Skin and Soft Tissue Infections

Total Page:16

File Type:pdf, Size:1020Kb

Skin and Soft Tissue Infections SKIN AND SOFT TISSUE INFECTIONS Clinical Setting Empiric Therapy Duration Comments Minor Skin Infections Impetigo • Secondarily Mupirocin 2% topical ointment BID 7 days infected skin lesions such eczema, ulcers, or lacerations INCISION AND DRAINAGE (I&D) IS RECOMMENDED AS PRIMARY MANAGEMENT, AND ANTIBIOTICS ARE NOT INDICATED UNLESS PATIENT MEETS ONE OF THE Abscess, Furuncles, FOLLOWING CRITERIA: • Close clinical follow-up is and Carbuncles • Severe, extensive, rapidly recommended, especially in progressive cellulitis, or abscess >2 patients no receiving antibiotic Abscesses - cm therapy collections of pus • Signs or symptoms of systemic illness • Cultures and susceptibility are within the dermis • Elderly, immunosuppressed, active recommended when I&D is and deeper skin neoplasm or diabetes mellitus performed tissues • Circumstances where abscess is difficult to drain • Renal dose adjustment may be Furuncle - infection • Associated septic phlebitis required for vancomycin and of the hair follicle in • Inadequate response to I&D alone trimethoprim-sulfamethoxazole which purulent 5-7 days • Staphylococcus aureus resistance material extends EMPIRIC ORAL ANTIBIOTIC THERAPY FOR rates are lowest for TMP-SMX through the dermis OUTPATIENT THERAPY, OR ORAL STEP-DOWN (3%) and doxycycline (4%), into the THERAPY MEETING ABOVE CRITERIA: compared to clindamycin (43%). subcutaneous tissue, Preferred: where a small TMP-SMX* 1-2 DS tabs PO BID • Empiric therapy should target abscess forms MRSA until susceptibilities are Alternative: known, and then therapy should Carbuncle - Doxycycline 200 mg PO x1, then 100 be tailored. For patients with coalescence of mg PO BID MSSA, preferred oral step-down several furuncles therapy is cephalexin, TMP-SMX, into a single EMPIRIC IV ANTIBIOTIC THERAPY FOR or doxycycline if patient has inflammatory mass HOSPITALIZED PATIENTS: severe beta-lactam allergy Preferred: Vancomycin* IV (see nomogram, AUC goal 400-600) Clinical Setting Empiric Therapy Duration Comments EMPIRIC IV ANTIBIOTIC THERAPY FOR HOSPITALIZED PATIENTS: Preferred: Cefazolin*2 g IV q8h Alternative for patients with life- threatening penicillin allergy (in patients with or without risk for MRSA) Clindamycin 600 mg IV q8h Non-Purulent Cellulitis Alternative for patients at risk for MRSA non-purulent cellulitis: (Absence of purulent Vancomycin* IV (see nomogram, AUC drainage or exudate, goal 400-600) if MRSA coverage is • Blood cultures and cultures from ulceration, and no indicated 5 days for purulent SSTI are recommended associated abscess) patients with for patients with fever, rapidly Patients at risk for MRSA: rapid clinical progressive cellulitis, or signs of Empiric therapy for • Cellulitis worse on >48 hours of IV response. systemic illness β-hemolytic β-lactam therapy streptococcus is • Known MRSA colonization Longer duration • Adjust antimicrobial therapy recommended. • Prior history of MRSA infection of therapy is based on culture results • Recent intravenous drug use indicated if If there is a concern • Severe sepsis or septic shock infection has • Consider initial aggressive dosing for necrotizing not improved of antibiotics if severe sepsis or fasciitis, please see EMPIRIC ORAL ANTIBIOTIC THERAPY FOR morbidly obese patient treatment OUTPATIENT THERAPY, OR ORAL STEP-DOWN recommendations THERAPY: listed under that Preferred section Cephalexin* 500 mg PO QID or 1000 mg PO TID + TMP-SMZ* 1-2 DS BID to cephalexin, if patient presents with risk factors for MRSA (listed above) ALTERNATIVE FOR PATIENTS WITH LIFE- THREATENING PENICILLIN ALLERGY (IN PATIENTS WITH OR WITHOUT RISK FOR MRSA): Clindamycin 450 mg PO TID Page 2 of 10 Clinical Setting Empiric Therapy Duration Comments EMPIRIC IV ANTIBIOTIC THERAPY FOR • Blood cultures and cultures from HOSPITALIZED PATIENTS: purulent SSTI are recommended Preferred: for patients with fever, rapidly Purulent Cellulitis Vancomycin* IV (see nomogram, AUC progressive cellulitis, or signs of goal 400-600) systemic illness (Purulent drainage or exudate without Alternative for vancomycin, if 5-10 days • Staphylococcus aureus resistance a drainable abscess) documented