respectively. Conclusion: Our results showed a high negative predictive value of hybrid capture for cervical lesions detection, in patients with previous diagnosis of ASC, when the high-risk HPV DNA research was negative.


RESUMEN Introducción: La colpocitología y la investigación del ácido desoxirribonucleico (ADN) del virus del papiloma humano (VPH) de alto riesgo son herramientas bien conocidas para la detección de lesiones cervicales, puesto que permiten el diagnóstico precoz del cáncer y sus lesiones precursoras. Objetivo: El objetivo de este estudio es evaluar la capacidad de detección del ADN-VPH de alto riesgo por captura híbrida en predecir lesiones intraepiteliales y cáncer en pacientes con diagnóstico colpocitológico inicial de atipia de células escamosas (ASC). Método: Análisis retrospectivo de resultados histológicos y citológicos después de un año de seguimiento desde la captura híbrida para investigación de ADN-VPH de alto riesgo en pacientes con diagnóstico previo de ASC. Se calcularon sensibilidad, especificidad y valores predictivos positivo y negativo en relación con la identificación de lesiones intraepiteliales escamosas. Resultados: Entre las 163 pacientes con diagnóstico de ASC previo y ausencia de ADN-VPH de alto riesgo, nueve (5,5%) presentaron lesiones escamosas intraepiteliales de bajo grado (LEIBG) o alto grado (LEIAG) durante el seguimiento. Por otra parte, entre las 110 pacientes con ASC y positividad para ADN-VPH de alto riesgo, 43 (39%) presentaron lesiones cervicales en un plazo de un año. Los valores de sensibilidad y especificidad y los valores predictivos positivo y negativo empleados en la captura híbrida para identificar lesiones escamosas intraepiteliales fueron 82,3%, 69,3%, 38,1% y 94,4%, respectivamente. Conclusión: Nuestros resultados demostraron alto valor predictivo negativo de la captura híbrida para detectar lesiones cervicales en pacientes con diagnóstico previo de ASC, cuando la investigación de ADN-VPH de alto riesgo ha sido negativa.


RESUMO Introdução: O exame colpocitológico e a investigação do ácido desoxirribonucleico (DNA)-papilomavírus humano (HPV) de alto risco são ferramentas bem conhecidas para o rastreamento das lesões cervicais, pois permitem o diagnóstico precoce do câncer e suas lesões precursoras. Objetivo: Este estudo tem o objetivo de avaliar a capacidade da detecção do DNA-HPV de alto risco pela captura híbrida em predizer lesões intraepiteliais e câncer em pacientes com diagnóstico colpocitológico inicial de atipia de células escamosas (ASC). Método: Análise retrospectiva de resultados histológicos e colpocitológicos após um ano de seguimento a partir da captura híbrida para pesquisa de DNA-HPV de alto risco em pacientes com diagnóstico prévio de ASC. Sensibilidade, especificidade e valores preditivos positivo e negativo da captura híbrida foram calculados em relação à identificação de lesões intraepiteliais escamosas. Resultados: Entre as 163 pacientes com diagnóstico de ASC prévio e ausência do DNA-HPV de alto risco, nove (5,5%) apresentaram lesões intraepiteliais escamosas de baixo grau (LIEBG) ou alto grau (LIEAG) durante o acompanhamento. Por outro lado, das 110 pacientes com ASC e positividade para o DNA-HPV de alto risco, 43 (39%) apresentaram lesões cervicais em até um ano. Os valores de sensibilidade e especificidade e os valores preditivos positivo e negativo aplicados à captura híbrida para a identificação de lesões intraepiteliais escamosas foram 82,3%, 69,3%, 38,1% e 94,4%, respectivamente. Conclusão: Nossos resultados mostraram alto valor preditivo negativo da captura híbrida para detecção de lesões cervicais em pacientes com diagnóstico prévio de ASC, quando a pesquisa do DNA-HPV de alto risco foi negativa.

9.
Rev. bras. ter. intensiva ; 31(4): 511-520, out.-dez. 2019. tab, graf
Article in Portuguese | LILACS | ID: biblio-1058052

