Surgical Site Infection: Prevention and Treatment [A] Evidence Review for Effectiveness of Nasal Decolonisation in Prevention of Surgical Site Infection

Total Page:16

File Type:pdf, Size:1020Kb

Surgical Site Infection: Prevention and Treatment [A] Evidence Review for Effectiveness of Nasal Decolonisation in Prevention of Surgical Site Infection National Institute for Health and Care Excellence Guideline version (FINAL) Surgical site infection: prevention and treatment [A] Evidence review for effectiveness of nasal decolonisation in prevention of surgical site infection NICE guideline NG125 Evidence reviews April 2019 FINAL These evidence reviews were developed by NICE Guideline Updates Team FINAL Error! No text of specified style in document. Disclaimer The recommendations in this guideline represent the view of NICE, arrived at after careful consideration of the evidence available. When exercising their judgement, professionals are expected to take this guideline fully into account, alongside the individual needs, preferences and values of their patients or service users. The recommendations in this guideline are not mandatory and the guideline does not override the responsibility of healthcare professionals to make decisions appropriate to the circumstances of the individual patient, in consultation with the patient and/or their carer or guardian. Local commissioners and/or providers have a responsibility to enable the guideline to be applied when individual health professionals and their patients or service users wish to use it. They should do so in the context of local and national priorities for funding and developing services, and in light of their duties to have due regard to the need to eliminate unlawful discrimination, to advance equality of opportunity and to reduce health inequalities. Nothing in this guideline should be interpreted in a way that would be inconsistent with compliance with those duties. NICE guidelines cover health and care in England. Decisions on how they apply in other UK countries are made by ministers in the Welsh Government, Scottish Government, and Northern Ireland Executive. All NICE guidance is subject to regular review and may be updated or withdrawn. Copyright © NICE 2019. All rights reserved. Subject to Notice of rights. ISBN: 978-1-4731-3394-5 FINAL Contents Effectiveness of nasal decolonisation in the prevention of surgical site infection ........ 6 Review question ............................................................................................................. 6 Introduction ........................................................................................................... 6 Table 1 PICO: Does the use of nasal decolonisation to eliminate Staphylococcus aureus (alone or in combination with other interventions) affect the rate of surgical site infection? ............................... 6 Methods and process ............................................................................................ 7 Clinical evidence ................................................................................................... 8 Summary of clinical studies included in the evidence review ................................. 8 Quality assessment of clinical studies included in the evidence review ............... 12 Economic evidence ............................................................................................. 12 Summary of studies included in the economic evidence review ........................... 12 Economic model .................................................................................................. 14 Evidence statements ........................................................................................... 17 The committee’s discussion of the evidence ........................................................ 20 Appendices ........................................................................................................................ 27 Appendix A – Review protocols .................................................................................... 27 Appendix B- Methods ................................................................................................... 37 Priority screening ................................................................................................. 37 Evidence of effectiveness of interventions ........................................................... 38 Health economics ................................................................................................ 41 Appendix C – Literature search strategies .................................................................... 43 Appendix D – Clinical evidence study selection ............................................................ 49 Appendix E – Clinical evidence tables .......................................................................... 50 E.1 Bode (2010) .................................................................................................. 50 E.2 Kalmeijer (2002) ............................................................................................ 52 E.3 Konvalinka (2006) ......................................................................................... 56 E.4 Perl (2002) .................................................................................................... 58 E.5 Philips (2014) ................................................................................................ 62 E.6 Segers (2006) ............................................................................................... 65 E.7 Sousa (2016) ................................................................................................ 68 E.8 Suzuki (2003) ................................................................................................ 70 E.9 Tai (2013) ..................................................................................................... 73 Appendix F – Forest plots ............................................................................................. 76 F.1 Mupirocin versus placebo .............................................................................. 76 F.2 Mupirocin versus no nasal decontamination .................................................. 81 F.3 Mupirocin versus 5% Povidone Iodine ........................................................... 82 F.4 Mupirocin + CH wash versus no treatment .................................................... 83 4 FINAL F.5 Mupirocin + CH wash versus placebo ........................................................... 84 F.6 Mupirocin (with or without CH was) versus all non-active interventions ......... 