allergy or intolerance: rates are lowest for TMP-SMX Linezolid** 600 mg IV/PO BID Longer duration (3%) and doxycycline (4%), Empiric therapy for of therapy is compared to clindamycin (43%). CA-MRSA is EMPIRIC ORAL ANTIBIOTIC THERAPY FOR indicated if recommended OUTPATIENT THERAPY, OR ORAL STEP-DOWN infection has • Empiric therapy should target THERAPY: not improved MRSA until susceptibilities are Therapy for β- Preferred: known, and then therapy should hemolytic TMP-SMX* 1-2 DS tabs PO BID be tailored. For patients with streptococci is likely MSSA, preferred oral step-down to be unnecessary Alternative: therapy is cephalexin, or TMP- Doxycycline 200 mg x1, then 100 mg SMX or doxycycline if patient has PO BID severe beta-lactam allergy Page 3 of 10 Clinical Setting Empiric Therapy Duration Comments PREFERRED: Piperacillin-tazobactam* 4.5 g IV q6h + Clindamycin 900 mg IV q8h + Vancomycin* (see nomogram, AUC • Emergent surgical and infectious goal 400-600) disease consultation is Necrotizing Fasciitis Optimal recommended duration is ALTERNATIVE FOR PATIENTS WITH PENICILLIN Early and aggressive unknown but ALLERGY: • Clindamycin is initiated for anti- surgical exploration should be Mild Allergy- Rash: toxin activity for Streptococcal and debridement is continued for a Cefepime* 2 g IV q8h and Staphylococcal infections, critical minimum of 2-3 + Clindamycin 900 mg IV q8h and could be discontinued after 1- days after + Vancomycin* (see nomogram, 3 days if infection has improved Emergent surgical completion of AUC goal 400-600) and patient is stable (assuming consultation is surgical another antibiotic with anti- recommended debridement Anaphylaxis: anaerobic activity is also Aztreonam* 2 g IV q8h administered). + Clindamycin 900 mg IV q8h + Vancomycin* (see nomogram, AUC goal 400-600) Page 4 of 10 Clinical Setting Empiric Therapy Duration Comments All systemic antimicrobial therapy should be used in combination with opening the incision and evacuation of infected material PREFERRED EMPIRIC INPATIENT THERAPY FOR Superficial Surgical SUPERFICIAL SSI, WITHOUT RISK FOR MRSA OR • Risk factors for MRSA include: Site Infections GNR (SEE BELOW): o nasal colonization Cefazolin* 2 g IV q8h o prior MRSA infection Infections involving OR o recent hospitalization the subcutaneous Cephalexin 500 mg PO QID or 1000 mg o recent antibiotics tissue within 30 days PO TID for mild-moderate infection, or of operation oral step-down therapy • Adjunctive systemic antimicrobial therapy is not routinely For SSI involving ALTERNATIVE EMPIRIC INPATIENT THERAPY FOR recommended unless associated deep tissue or organ PATIENTS WITH HIGH RISK OF MRSA OR with significant systemic response space or PCN/CEPHALOSPORIN ALLERGY: complicated by Vancomycin* IV (see nomogram, AUC • Indications for systemic sepsis/septic shock, goal 400-600) antimicrobials include: erythema 5 -7 days see below or organ and induration extending >5 cm specific guidelines EMPIRIC INPATIENT THERAPY FOR PATIENTS WITH Therapy may from wound edge, fever >38.5°C, (Intra-abdominal, HIGH RISK OF MRSA AND VANCOMYCIN ALLERGY need to be HR >110 beats/minute, WBC (NOT VANCOMYCIN INFUSION REACTION): Gynecology, extended based >12,000 Linezolid** 600 mg IV/PO q12h Meningitis, on severity of OR • Antibiotics should be adjusted Endocarditis, Bone infection and TMP-SMX* 1-2 DS tabs PO BID for mild- based on Gram stain, cultures and and Joint) response to moderate infection, or oral step-down sensitivities obtained from I&D treatment Suture removal plus therapy • Wound infection and systemic incision and EMPIRIC THERAPY FOR PATIENTS WITH SUPERFICIAL illness in the first 4 days drainage should be SSI FOLLOWING OPERATIONS OF THE AXILLA, (especially the first 48 hours) performed GASTROINTESTINAL TRACT, PERINEUM, OR FEMALE should prompt close wound If there is a concern GENITAL TRACT: examination for evidence of for necrotizing Cefazolin* 2 g IV q8h streptococcal or clostridial fasciitis, please refer + Metronidazole 500 mg PO/IV q8h necrotizing infection. See + Vancomycin* IV (see nomogram, AUC to that section necrotizing fasciitis section if goal 400-600), if risk for MRSA concern exists. OR Amoxicillin-clavulanate 875 mg PO BID • Consider initial aggressive