ABSTRACT

RESUMO Objetivo: Caracterizar os pacientes com doença crítica crônica e identificar os preditores relacionados à evolução para doença crítica crônica. Métodos: Coleta prospectiva de dados por 1 ano realizada na unidade de terapia intensiva de um hospital geral localizado na Região Sul do país. Construíram-se três modelos de regressão logística para identificar os fatores associados com doença crítica crônica. Resultados: Dentre os 574 pacientes admitidos à unidade de terapia intensiva durante o período do estudo, 200 foram submetidos à ventilação mecânica. Destes, 85 (43,5%) pacientes desenvolveram doença crítica crônica, totalizando 14,8% de todos os pacientes admitidos à unidade de terapia intensiva. O modelo de regressão que avaliou os fatores prévios à admissão à unidade de terapia intensiva associados com doença crítica crônica identificou insuficiência renal crônica submetida à diálise (OR 3,57; p = 0,04) e diagnóstico neurológico quando da admissão ao hospital (OR 2,25; p = 0,008) como fatores independentes. No modelo que avaliou a associação de doença crítica crônica com situações ocorridas durante a permanência na unidade de terapia intensiva, destacaram-se fraqueza muscular (OR 2,86; p = 0,01) e úlceras por pressão (OR 9,54; p < 0,001). Na análise multivariada global (fatores prévios e situações ocorridas durante a permanência na unidade de terapia intensiva), destacaram-se admissão ao hospital por doenças neurológicas (OR 2,61; p = 0,03) e desenvolvimento de úlceras por pressão (OR 9,08; p < 0,001). Conclusão: A incidência de doença crítica crônica foi similar à observada em outros estudos e teve associação mais forte com o diagnóstico de doenças neurológicas quando da admissão ao hospital e insuficiência renal crônica submetida à hemodiálise, assim como com complicações desenvolvidas durante a hospitalização, como úlceras por pressão e fraqueza muscular.


ABSTRACT Objective: To characterize patients with chronic critical illness and identify predictors of development of chronic critical illness. Methods: Prospective data was collected for 1 year in the intensive care unit of a general hospital in Southern Brazil. Three logistic regression models were constructed to identify factors associated with chronic critical illness. Results: Among the 574 subjects admitted to the intensive care unit, 200 were submitted to mechanical ventilation. Of these patients, 85 (43.5%) developed chronic critical illness, composing 14.8% of all the patients admitted to the intensive care unit. The regression model that evaluated the association of chronic critical illness with conditions present prior to intensive care unit admission identified chronic renal failure in patients undergoing hemodialysis (OR 3.57; p = 0.04) and a neurological diagnosis at hospital admission (OR 2.25; p = 0.008) as independent factors. In the model that evaluated the association of chronic critical illness with situations that occurred during intensive care unit stay, muscle weakness (OR 2.86; p = 0.01) and pressure ulcers (OR 9.54; p < 0.001) had the strongest associations. In the global multivariate analysis (that assessed previous factors and situations that occurred in the intensive care unit), hospital admission due to neurological diseases (OR 2.61; p = 0.03) and the development of pressure ulcers (OR 9.08; p < 0.001) had the strongest associations. Conclusion: The incidence of chronic critical illness in this study was similar to that observed in other studies and had a strong association with the diagnosis of neurological diseases at hospital admission and chronic renal failure in patients undergoing hemodialysis, as well as complications developed during hospitalization, such as pressure ulcers and muscle weakness.


Subject(s)
Humans , Male , Female , Adult , Aged , Respiration, Artificial/statistics & numerical data , Critical Illness/epidemiology , Critical Care , Intensive Care Units , Brazil , Chronic Disease , Prospective Studies , Risk Factors , Muscle Weakness/epidemiology , Pressure Ulcer/epidemiology , Hospitalization/statistics & numerical data , Length of Stay , Middle Aged
10.
Rev. epidemiol. controle infecç ; 9(4): 281-286, out.-dez. 2019. ilus
Article in Portuguese | LILACS | ID: biblio-1152242

ABSTRACT

Justificativa e objetivos: Infecções Relacionadas à Assistência à Saúde (IRAS) causadas por bacilos Gram negativos multirresistentes (BGN-MDR) são consideradas um problema de saúde pública e um impacto nas taxas de mortalidade nas Unidades de Terapia Intensiva (UTI). O objetivo deste estudo foi verificar o perfil fenotípico de resistência à colistina e à tigeciclina, consideradas como último recurso terapêutico aos BGN-MDR. Métodos: Os dados foram coletados nas fichas de busca ativa do serviço de controle de infecções e prontuários médicos de pacientes internados em duas UTIs de um hospital público de Joinville, entre janeiro de 2016 e junho de 2017. Resultados: Ocorreram 256 IRAS por BGN, acometendo principalmente o gênero masculino (62%), com mediana de idade de 65 anos. Entre os BGN, 37% expressaram MDR; sendo as espécies mais frequentes: Klebsiella pneumoniae e (47%), Acinetobacter baumannii (23%) e Stenotrophomonas maltophilia (11%). A resistência de BGN-MDR à colistina e tigeciclina foi de 5% e de 12%, respectivamente; 5% dos isolados foram resistentes aos dois antibióticos. A taxa de óbito entre os pacientes com IRAS por BGN-MDR resistentes à colistina foi mais alta (60%) que aquelas à tigeciclina (45%). Conclusão: K. pneumoniae e A. baumannii produtores de carbapenemases, resistentes a colistina e tigeciclina prevaleceram entre os BGN-MDR, e estiveram associadas a maioria dos óbitos. Essas observações, junto com o alto uso de carbapenêmicos na terapia empírica, mostra a necessidade do uso racional de antimicrobianos.(AU)