86 F.7 Chlorhexidine + CH wash versus placebo ..................................................... 86 Appendix G – GRADE tables ........................................................................................ 89 G.1 Mupirocin versus placebo ............................................................................. 89 G.2 Mupirocin versus no nasal decontamination ................................................. 93 G.3 Mupirocin versus 5% povidone iodine ........................................................... 94 G.4 Mupirocin and chlorhexidine body wash vs No nasal decontamination ......... 95 G.5 Mupirocin and chlorhexidine body wash vs placebo ...................................... 97 G.6 Mupirocin (with or without chlorhexidine body wash) vs all non-active interventions ............................................................................................ 98 G.7 Chlorhexidine vs. placebo ............................................................................. 99 Appendix H – Economic evidence tables .................................................................... 101 Appendix I – Economic evidence study selection ....................................................... 106 Appendix J – Excluded studies ................................................................................... 107 Clinical studies .................................................................................................. 107 Economic studies .............................................................................................. 112 Appendix K – Research recommendations ................................................................. 115 1. What is the clinical effectiveness of preoperative nasal decolonisation using mupirocin in combination with a chlorhexidine body wash in the whole population? .................................................................................. 115 2. What is the contribution to clinical effectiveness of the timing of nasal decolonisation and body wash for the prevention of surgical site infection? ............................................................................................... 116 3. Is the use of chlorhexidine body wash associated with increased antimicrobial resistance? ........................................................................ 117 4. What is the effectiveness of decolonisation using alternative interventions in combination with nasal decolonisation in the prevention of surgical site infections when chlorhexidine is contraindicated? .......... 118 Appendix L - References ............................................................................................ 119 Included studies ................................................................................................ 119 Excluded studies ............................................................................................... 120 5 FINAL Effectiveness of nasal decolonisation in the prevention of surgical site infection Effectiveness of nasal decolonisation in the prevention of surgical site infection Review question Does the use of nasal decolonisation to eliminate Staphylococcus aureus (alone or in combination with other interventions)
Recommended publications
  • Chlorhexidine Soap Instructions
    Pre-Operative Bathing Instructions Infection Prevention Because skin is not sterile, we need to be sure that your skin is as free of germs as possible before your admission. You can reduce the number of germs on your skin and decrease the risk of surgical site infection by preparing your skin with a special soap called chlorhexidine gluconate (CHG). The instructions for use are attached. What is CHG? CHG is a chemical antiseptic that is effective on both gram-positive and gram-negative bacteria. It is both bacteriocidal (kills) and bacteriostatic (stops reproductions) of any bacteria on the skin. CHG is in several products such as mouthwash, contact lens solution, wound wash, acne skin wash topical skin cleansers (chloraprep-what is used to clean your skin before an IV), thus we do not expect using this soap will cause skin irritation but please speak with your primary care physician to discuss any allergies. Studies show that repeated use of CHG soap enhances the ability of CHG to reduce bacterial counts on the skin; not only during the immediate period after the shower, but for a number of hours afterward. Studies suggest that patients may benefit from bathing or showering with CHG soap for at least 3 days before surgery in order to achieve the most benefit. It is unknown whether using CHG soap for less than or more than 3 days is beneficial. We recommend 3 days of treatment but understand this is not always possible and bathing the night before and the day of using CHG is acceptable. CHG soap can be purchased at any local pharmacy.
    [Show full text]
  • Health Evidence Review Commission's Value-Based Benefits Subcommittee
    Health Evidence Review Commission's Value-based Benefits Subcommittee September 28, 2017 8:00 AM - 1:00 PM Clackamas Community College Wilsonville Training Center, Room 111-112 29373 SW Town Center Loop E, Wilsonville, Oregon, 97070 Section 1.0 Call to Order AGENDA VALUE-BASED BENEFITS SUBCOMMITTEE September 28, 2017 8:00am - 1:00pm Wilsonville Training Center, Rooms 111-112 29353 SW Town Center Loop E Wilsonville, Oregon 97070 A working lunch will be served at approximately 12:00 PM All times are approximate I. Call to Order, Roll Call, Approval of Minutes – Kevin Olson 8:00 AM II. Staff report – Ariel Smits, Cat Livingston, Darren Coffman 8:05 AM A. Chronic Pain Task Force meeting report B. Errata C. Retreat III. Straightforward/Consent agenda – Ariel Smits 8:15 AM A. Consent table B. Straightforward Modifications to the Prioritized List Changes: Continuous Glucose Monitoring in Diabetes Mellitus C. Straightforward changes to the PPI guideline for Barrett’s esophagus with dysplasia D. Tobacco cessation guideline clarification IV. Advisory Panel reports 8:25 AM A. OHAP 1. 2018 CDT code placement recommendations V. Previous discussion items 8:30 AM A. Consideration for prioritization on lines 500/660, Services with Minimal or No Clinical Benefit and/or Low Cost-Effectiveness 1. New medications for the treatment of Duchenne muscular dystrophy i. deflazacort (Emflaza) ii. etepliren (Exondys 51) VI. New discussion items 9:30 AM A. Testicular prostheses B. Capsulorrhaphy for recurrent shoulder dislocation C. Transcutaneous neurostimulators D. Physical therapy for interstitial cystitis E. Acute peripheral nerve injuries F. SOI on role of Prioritized List in Coverage G.