dosing for mild-moderate infection, or oral of antibiotics in morbidly obese step-down therapy patient CEPHALOSPORIN/PCN ANAPHYLAXIS: Aztreonam* 2 g IV q8h + Metronidazole 500 mg PO/IV q8h + Vancomycin* IV (see nomogram, AUC goal 400-600) Page 5 of 10 Clinical Setting Empiric Therapy Duration Comments Deep tissue Surgical All systemic antimicrobial therapy should Site Infections or be used in combination with opening the any SSI complicated incision and evacuation of infected by sepsis/septic material shock EMPIRIC INPATIENT THERAPY FOR DEEP TISSUE SSI Infections involving OR COMPLICATED BY SEPSIS/SEPTIC SHOCK: the deep fascia or Piperacillin-tazobactam* 4.5 g IV q6h muscle within 30 7-10 days + Vancomycin* IV (see nomogram, AUC days of operation goal 400-600) Therapy may For SSI with organ need to be ALTERNATIVE WITH PCN ALLERGY WITHOUT space involvement, extended • Consider initial aggressive dosing of ANAPHYLAXIS, ANGIOEDEMA OR URTICARIA: see specific based on antibiotics if severe sepsis or Cefepime* 2 g IV q8h guidelines for Intra- severity of morbidly obese patient + Vancomycin* IV (see nomogram, AUC abdominal, goal 400-600) infection and Gynecologic, response to Meningitis,
Recommended publications
  • Abscess Prevention
    ABSCESS PREVENTION ▪ Chest pains may occur if infection How do you soak/use Avoiding abscesses goes to heart or lungs compresses? • Wash your hands and the injection site. What should I do if I get ▪ Use warm/hot water (that doesn’t burn your skin) • Use alcohol pads and wipe an abscess? ▪ Soak in tub of plain hot water or hot back & forth (rub hard) over ▪ Treat at home with warm soaks water with Epsom salts injection site to remove dirt. only if: ▪ Use hot, wet, clean washcloth and - No red streaks hold on abscess, if abscess cannot • Then use another new alcohol - Skin not hot and puffy be soaked in tub pad for the final cleaning. ▪ Soak abscess 3 to 4 times a day for ▪ Go to a clinic if abscess: 10-15 minutes each time, if possible What is a skin abscess? - Not improving, especially ▪ Cover with a clean dry bandage after after 5-7 days soaking ▪ Pocket of pus - Gets bigger and/or very ▪ soaking/using compresses ▪ Often found at injection sites, but STOP painful when abscess starts draining can be found elsewhere - Is hot and puffy ▪ More likely with Red streaks start spreading skin-popping from the abscess-go ASAP! muscling What about missing a vein ▪ Go to emergency room if: ▪ May occur even after you stop Chest pain antibiotics? injecting High fever, chills ▪ Take all antibiotics, if Infection looks like it is How do you know it’s an spreading fast prescribed, even if you feel better abscess? ▪ Take antibiotics after you fix (if ▪ using heroin) ▪ Pink or reddish lump on skin ▪ Do not take antibiotics with ▪ Tender or painful Warning
    [Show full text]
  • Coexistence of Antibodies to Tick-Borne
    Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 98(3): 311-318, April 2003 311 Coexistence of Antibodies to Tick-borne Agents of Babesiosis and Lyme Borreliosis in Patients from Cotia County, State of São Paulo, Brazil Natalino Hajime Yoshinari/+, Milena Garcia Abrão, Virginia Lúcia Nazário Bonoldi, Cleber Oliveira Soares*, Claudio Roberto Madruga*, Alessandra Scofield**, Carlos Luis Massard**, Adivaldo Henrique da Fonseca** Laboratório de Investigação em Reumatologia (LIM-17), Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, Av. Dr. Arnaldo 455, 3º andar, 01246-903 São Paulo, SP, Brasil *Embrapa Gado de Corte, Campo Grande, MS, Brasil **Universidade Federal Rural do Rio de Janeiro, Seropédica, RJ, Brasil This paper reports a case of coinfection caused by pathogens of Lyme disease and babesiosis in brothers. This was the first case of borreliosis in Brazil, acquired in Cotia County, State of São Paulo, Brazil. Both children had tick bite history, presented erythema migrans, fever, arthralgia, mialgia, and developed positive serology (ELISA and Western-blotting) directed to Borrelia burgdorferi G 39/40 and Babesia bovis antigens, mainly of IgM class antibodies, suggestive of acute disease. Also, high frequencies of antibodies to B. bovis was observed in a group of 59 Brazilian patients with Lyme borreliosis (25.4%), when compared with that