Assuntos
Papillomaviridae , Infecções por Papillomavirus/prevenção & controle , Neoplasias do Colo do Útero/virologia , Vacinas Virais/administração & dosagem , Adolescente , Feminino , Seguimentos , Humanos , Masculino , Sistema de Registros , Suécia , Neoplasias do Colo do Útero/prevenção & controle , Vacinação/economia , Vacinas Virais/efeitos adversos , Vacinas Virais/normasRESUMO
Similar changes in the periurethral and vaginal microflora were observed in 19 women with recurrent urinary tract infection following treatment with norfloxacin (NOR) or pivmecillinam (PIV). Escherichia coli strains were suppressed by both treatments. Staphylococcus spp. and enterococci colony counts increased following PIV treatment in the periurethral flora but remained stable with NOR.
Assuntos
Andinocilina Pivoxil/uso terapêutico , Bactérias/isolamento & purificação , Norfloxacino/uso terapêutico , Infecções Urinárias/tratamento farmacológico , Adolescente , Adulto , Bactérias/efeitos dos fármacos , Método Duplo-Cego , Feminino , Humanos , Pessoa de Meia-Idade , Recidiva , Uretra/microbiologia , Infecções Urinárias/microbiologia , Vagina/microbiologiaRESUMO
OBJECTIVE: Renal concentrating capacity (RCC) has been used as a tool in the diagnosis of the site of urinary tract infection (UTI). In this study, RCC was measured in women with symptoms of UTI in relation to the clinical picture and the bacterial species isolated. MATERIAL AND METHODS: In 633 outpatients aged > or =18 years with symptoms of UTI, a renal concentration test with desmopressin was performed at baseline. The test was repeated after antibiotic treatment in a subset of patients with osmolality values below the reference levels at entry. The bacterial species were identified and patients were classified as having either pyelonephritis or cystitis. RESULTS: RCC was reduced in patients infected with Escherichia coli or Staphylococcus saprophyticus compared to those who had negative urine cultures and increased after antibiotic treatment. Patients with symptoms of both pyelonephritis and cystitis had reduced RCC: 44/68 (65%) and 205/457 (45%), respectively. CONCLUSIONS: These findings demonstrate a considerable overlap in RCC between patients with pyelonephritis and cystitis, making the osmolality test unreliable for the purpose of diagnosis of the site of UTI.
Assuntos
Capacidade de Concentração Renal/fisiologia , Pacientes Ambulatoriais , Infecções Urinárias/fisiopatologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antibacterianos/uso terapêutico , Antidiuréticos , Desamino Arginina Vasopressina , Feminino , Seguimentos , Humanos , Capacidade de Concentração Renal/efeitos dos fármacos , Pessoa de Meia-Idade , Concentração Osmolar , Infecções Urinárias/tratamento farmacológico , Infecções Urinárias/urinaAssuntos
Vacinação em Massa , Vacinação , Vacinas Virais/administração & dosagem , Pré-Escolar , Humanos , Esquemas de Imunização , Lactente , Vacinação em Massa/economia , Vacinação em Massa/normas , Guias de Prática Clínica como Assunto , Suécia , Vacinação/economia , Vacinação/normas , Vacinas Virais/economia , Organização Mundial da SaúdeAssuntos
Guerra Biológica , Bioterrorismo , Planejamento em Desastres , Surtos de Doenças/prevenção & controle , Vacina Antivariólica/provisão & distribuição , Varíola/prevenção & controle , Guerra Biológica/prevenção & controle , Bioterrorismo/prevenção & controle , Guias como Assunto , Humanos , Varíola/transmissão , Vacina Antivariólica/administração & dosagemRESUMO
The introduction of the 2 neuraminidase inhibitors (NAIs) zanamivir and oseltamivir has offered new options for the prevention and treatment of influenza. This article summarizes a Swedish consensus guidance document on the rational use of antiviral drugs in the management of influenza virus infections. Vaccination remains the cornerstone for influenza prophylaxis. Target groups for the annual vaccination programme are the 'at-risk' individuals, i.e. elderly patients ( > or = 65 y) and patients with chronic pulmonary disease or cardiovascular disease or other chronic diseases predisposing for a complicated course of influenza. Antiviral drugs are not a substitute for influenza vaccination, but could be used as adjuncts. Currently, 3 drugs have been approved for the treatment of influenza, including zanamivir and oseltamivir and the M2 inhibitor amantadin. Amantadin has come to very limited use, has recently been withdrawn from the Swedish market and is available only on a named patient basis. Compared with amantadin, the