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1.
J Hosp Infect ; 68(2): 123-9, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18192077

ABSTRACT

The aim was to evaluate the effect of control selection on risk factor analysis for extended-spectrum beta-lactamase-producing Klebsiella pneumoniae (ESBL-KP) infections. Four contemporaneous case-control studies were conducted prospectively with 372 patients: Study 1 (ESBL-KP-infected vs non-infected); Study 2 (ESBL-KP-infected vs non-ESBL-KP-infected); Study 3 (all KP-infected vs non-infected); Study 4 (non-ESBL-KP-infected vs non-infected). Time at risk (TAR, i.e. duration of hospital stay) was the most significant risk factor [Study 1: odds ratio (OR): 5.74 (95% CI: 2.26-14.59; P<0.001); Study 2: 3.52 (1.47-8.43; P=0.005); Study 3: 2.68 (1.57-4.58; P<0.001)]; central venous catheterisation (CVC) was a risk factor in Study 1: 5.31 (1.67-16.82; P=0.005) and Study 3: 2.10 (1.04-4.27; P=0.04). Prior use of cephalosporins (PUC) was a risk factor only in studies with non-infected patients as controls [Study 1: 5.64 (1.90-16.72; P=0.002) and Study 3: 4.60 (2.09-10.13; P<0.001)]. The ORs were uniformly lower with 'non-ESBL-KP-infected' (TAR: 3.52; CVC: 2.07; PUC: 1.97) compared with 'non-infected' patients (TAR: 5.74; CVC: 5.31; PUC: 5.64) as control groups. Selection of control patients has a crucial role in the evaluation of risk factors for ESBL-KP infections. A consistent underestimation of the magnitude of the risk factors is observed when the control group is defined by the non-ESBL-KP-infected patients.


Subject(s)
Control Groups , Cross Infection/epidemiology , Klebsiella Infections/epidemiology , Klebsiella pneumoniae/enzymology , Patient Selection , Anti-Bacterial Agents/therapeutic use , Bias , Brazil/epidemiology , Case-Control Studies , Cross Infection/drug therapy , Cross Infection/microbiology , Equipment Contamination , Humans , Klebsiella Infections/drug therapy , Klebsiella Infections/microbiology , Klebsiella pneumoniae/isolation & purification , Length of Stay , Logistic Models , Prospective Studies , Risk Factors , Surveys and Questionnaires , beta-Lactamases/biosynthesis
2.
Int J Gynecol Cancer ; 18(3): 387-99, 2008.
Article in English | MEDLINE | ID: mdl-17692084

ABSTRACT

To determine the efficacy, safety, and cost of laparoscopic surgery compared with laparotomy in women with ovarian tumors assumed to be benign. This study is a systematic review. We searched (MEDLINE, EMBASE, LILACS, and COCHRANE LIBRARY) trials registers and reference lists of published trial reports. Six randomized controlled trials were identified involving 324 patients. Duration of surgery, adverse effects of surgery, pain, length of hospital stay, and economic outcomes were compared. The mean duration of surgery was longer in the laparoscopy group overall (weighted mean difference 11.39, 95% CI 0.57-22.22). The pooled estimate for febrile morbidity decreased for laparoscopy (Peto OR 0.34, 95% CI 0.13-0.88). The odds of any adverse effect were decreased after laparoscopic procedures (Peto OR 0.26, 95% CI 0.12-0.55). The odds of being pain free were significantly greater for the laparoscopy group (Peto OR 7.35, 95% CI 4.3-12.56). Mean length of hospital stay was shorter in the laparoscopy group with reduction of 2.79 days (95% CI -2.95 to -2.62). In economic outcomes, there was a significant reduction of US$1045 (95% CI -1361 to -726.97) in the laparoscopy group. Laparoscopy is associated with a reduction in the following: febrile morbidity, urinary tract infection, postoperative complications, postoperative pain, days in hospital, and total cost. These findings should be interpreted with caution as only a small number of studies were identified including a total of only 324 women.


