Acute Rhinosinusitis: When to Prescribe an Antibiotic

Total Page:16

File Type:pdf, Size:1020Kb

Acute Rhinosinusitis: When to Prescribe an Antibiotic Pamela R. Hughes, MD; Carol H. Hungerford, DO; Acute rhinosinusitis: Kevin N. Jensen, DO Family Medicine Residency Clinic (Dr. Hughes) and When to prescribe an antibiotic Family Health Clinic (Dr. Hungerford), Mike O’Callaghan Military Medical Center, Las Vegas, Yes, the majority of antibiotics prescribed for acute NV; Ear Nose and Throat Specialists of Alaska, rhinosinusitis are unnecessary, but when should you Wasilla (Dr. Jensen) prescribe one and which one(s) should you use? pamela.r.hughes4.mil@ mail.mil The authors reported no potential conflict of interest relevant to this article. n estimated 30 million cases of acute rhinosinusitis PRACTICE The opinions and assertions (ARS) occur every year in the United States.1 More than contained herein are those RECOMMENDATIONS 80% of people with ARS are prescribed antibiotics in of the authors and are not to ❯ Reserve antibiotics for A be construed as official or as North America, accounting for 15% to 20% of all antibiotic pre- reflecting the views of the US Air patients who meet diagnostic scriptions in the adult outpatient setting.2,3 Many of these pre- Force Medical Department, the criteria for acute bacterial US Air Force at large, or the US scriptions are unnecessary, as the most common cause of ARS Department of Defense. rhinosinusitis (ABRS). 4,5 Patients must have purulent is a virus. Evidence consistently shows that symptoms of ARS nasal drainage that is will resolve spontaneously in most patients and that only those accompanied by either nasal patients with severe or prolonged symptoms require consider- obstruction or facial pain/ ation of antibiotic therapy.1,2,4,6 Nearly half of all patients will pressure/fullness and EITHER improve within 1 week and two-thirds of patients will improve symptoms that persist within 2 weeks without the use of antibiotics.7 In children, only without improvement for at about 6% to 7% presenting with upper respiratory symptoms least 10 days OR symptoms meet the criteria for acute bacterial rhinosinusitis (ABRS),8 that worsen within 10 days which we’ll detail in a bit. For most patients, treatment should of initial improvement consist of symptom management.5 (“double sickening”). A But what about the minority who require antibiotic ther- ❯ Offer watchful waiting apy? This article reviews how to evaluate patients with ARS, and delay antibiotics for up identify those who require antibiotics, and prescribe the most to 7 days after diagnosing appropriate antibiotic treatment regimens. ABRS in a patient if adequate access to follow- up is available; otherwise, treat with amoxicillin (with Diagnosis: Distinguishing or without clavulanate) viral from bacterial disease for 5 to 10 days. A ARS is defined as the sudden onset of purulent nasal discharge plus either nasal blockage or facial pressure/pain lasting Strength of recommendation (SOR) < 4 weeks.3,9 Additional signs and symptoms may include post- A Good-quality patient-oriented evidence nasal drip, a reduced sense of smell, sinus tenderness to palpa- B Inconsistent or limited-quality tion, and maxillary toothaches.10,11 patient-oriented evidence ARS may be viral or bacterial in etiology, with the most C Consensus, usual practice, opinion, disease-oriented common bacterial organisms being Streptococcus pneumoni- evidence, case series ae, Haemophilus influenzae, and Moraxella catarrhalis.1,3,5 The most common viral causes are influenza, parainfluenza, and rhinovirus. Approximately 90% to 98% of cases of ARS are vi- ral6,11; only about 0.5% to 2% of viral rhinosinusitis episodes are 244 THE JOURNAL OF FAMILY PRACTICE | JUNE 2020 | VOL 69, NO 5 complicated by bacterial infection.1,10-12 or lavage) was unilateral tenderness of the Diagnose ABRS when symptoms of ARS maxillary