    [Show full text]
  • Thoracic Actinomycosis P
    Thorax (1973), 28, 73. Thoracic actinomycosis P. R. SLADE, B. V. SLESSER, and J. SOUTHGATE Groby Road Hospital, Leicester Six cases of pulmonary infection with Actinomyces Israeli and one case of infection with Nocardia asteroides are described. The incidence of thoracic actinomycosis has declined recently and the classical presentation with chronic discharging sinuses is now uncommon. The cases described illustrate some of the forms which the disease may take. Actinomycotic infection has been noted, not infrequently, to co-exist with bronchial carcinoma and a case illustrating this association is described. Sputum cytology as practised for the diagnosis of bronchial carcinoma has helped to identify the fungi in the sputum. Treatment is discussed, particularly the possible use of oral antibiotics rather than penicillin by injection. Actinomycosis is not common in this country. showed only submucosal fibrosis. Cytological exam- The Table shows the number of cases reported to ination of the sputum showed the presence of fungus Health Laboratory Service from public (Figs 2 and 3) and cultures gave a growth of the Public Actinomyces Israeli. The patient was hypersensitive to health and hospital laboratories in the United penicillin and was treated with oral tetracycline, 2 g Kingdom and Republic of Ireland in recent years. daily for six months. There was marked reduction It is usually considered that the chest may be in the shadowing on the chest film after only six involved in about 15% of cases (Cecil and Loeb, weeks of treatment (Fig. 4) and subsequently com- 1963). But, of the 36 cases reported in 1970, the plete disappearance. The patient has remained well chest was involved in only one case.
    [Show full text]
  • Quantitative Sputum Culture As a Means of Excluding False Positive Reports in the Routine Microbiology Laboratory
    J Clin Pathol: first published as 10.1136/jcp.25.8.697 on 1 August 1972. Downloaded from J. clin. Path., 1972, 25, 697-700 Quantitative sputum culture as a means of excluding false positive reports in the routine microbiology laboratory M. J. B. WILSON AND D. E. MARTIN From the Department of Microbiology, Royal Perth Hospital, Perth, Western Australia SYNOPSIS A relatively simple technique for sputum homogenization and dilution is described. Results show that this technique is reliable for isolation and quantitative culture of organisms from cases of chest infection. The technique has resulted in significant reduction in false positive reports, particularly when a system of interpretative reporting is utilized based on 107 organisms per millilitre of sputum being accepted as evidence of significant infection. The bacteriology of human excretions, particularly A critical analysis of sputum culture results from sputum and urine, has given rise to considerable our laboratory showed that there was frequently a difficulties in interpretation. Kass (1957) contributed good growth of a potential pathogen when clinical much to the better understanding of the significance evidence for infection was equivocal and there was a of non-catheter urine culture when he introduced the tendency for the laboratory to make an excessive copyright. concept of colony counts, in an effort to distinguish number of false positive reports using standard between infected urine and urine from normal culture methods. These false positive reports are persons contaminated by urethral flora. Lower misleading and make it difficult to manage cases respiratory tract infections may likewise show a effectively, and they may lead to unwarranted and heavy growth of commensal organisms, because of undesirable antibiotic usage.
    [Show full text]
  • Antibiotic Resistant Organisms Prevention and Control Guidelines for Healthcare Facilities
    Antibiotic Resistant Organisms Prevention and Control Guidelines for Healthcare Facilities Reference Document for use by Health Care Organizations for Internal Policy/Protocol Development Revised from Provincial Infection Control Network Antibiotic Resistant Organisms Prevention and Control Guidelines 2008 Provincial Infection Control Network 2013 PICNet Antibiotic Resistant Organism (ARO) Guidelines Table of Contents Revisions Working Group ................................................................................................................... 3 Acronyms .......................................................................................................................................... 4 1 Introduction ................................................................................................................................ 5 2 Purpose ....................................................................................................................................... 5 3 Scope .......................................................................................................................................... 5 4 Literature Search Strategy ............................................................................................................ 6 5 Methods ...................................................................................................................................... 6 6 Background ................................................................................................................................