obtained in a normal control group (10.2%) (chi-square = 5.6; p < 0.05). Interestingly, both children presented the highest titers for IgM antibodies directed to both infective diseases, among all patients with Lyme borreliosis. Key words: lyme borreliosis - lyme disease - spirochetosis - borreliosis - babesiosis - coinfection - tick-borne disease - Brazil Babesiosis is a tick-borne disease distributed world- The first case of babesiosis in a healthy person, with wide, caused by hemoprotozoans of the genus Babesia, intact spleen, was reported in 1969 in a woman from Nan- which infects wild and domestic animals, promoting eco- tucket Island (Massachusetts, USA)(Wester et al.
    [Show full text]
  • Bacterial Infections Diseases Picture Cause Basic Lesion
    page: 117 Chapter 6: alphabetical Bacterial infections diseases picture cause basic lesion search contents print last screen viewed back next Bacterial infections diseases Impetigo page: 118 6.1 Impetigo alphabetical Bullous impetigo Bullae with cloudy contents, often surrounded by an erythematous halo. These bullae rupture easily picture and are rapidly replaced by extensive crusty patches. Bullous impetigo is classically caused by Staphylococcus aureus. cause basic lesion Basic Lesions: Bullae; Crusts Causes: Infection search contents print last screen viewed back next Bacterial infections diseases Impetigo page: 119 alphabetical Non-bullous impetigo Erythematous patches covered by a yellowish crust. Lesions are most frequently around the mouth. picture Lesions around the nose are very characteristic and require prolonged treatment. ß-Haemolytic streptococcus is cause most frequently found in this type of impetigo. basic lesion Basic Lesions: Erythematous Macule; Crusts Causes: Infection search contents print last screen viewed back next Bacterial infections diseases Ecthyma page: 120 6.2 Ecthyma alphabetical Slow and gradually deepening ulceration surmounted by a thick crust. The usual site of ecthyma are the legs. After healing there is a permanent scar. The pathogen is picture often a streptococcus. Ecthyma is very common in tropical countries. cause basic lesion Basic Lesions: Crusts; Ulcers Causes: Infection search contents print last screen viewed back next Bacterial infections diseases Folliculitis page: 121 6.3 Folliculitis
    [Show full text]
  • Intravenous Iron Replacement Therapy (Feraheme®, Injectafer®, & Monoferric®)
    UnitedHealthcare® Commercial Medical Benefit Drug Policy Intravenous Iron Replacement Therapy (Feraheme®, Injectafer®, & Monoferric®) Policy Number: 2021D0088F Effective Date: July 1, 2021 Instructions for Use Table of Contents Page Community Plan Policy Coverage Rationale ....................................................................... 1 • Intravenous Iron Replacement Therapy (Feraheme®, Definitions ...................................................................................... 3 Injectafer®, & Monoferric®) Applicable Codes .......................................................................... 3 Background.................................................................................... 4 Benefit Considerations .................................................................. 4 Clinical Evidence ........................................................................... 5 U.S. Food and Drug Administration ............................................. 7 Centers for Medicare and Medicaid Services ............................. 8 References ..................................................................................... 8 Policy History/Revision Information ............................................. 9 Instructions for Use ....................................................................... 9 Coverage Rationale See Benefit Considerations This policy refers to the following intravenous iron replacements: Feraheme® (ferumoxytol) Injectafer® (ferric carboxymaltose) Monoferric® (ferric derisomaltose)* The following
    [Show full text]
  • Study Guide Medical Terminology by Thea Liza Batan About the Author
    Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails ­proficiency­in­communicating­with­healthcare­professionals­such­as­physicians,­nurses,­ or dentists.
