Avaliação da ação germicida da luz ultravioleta de cabine de segurança biológica frente às espécies bacterianas / Evaluation of the germicidal action of ultraviolet light in biosafety cabinet concerning bacterial species

RESUMO: Introdução: A cabine de segurança biológica (CBS) é um equipamento de proteção coletiva, utilizado para efe-tuar a contenção de aerossóis produzidos nos procedimentos laboratoriais. A CBS protege tanto os trabalhadores, quanto o material manipulado e o meio ambiente. Dispõe de lâmpadas de luz ultravioleta (UV) que possui ação germicida, alterando os ácidos nucleicos dos micro-organismos. Objetivo: O objetivo do presente estudo foi avaliar a ação germicida da luz UV da CBS classe II, tipo A2, frente à cultura de duas espécies de bactérias com diferentes condições de exposição a luz UV. Material e Métodos: Para o desenvolvimento da pesquisa foram utilizadas as bactérias Staphylococcus aureus ATCC 25923 e Klebsiella pneumoniae ATCC 10031, na concentração de 1,5x108 Unidades Formadoras de Colônias/ml (UFC/ml), que após a semeadura em biplacas de Petri foram expostas à luz UV em diferentes condições e tempos. Resultados: Os resultados obtidos revelaram que as espécies de bactérias apresentaram igual perfil de crescimento ou inibição quando submetidas às diferentes condições de exposição. As biplacas de Petri com as tampas abertas e protegidas ou não com embalagem de esterilização apresentaram, nos tempos 15 e 20 minutos, inibição bacteriana. Nas biplacas protegidas pelo papel alumínio e nas biplacas com a tampa fechada, independentemente do tempo e da condição, os micro-organismos apresentaram crescimento bacteriano. Conclusão: Com os resultados obtidos, sugere-se que a ação germicida da luz UV foi eficaz, garantindo a descontaminação adequada e assegurando a qualidade na biossegurança laboratoria. (AU)

ABSTRACT: Introduction: The biological safety cabinet (BSC) is a collective protective device used to hold aerosols produced in laboratory procedures. The BSC protects workers, material handling, and the environment. It relies on ultraviolet light (UV) lamps that have germicidal action, altering the nucleic acids of microorganisms. Objective: The objective of the present study was to evaluate the germicidal action of BSC class II type A2 UV light against the culture of two bacterial species with different conditions of exposure to UV light. Methods: For the research, the bacteria Sta-phylococcus aureus ATCC 25923 and Klebsiella pneumoniae ATCC 10031 were used, at a concentration of 1.5x108Colony Forming Units/ml (CFU/ml), which were seeded in Petri biplates. Use UV light under different conditions and times. Results: The bacterial species showed the same growth or inhibition profile when subjected to different exposure conditions. Petri dishes with the cover open and protected or not with sterilization packaging showed bacterial inhibition at 15 and 20 minutes. The microorganisms in the biplates protected by the aluminum foil and in the biplates with the cover on, regardless of the time and condition, showed bacterial growth. Conclusion: With the results obtained, it is suggested that the germicidal action of UV light was effective, ensuring adequate decon-tamination and ensuring quality in laboratory biosafety. (AU)

Ten- to 14-year clinical followup of the cementless Natural Knee system.

Of 300 consecutive knees (238 patients) that had undergone arthroplasty with the cementless Natural Knee prosthesis from 1985 to 1989, 176 knees (141 patients) were available for followup at an average of 12 +/- 1 years after the operation. Knee function was improved significantly. Modified Hospital for Special Surgery knee scores improved from 59.1 +/- 13.2 points preoperatively to 97.8 +/- 4.7 points at last followup. At last followup, knee range of motion averaged 0 degrees +/- 2 degrees to 120 degrees +/- 10 degrees. Implant survival was 93.4% (including infection and simple polyethylene exchanges) and 95.1% (excluding infection and simple polyethylene exchanges) at 10 years when applying the Kaplan-Meier survival analysis, using loose components, revision, or both as failure criteria. Besides the three revisions for infection, only two femoral and one tibial component required revision. The patellar component survivorship at 10 years was 95.1%. All patellar revisions were attributed to edge wear. Subsequent operative and design changes, including patellar component medialization and countersinking, have decreased the incidence of patellar revision. The long-term results of this cementless knee system compare favorably with those of cemented systems. The Natural Knee design has provided excellent and predictable long-term clinical results in the current series of active patients.