Background and objectives: Healthcare-associated Infections (HAIs) caused by multidrug-resistant Gram-negative bacilli (GNB-MDR) are considered a public health problem and have an impact on mortality rates in Intensive Care Units (ICU). The aim of this study was to verify the phenotypic profile of resistance to colistin and tigecycline, considered as the last antimicrobial choice to treat BGNMDR infections. Methods: Data were collected on the active search records of the infection control service and medical records of patients admitted to two ICUs at a public hospital in Joinville between January 2016 and June 2017. Results: There were 256 HAIs caused by GNB, mainly affecting males (62%), with a median age of 65 years. Among GNBs, 37% expressed MDR; the most frequent species were: Klebsiella pneumoniae (47%), Acinetobacter baumannii (23%) and Stenotrophomonas maltophilia (11%). The resistance of GNB-MDR to colistin and tigecycline was 5% and 12%, respectively; 5% of the isolates were resistant to both antibiotics. The death rate among patients with HAIs caused by colistin-resistant GNB-MDR was higher (60%) than those to tigecycline (45%). Conclusion: Carbapenemase-producing K. pneumoniae and A. baumannii, resistant to colistin and tigecycline, prevailed among GNB-MDRs, and were associated with most deaths. These observations, coupled with the high use of carbapenems in empirical therapy, show the need for rational use of antimicrobials.(AU)


Justificación y objetivos: Las Infección nosocomial (IHs) causadas por bacilos Gram negativos multirresistentes (BGN-MDR) se consideran un problema de salud pública y un impacto en las tasas de mortalidad en las Unidades de Terapia Intensiva (UTI). El objetivo de este estudio fue verificar el perfil fenotípico de resistencia a la colistina ya la tigeciclina, consideradas como último recurso terapéutico a los BGN-MDR. Métodos: Los datos fueron recolectados en las fichas de búsqueda activa del servicio de control de infecciones y prontuarios médicos de pacientes internados en dos UTIs de un hospital público de Joinville, entre enero de 2016 y junio de 2017. Resultados: Ocurrieron 256 IHs por BGN, que afectan principalmente al género masculino (62%), con mediana de edad de 65 años. Entre los BGN, el 37% expresó MDR; siendo las especies más frecuentes: Klebsiella pneumoniae (47%), Acinetobacter baumannii (23%) y Stenotrophomonas maltophilia (11%). La resistencia de BGN-MDR a la colistina y tigeciclina fue del 5% y del 12%, respectivamente; 5% de los aislados fueron resistentes a los dos antibióticos. La tasa de muerte entre los pacientes con IH causadas por los BGN-MDR resistentes la colistina fue más alta (60%) que aquellas a tigeciclina (45%). Conclusión: K. pneumoniae y A. baumannii productoras de carbapenemases, resistentes la colistina y la tigeciclina, fueron más frecuentes entre los BGN-MDR y su asociación estuvo presente en la mayoría de las muertes. Estas observaciones, junto con el alto uso de carbapenems en la terapia empírica, muestran la necesidad de un uso racional de los antimicrobianos.(AU)


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Aged , Young Adult , Colistin/pharmacology , Drug Resistance, Multiple, Bacterial , Tigecycline/pharmacology , Gram-Negative Bacteria/drug effects , Anti-Bacterial Agents/pharmacology , Phenotype , Cross Infection/drug therapy , Gram-Negative Bacterial Infections/drug therapy , Colistin/therapeutic use , Stenotrophomonas maltophilia/drug effects , Stenotrophomonas maltophilia/genetics , Acinetobacter baumannii/drug effects , Acinetobacter baumannii/genetics , Tigecycline/therapeutic use , Gram-Negative Bacteria/genetics , Hospitalization , Klebsiella pneumoniae/drug effects , Klebsiella pneumoniae/genetics , Anti-Bacterial Agents/therapeutic use
11.
Rev. Soc. Bras. Med. Trop ; 52: e20180348, 2019.
Article in English | LILACS | ID: biblio-1013316

ABSTRACT

Abstract We report the occurrence in Brazil of the bla NDM-1 gene in Acinetobacter pittii, prior to the previously described first reports regarding the species Providencia rettgeri and Enterobacter hormaechei. Clinical isolates were investigated by polymerase chain reaction followed by bidirectional sequencing, and species was confirmed by 16S rDNA sequencing and matrix-assisted laser desorption-ionization time-of-flight spectrometry. A. pittii carrying bla NDM-1 was confirmed in a patient with no national or international travel history, or transfer from another hospital. The findings warn of the possibility of silent spread of bla NDM-1 to the community.


