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1.
J Inj Violence Res ; 14(1): 115-124, 2022 Jan.
Article in English | MEDLINE | ID: mdl-35137693

ABSTRACT

BACKGROUND: The precision of emergency medical services (EMS) triage criteria dictates whether an injured patient receives appropriate care. The trauma triage protocol is a decision scheme that groups patients into triage categories of major, moderate and minor. We hypothesized that there is a difference between trauma triage category and injury severity score (ISS). METHODS: This retrospective, observational study was conducted to investigate a difference between trauma triage category and ISS. Bivariate analysis was used to test for differences between the subgroup means. The differences between the group means on each measure were analyzed for direction and statistical significance using ANOVA for continuous variables and chi square tests for categorical variables. Logistic and linear regressions were performed to evaluate factors predicting mortality, ICU length of stay. RESULTS: With respect to trauma triage category, our findings indicate that minor and moderate triage categories are similar with respect to ISS, GCS, ICU LOS, hospital LOS, and mortality. However, after excluding for low impact injuries (falls), differences between the minor and moderate categories were evident when comparing to ISS, GCS, ICU LOS, and hospital LOS. Additionally, after excluding for low impact injures, ISS, ICU LOS, and hospital stay were found to correlate well with trauma triage category. CONCLUSIONS: In this retrospective, observational study significant differences were not seen when comparing ISS with the trauma triage categories of moderate and minor during our initial analysis. However, a difference was found after excluding for low impact injuries. These findings suggest that CDC criteria accurately predicts outcomes in high impact trauma.


Subject(s)
Triage , Wounds and Injuries , Centers for Disease Control and Prevention, U.S. , Humans , Injury Severity Score , Retrospective Studies , Trauma Centers , Triage/methods , United States , Wounds and Injuries/therapy
2.
Infect Control Hosp Epidemiol ; 16(8): 488-90, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7594395

ABSTRACT

The gown-glove interface is the weakest point in the present barrier system of gown and glove protection for the surgeon and other healthcare professionals who come into direct contact with body liquids. Try it yourself: put on a fluid-resistant gown and surgical gloves. See that the glove cuff is well proximal to the stockinette. Hold your wrist and forearm for a moment under running water. Wait a minute to see if your forearm is wet. A wet forearm during surgery would be a blooded one. We propose a gown redesign that creates a dart at the terminal forearm, sealed by a liquid-proof method, and then similarly sealing the proximal end of the glove to the sleeve.


Subject(s)
Gloves, Surgical , Infectious Disease Transmission, Patient-to-Professional/prevention & control , Protective Clothing , Universal Precautions/methods , Humans
3.
Am Surg ; 61(6): 486-91, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7762895

ABSTRACT

OBJECTIVE: To evaluate the effect of topical povidone iodine ointment on wound healing. MATERIALS AND METHODS: 60 female mice randomly divided into four groups, A-D. Each mouse had a 2 cm linear incision made on the dorsal skin. Group A had povidone iodine ointment, and group B had ointment base applied for 7 days to the healing incision. Group C were given steroids for 7 days, and group D were allowed to heal without treatment. On Day 8, the strength of the incision was tested with an in vivo tensometer, and the hydroxyproline content of the incision was determined. RESULTS: Using ANOVA and Fischer's LSD test (P < 0.05), povidone iodine as well as steroid groups had significantly reduced wound strengths as compared to the controls and the group with ointment base. No significant difference in the hydroxyproline content was seen. CONCLUSIONS: Povidone iodine significantly reduces wound strength without reducing the total hydroxyproline content of the wound.


Subject(s)
Povidone-Iodine/therapeutic use , Wound Healing/drug effects , Administration, Cutaneous , Animals , Cortisone/adverse effects , Cortisone/analogs & derivatives , Female , Hydroxyproline/analysis , Mice , Ointments , Surgical Wound Infection/pathology , Surgical Wound Infection/prevention & control , Tensile Strength
5.
J Am Coll Surg ; 178(2): 185-6, 1994 Feb.
Article in English | MEDLINE | ID: mdl-8173735
6.
J Long Term Eff Med Implants ; 4(2-3): 127-32, 1994.
Article in English | MEDLINE | ID: mdl-10155134

ABSTRACT

The barrier properties of natural rubber latex gloves have been of clinical interest since the concept of using an integrity monitor was introduced by me over 30 years ago. Although surgeons expect their gloves to serve as an effective barrier during use, products can and do fail. Failure is often unrecognized, resulting in the wearer's exposure to potential pathogens and the patient to microorganisms shed by surgical team members. Although a variety of solutions have been suggested (double gloving, cut-resistant gloves), these remedies do not alert the surgeon to a breach of barrier, the cost and consequences of which are astronomical to the health system. As a result, some form of breach detection device is now recommended to minimize the likelihood of exposure, infection, and/or allergy.


Subject(s)
General Surgery , Gloves, Surgical/standards , Infection Control/methods , Occupational Exposure , Equipment Failure , Humans
7.
Infect Control Hosp Epidemiol ; 14(9): 510, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8228155
8.
J Healthc Mater Manage ; 11(9): 34-5, 1993 Oct.
Article in English | MEDLINE | ID: mdl-10129224

ABSTRACT

A letter appearing in the AORN Journal questioned whether flash sterilization is appropriate for instruments coded with color identification tape. The reply stated that porous, colored tape required a longer time to penetrate and sterilize the area beneath, and thus if it should peel off, the zone beneath might not be sterile. This conclusion was, as far as we can determine, reached by intuitive reasoning and not by experimental evidence. Therefore, the following experimental approach was undertaken to test the hypothesis. Spores on discs were placed between the color-code tape and a metal instrument. Exposure to heat (135 degrees C) and time (3 min.) was in a gravity displacement sterilizer. We then determined whether spore kill has been achieved. The test organism was B. stearothermophilus. None of the discs that were in contact with the instruments while being sterilized showed any growth. Thus, it appears that sterility can be achieved on the instrument surfaces that are beneath color-code tape in three minutes.