Cementless primary total hip arthroplasty with a tapered, proximally porous-coated titanium prosthesis: a 4- to 8-year retrospective review.

A consecutive series of 100 primary total hip arthroplasties were performed at a single institution on 87 patients using a cementless collared titanium press-fit stem. Of patients, 87% received a hemispheric porous-coated cup, and 13% received a nonmodular titanium fibermesh press-fit cup. Ten hips were excluded from the longer-term evaluation: 6 were lost to follow-up, and 4 patients were deceased. Ninety hips, with an average follow-up of 81 +/- 12 months, were retrospectively reviewed. The average postoperative hip score was 94, compared with an average preoperative hip score of 42. No postoperative infections were observed, but there were 2 cases of postoperative dislocation (2%) and 1 case of thigh pain (1%) at last follow-up. There were 2 revisions, both for cup failures. There were no femoral component loosenings or revisions. There was no evidence of stem subsidence or instability. These midterm results are encouraging with this stem design.

Posterior stabilization in total knee arthroplasty with use of an ultracongruent polyethylene insert.

Fifty-three primary and 47 revision posterior cruciate ligament (PCL)-substituting total knee arthroplasties (TKAs) using a highly conforming (ultracongruent) polyethylene insert were retrospectively reviewed over a 48- to 106-month (mean, 60+/-11 months) follow-up period. These 100 knees were age and sex matched with another 100 TKAs performed using a PCL-sparing design. The ultracongruent design has an anterior buildup of 12.5 mm and a more conforming articular surface to match better the radius of the femoral component. In primary and revision TKAs, the average Hospital for Special Surgery knee score (P = .3) and range of motion (P = .43) were similar between the PCL-sparing and ultracongruent groups. In primary and revision TKAs, there were no revisions resulting from instability for patients receiving an ultracongruent insert versus 5 knees in the PCL-sparing control group secondary to subsequent postoperative anteroposterior instability and PCL insufficiency.

High tibial osteotomy with a calibrated osteotomy guide, rigid internal fixation, and early motion. Long-term follow-up.

BACKGROUND: We studied the results of sixty-four valgus-producing high tibial osteotomies performed with the use of a calibrated osteotomy cutting guide and rigid internal fixation, and followed by early motion, in fifty-six patients who had medial unicompartmental osteoarthritis and varus malalignment. Long-term studies have demonstrated that a high tibial osteotomy performed with staple fixation and followed by immobilization in a cast has an expected survival rate of approximately 85 percent at five years and 60 percent at ten years (in studies of ninety-five knees and 213 knees, respectively). To the best of our knowledge, there are no long-term reports on high tibial osteotomies performed with a calibrated osteotomy cutting guide and rigid internal fixation and followed by early motion. METHODS: The indications for high tibial osteotomy were medial unicompartmental osteoarthritis and varus malalignment. A lateral closing-wedge osteotomy was performed. The patients were reexamined to obtain a knee score, to make lateral radiographs of both knees, and to make a full-length anteroposterior radiograph (showing the entire lower extremity, including the hip and ankle) of the involved knee with the patient standing. RESULTS: Twenty-one knees were treated with a subsequent total knee arthroplasty at an average of sixty-five months after the high tibial osteotomy. The remaining forty-three knees had a good or excellent clinical result, with an average knee score of 94 points at an average of 8.5 years after the osteotomy. Survivorship analysis showed an expected rate of survival, with conversion to a total knee arthroplasty as the end point, of 85 percent at five years and 53 percent at ten years. No patient had patella baja postoperatively. There were six complications: four superficial wound infections, one superficial-vein thrombosis, and one delayed union (union occurred at five months). CONCLUSIONS: High tibial osteotomy has been criticized because of a high rate of complications, a loss of effectiveness with time, and the difficulty of conversion to a total knee arthroplasty secondary to patella baja. In our series, in which an osteotomy was performed with a calibrated osteotomy cutting guide and rigid internal fixation and was followed by early motion, the rate of complications was low and approximately two-thirds of the knees had a good or excellent clinical result at an average of 8.5 years. Conversion to a total knee arthroplasty was accomplished without difficulty in the patients who had this procedure. We highly recommend high tibial osteotomy with a calibrated osteotomy cutting guide, rigid internal fixation, and early motion for patients who wish to continue an active lifestyle.