Subject(s)
Humans , Female , Aged, 80 and over , Acinetobacter/isolation & purification , beta-Lactamases/isolation & purification , Acinetobacter Infections/microbiology , Anti-Bacterial Agents/therapeutic use , beta-Lactamases/genetics , Brazil , Acinetobacter Infections/drug therapy , Microbial Sensitivity Tests
12.
J. Bras. Patol. Med. Lab. (Online) ; 54(6): 407-411, Nov.-Dec. 2018. tab
Article in English | LILACS-Express | LILACS | ID: biblio-975866

ABSTRACT

ABSTRACT Introduction: The thyroid cytopathologic classification based on The Bethesda System for Reporting Thyroid Cytopathology (TBSRTC) standardized results derived from fine-needle aspiration (FNA). It has facilitated communication among clinicians, seems to reduce the number of unnecessary thyroidectomies and also improves the quality of malignancy detection. Objective: To evaluate the correlation between cytopathological samples classified according to TBSRTC and their histological finding after specimen examination following surgical procedure. Methods: Cytopathological samples classified according to TBSRTC were correlated with the respective anatomopathological finding after thyroidectomy. There were retrospectively included all cases of thyroidectomy with previous FNA in the same lateral position of the organ that occurred within two years. Results: The 200 cases of thyroid FNA analyzed were distributed in 25 nondiagnostic or unsatisfactory cases (I; 12.5%), 45 benign cases (II; 22.5%), 48 atypia or follicular lesions of undetermined significance [(AUS/FLUS), III; 24%], 23 suspected cases for follicular neoplasia or follicular neoplasias [(SFN/FN), IV; 11.5%], 40 cases suspected for malignancy (V; 20%), and 19 malignant cases (VI; 9.5%). The malignancy rates observed for categories I to VI were 12%, 13.3%, 29.2%, 43.5%, 85%, and 100%, respectively. Conclusion: The prevalence of Bethesda II category was lower than predicted by TBSRTC (60%-70%), as well as Bethesda III was higher than recommended (7%). Nevertheless, the corresponding malignancy rates were within the expected ranges.


RESUMO Introdução: A classificação citopatológica tireoidiana com base no Sistema de Bethesda para Relatos de Citopatologia da Tireoide (SBRCT) padronizou os resultados provenientes de punção aspirativa por agulha fina (PAAF). Seu uso tem facilitado a comunicação entre clínicos, parece reduzir o número de tireoidectomias não necessárias e também melhora a qualidade na detecção de malignidade. Objetivo: Avaliar a correlação entre amostras citopatológicas classificadas de acordo com o SBRCT e seu achado histológico após análise da amostra pós procedimentos cirúrgico. Métodos: Amostras citopatológicas classificadas de acordo com Sistema de Bethesda foram correlacionadas com o achado anatomopatológico respectivo após tireoidectomia. Foram incluídos todos os casos de tireoidectomia com PAAF anterior, na mesma lateralidade do órgão, ocorridos no período de dois anos. Resultados: Os 200 casos de PAAF de tireoide analisados foram distribuídos em 25 casos não diagnósticos ou insatisfatórios (I; 12,5%), 45 casos benignos (II; 22,5%), 48 atipias ou lesões foliculares de significado indeterminado [(AUS/FLUS), III, 24%], 23 casos suspeitos para neoplasia folicular ou neoplasias foliculares [(SFN/FN), IV; 11,5%), 40 casos suspeitos para malignidade (V; 20%) e 19 casos malignos (VI; 9,5%). As taxas de malignidade observadas para as categorias I a VI foram 12%, 13,3%, 29,2%, 43,5%, 85% e 100%, respectivamente. Conclusão: A prevalência da categoria II de Bethesda foi menor do que a recomendada pelo SBRCT (60%-70%), bem como a categoria III, a qual foi maior do que a recomendada (7%), porém os índices correspondentes de malignidade encontraram-se dentro das variações esperadas.