sinuses. The presence of purulent fail to improve after 10 days or symptoms of drainage in the nose or posterior pharynx ARS worsen within 10 days after initial im- also has significant diagnostic value, as it pre- provement (“double sickening”).1,11 Symp- dicts the presence of bacteria on antral aspi- toms that are significantly associated with ration.1 Purulent discharge in the pharynx is ABRS are unilateral sinus pain and reported associated with a higher likelihood of benefit maxillary pain. The presence of facial or den- from antibiotic therapy compared to placebo tal pain correlates with ABRS but does not (number needed to treat [NNT] = 8).16 How- identify the specific sinus involved.1 ever, colored nasal discharge indicates the There isn’t good correlation between pa- presence of neutrophils—not bacteria—and tients saying they have sinusitis and actually does not predict the likelihood of bacterial having it.13 A 2019 meta-analysis by Ebell et sinus infection.14,17 Therefore, the history and al14 reported that based on limited data, the physical exam should focus on location of overall clinical impression, fetid odor on the pain (sinus and/or teeth), duration of symp- breath, and pain in the teeth are the best in- toms, presence of fever, change in symptom dividual clinical predictors of ABRS. severity, attempted home therapies, sinus As recommended by the Infectious Dis- tenderness on exam, breath odor, and puru- ease Society of America (IDSA), a diagnosis lent drainage seen in the nasal cavity or pos- of ABRS is also reasonable in patients who terior pharynx.13,14 Approximately present with severe symptoms at the onset.6 ❚ Radiographic imaging has no role 90% to 98% of Although there is no consensus about what in the diagnosis or treatment of uncom- cases of acute constitutes “severe symptoms,” they are often plicated ABRS because viral and bacterial rhinosinusitis described as a temperature ≥ 102°F (39°C) etiologies have similar radiographic appear- are viral; only plus 3 to 4 days of purulent nasal drainage.1,4,6 ances. Additionally, employing radiologic about 0.5% Additional symptoms of ABRS may in- imaging would increase health care costs by to 2% of viral clude cough, fatigue, decreased or lack of at least 4-fold.5,6,8,17 The American Academy rhinosinusitis sense of smell (hyposmia or anosmia), and of Otolaryngology-Head and Neck Surgery episodes are ear pressure.10 Another sign of “double sick- (AAO-HNS) clinical practice guidelines rec- complicated ening” is the development of a fever after ommend against radiographic imaging for by bacterial several days of symptoms.1,9,15 Viral sinusitis patients who meet the diagnostic criteria for infection. typically lasts 5 to 7 days with a peak at days ABRS unless concern exists for a complica- 2 to 3.1,15 If symptoms continue for 10 days, tion or an alternate diagnosis is suspected.1 there is a 60% chance of bacterial sinusitis, Computed tomography (CT) imaging of the although some viral rhinosinusitis symptoms sinuses may be warranted in patients with se- persist for > 14 days.1,5 Beyond 4 to 12 weeks, vere headaches, facial swelling, cranial nerve sinusitis is classified as subacute or chronic.3 palsies, or bulging of the eye (proptosis), all of which indicate a potential complication of ABRS.1 Physical exam findings and the ❚ Laboratory evaluations. ABRS is a limited roles of imaging and labs clinical diagnosis; therefore, routine lab Common physical exam findings associated work, such as a white blood cell count, with the diagnosis of ABRS include altered C- reactive protein (CRP) level, and/or eryth- speech indicating nasal obstruction; edema rocyte sedimentation rate (ESR), are not or erythema of the skin indicating congested indicated unless an alternate diagnosis is capillaries; tenderness to palpation over the suspected.1,5,13,18,19 cheeks or upper teeth; odorous breath; and In one study, CRP > 10 mg/L and ESR purulent drainage from the nose or in the > 10 mm/h were the strongest individual pre- posterior pharynx. dictors of purulent antral puncture aspirate In a study by Hansen et al13 (N = 174), the or positive bacterial culture of aspirate, which only sign that showed significant association is considered diagnostic for ABRS. 20 However, with ABRS (diagnosed by sinus aspiration CRP and ESR by themselves are not adequate MDEDGE.COM/FAMILYMEDICINE VOL 69, NO 5 | JUNE 2020 | THE JOURNAL OF FAMILY PRACTICE 245 TABLE 1 Diagnostic criteria for acute bacterial rhinosinusitis AAO-HNS1 ARS symptoms (purulent nasal discharge plus either nasal obstruction or facial pain/pressure) plus 1 of the following: Persistent symptoms for 10 days after onset without improvement OR Acute worsening of symptoms after an initial improvement (“double sickening”) IDSA6 Presence of ARS symptoms with any of the following: • Severe features (temperature ≥ 102ºF [39ºC] and facial pain) for at least 3 days • “Double sickening” • Persistent and not improving symptoms for at least 10 days AAO-HNS, American Academy of Otolaryngology-Head and Neck Surgery; ARS, acute rhinosinusitis; IDSA, Infectious Diseases Society of America. to diagnose ABRS.20 This study developed a ARS and ABRS is recommended as first-line clinical decision rule that used symptoms, therapy; it should be offered to patients before signs, and laboratory values to rate the likeli- making a diagnosis of ABRS.1,5,9,25 Consider hood of ABRS as being either low, moderate, using analgesics, topical intranasal steroids, or high. However, this clinical decision rule and/or nasal saline irrigation to alleviate has not been prospectively validated. symptoms and improve quality of life.1,5,25 In- Thus, CRP and ESR elevations can sup- terventions with questionable or unproven port the diagnosis of ABRS, but the low sen- efficacy
Recommended publications
  • Overtreatment and Underutilization of Watchful Waiting in Men with Limited
    ARTICLE IN PRESS Oncology Overtreatment and Underutilization of Watchful Waiting in Men With Limited Life Expectancy: An Analysis of the Michigan Urological Surgery Improvement Collaborative Registry Udit SinghalC, Jeffrey J. TosoianC, Ji Qi, David C. Miller, Susan M. Linsell, Michael Cher, Brian Lane, Michael Cotant, James E. Montie, Wassim Bazzi, Mohammad Jafri, Bradley Rosenberg, and Arvin K. George, Michigan Urological Surgery Improvement Collaborative OBJECTIVE To determine rates of watchful waiting (WW) vs treatment in prostate cancer (PCa) and limited life expectancy (LE) and assess determinants of management. MATERIALS AND Patients diagnosed with PCa between 2012 and 2018 with <10 years LE were identified from the METHODS Michigan Urologic Surgery Improvement Collaborative registry. Multinomial logistic regression models were used to identify factors associated with management choice among NCCN low-risk PCa patients. Data from high-volume practices were analyzed to understand practice variation. RESULTS Total 2393 patients were included. Overall, WW was performed in 8.1% compared to 23.3%, 25%, 11.2%, and 3.6% who underwent AS, radiation (XRT), prostatectomy (RP), and brachytherapy (BT), respectively. In men with NCCN low-risk disease (n = 358), WW was performed in 15.1%, compared to AS (69.3%), XRT (4.2%), RP (6.7%), and BT (2.5%). There was wide variation in management among practices in low-risk men; WW (6%-35%), AS (44%-81%), and definitive treatment (0%-30%). Older age was associated with less likelihood of undergoing AS vs WW (odds ratio [OR] 0.88, P < .001) or treatment vs WW (OR 0.83, P < .0001). Presence of ≥cT2 disease (OR 8.55, P = .014) and greater number of positive biopsy cores (OR 1.41, P = .014) was associated with greater likelihood of treatment vs WW and Charlson comorbidity score of 1 vs 0 (OR 0.23, P = .043) was associated with less likelihood of treatment vs WW.