Subject(s)
Equipment Contamination/prevention & control , Operating Rooms/standards , Sterilization/standards , Evaluation Studies as Topic , Humans , Sterilization/methods , Surgical Instruments/standards
9.
Arch Surg ; 127(11): 1354-7, 1992 Nov.
Article in English | MEDLINE | ID: mdl-1444798

ABSTRACT

Latex surgical gloves have recently been identified as a potential source of allergens. Much of the current information suggests that the soluble proteins in latex may cause significant reactions in sensitive individuals. The starch powders used as a lubricant on some latex gloves have also been identified as potential allergens in some patients. In this study, we determined these powders to act as potential carriers of latex allergens. We have produced a polyclonal antiserum to be used as a reagent to study latex proteins. By Western blot analysis, we identified a significant interaction between latex proteins and starch powders. The binding of latex proteins to starch particles results in a glove particle that may have an increased potential to act as an allergen. The latex protein-starch particles represent a potential mechanism for exposure and sensitization of health care workers to latex allergens. Elimination of these particles from the operating room should reduce the route of sensitization and the potential for adverse reactions to latex.


Subject(s)
Antigens/immunology , Drug Hypersensitivity/immunology , Gloves, Surgical/standards , Latex/adverse effects , Starch/adverse effects , Adsorption , Animals , Antigens/metabolism , Blotting, Western , Disease Models, Animal , Drug Hypersensitivity/blood , Drug Hypersensitivity/etiology , Electrophoresis, Polyacrylamide Gel , Enzyme-Linked Immunosorbent Assay , Evaluation Studies as Topic , Humans , Immune Sera , Latex/metabolism , Powders , Protein Binding , Rabbits , Starch/immunology , Starch/metabolism
12.
AORN J ; 55(4): 955-7, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1558384
15.
Am Surg ; 57(5): 301-5, 1991 May.
Article in English | MEDLINE | ID: mdl-2039128

ABSTRACT

A startling 31 per cent rate of perforated appendicitis in 1984 prompted a 5-year review at the Guthrie Medical Center. An increase over previous rates of 13 per cent and 0 per cent in 1964 and 1944 was confirmed in this study. Perforation accompanied 44 of 240 cases of appendicitis (18.3%); diagnostic accuracy in 295 cases undergoing operation was 81.4 per cent. Groups at risk for perforation were patients in the first decade of life (34.3% with perforations) and those over 50 years of age (48% perforated). Perforation rates were generally inversely related to accuracy. Accuracy was poorest in women in the second to fourth decade or those in the mid-portion of the menstrual cycle. When the appendix was not perforated, complications occurred in 8.7 per cent of patients while 29.5 per cent with a perforation had a complication. The mean hospital stay was prolonged by 2.5 days if the appendix was perforated. An increased awareness of the risk by both the public and physicians is essential to reduce the number of perforations.


Subject(s)
Appendicitis/epidemiology , Intestinal Perforation/epidemiology , Adolescent , Adult , Aged , Aged, 80 and over , Appendectomy/adverse effects , Appendicitis/complications , Appendicitis/pathology , Child , Child, Preschool , Female , Humans , Incidence , Infant , Intestinal Perforation/complications , Intestinal Perforation/pathology , Male , Middle Aged , Pennsylvania/epidemiology , Peritonitis/etiology , Rupture, Spontaneous
17.
AORN J ; 51(6): 1493-7, 1500-8, 1990 Jun.
Article in English | MEDLINE | ID: mdl-2357060

ABSTRACT

When addressing the impact of medical waste management and regulatory controls on the health care industry, it is important to remember that as long as modern medicine continues to maintain and sustain its current quality of life and wellness standards, industry will continue to generate various byproducts that have adverse effects on both people and the environment. It is important, therefore, to carefully evaluate the impact of societal demands. Unless government, industry, environmental groups, and health care providers abandon their current adversarial relationships and work together to solve shared problems, there will be no improvement in the growing problem of medical waste. The long-term solutions to today's growing waste problems depend to a great extent on human factors and the willingness of industry, medical community, and governmental bodies to cooperate with each other, recognizing the cause-effect relationship of a continued demand for disposable products. There are many pieces to the waste management puzzle. Obviously, surgeons cannot perform surgery without exposure to blood, tissue or body fluids, and nurses cannot maintain asepsis without sterile products. Because the health care team cannot totally eliminate the source of medical waste, they must learn to more effectively manage and control it. Health care professionals must encourage industry and government to work together to develop standards for products and materials used as barriers and use more biodegradable materials. Health care facilities must learn to minimize the amount of medical waste designated as regulated or infectious. Segregating potentially infectious material from clean waste at the point of generation may reduce both volume and cost.


Subject(s)
Medical Waste , Refuse Disposal/methods , Waste Products , Humans , Refuse Disposal/legislation & jurisprudence , Refuse Disposal/standards , United States
18.
JAMA ; 263(12): 1632-3, 1990.
Article in English | MEDLINE | ID: mdl-2308196
19.
AORN J ; 50(1): 157-8, 1989 Jul.
Article in English | MEDLINE | ID: mdl-2751296
20.
Br J Surg ; 76(7): 764, 1989 Jul.
Article in English | MEDLINE | ID: mdl-2765822
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