    [Show full text]
  • Abscesses Are a Serious Problem for People Who Shoot Drugs
    Where to Get Your Abscess Seen Abscesses are a serious problem for people who shoot drugs. But what the hell are they and where can you go for care? What are abscesses? Abscesses are pockets of bacteria and pus underneath you skin and occasionally in your muscle. Your body creates a wall around the bacteria in order to keep the bacteria from infecting your whole body. Another name for an abscess is a “soft tissues infection”. What are bacteria? Bacteria are microscopic organisms. Bacteria are everywhere in our environment and a few kinds cause infections and disease. The main bacteria that cause abscesses are: staphylococcus (staff-lo-coc-us) aureus (or-e-us). How can you tell when you have an abscess? Because they are pockets of infection abscesses cause swollen lumps under the skin which are often red (or in darker skinned people darker than the surrounding skin) warm to the touch and painful (often VERY painful). What is the worst thing that can happen? The worst thing that can happen with abscesses is that they can burst under your skin and cause a general infection of your whole body or blood. An all over bacterial infection can kill you. Another super bad thing that can happen is a endocarditis, which is an infection of the lining of your heart, and “septic embolism”, which means that a lump of the contaminates in your abscess get loose in your body and lodge in your lungs or brain. Why do abscesses happen? Abscesses are caused when bad bacteria come in to contact with healthy flesh.
    [Show full text]
  • Intra-Abdominal Ventriculoperitoneal Shunt Abscess from Streptococcus Pyogenes After Pharyngitis with Scarlet Fever
    NEURO ISSN 2377-1607 http://dx.doi.org/10.17140/NOJ-1-107 Open Journal Case Report Intra-Abdominal Ventriculoperitoneal Shunt *Corresponding author Abscess from Streptococcus Pyogenes Edward A. Monaco 3rd, MD, PhD Assistant Professor after Pharyngitis with Scarlet Fever: Case Department of Neurological Surgery University of Pittsburgh Medical Center, Suite F158, 200 Lothrop Report and Review of the Literature Street, Pittsburgh, PA 15213, USA Tel. 412-647-6777 Stephanie H. Chen and Edward A. Monaco 3rd* Fax: 412-647-6483 E-mail: [email protected] Department of Neurological Surgery, University of Pittsburgh Medical Center, Suite F158, 200 Lothrop Street, Pittsburgh, PA 15213, USA Volume 1 : Issue 1 Article Ref. #: 1000NOJ1107 ABSTRACT Article History Received: November 13th, 2014 Objective: Infection is one of the most frequent complications of ventriculoperitoneal shunts. th Accepted: December 15 , 2014 However, Streptococcus pyogenes (Group A Streptococcus, GAS) as a causative agent appears th Published: December 16 , 2014 to be extremely rare. We present an unusual case of a peritoneal shunt infection due to GAS that occurred after pharyngitis with scarlet fever. Case Description: A 31 year-old woman with congenital shunt-dependent hydrocephalus pre- Citation sented with fever, vomiting, and acute abdominal symptoms several weeks after being treated Chen SH, Monaco EA 3rd. Intra-ab- dominal ventriculoperitoneal shunt for pharyngitis and scarlet fever. She was found to have a large intra-abdominal peritoneal abscess from Streptococcus pyo- catheter-associated abscess that grew out GAS. genes after pharyngitis with scarlet Results: The patient’s shunt was externalized at the clavicle and the cerebrospinal fluid (CSF) fever: Case report and review of the was sterile.