NAIs have clear advantages because of their broader anti-influenza activity against both type A and B, improved safety profiles and low potential for inducing drug resistance. The NAls are therefore recommended as first options in the treatment of influenza. Oseltamivir can be taken orally, whereas zanamivir is for oral inhalation. Limited in vitro and in vivo data suggest that oseltamivir is less potent against influenza B, whereas zanamivir seems equally effective against influenza A and B. In influenza-positive healthy adults and children, treated within 48 h after symptom onset, the NAIs shorten the duration of illness by about 1 d. No significant effect on the duration of symptoms has been documented in treated at-risk patients with influenza. Owing to their limited therapeutic benefit, general use of the NAIs in the treatment of influenza is not recommended, but they can be advocated on an individualized basis for patients with severe influenza who can start therapy within 48 h of the onset of symptoms. Zanamivir is the preferred choice in a confirmed influenza B epidemic. For prevention of influenza, 2 drugs are approved, oseltamivir in adults above 12 y old and amantadin in people above 10 y old. The 70-90% protective efficacy of oseltamivir for household postexposure prophylaxis and for seasonal prophylaxis is comparable to that reported for amantadin. Oseltamivir is the preferred drug for prophylactic use. Chemoprophylaxis is targeted at high-risk groups and should be considered on a case-by-case basis depending on the circumstances and the population requiring protection. A broader preventive use of oseltamivir can be advocated in at-risk groups during seasons when there is a poor antigenic match between the epidemic strains and the vaccine strains. Oseltamivir prophylaxis is otherwise recommended for patients unable to be vaccinated and for families exposed to influenza which include a member of the at-risk groups. In high-risk hospital units and in institutions caring for the elderly, oseltamivir prophylaxis, in combination with vaccination, can be recommended as measures to control an influenza outbreak.
Assuntos
Acetamidas/uso terapêutico , Antivirais/uso terapêutico , Vacinas contra Influenza/administração & dosagem , Influenza Humana/tratamento farmacológico , Influenza Humana/prevenção & controle , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Feminino , Diretrizes para o Planejamento em Saúde , Humanos , Esquemas de Imunização , Incidência , Influenza Humana/epidemiologia , Masculino , Pessoa de Meia-Idade , Oseltamivir , Prevenção Primária/organização & administração , Medição de Risco , Distribuição por Sexo , Taxa de Sobrevida , Suécia/epidemiologiaRESUMO
We have studied the immune response to a variable surface-exposed loop region of the P66 outer membrane protein from Borrelia burgdorferi sensu lato by using an enzyme immunoassay. Lyme borreliosis populations found in North America and Sweden were preferentially more seroreactive to P66 from their respective regional species, namely, B. burgdorferi sensu stricto and B. garinii and B. afzelii, respectively.
Assuntos
Anticorpos Antibacterianos/sangue , Antígenos de Bactérias/imunologia , Proteínas de Bactérias , Borrelia burgdorferi/imunologia , Doença de Lyme/diagnóstico , Porinas/imunologia , Sequência de Bases , Reações Cruzadas , Humanos , Técnicas Imunoenzimáticas , Dados de Sequência Molecular , Proteínas Recombinantes/imunologia , Especificidade da EspécieRESUMO
The Lyme Borrelia genospecies Borrelia afzelii and B. garinii have previously been isolated using a culture method in Swedish patients with Lyme borreliosis (LB). There are reports suggesting that the genospecies distribution in human tissue specimens as determined by molecular methods is different from that obtained by culture. In the present study, we developed a nested PCR for detection of Lyme Borrelia-specific DNA in cerebrospinal fluid from Swedish patients with LB. The genospecies were subsequently identified by sequence analysis in a total of 7 PCR-positive patients. Two sequences were identified as B. burgdorferi sensu stricto (s. s.), 1 as B. afzelii and 4 as B. garinii. These are the first reported cases in which B. burgdorferi s. s. has been shown to be the causative agent of human LB in Sweden. The results of our study confirm that the use of direct molecular analytical methods for Borrelia genospecies identification in clinical specimens can provide epidemiological information additional to that obtained by culture.