Subject(s)
Laparoscopy/methods , Laparotomy/methods , Ovarian Neoplasms/pathology , Ovarian Neoplasms/surgery , Ovariectomy/methods , Aged , Biopsy, Needle , Cost-Benefit Analysis , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Immunohistochemistry , Laparoscopy/economics , Laparotomy/economics , Length of Stay , Middle Aged , Ovarian Neoplasms/mortality , Pain, Postoperative/physiopathology , Randomized Controlled Trials as Topic , Risk Assessment , Survival Rate , Treatment Outcome , United States
3.
Int J Gynecol Cancer ; 17(6): 1205-14, 2007.
Article in English | MEDLINE | ID: mdl-17506842

ABSTRACT

The detection of telomerase activity in cervix may provide information on cervical carcinogenesis and may be a marker to monitor cervical intraepithelial neoplasia transition. A quantitative systematic review was performed to estimate the accuracy of telomerase assay in cervical lesions. Studies that evaluated the telomerase test (telomerase repeated amplification protocol) for the diagnosis of cervix lesions and compared it to paraffin-embedded sections as the diagnostic standard were included. Ten studies were analyzed, which included 1069 women. The diagnostic odds ratio (DOR) for a positive telomerase test for low-grade squamous intraepithelial lesions (Lo-SIL) vs normal or benign lesions was 3.2 (95% CI, 1.9-5.6). The DOR for a positive telomerase test for high-grade squamous intraepithelial lesions (Hi-SIL) vs Lo-SIL, normal or benign lesions was 5.8 (95% CI, 3.1-10). For cervix cancer vs Hi-SIL, the DOR for a positive telomerase test was 8.1 (95% CI, 3.2-20.3) and for cervix cancer vs Lo-SIL, normal or benign lesions, it was 40.9 (95% CI, 18.2-91). Our data support the current hypothesis that telomerase may activate an early event in cervical carcinogenesis that could be associated with the initiation and progression of cervical lesions.


Subject(s)
Telomerase/metabolism , Uterine Cervical Dysplasia/enzymology , Uterine Cervical Neoplasms/enzymology , Female , Humans , Odds Ratio , Sensitivity and Specificity , Uterine Cervical Dysplasia/diagnosis , Uterine Cervical Neoplasms/diagnosis
4.
J Hosp Infect ; 65(4): 361-7, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17350721

ABSTRACT

Initial antibiotic therapy is an important determinant of clinical outcomes in ventilator-associated pneumonia (VAP). Several studies have investigated this issue, with conflicting results. This study investigated risk factors of inadequate empirical antimicrobial therapy and its impact on outcomes for patients with a clinical diagnosis of VAP. The primary outcome was adequacy of antimicrobial therapy. Secondary outcomes were duration of mechanical ventilation, hospital and intensive care unit (ICU) lengths of stay, and mortality due to VAP. Mean age was 62.9+/-15.2 years, mean APACHE (Acute Physiological Assessment and Chronic Health Evaluation) II score was 20.1+/-8.1 and mean MODS (Multiple Organ Dysfunction Score) was 3.7+/-2.5. Sixty-nine (45.7%) of 151 patients with a clinical diagnosis of VAP received inadequate antimicrobial treatment for VAP initially. There were 100 (66.2%) episodes of VAP caused by multidrug-resistant pathogens, of which 56% were inadequately treated, whereas the rate of inadequate antimicrobial therapy for VAP caused by susceptible-drug pathogens was 25.5% (P<0.001). Multiple logistic regression analysis revealed that the risk of inadequate antimicrobial treatment was more than twice as great for patients with late-onset VAP [odds ratio (OR), 2.93; 95% confidence interval (CI), 1.30-6.64; P=0.01], and more than three times for patients with VAP caused by multidrug-resistant pathogens (OR, 3.07; 95% CI, 1.29-7.30; P=0.01) or with polymicrobial VAP (OR, 3.67; 95% CI, 1.21-11.12; P=0.02). Inadequate antimicrobial treatment was associated with higher mortality for patients with VAP. Two of three independent risk factors for treatment inadequacy were associated with the isolation and identification of micro-organisms.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Length of Stay , Pneumonia/etiology , Respiration, Artificial/adverse effects , APACHE , Aged , Brazil , Female , Humans , Male , Middle Aged , Pneumonia/drug therapy , Pneumonia/mortality , Retrospective Studies , Risk Factors , Treatment Failure
5.
Cochrane Database Syst Rev ; (3): CD004751, 2005 Jul 20.
Article in English | MEDLINE | ID: mdl-16034946