13.
Arq. neuropsiquiatr ; 75(12): 881-889, Dec. 2017. tab, graf
Article in English | LILACS | ID: biblio-888281

ABSTRACT

ABSTRACT Aiming to contribute to studies that use detailed clinical and genomic information of biobanks, we present the initial results of the first Latin American Stroke Biobank. Methods: Blood samples were collected from patients included in the Joinville Stroke Registry and four Brazilian cities. Demographic socio-economic data, cardiovascular risk factors, Causative Classification System for Ischemic Stroke, Trial of Org 10172 in Acute Stroke Treatment and National Institutes of Health scores, functional stroke status (modified Rankin) and brain images were recorded. Additionally, controls from both geographic regions were recruited. High-molecular-weight genomic DNA was obtained from all participants. Results: A total of 2,688 patients and 3,282 controls were included. Among the patients, 76% had ischemic stroke, 12% transient ischemic attacks, 9% hemorrhagic stroke and 3% subarachnoid hemorrhage. Patients with undetermined ischemic stroke were most common according the Trial of Org 10172 in Acute Stroke Treatment (40%) and Causative Classification System for Ischemic Stroke (47%) criteria. A quarter of the patients were under 55 years of age at the first-ever episode. Conclusions: We established the Joinville Stroke Biobank and discuss its potential for contributing to the understanding of the risk factors leading to stroke.


RESUMO Com o objetivo de contribuir para estudos que utilizam informações clínicas e genômicas de biobancos, apresentamos os resultados iniciais do primeiro Biobanco Latinoamericano em Acidente Vascular Cerebral (AVC). Métodos: Foram coletadas amostras de sangue de pacientes recrutados pelo Registro de AVC de Joinville e posteriormente de quatro cidades brasileiras. Foram registrados dados socioeconômicos demográficos, fatores de risco cardiovasculares, Causative Classification System (CCS), Trial of Org 10172 in Acute Stroke Treatment, National Institutes of Health, estado funcional (Rankin modificado) e imagens cerebrais. Adicionalmente, foram recrutados controles das regiões geográficas correspondentes. Obteve-se DNA genômico de todos participantes. Resultados: Foram incluídos 2688 pacientes e 3282 controles. Entre os pacientes, 76% tiveram AVC isquêmico, 12% ataques isquêmicos transitórios, 9% AVC hemorrágico e 3% hemorragia subaracnóidea. Os casos indeterminados foram os mais frequentes e classificados de acordo com TOAST (40%) e CCS (47%). Um quarto dos pacientes tinham menos de 55 anos no primeiro evento. Conclusões: Estabelecemos o Joinville Stroke Biobank, e discutimos aqui seu potencial na compreensão dos fatores de risco do AVC.


Subject(s)
Humans , Male , Female , Middle Aged , Aged , Genome, Human/genetics , Biological Specimen Banks/statistics & numerical data , Stroke/genetics , Socioeconomic Factors , Brazil , Case-Control Studies , Risk Factors , Stroke/blood
14.
An. acad. bras. ciênc ; 89(1,supl): 675-684, May. 2017. tab, graf
Article in English | LILACS | ID: biblio-886657

ABSTRACT

ABSTRACT The BK virus (BKV) produces a subclinical kidney infection in immunocompetent individuals. However, viremia may occur in kidney transplant patients with ongoing immunosuppression. BKV-associated nephropathy (BKVN) has no specific treatment and is a leading cause of organ transplant loss. In this study, we evaluated the predisposition and the clinical impact of BKV replication in kidney transplant patients during post-transplant monitoring in a reference institution in Brazil. Demographic, clinical and laboratory data generated during routine outpatient follow-up were retrospectively collected. BK viremia was investigated using real-time polymerase chain reaction. Of the 553 participants, 7.4% (n = 41) presented BKV replication. Of these, 16 (39%) lost their kidney graft and interstitial nephritis was identified on kidney biopsy in 50% of the cases. Among the evaluated variables, only the use of the immunosuppressant mycophenolate sodium was identified as a risk factor for viremia (OR 7.96; 95% CI 2.35 to 26.98). The graft survival estimate in BKV-positive patients was significantly reduced (24.8% vs. 85.6%) after 10 years of transplantation. We concluded that defining predisposing factors remains an important challenge for the prevention and control of BKV activity following kidney transplantation, especially considering the development of BKVN and its strong effect on graft maintenance.