    [Show full text]
  • Appropriateness Criteria for Active Surveillance of Prostate Cancer
    Appropriateness Criteria for Active Surveillance of Prostate Cancer Michael L. Cher,* Apoorv Dhir, Gregory B. Auffenberg, Susan Linsell, Yuqing Gao, Bradley Rosenberg,† S. Mohammad Jafri, Laurence Klotz, David C. Miller,‡ Khurshid R. Ghani, Steven J. Bernstein, James E. Montie and Brian R. Lane for the Michigan Urological Surgery Improvement Collaborative From the Department of Urology, Wayne State University, Detroit (MLC), Department of Urology (AD, GBA, SL, YG, DCM, KRG, JEM) and Department of Medicine (SJB), University of Michigan, Center for Clinical Management Research, VA Ann Arbor Healthcare System (SJB), Ann Arbor, Comprehensive Urology, Royal Oak (BR, SMJ), Division of Urology, Spectrum Health, Grand Rapids (BRL), Michigan, and the Division of Urology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada (LK) Purpose: The adoption of active surveillance varies widely across urological communities, which suggests a need for more consistency in the counseling of Abbreviations and Acronyms patients. To address this need we used the RAND/UCLA Appropriateness ¼ Method to develop appropriateness criteria and counseling statements for active AA African-American surveillance. AS ¼ active surveillance Materials and Methods: Panelists were recruited from MUSIC urology practices. LE ¼ life expectancy Combinations of parameters thought to influence decision making were used to MUSIC ¼ Michigan Urological create and score 160 theoretical clinical scenarios for appropriateness of active Surgery Improvement surveillance. Recent rates of active surveillance among real patients across the Collaborative state were assessed using the MUSIC registry. PC ¼ prostate cancer Results: Low volume Gleason 6 was deemed highly appropriate for active sur- PSA ¼ prostate specific antigen veillance whereas high volume Gleason 6 and low volume Gleason 3þ4 were PSAD ¼ prostate specific antigen deemed appropriate to uncertain.
    [Show full text]
  • Vaginal Bleeding in the Early Stages of Pregnancy
    n LEARNING OBJECTIVES: • Tex t here • Tex t here CME • Tex t here • Tex t here CE n COMPLETE THE POSTTEST: Page xx n ADDITIONAL CME/CE: Pages xx FEATURE Turn to page 27 for additional information on this month’s CME/CE courses. KIMBERLY D. WALKER; KATHY DEXTER, MLS, MHA, MPA, PA-C; AND BONNIE A. DADIG, ED.D., PA-C Vaginal bleeding in the early stages of pregnancy A number of potential causes of early pregnancy vaginal bleeding must be considered when deciding what type of management is required. p to 25% of all women in the early stages of pregnancy will experience vaginal bleeding Uor spotting. Even more sobering, half of those women will go on to experience intrauterine fetal demise prior to the 20th week.1 To reduce morbidity and mortality, the astute practitioner should be able to effectively assess and manage a patient with vaginal bleeding in the first half of her pregnancy. Causes Appropriate assessment and management of the patient requires an understanding of the differential diagnoses of vaginal bleeding in early pregnancy (Table 1). Fifty percent of early pregnancy bleeds— defined as bleeding at< 20 weeks’ gestation—occur in viable intrauterine pregnancies (IUP). A total of 30% to 50% of early pregnancy bleeds indicate fetal demise, In an ectopic pregnancy, 7% of which are attributable to ectopic pregnancy the embryo (shown) (EP), and fewer than 1% are caused by trophoblastic implants outside the 2 uterine cavity. disease and/or lesions of the cervix/vagina. While chromosomal abnormalities are the most © SCIENCE SOURCE / BIOPHOTO ASSOCIATES common cause of fetal demise and subsequent 1 THE CLINICAL ADVISOR • APRIL 2013 • www.ClinicalAdvisor.comwww.ClinicalAdvisor.com • THE CLINICAL ADVISOR • APRIL 2013 1 CME CE EARLY PREGNANCY BLEEDING The patient will present with vaginal bleeding and mild-to-moderate subrapubic or midline lower abdominal pain that may radiate to the lower back.