    [Show full text]
  • Hereditary Gingival Fibromatosis CASE REPORT
    Richa et al.: Management of Hereditary Gingival Fibromatosis CASE REPORT Hereditary Gingival Fibromatosis and its management: A Rare Case of Homozygous Twins Richa1, Neeraj Kumar2, Krishan Gauba3, Debojyoti Chatterjee4 1-Tutor, Unit of Pedodontics and preventive dentistry, ESIC Dental College and Hospital, Rohini, Delhi. 2-Senior Resident, Unit of Pedodontics and preventive dentistry, Oral Health Sciences Centre, Post Correspondence to: Graduate Institute of Medical Education and Research , Chandigarh, India. 3-Professor and Head, Dr. Richa, Tutor, Unit of Pedodontics and Department of Oral Health Sciences Centre, Post Graduate Institute of Medical Education and preventive dentistry, ESIC Dental College and Research, Chandigarh, India. 4-Senior Resident, Department of Histopathology, Oral Health Sciences Hospital, Rohini, Delhi Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India. Contact Us: www.ijohmr.com ABSTRACT Hereditary gingival fibromatosis (HGF) is a rare condition which manifests itself by gingival overgrowth covering teeth to variable degree i.e. either isolated or as part of a syndrome. This paper presented two cases of generalized and severe HGF in siblings without any systemic illness. HGF was confirmed based on family history, clinical and histological examination. Management of both the cases was done conservatively. Quadrant wise gingivectomy using ledge and wedge method was adopted and followed for 12 months. The surgical procedure yielded functionally and esthetically satisfying results with no recurrence. KEYWORDS: Gingival enlargement, Hereditary, homozygous, Gingivectomy AA swollen gums. The patient gave a history of swelling of upper gums that started 2 years back which gradually aaaasasasss INTRODUCTION increased in size. The child’s mother denied prenatal Hereditary Gingival Enlargement, being a rare entity, is exposure to tobacco, alcohol, and drug.
    [Show full text]
  • Specimen Collection: Sputum (Home Health Care) - CE
    Specimen Collection: Sputum (Home Health Care) - CE ALERT Don appropriate personal protective equipment (PPE) based on the patient’s signs and symptoms and indications for isolation precautions. Bronchospasm or laryngospasm, as a result of suctioning, can be severe and prolonged, and, in some cases, can be life-threatening without intervention. OVERVIEW Sputum is produced by cells that line the respiratory tract. Although production is minimal in the healthy patient, disease processes can increase the amount or change the character of sputum. Examination of sputum aids in the diagnosis and treatment of many conditions such as bronchitis, bronchiectasis, tuberculosis (TB), pneumonia, and pulmonary abscess, or lung cancer.3 In many cases, suctioning is indicated to collect sputum from a patient who cannot spontaneously produce a sample for laboratory analysis. Suctioning may provoke violent coughing, induce vomiting, and result in aspiration of stomach contents. Suctioning may also induce constriction of the pharyngeal, laryngeal, and bronchial muscles. In addition, suctioning may cause hypoxemia or vagal overload, causing cardiopulmonary compromise and an increase in intracranial pressure. Sputum for cytology, culture and sensitivity, and acid-fast bacilli (AFB) are three major types of sputum specimens.3 Cytologic or cellular examination of sputum may identify aberrant cells or cancer. Sputum collected for culture and sensitivity testing can be used to identify specific microorganisms and determine which antibiotics are the most sensitive. The AFB smear is used to support a diagnosis of TB. A definitive diagnosis of TB also requires a sputum culture and sensitivity.3 Regardless of the test ordered, a sputum specimen should be collected first thing in the morning due to a greater accumulation of bronchial secretions overnight.