Subject(s)
Humans , Male , Female , Adult , Tumor Virus Infections/complications , Viremia/complications , Virus Replication/immunology , Kidney Transplantation/adverse effects , BK Virus/physiology , Polyomavirus Infections/complications , Tumor Virus Infections/virology , Viremia/virology , Cross-Sectional Studies , Retrospective Studies , Risk Factors , Polyomavirus Infections/virology , Graft Rejection
15.
Rev. Soc. Bras. Med. Trop ; 49(4): 433-440, July-Aug. 2016. tab, graf
Article in English | LILACS | ID: lil-792800

ABSTRACT

Abstract: INTRODUCTION: Members of the Acinetobacter genus are key pathogens that cause healthcare-associated infections, and they tend to spread and develop new antibiotic resistance mechanisms. Oxacillinases are primarily responsible for resistance to carbapenem antibiotics. Higher rates of carbapenem hydrolysis might be ascribed to insertion sequences, such as the ISAba1 sequence, near bla OXA genes. The present study examined the occurrence of the genetic elements bla OXA and ISAba1 and their relationship with susceptibility to carbapenems in clinical isolates of the Acinetobacter calcoaceticus-Acinetobacter baumannii complex. METHODS: Isolates identified over 6 consecutive years in a general hospital in Joinville, Southern Brazil, were evaluated. The investigation of 5 families of genes encoding oxacillinases and the ISAba1 sequence location relative to bla OXA genes was conducted using polymerase chain reaction. RESULTS: All isolates presented the bla OXA-51-like gene (n = 78), and 91% tested positive for the bla OXA-23-like gene (n = 71). The presence of ISAba1 was exclusively detected in isolates carrying the bla OXA-23-like gene. All isolates in which ISAba1 was found upstream of the bla OXA-23-like gene (n = 69) showed resistance to carbapenems, whereas the only isolate in which ISAba1 was not located near the bla OXA-23-like gene was susceptible to carbapenems. The ISAba1 sequence position of another bla OXA-23-like-positive isolate was inconclusive. The isolates exclusively carrying the bla OXA-51-like gene (n = 7) showed susceptibility to carbapenems. CONCLUSIONS: The presence of the ISAba1 sequence upstream of the bla OXA-23-like gene was strongly associated with carbapenem resistance in isolates of the A. calcoaceticus-A. baumannii complex in the hospital center studied.


Subject(s)
Humans , Bacterial Proteins/genetics , DNA, Bacterial/genetics , Carbapenems/pharmacology , Acinetobacter calcoaceticus/drug effects , beta-Lactam Resistance/genetics , Acinetobacter baumannii/drug effects , Anti-Bacterial Agents/pharmacology , Phenotype , Bacterial Proteins/metabolism , Brazil , Acinetobacter Infections/microbiology , Polymerase Chain Reaction , Electrophoresis, Gel, Pulsed-Field , Acinetobacter calcoaceticus/isolation & purification , Acinetobacter calcoaceticus/genetics , Acinetobacter baumannii/isolation & purification , Acinetobacter baumannii/genetics , Genotype
16.
Rev. Soc. Bras. Med. Trop ; 48(6): 699-705, Nov.-Dec. 2015. tab, graf
Article in English | LILACS | ID: lil-767825

ABSTRACT

Abstract: INTRODUCTION: Carbapenems are the therapy of choice for treating severe infections caused by the Acinetobacter calcoaceticus-Acinetobacter baumannii complex. We aimed to assess the prevalence and antimicrobial susceptibility profiles of producers of distinct oxacillinases among nosocomial isolates of the A. calcoaceticus-A. baumannii complex in a 249-bed general hospital located in Joinville, Southern Brazil. METHODS: Of the 139 A. baumannii clinical isolates with reduced susceptibility to carbapenems between 2010 and 2013, 118 isolates from varying anatomical sites and hospital sectors were selected for genotypic analysis. Five families of genes encoding oxacillinases, namely blaOXA-23-like, blaOXA-24-like, blaOXA-51-like, blaOXA-58-like, and blaOXA-143-like, wereinvestigated by multiplex polymerase chain reaction (PCR). RESULTS: Most (87.3%) isolates simultaneously carried the blaOXA-23-likeand blaOXA-51-likegenes, whereas three (2.5%) isolates harbored only blaOXA-51-likeones. The circulation of carbapenem-resistant isolates increased during the study period: from none in 2010, to 22 in 2011, 64 in 2012, and 53 in 2013. CONCLUSIONS: Isolates carrying the blaOXA-23-likeand blaOXA-51-likegenes were widely distributed in the hospital investigated. Because of the worsening scenario, the implementation of preventive measures and effective barriers is needed.