    [Show full text]
  • Watchful Waiting
    Treatment Specialist Nurses 0800 074 8383 prostatecanceruk.org 1 Watchful waiting In this fact sheet: • What is watchful waiting? • Making a decision about treatment • Who can go on watchful waiting? • Dealing with prostate cancer • Can I have treatment instead? • Questions to ask your doctor or nurse • What are the advantages and • More information disadvantages of watchful waiting? • About us • What does watchful waiting involve? This fact sheet is for men who want to know What is watchful waiting? more about watchful waiting, which is a way Watchful waiting is a way of monitoring prostate of monitoring prostate cancer. Your partner, cancer that isn’t causing any symptoms or family or friends might also find it helpful. problems. The aim is to keep an eye on the cancer over the long term, and avoid treatment Watchful waiting isn’t the same as active unless you get symptoms. surveillance, which is another way of monitoring prostate cancer. We explain the It might seem strange not to have treatment, differences between them on page 2. but prostate cancer often grows slowly and may never cause any problems or symptoms. Each hospital or GP surgery will do things differently, so use this fact sheet as a Also, many treatments for prostate cancer, like general guide and ask your doctor or nurse radiotherapy, surgery or hormone therapy, can for more information. You can also speak cause side effects. These include urinary, erection to our Specialist Nurses, in confidence, on and bowel problems, and fatigue. For some men, 0800 074 8383, or chat to them online.
    [Show full text]
  • Pyelonephritis (Acute): Antimicrobial Prescribing Guideline Evidence Review
    National Institute for Health and Care Excellence Final Pyelonephritis (acute): antimicrobial prescribing guideline Evidence review NICE guideline 111 October 2018 Contents 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 2018. All rights reserved. Subject to Notice of rights. ISBN: 978-1-4731-3124-8 Contents Contents Contents .............................................................................................................................
    [Show full text]
  • Arc-Staghorn-Calculi.Pdf
    American Urological Association, Inc.® Nephrolithiasis Clinical Guidelines Panel: Report on the Management of Staghorn Calculi Archived Document— For Reference Only Clinical Practice Guidelines Nephrolithiasis Clinical Guidelines Panel Members and Consultants Joseph W. Segura, M.D., Chairman Glenn M. Preminger, M.D., Facilitator The Carl Rosen Professor of Urology Professor, Department of Urology Department of Urology Duke University Medical Center The Mayo Clinic Durham, North Carolina Rochester, Minnesota Dean G. Assimos, M.D. Joseph N. Macaluso, Jr., M.D. Assoc. Professor of Surgical Sciences Medical Dir.; Dir. of Grants & Research Department of Urology Urologic Institute of New Orleans The Bowman Gray School of Medicine Assoc. Professor & Dir. of Endourology, Wake Forest University Lithotripsy & Stone Disease Winston-Salem, North Carolina Louisiana State Univ. Medical Center Stephen P. Dretler, M.D. School of Medicine Director, Kidney Stone Center New Orleans, Louisiana Massachusetts General Hospital David L. McCullough, M.D. Boston, Massachusetts William H. Boyce Professor Robert I. Kahn, M.D. Chairman, Department of Urology Chief of Endourology The Bowman Gray School of Medicine California Pacific Medical Center Wake Forest University San Francisco,Archived California Document—Winston-Salem, North Carolina James E. Lingeman, M.D. Claus G. Roehrborn, M.D. Director of Research Facilitator Coordinator Methodist HospitalFor ReferenceHanan Bell, Ph.D. Only Institute for Kidney Stone Disease Methodology and Statistical Consultant Associate Clinical Instructor in Urology Curtis Colby Indiana University School of Medicine Editor Indianapolis, Indiana Patrick Florer Computer Database Design Consultant The Nephrolithiasis Clinical Guidelines Panel consists of board-certified urologists who are experts in stone disease. This Report on the Management of Staghorn Calculi was extensively reviewed by over 50 urolo- gists throughout the country in the Fall of 1993.