ABSTRACT

BACKGROUND: Over the last ten years laparoscopy has become an increasingly common approach for the surgical removal of benign ovarian tumours. There remains uncertainty as to the value of this intervention. This review has been undertaken to assess the available evidence for the benefits and harms of laparoscopic surgery for benign ovarian tumours compared to laparotomy. OBJECTIVES: To determine the efficacy, safety and cost of laparoscopic surgery compared with laparotomy in women with ovarian tumours assumed to be benign. SEARCH STRATEGY: We searched electronic databases, trials registers and reference lists of published trial reports. Review articles were also searched. SELECTION CRITERIA: All randomised controlled trials comparing laparoscopy versus laparotomy for benign ovarian tumours. DATA COLLECTION AND ANALYSIS: Three reviewers independently assessed each study's eligibility and quality and extracted data. MAIN RESULTS: Six randomised controlled trials were identified involving 324 patients. Three subgroups of ovarian tumours were considered: any histological type of benign ovarian tumour, dermoid cysts and endometriomata. Surgical outcomes: The mean duration of surgery was longer in the laparoscopy group compared to the laparotomy group overall (WMD 11.39; 95% CI 0.57 to 22.22). However, heterogeneity was present with substantial inconsistency (I(2)=87%) . The heterogeneity found in these analyses was likely to reflect differences in the patient populations. Adverse effects of surgery: The pooled estimate for febrile morbidity decreased for laparoscopy compared to laparotomy (Peto OR 0.34; 95% CI 0.13 to 0.88). The odds of any adverse effect of surgery (total number of complications - surgical injury and/or post operative complications) were decreased after laparoscopic procedures (Peto OR 0.26; 95% CI 0.12 to 0.55). Short-term recovery: VAS pain scores favoured laparoscopy (WMD -2.36; 95% CI -2.07 to -2.03) andt he odds of being pain free were significantly greater for the laparoscopy group compared to laparotomy (Peto OR 7.35; 95% CI 4.3 to 12.56). Mean length of hospital stay was shorter in the laparoscopy group with reduction 2.79 days (95% CI -2.95 to -2.62) compared to laparotomy. Economic outcomes: There was a significant reduction of US$1045 (95% CI -1361 to -726.97) in the laparoscopy group compared to the laparotomy group in one trial of women with any type of benign ovarian tumour. AUTHORS' CONCLUSIONS: In women undergoing surgery for benign ovarian tumours, laparoscopy is associated with a reduction in the following; febrile morbidity, urinary tract infection, post operative complications, post operative pain, days in hospital and total cost. These findings should be interpreted with caution as only a small number of studies were identified including a total of only 324 women and not all of the important outcomes were reported in each study.


Subject(s)
Laparoscopy , Laparotomy , Ovarian Neoplasms/surgery , Female , Humans , Laparoscopy/adverse effects , Laparoscopy/economics , Laparotomy/adverse effects , Laparotomy/economics , Randomized Controlled Trials as Topic
6.
Rev Saude Publica ; 30(2): 168-78, 1996 Apr.
Article in Portuguese | MEDLINE | ID: mdl-9077016

ABSTRACT

In epidemiological investigations of infant diseases, data are usually collected on a large set of variables. The associations between presumptive risk factors and the outcome is commonly evaluated through statistical modeling, but the model-building strategies are seldom described. In the project, data collected in a case-control study of risk factors for dehydrating diarrhea in infants have been used to present a hierarchized approach to the assessment of risk factors. The variables were grouped into a hierarchy of categories, ranging from distal determinants to proximate ones. These categories included, in this order, socioeconomic, environmental, reproductive maternal, nutritional and demographic sets. According to the univariate analyses all variables were associated with the outcome. As the purpose was to identify a parsimonious model to explain the data, in each set the confounders were selected through backward elimination, according to an alpha level of 0.10. The risk factors were evaluated through logistic regression after adjustment for confounders in the same set or in hierarchically superior sets. This approach allows researchers to quantify the contribution of each level of adjustment, to understand the model-building strategy as well as interpret the independent associations. The goodness-of-fit assessed at each set showed significant improvements in the model. The gamma coefficient of association was employed to quantify the proportion of cases and controls correctly identified by comparing the observed value with that predicted by the variables in the model. The final model resulted in a gamma of 0.74. The children's ages did not improve the prediction of cases and controls, but they have been kept in the model as they affect some exposures such as breastfeeding.


Subject(s)
Diarrhea, Infantile/epidemiology , Models, Statistical , Case-Control Studies , Confounding Factors, Epidemiologic , Female , Humans , Infant , Infant, Newborn , Male , Risk Factors , Severity of Illness Index , Socioeconomic Factors
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