Subject(s)
Humans , Acinetobacter Infections/microbiology , Acinetobacter baumannii/drug effects , Anti-Bacterial Agents/pharmacology , Carbapenems/pharmacology , Cross Infection/microbiology , beta-Lactamases/genetics , Acinetobacter baumannii/enzymology , Acinetobacter baumannii/genetics , Brazil , Disk Diffusion Antimicrobial Tests , Genotype , Multiplex Polymerase Chain Reaction , Phenotype , beta-Lactamases/drug effects
17.
Rev. bras. ginecol. obstet ; 37(8): 353-358, ago. 2015. tab
Article in Portuguese | LILACS | ID: lil-756557

ABSTRACT

OBJETIVO:

Investigar a associação entre fatores de risco genéticos, comportamentais, biológicos e médicos e a ocorrência da prematuridade.

MÉTODOS:

Realizou-se estudo retrospectivo do tipo caso-controle. A técnica de reação em cadeia da polimerase em tempo real foi utilizada para analisar a influência dos polimorfismos rs12473815 do gene codificante para o receptor do hormônio folículo estimulante (FSHR) e rs1942836 do gene codificante para o receptor da progesterona (PGR). A avaliação dos outros fatores de risco se deu por meio da aplicação de questionários validados ou especificamente desenvolvidos e análise de dados em prontuário eletrônico. Foram incluídas 157 gestantes (45 casos com gestação <37 semanas e 112 controles com gestação >37 e ≤42 semanas).

RESULTADOS:

Os genótipos CT do polimorfismo rs12473815 e TC e CC do polimorfismo rs1942836 mostraram-se associados a uma maior chance de desenvolver parto prematuro. Observou-se associação entre o nascimento prematuro e a ingestão alcoólica quando o consumo ocorreu em duas ou mais ocasiões mensais. O baixo índice de massa corporal pré-gestacional se mostrou preditor do nascimento prematuro espontâneo, enquanto o elevado índice de massa corporal reduziu a sua probabilidade.

CONCLUSÕES:

Os resultados encontrados sugerem que a ingestão alcoólica excessiva, o baixo índice de massa corporal pré-gestacional e os alelos de risco dos polimorfismos rs12473815 e rs1942836 dos genes FSHRe PGR, respectivamente, influenciam a ocorrência de nascimento prematuro.

.

PURPOSE:

To investigate the association between genetic, behavioral, biological and medical risk factors and the occurrence of preterm birth.

METHODS:

A retrospective case-control study was conducted. The real-time polymerase chain reaction was used to analyze the influence of the rs12473815 polymorphism of the follicle stimulating hormone receptor gene (FSHR) and the rs1942836 polymorphism of the progesterone receptor gene (PGR). Other proposed risk factors were assessed using validated or specifically developed questionnaires and analysis of electronically recorded medical data. A total of 157 patients were included (45 cases who went into labor before 37 weeks of pregnancy and 112 controls who went into labor after 37 and before 42 weeks of pregnancy).

RESULTS:

The genotypes CT of rs12473815 and CT and CC of rs1942836 were associated with a higher chance of premature delivery. There was an association between preterm birth and alcohol intake when consumption occurred 2 or more times per month. Low pre-pregnancy body mass index was a predictor of spontaneous preterm birth, while high body mass index reduced this likelihood.

CONCLUSIONS:

The results suggest that excessive alcohol intake, a low level of pre-pregnancy body mass and the risk alleles of rs12473815 and rs1942836 polymorphisms of the FSHR and PGR genes, respectively, influence the occurrence of preterm birth.

.


Subject(s)
Humans , Female , Pregnancy , Young Adult , Premature Birth/epidemiology , Case-Control Studies , Disease Susceptibility , Maternal Behavior , Premature Birth/etiology , Premature Birth/genetics , Retrospective Studies , Risk Factors , Socioeconomic Factors
18.
J. bras. patol. med. lab ; 51(1): 28-32, Jan-Feb/2015. tab
Article in English | LILACS | ID: lil-746525

ABSTRACT

Introduction: Cancer of the cervix is the second most common cancer among women worldwide and the frequency of precancerous lesions is increasing among adolescents. Objective: To study and compare the frequency of epithelial abnormalities in cervical cytology exams in adolescents and adults. Materials and methods: Retrospective study based on analysis of reports of cytology exams performed in the years 2000 and 2010 in adolescents (12-18 years old) and in adult women. The frequency of cytological alterations was explored, stratifying them into high-grade/carcinoma and low-grade lesions. Results: In 2000, rates of epithelial abnormalities were 3.08% in adolescents and 1.39% in adult females, and were 4.76% and 1.83% in 2010, respectively. The high-grade lesions/carcinomas were more common among adults in both years. Discussion: There was an increase in prevalence of epithelial abnormalities in the last decade, both in adolescents and in adults. Proportionally, the increase was higher among adolescents (6.7%) than in adults (2.2%). However, the rate of high-grade lesions/carcinoma was higher among adult women in the two analyzed years. Conclusion: It was observed that the frequency of cervical epithelial abnormalities was higher among adolescents than adults and increased between 2000 and 2010. .