    [Show full text]
  • Being Aware of Chlorhexidine Allergy
    Being aware of chlorhexidine allergy If you have an immediate allergic reaction to chlorhexidine you may experience symptoms such as: x itching x skin rash (hives) x swelling x anaphylaxis. People who develop anaphylaxis to chlorhexidine may have experienced mild reactions, such as skin rash, to chlorhexidine before. Irritant contact dermatitis or allergic contact dermatitis Chlorhexidine can also cause irritant dermatitis. This is not a true allergic reaction. It is caused by chlorhexidine directly irritating skin and results in rough, dry and scaly Chlorhexidine is an antiseptic. Allergic reactions to skin, sometimes with weeping sores. chlorhexidine are rare but are becoming more common. Chlorhexidine is used in many products both in Chlorhexidine can also cause allergic contact hospitals and in the community. dermatitis. Symptoms look like irritant dermatitis, but the cause of the symptoms is delayed by 12-48 hours Why have I been given this factsheet? after contact with chlorhexidine. You have been given this brochure because you have had a reaction to a medication, a medical dressing Both irritant dermatitis and allergic contact dermatitis or antiseptic. This may or may not be caused by a caused by chlorhexidine are annoying but not chlorhexidine allergy. dangerous. It is important that you are aware of the possibility of an It is recommended that you avoid chlorhexidine if you allergy. experience these responses as some people have gone on to develop immediate allergic reaction to chlorhexidine. Allergic reactions to chlorhexidine Severe allergic reactions to chlorhexidine are rare, but How do I know which products contain they can be serious. Immediate allergic reactions can chlorhexidine? cause anaphlaxis (a very severe allergic reaction which can be life-threatening).
    [Show full text]
  • 3Rd Quarter 2001 Bulletin
    In This Issue... Promoting Colorectal Cancer Screening Important Information and Documentaion on Promoting the Prevention of Colorectal Cancer ....................................................................................................... 9 Intestinal and Multi-Visceral Transplantation Coverage Guidelines and Requirements for Approval of Transplantation Facilities12 Expanded Coverage of Positron Emission Tomography Scans New HCPCS Codes and Coverage Guidelines Effective July 1, 2001 ..................... 14 Skilled Nursing Facility Consolidated Billing Clarification on HCPCS Coding Update and Part B Fee Schedule Services .......... 22 Final Medical Review Policies 29540, 33282, 67221, 70450, 76090, 76092, 82947, 86353, 93922, C1300, C1305, J0207, and J9293 ......................................................................................... 31 Outpatient Prospective Payment System Bulletin Devices Eligible for Transitional Pass-Through Payments, New Categories and Crosswalk C-codes to Be Used in Coding Devices Eligible for Transitional Pass-Through Payments ............................................................................................ 68 Features From the Medical Director 3 he Medicare A Bulletin Administrative 4 Tshould be shared with all General Information 5 health care practitioners and managerial members of the General Coverage 12 provider/supplier staff. Hospital Services 17 Publications issued after End Stage Renal Disease 19 October 1, 1997, are available at no-cost from our provider Skilled Nursing Facility
    [Show full text]
  • 11736 Lab Req Red-Blue
    3550 W. Peterson Ave., Ste. 100 ACCOUNT: Chicago, Illinois 60659 Tel: 773-478-6333 Fax: 773-478-6335 LABORATORY REQUISITION PATIENT NAME - LAST FIRST MIDDLE INITIAL PATIENT IDENTIFICATION SOCIAL SECURITY NO. DATE OF BIRTH SEX N O I NAME OF INSURED SS# OF INSURED RELATIONSHIP TO PATIENT T A M R O PATIENT/INSURED ADDRESS PHONE NUMBER MEDICARE NO. (INCLUDING ALPHA CHARACTERS) F Please attach an ABN form. N I G N CITY STATE ZIP CODE I L L I MEDICAID NO. B BILL I PHYSICIAN I PATIENT I MEDICARE I MEDICAID I INSURANCE (attach copy of both sides of card) TO ACCOUNT DIAGNOSIS (CD-9 CODE(S)) (REQUIRED FOR 3RD PARTY BILLING) PLEASE WRITE PATIENT’S NAME ON ALL SPECIMENS DATE COLLECTED COLLECTED BY AM DR. NAME / NPI # DR. OR RN SIGNATURE PM 001 GENERAL HEALTH PROFILE ( Male ) - CBC, CMP, LIPID, TSH, FT4, TT3, FERRITIN, PSA, H-PYLORI, MAG, ESR, UA, IRON/TIBC SST, L, U 002 GENERAL HEALTH PROFILE ( Female ) - CBC, CMP, LIPID, TSH, FT4, TT3, FERRITIN, H-PYLORI, MAG, ESR, UA, IRON/TIBC SST, L, U 003 AMENOR/MENSTR. DISORDER - CMP, LIPID, CBC, TSH, FT4, TT3, ESR, IRON/TIBC, FERRITIN, MAG, UA, HCG, FSH, LH, PROLACTIN, RET COUNT SST, L, U 004 ANEMIA - CMP, LIPID, IRON/TIBC, CBC, FERRITIN, TSH, FT4, TT3, H-PYLORI, UA, G6PD, RET COUNT SST, L, U 005 ARTHRITIS - CMP, LIPID, CBC, URIC ACID, ESR, ASO, CRP, ANA, RH, SLE SST, L, U 006 DIABETES - CMP, LIPID, CBC, HBA1C, CORTISOL, TSH, FT4, TT3, UA, RET COUNT SST, L, U 007 HEPATITIS - HAAB IGM, HBCAB IGM, HBSAB, HBSAG, HCAB, SGOT, SGPT SST 008 HYPERTENSION/CARDIAC - CMP, LIPID, CBC, TSH, FT4, TT3, IRON/TIBC, CPK, CORTISOL,
    [Show full text]
  • Detecting Carbapenem-Resistant Acinetobacter Baumannii (CRAB) Carriage: Which Body Site Should Be Cultured?