    [Show full text]
  • Strep Throat and Scarlet Fever N
    n Strep Throat and Scarlet Fever n After a few days, the rash begins to fade. The skin usually Strep throat is caused by infection with the bac- begins to peel, as it often does after a sunburn. teria Streptococcus. In addition to sore throat, swollen glands, and other symptoms, some chil- What are some possible dren develop a rash. When this rash is present, the infection is called scarlet fever. If your child complications of scarlet fever? has a strep infection, he or she will need antibio- Strep infection has some potentially serious complica- tics to treat it and to prevent rheumatic fever, tions. With proper treatment, most of these can be pre- which can be serious. vented. Complications include: Strep infection may cause an abscess (localized area of pus) in the throat. What are strep throat and scarlet Rheumatic fever. This disease develops a few weeks after fever? the original strep infection. It is felt to be caused by our immune system. It can be serious and can cause fever, heart Most sore throats are caused by virus, but strep throat is inflammation, arthritis, and other symptoms. Your child caused by the bacteria Group A Strepococcus. Treatment can be left with heart problems called rheumatic disease. of this infection with antibiotics may help your child feel Rheumatic fever is uncommon now and can be prevented better and prevent rheumatic fever. by treating the strep infection properly with antibiotics. Some children with strep throat or strep infections else- where may develop a rash. When that occurs, the infection Acute glomerulonephritis.
    [Show full text]
  • Mir-205: a Potential Biomedicine for Cancer Therapy
    cells Review miR-205: A Potential Biomedicine for Cancer Therapy Neeraj Chauhan 1,2 , Anupam Dhasmana 1,2, Meena Jaggi 1,2, Subhash C. Chauhan 1,2 and Murali M. Yallapu 1,2,* 1 Department of Immunology and Microbiology, School of Medicine, University of Texas Rio Grande Valley, McAllen, TX 78504, USA; [email protected] (N.C.); [email protected] (A.D.); [email protected] (M.J.); [email protected] (S.C.C.) 2 South Texas Center of Excellence in Cancer Research, School of Medicine, University of Texas Rio Grande Valley, McAllen, TX 78504, USA * Correspondence: [email protected]; Tel.: +1-(956)-296-1734 Received: 3 June 2020; Accepted: 21 August 2020; Published: 25 August 2020 Abstract: microRNAs (miRNAs) are a class of small non-coding RNAs that regulate the expression of their target mRNAs post transcriptionally. miRNAs are known to regulate not just a gene but the whole gene network (signaling pathways). Accumulating evidence(s) suggests that miRNAs can work either as oncogenes or tumor suppressors, but some miRNAs have a dual nature since they can act as both. miRNA 205 (miR-205) is one such highly conserved miRNA that can act as both, oncomiRNA and tumor suppressor. However, most reports confirm its emerging role as a tumor suppressor in many cancers. This review focuses on the downregulated expression of miR-205 and discusses its dysregulation in breast, prostate, skin, liver, gliomas, pancreatic, colorectal and renal cancers. This review also confers its role in tumor initiation, progression, cell proliferation, epithelial to mesenchymal transition, and tumor metastasis.
    [Show full text]
  • A Case of Severe Human Granulocytic Anaplasmosis in an Immunocompromised Pregnant Patient
    Elmer ress Case Report J Med Cases. 2015;6(6):282-284 A Case of Severe Human Granulocytic Anaplasmosis in an Immunocompromised Pregnant Patient Marijo Aguileraa, c, Anne Marie Furusethb, Lauren Giacobbea, Katherine Jacobsa, Kirk Ramina Abstract festations include respiratory or neurologic involvement, acute renal failure, invasive opportunistic infections and a shock- Human granulocytic anaplasmosis (HGA) is a tick-borne disease that like illness [2-4]. Recent delineation of the various species can often result in persistent fevers and other non-specific symptoms associated with ehrlichia infections and an increased under- including myalgias, headache, and malaise. The incidence among en- standing of the epidemiology has augmented our knowledge of demic areas has been increasing, and clinician recognition of disease these tick-borne diseases. However, a detailed understanding symptoms has aided in the correct diagnosis and treatment of patients of HGA infections in both immunocompromised and pregnant who have been exposed. While there have been few cases reported of patients is limited. We report a case of a severe HGA infection HGA disease during pregnancy, all patients have undergone a rela- presenting as an acute exacerbation of Crohn’s disease in a tively mild disease course without complications. HGA may cause pregnant immunocompromised patient. more severe disease in the elderly and immunocompromised. Herein, we report an unusual presentation and severe disease complications of HGA in a pregnant female who was concomitantly immunocompro- Case Report mised due to azathioprine treatment of her Crohn’s disease. Follow- ing successful treatment with rifampin, she subsequently delivered a A 34-year-old primigravida at 17+2 weeks’ gestation presented healthy female infant without any disease sequelae.