Introdução: O câncer do colo do útero é o segundo tipo de câncer mais comum entre as mulheres em todo o mundo, e a frequência de lesões pré-neoplásicas vem aumentando entre as adolescentes. Objetivos: Estudar e comparar a frequência de anormalidades epiteliais em exames colpocitológicos em adolescentes e adultas. Materiais e métodos: Estudo retrospectivo com base na análise de laudos de exames colpocitológicos realizados nos anos de 2000 e 2010 em adolescentes (12 a 18 anos de idade) e em mulheres adultas. A frequência de alterações citológicas foi explorada, estratificando-as em lesões de alto grau/carcinoma e lesões de baixo grau. Resultados: Em 2000, as taxas de anormalidades epiteliais foram de 3,08% nas adolescentes e de 1,39% nas mulheres adultas; em 2010, de 4,76% e 1,83%, respectivamente. As lesões de alto grau/carcinoma foram mais frequentes entre as adultas em ambos os anos. Discussão: Tanto em adolescentes como em adultas, verificou-se aumento da prevalência de anormalidades epiteliais na última década. Proporcionalmente, o aumento foi maior entre adolescentes (6,7%) do que em adultas (2,2%). No entanto, a taxa de lesões de alto grau/carcinoma foi maior entre as adultas nos dois anos analisados. Conclusão: Observou-se que a frequência de anormalidades epiteliais cervicais é maior em adolescentes do que em adultas, tendo aumentado entre os anos de 2000 e 2010. .

20.
Rev. bioét. (Impr.) ; 23(3): 456-467, 2015. tab, graf
Article in Spanish, English | LILACS | ID: lil-768363

ABSTRACT

O uso de placebo em pesquisa clínica tem sido motivo de debate nos últimos anos, sobretudo após a Associação Médica Mundial publicar, em 2002, nota de esclarecimento do parágrafo 29 da Declaração de Helsinki. O Brasil tem se destacado por sua posição firme e contrária ao uso flexível de placebo. Tanto o Conselho Federal de Medicina quanto o Conselho Nacional de Saúde editaram resoluções que normatizam seu uso no Brasil, de forma a não admiti-lo em caso da existência de um método terapêutico melhor. O presente artigo reforça essa posição e tem por objetivo descrever as diversas aplicações de placebo em pesquisa clínica, bem como trazer à luz a complexa decisão sobre a eticidade de seu uso. Além disso, os autores propõem uma reflexão acerca da utilização de placebo no âmbito da pesquisa, por meio de algoritmos decisórios baseados nas normativas éticas brasileiras...


The use of placebos in clinical research has been a matter of considerable debate in recent years, notably when the World Medical Association published, in 2002, a note of clarification for paragraph 29 of the Helsinki Declaration. Brazil is known for its strong opposition to the flexible use of placebos. Both the Federal Council of Medicine and the National Health Council have published resolutions regulating the use of placebos in Brazil, preventing their use if there is a more effective therapeutic method already in place. The present study reinforces that position and aims to describe the various uses of placebos in clinical research, as well as examining the complex decisions relating to the ethics of their use. Additionally, the authors propose a reflection on the use of placebos through decision-making algorithms based on Brazilian ethical standards...


El uso del placebo en la investigación clínica ha sido un tema de debate en los últimos años, sobre todo después de que la Asociación Médica Mundial publicara, en 2002, una nota aclaratoria del párrafo 29 de la Declaración de Helsinki. Brasil se ha destacado por su firme posición en contra de la utilización flexible del placebo. Tanto el Consejo Federal de Medicina como el Consejo Nacional de Salud editaron resoluciones que regulan el uso del placebo en Brasil, no admitiéndose su uso cuando existe un mejor método terapéutico. El presente artículo refuerza esa posición y tiene como objetivo describir diferentes usos del placebo en la investigación clínica, así como contribuir en la discusión sobre la ética de su uso. Además, los autores proponen una reflexión sobre el uso del placebo en la investigación a través de algoritmos para la toma de decisiones, los cuales se basan en las normativas éticas de Brasil...


Subject(s)
Humans , Male , Female , Algorithms , Bioethics , Clinical Trials as Topic , Placebos , Decision Support Techniques , Ethics, Research , Helsinki Declaration , Human Rights , Ethicists , Methodology as a Subject
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