    Infection Control & Hospital Epidemiology (2020), 41, 965–967 doi:10.1017/ice.2020.197 Concise Communication Detecting carbapenem-resistant Acinetobacter baumannii (CRAB) carriage: Which body site should be cultured? Amir Nutman MD, MPH1,2 , Elizabeth Temkin DrPH1, Jonathan Lellouche PhD1, Debby Ben David MD1,2, David Schwartz PhD1 and Yehuda Carmeli MD, MPH1,2 1National Institute for Antibiotic Resistance and Infection Control, Ministry of Health, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel and 2Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel Abstract We compared the yield of culturing various body sites to detect carriage of carbapenem-resistant Acinetobacter baumannii (CRAB). Culturing the skin using a premoistened sponge, with overnight enrichment and plating on CHROMagar MDR Acinetobacter, had the highest yield: 92%. Skin is satisfactory as a single site for active surveillance of CRAB. (Received 8 January 2020; accepted 28 April 2020; electronically published 19 June 2020) Acinetobacter baumannii is a multidrug-resistant pathogen caus- The primary outcome was screening yield for each body site ing severe infections in hospitals and long-term care facilities. sampled. Because there is no gold standard for CRAB screening, Detecting carriers is a mainstay of controlling nosocomial spread a patient was defined as a CRAB carrier if a culture from any of of resistant organisms. Screening for carbapenem-resistant the sites sampled was positive. Acinetobacter baumannii (CRAB) has been recommended to control outbreaks, but no specific recommendations have been Specimen collection methods made regarding which body sites to culture.1 In 2007, we studied the yield of culturing the nose, throat, axilla, groin, rectum, open Buccal mucosa and rectal specimens were collected using swabs wounds, and tracheal aspirates, and no site or combination of (Amies agar gel transport swab; Copan Italia S.P.A., Brescia, sites had high enough sensitivity to be recommended for CRAB Italy).
    [Show full text]
  • Clinical Practice Guidelines for Antimicrobial Prophylaxis in Surgery
    SURGICAL INFECTIONS Volume 14, Number 1, 2013 Surgical Infection Mary Ann Liebert, Inc. DOI: 10.1089/sur.2013.9999 Society Guidelines Clinical Practice Guidelines for Antimicrobial Prophylaxis in Surgery Dale W. Bratzler,1 E. Patchen Dellinger,2 Keith M. Olsen,3 Trish M. Perl,4 Paul G. Auwaerter,5 Maureen K. Bolon,6 Douglas N. Fish,7 Lena M. Napolitano,8 Robert G. Sawyer,9 Douglas Slain,10 James P. Steinberg,11 and Robert A. Weinstein12 hese guidelines were developed jointly by the Ameri- the project. Panel members and contractors were required to Tcan Society of Health-System Pharmacists (ASHP), the disclose any possible conflicts of interest before their ap- Infectious Diseases Society of America (IDSA), the Surgical pointment and throughout the guideline development pro- Infection Society (SIS), and the Society for Healthcare Epide- cess. Drafted documents for each surgical procedural section miology of America (SHEA). This work represents an update were reviewed by the expert panel and, once revised, were to the previously published ASHP Therapeutic Guidelines on available for public comment on the ASHP website. After Antimicrobial Prophylaxis in Surgery [1], as well as guide- additional revisions were made to address reviewer com- lines from IDSA and SIS [2,3]. The guidelines are intended to ments, the final document was approved by the expert panel provide practitioners with a standardized approach to the and the boards of directors of the above-named organizations. rational, safe, and effective use of antimicrobial agents for the prevention of surgical site infections (SSIs) based on currently Strength of evidence and grading of recommendations available clinical evidence and emerging issues.
    [Show full text]