    [Show full text]
  • EAU Guidelines on Urolithiasis 2019
    EAU Guidelines on Urolithiasis C. Türk (Chair), A. Skolarikos (Vice-chair), A. Neisius, A. Petrik, C. Seitz, K. Thomas Guidelines Associates: J.F. Donaldson, T. Drake, N. Grivas, Y. Ruhayel © European Association of Urology 2019 TABLE OF CONTENTS PAGE 1. INTRODUCTION 6 1.1 Aims and scope 6 1.2 Panel composition 6 1.3 Available publications 6 1.4 Publication history and summary of changes 6 1.4.1 Publication history 6 1.4.2 Summary of changes 6 2. METHODS 7 2.1 Data identification 7 2.2 Review 8 2.3 Future goals 8 3. GUIDELINES 8 3.1 Prevalence, aetiology, risk of recurrence 8 3.1.1 Introduction 8 3.1.2 Stone composition 9 3.1.3 Risk groups for stone formation 9 3.2 Classification of stones 10 3.2.1 Stone size 10 3.2.2 Stone location 10 3.2.3 X-ray characteristics 10 3.3 Diagnostic evaluation 11 3.3.1 Diagnostic imaging 11 3.3.1.1 Evaluation of patients with acute flank pain/suspected ureteral stones 11 3.3.1.2 Radiological evaluation of patients with renal stones 11 3.3.1.3 Summary of evidence and guidelines for diagnostic imaging 12 3.3.2 Diagnostics - metabolism-related 12 3.3.2.1 Basic laboratory analysis - non-emergency urolithiasis patients 12 3.3.2.2 Analysis of stone composition 12 3.3.2.3 Guidelines for laboratory examinations and stone analysis 12 3.3.3 Diagnosis in special groups and conditions 13 3.3.3.1 Diagnostic imaging during pregnancy 13 3.3.3.1.1 Summary of evidence and guidelines for diagnostic imaging during pregnancy 13 3.3.3.2 Diagnostic imaging in children 14 3.3.3.2.1 Summary of evidence and guidelines for diagnostic
    [Show full text]
  • Genitourinary Prostate Cancer
    PRINCESS MARGARET CANCER CENTRE CLINICAL PRACTICE GUIDELINES GENITOURINARY PROSTATE CANCER GU Site Group – Prostate Cancer Authors: Dr. Charles Catton, Dr. Anthony Joshua 1. INTRODUCTION 3 2. PREVENTION 3 3. SCREENING AND EARLY DETECTION 3 4. DIAGNOSIS 4 5. PATHOLOGY 5 6. MANAGEMENT 6 6.1 ADENOCARCINOMA OF PROSTATE 6 6.2 LOW RISK 6.3 INTERMEDIATE RISK 6.4 HIGH RISK 6.5 PRESENTATION WITH N1 OR M1 DISEASE 6.6 MANAGEMENT OF PROGRESSION AFTER INITIAL THERAPY 6.7 ONCOLOGY NURSING PRACTICE 13 7. SUPPORTIVE CARE 14 7.1 PATIENT EDUCATION 14 7.2 PSYCHOSOCIAL CARE 14 7.3 SYMPTOM MANAGEMENT 14 7.4 CLINICAL NUTRITION 14 7.5 PALLIATIVE CARE 14 7.6 OTHER 14 8. FOLLOW-UP CARE 15 9. APPENDIX 1 – PATHOLOGICAL CLASSIFICATION 16 10. APPENDIX 2 – TESTICULAR CANCER STAGING 18 2 Last Revision Date – October 2015 1. UINTRODUCTIONU Prostate cancer is the most frequently diagnosed cancer in Canadian males accounting for 28.4% of new cases and 11% of all cancer deaths (Canadian Cancer Statistics 2008). Diagnosis is most frequently made between the ages of 60-69. The average annual change in age-standardized incidence increased by 1.2%/year from 1995-2004. This increase is attributed to the introduction of prostate cancer screening during the interval. The natural history of prostate cancer is variable, but it is frequently indolent with an age standardized mortality rate of 23.6/100,000 in 2008 compared to 209/100,000 for all cancers. Death from prostate cancer most frequently occurs over the age of 79 (53.4% of deaths), and is uncommon before the age of 70 (14.8% of deaths).