    [Show full text]
  • Allied Health Professionals Consumer Fact Sheet Board of Registration of Allied Health Professionals
    Allied Health Professionals Consumer Fact Sheet Board of Registration of Allied Health Professionals The Board of Registration in Allied Health evaluates the qualifications of applicants for licensure and grants licenses to those who qualify. It establishes rules and regulations to ensure the integrity and competence of licensees. The Board is the link between the consumer and the allied health professional and, as such, promotes the public health, welfare and safety. Allied health professionals are occupational therapists and assistants, athletic trainers, and physical therapists and assistants. Occupational Therapists/Occupational Therapist Assistants Occupational therapists are health professionals who use occupational activities with specific goals in helping people of all ages to prevent, lessen or overcome physical, psychological or developmental disabilities. Occupational Therapists and Occupational Therapist Assistants help people with physical, psychological, or developmental problems regain abilities or adjust to handicaps. They work with physicians, physical and speech therapists, nurses, social workers, psychologists, teachers and other specialists. Patients may face handicaps, injuries, illness, psychological or social problems, or barriers due to age, economic, and cultural factors. Occupational Therapists: Consult with treatment teams to develop individualized treatment programs. Select and teach activities based on the needs and capabilities of each patient Evaluate each patient's progress, attitude and behavior. Design special equipment to aid patients with disabilities. Teach patients how to adjust to home, work, and social environments. Test and evaluate patients' physical and mental abilities. Educate others about occupational therapy. The goal of occupational therapy (OT) is for persons to achieve the highest level of independence after an injury or illness. OT addresses the whole person - cognitive, physical and emotional status.
    [Show full text]
  • Skin Disease and Disorders
    Sports Dermatology Robert Kiningham, MD, FACSM Department of Family Medicine University of Michigan Health System Disclosures/Conflicts of Interest ◼ None Goals and Objectives ◼ Review skin infections common in athletes ◼ Establish a logical treatment approach to skin infections ◼ Discuss ways to decrease the risk of athlete’s acquiring and spreading skin infections ◼ Discuss disqualification and return-to-play criteria for athletes with skin infections ◼ Recognize and treat non-infectious skin conditions in athletes Skin Infections in Athletes ◼ Bacterial ◼ Herpetic ◼ Fungal Skin Infections in Athletes ◼ Very common – most common cause of practice-loss time in wrestlers ◼ Athletes are susceptible because: – Prone to skin breakdown (abrasions, cuts) – Warm, moist environment – Close contacts Cases 1 -3 ◼ 21 year old male football player with 4 day h/o left axillary pain and tenderness. Two days ago he noticed a tender “bump” that is getting bigger and more tender. ◼ 16 year old football player with 3 day h/o mildly tender lesions on chin. Started as a single lesion, but now has “spread”. Over the past day the lesions have developed a dark yellowish crust. ◼ 19 year old wrestler with a 3 day h/o lesions on right side of face. Noticed “tingling” 4 days ago, small fluid filled lesions then appeared that have now started to crust over. Skin Infections Bacterial Skin Infections ◼ Cellulitis ◼ Erysipelas ◼ Impetigo ◼ Furunculosis ◼ Folliculitis ◼ Paronychea Cellulitis Cellulitis ◼ Diffuse infection of connective tissue with severe inflammation of dermal and subcutaneous layers of the skin – Triad of erythema, edema, and warmth in the absence of underlying foci ◼ S. aureus or S. pyogenes Erysipelas Erysipelas ◼ Superficial infection of the dermis ◼ Distinguished from cellulitis by the intracutaneous edema that produces palpable margins of the skin.
    [Show full text]