6- to 10-year experience using countersunk metal-backed patellas.

Three hundred two consecutive cementless total knee arthroplasties (Natural Knee, Intermedics Orthopedics, Inc., Austin, TX) were performed using a metal-backed, porous-coated patellar component. Fifty-nine patients died and 31 were lost to follow-up evaluation, resulting in 212 knees available for evaluation at 6 to 10 years. The mean follow-up period was 91 months. The mean modified Hospital for Special Surgery total knee score improved from 58 before surgery to 98 at the most recent follow-up visit. Mean patellar translation and tilt were 2.75 mm and 3.5 degrees, respectively. There were no patellar lucencies nor loosening. Eleven patients (5%) underwent revision of the patellar component. Overall patellar survivorship was 96%. Comparatively good results can be achieved with the use of a metal-backed patellar component if component design, surgical technique, and patellar alignment are properly addressed.

Patellar component medialization in total knee arthroplasty.

Intraoperative correction of patellar maltracking has traditionally involved the use of a lateral retinacular release. Problems, however, related to lateral retinacular release include increased postoperative pain and wound healing complications, compromised patellar blood flow, and longer rehabilitation. The purpose of this study was to assess the effect of patellar medialization in total knee arthroplasty. One hundred forty patients underwent total knee arthroplasty using the same components. Two groups of 70 patients each made up the study. Group 1 included patients whose patellar components were centralized on the patella, and group 2 consisted of patients in whom the patellar component was medialized to reproduce the patient's anatomic high point (ie, sagittal ridge). Lateral retinacular release was required in 45.5% of the patients in group 1 compared with 17% in group 2. The technique of patellar medialization is described.

Treatment of infected total knee arthroplasty using an articulating spacer.

Twenty-six patients with late infected total knee arthroplasties were treated by debridement and removal of components and all cement, preserving collateral ligaments. At time of debridement, an articulating spacer was fashioned to allow partial weightbearing and knee range of motion (ROM) during rehabilitation. This spacer was implanted using antibiotic-impregnated bone cement. For this purpose, 4.8 g of powdered tobramycin was mixed with each 40-g batch of Simplex cement. Cement was applied early to the components, but applied late to the femur, tibia, and patella to allow molding to the defects and bone without adherence to bone. Patients received tailored intravenous antibiotic therapy for 6 weeks in addition to this antibiotic-impregnated cement for treatment of a variety of gram positive and gram negative organisms. All patients had cemented revision total knee arthroplasty using antibiotic-impregnated cement with standard cementing techniques used. All patients but 1 had reimplantation; this patient died of unrelated causes before revision. Range of motion before revision was 10 degrees to 95 degrees. Followup averaged 30 months (range, 13-70 months). The average Modified Hospital for Special Surgery Knee Score after revision was 87 points (range, 53-100 points), with 92% good to excellent results. Range of motion after reimplantation was 5 degrees to 106 degrees. There have been no recurrences of infection. Use of an articulating spacer to treat infected total knee arthroplasty improves ultimate ROM and soft tissue health and significantly decreases the risk of reinfection.