    [Show full text]
  • Follow-Up of Prostatectomy Versus Observation for Early Prostate Cancer
    OUTCOMES RESEARCH IN REVIEW Follow-up of Prostatectomy versus Observation for Early Prostate Cancer Wilt T, Jones K, Barry M, et al. Follow-up of prostatectomy versus observation for early prostate cancer. N Engl J Med 2017;377:132–42. Objective. To determine differences in all-cause and sured from date of diagnosis to August 2014 or until prostate cancer–specific mortality between subgroups of the patient died. A third-party end-points committee patients who underwent watchful waiting versus radical blinded to patient arm in the trial determined the cause prostactectomy (RP) for early-stage prostate cancer. of death from medical record assessment. Design. Randomized prospective multicenter trial Main results. 731 men with a mean age of 67 were ran- (PIVOT study). domly assigned to RP or watchful waiting. The median PSA of patients was 7.8 ng/mL with 75% of patients Setting and participants. Study participants were having a Gleason score ≤ 7 and 74% of patients having Department of Veterans Affairs (VA) patients younger low- or intermediate-risk prostate cancer. As of August than age 75 with biopsy-proven local prostate cancer 2014, 468 of 731 men had died; cause of death was un- (T1–T2, M0 by TNM staging and centrally confirmed available in 7 patients (2 patients in the surgery arm and by pathology laboratory in Baylor) between November 5 in the observation arm). Median duration of follow-up 1994 and January 2002. They were patients at NCI to death or end of follow-up was 12.7 years. All-cause medical center–associated VA facilities.
    [Show full text]
  • Comparative Effectiveness of Treatments for Asymptomatic Bacteriuria Including Watchful Waiting
    October 2016 Comparative effectiveness of treatments for asymptomatic bacteriuria including watchful waiting Prepared for: Patient-Centered Outcomes Research Institute (PCORI) 1828 L St., NW, Suite 900 Washington, DC 20036 Phone: (202) 827-7700 Fax: (202) 355-9558 www.pcori.org Prepared by: Johns Hopkins Evidence-Based Practice Center Baltimore, Maryland Comparative effectiveness of treatments for asymptomatic bacteriuria including watchful waiting PCORI Scientific Program Area: Comparative Effectiveness Research Executive Summary Overall Comparative Research Question What is the comparative effectiveness of treatments (antibiotics, etc) for asymptomatic bacteriuria including watchful waiting? Brief Overview of the Topic Asymptomatic bacteriuria occurs when specific bacteria are present in the urine, without signs or symptoms of a urinary tract infection. Guidelines consistently recommend screening and treatment of asymptomatic bacteriuria in pregnant women. Some, but not all guidelines, recommend screening and treatment prior to urologic and urogynecologic procedures. Other populations, especially those in long-term care facilities and with urinary catheters, are screened despite the absence of guideline recommendations. Concerns have been raised that screening for asymptomatic bacteriuria may lead to overuse of antibiotics, which may contribute to antibiotic resistance. Impact on Health and Populations Asymptomatic bacteriuria is more common among women, older individuals, residents of long- term care facilities, people with indwelling urinary catheters, and those with diabetes mellitus, spinal cord injuries or who are undergoing hemodialysis. Assessment of Current Options In current clinical practice, individuals who are screened and test positive for asymptomatic bacteriuria often are prescribed antibiotics. However, clinicians may choose not to use antibiotics until symptoms occur which is called watchful waiting. Other terms for watchful waiting are expectant management or active surveillance.
    [Show full text]