infeccion necrotizante de tejidos blandos

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    INFECCION NECROTIZANTE DE

    TEJIDOS BLANDOS

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    ANTECEDENTES

    Jones 1871 and were termed hospital

    gangrene.

    In 1951,Wilson coined the term necrotizing

    fasciitis.

    infections of any of the layers within the soft

    tissue compartment (dermis, subcutaneous

    tissue, superficial fascia, deep fascia, or

    muscle) that are associated with necrotizing

    changes.

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    ANTECEDENTES

    incidence of NSTI in the United States is

    estimated to be 5001500 cases per year.

    0.04 cases per 1000 person-years.

    Establishing the diagnosis of NSTI is probably

    the greatest challenge in managing these

    infections.

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    DIAGNOSTICO

    Delay of diagnosis leads to delayed surgical

    debridement, which leads to higher mortality.

    The first and most important tool for early

    diagnosis of NSTI is to have a high index of

    suspicion.

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    FACTORES DE RIESGO

    injection drug use

    chronic debilitating comorbidities (e.g.,

    diabetes mellitus, immune suppression, and

    obesity).

    most large published series

    show that, in 20% of patients with NSTI, theetiology is unknown, and the patients are

    considered to have idiopathic NSTI

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    We have also observed that cases of NSTI

    without a recognized precipitating factor are

    more likely to be caused by group A

    streptococcal and community-acquired

    methicillin-resistant staphylococcal infection.

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    Initial signs and symptoms swelling, erythema, pain,and tachycardia.

    once the infection progresses: tense edema outsidethe area of compromised skin, pain disproportionate to

    appearance, skin, discoloration (ecchymosis),blisters/bullae and necrosis, crepitus and/orsubcutaneous gas.

    Systemic findings include: fever, tachycardia,hypotension, and shock (sensitivity is low, 1040%.

    Progression of these signs and symptoms is usuallyrelatively fast, particularly if group A Streptococcus orClostridium species are involved.

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    Even in the most experienced hands, clinical

    findings are not accurate enough for

    diagnosis, and both clinical clues and

    diagnostic tools should be used in

    combination to help make an early diagnosis.

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    PRUEBAS DE LABORATORIO

    Wall et al. WBC count

    115,400 cells/mm3 or a

    serum sodium level 135

    mmol/L was associated

    with NSTI.

    NPV of 99%, but not very

    specific, PPV of only 26%.

    Wong et al.

    PPV of 92% and a NPV of

    96%.

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    ESTUDIOS DE IMAGEN

    Radiography: identify subcutaneous gas

    Ultrasonography: increased thickness of

    the fascial layer with or without enhancement MRI

    CT: deep abscesses

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    OTROS METODOS

    Biopsy specimen from the compromised site

    that includes deep fascia and possibly muscle.

    These findings include gray necrotic tissue,

    lack of bleeding, thrombosed vessels,

    dishwater pus, noncontracting muscle, and

    a positive finger test result, which is

    characterized by lack of resistance to fingerdissection in normally adherent tissues.

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    MICROBIOLOGIA

    A wide spectrum of

    organisms are

    commonly recovered.

    2/3polymicrobial; 1/3Monomicrobial. gram-

    positive cocci.

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    TRATAMIENTO

    source control, antimicrobial therapy, support,

    and monitoring.

    when treatment is only based on antimicrobial

    therapy and support, mortality approaches

    100%.

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    TRATAMIENTO

    Broad-spectrum antimicrobial therapy shouldbe started early to include coverage for gram-positive, gram-negative, and anaerobic

    organisms. Special consideration for group A Streptococcus

    and Clostridium species should be taken.

    Acceptable regimens include monotherapyagents, such as imipenem, meropenem,ertapenem, piperacillin/tazobactam andtigecycline.

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    TRATAMIENTO

    Multidrug regimens have also been described,including triple-drug therapy regimens, suchas high-dose penicillin, high-dose clindamycin,

    and a fluoroquinolone or an aminoglycosidefor coverage of gram-negative organisms.

    Vancomycin, daptomycin, or linezolid shouldbe included in the regimen until methicillin-resistant staphylococcal infection has beenexcluded.

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    MORTALIDAD

    Since the first description by Jones [1], mortality

    in patients with NSTI remains high. He reported a

    mortality rate of 46%, and a recent pooled

    analysis determined it to be34%. More recent series have reported mortality rates

    with a range of 16%24%a rate that, although

    lower than the rate 100 years ago, still accountsfor high mortality associated with NSTI