Empyema medical therapy: Difference between revisions

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**** It should be noted, however, that the patients in Wait’s study had fibrinopurulent empyema, and not simple parapneumonic effusions or chronic empyema.
**** It should be noted, however, that the patients in Wait’s study had fibrinopurulent empyema, and not simple parapneumonic effusions or chronic empyema.
** Obviously, the definitive answer is still out on the optimal management of empyema, however, the above data may indicate a more aggressive approach in these patients.
** Obviously, the definitive answer is still out on the optimal management of empyema, however, the above data may indicate a more aggressive approach in these patients.
 
====Antibiotics====
*'''Empyema'''<ref>{{cite book | last = LastName | first = FirstName | title = Sanford guide to antimicrobial therapy | publisher = Antimicrobial Therapy | location = Place of publication not identified | year = 2007 | isbn = 9781930808386 }}</ref>
:* 1. '''Empiric antimicrobial therapy or culture negative therapy'''
:::*Causative pathogens:
::::*Streptococcus milleri
::::*Streptococcus pneumoniae
::::*Streptococcus intermedius
::::*Staphylococcus aureus
::::*Enterobacteriaceae
::::*Escherichia coli
::::*Fusobacterium spp.
::::*Bacteroides spp.
::::*Peptostreptococcus spp.
:::* Preferred regimen (1): [[Cefuroxime]] 1.5 g IV q8h {{and}} [[Metronidazole]] 500 mg IV q8h
:::* Preferred regimen (2): [[Ceftriaxone]] 1.5 g IV q8h {{and}} [[Metronidazole]] 500 mg IV q8h
:::* Preferred regimen (3): [[Piperacillin-Tazobactam]] 3.375 g IV q4h {{or}} [[Ticarcillin-clavulanate]] 3.1 g IV q4h {{or}} [[Ampicillin-Sulbactam]] 2/1 g IV q6h
:::* Preferred regimen (4): [[Meropenem]] 1 g IV q8h {{or}} [[Imipenem]] 500 mg IV q6h
:::* Note: Consider coverage for MRSA if high suspicion exists.
:* 2. '''Pathogen-based therapy'''
::* 2.1 '''Acute empyema'''
:::* 2.1.1 '''Streptococcus pneumoniae, Group A streptrococcus  '''
::::* Preferred regimen: [[Ceftriaxone]] 1.5 g IV/IM q24h
:::* 2.1.2 '''Staphylococcus aureus'''
::::* 2.1.2.1 '''MSSA'''
:::::* Preferred regimen: [[Nafcillin]] 2 g IV q4h {{or}} [[Oxacillin]] 2 g IV q4h
::::* 2.1.2.2 '''MRSA'''
:::::* Preferred regimen: [[Vancomycin]] 1 g IV q12h {{or}} [[Linezolid]] 600 mg PO/IV q12h
:::* 2.1.3 '''Hemophilus influenzae'''
::::* Preferred regimen: [[Ceftriaxone]] 1.5 g IV/IM q24h
::::* Alternative regimen: [[Trimethoprim-Sulfamethoxazole]] 8-20 mg TMP/kg/day IV q6-12h or [[Ampicillin-Sulbactam]] 2/1 g IV q6h
::* 2.2 '''Subacute/chronic empyema'''
:::* 2.2.1 '''Anaerobic streptococcus, Streptococcus milleri, Bacteroides species, Enterobacteriaceae, Mycobacterium tuberculosis'''
::::* Preferred regimen: [[Clindamycin]] 450–900 mg IV q8h {{and}} [[Ceftriaxone]] 1.5 g IV/IM q24h
::::* Alternative regimen: [[Imipenem]] 500 mg IV q6h {{or}} [[Piperacillin-Tazobactam]] 3.375 g IV q4h {{or}} [[Ticarcillin-clavulanate]] 3.1 g IV q4h {{or}} [[Ampicillin-Sulbactam]] 2/1 g IV q6h
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 14:33, 12 August 2015

Empyema Microchapters

Patient Information

Overview

Classification

Subdural empyema
Pleural empyema

Differential Diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Medical Therapy

Pharmacotherapy

Acute Pharmacotherapies

  • Obviously, appropriate antibiotics are indicated in all patients with an underlying infection. Drainage of the pleural space should be considered early, as delay of even a few days is associated with an increase in morbidity and mortality.
    • Indications for chest tube drainage include: a pH < 7.0, glucose < 40-50, gross pus, or organisms on Gram’s stain.
      • In borderline cases, reassessment with a repeat tap should be preformed in 12 – 24 hours. If the LDH is increasing, and the pH and glucose are decreasing, a chest tube should be placed immediately.
      • The chest tube should be at least a 28 F (smaller tubes become obstructed with fibrin clot), and left in place until the drainage is clear and yellow, and its volume is < 50 cc/day.
      • Patients will get better within 24 – 48 hours. If they don’t, suspect inadequate drainage due to loculations or inappropriate antibiotics.
    • Thrombolytics (mainly urokinase and streptokinase) have been used to break up loculations and assist drainage.
      • The typical streptokinase (SK) dose is 250,000 units in 30 – 100 cc normal saline solution (NS), and the typical urokinase dose in 100,000 units, also in 30 – 60 cc NS. They are instilled via the chest tube, left in place for 1-4 hours (chest tube clamped), and repeated daily as needed.
        • Two randomized studies comparing SK to chest tube drainage alone have shown an increase in the amount of drainage, however a statistical difference in the resolution of white blood cell (WBC) count and fever, the need for surgical drainage, or the duration of hospitalization has not been demonstrated.
    • More recently, however, VATS (video-assisted thoracoscopic surgery) has been compared to treatment by treatment with SK and chest tube drainage (SK-CT) in randomized trials.
      • Wait et.al. studied 20 patients and found that VATS was associated with a significantly higher primary treatment success (91% vs. 44%), lower chest tube duration (6 days vs. 10 days) and a lower number of hospital days (9 vs. 13). VATS was also associated with a non-significant trend towards lower hospital costs.
        • They felt that SK-CT only delayed, and did not prevent definitive treatment with VATS.
        • It should be noted, however, that the patients in Wait’s study had fibrinopurulent empyema, and not simple parapneumonic effusions or chronic empyema.
    • Obviously, the definitive answer is still out on the optimal management of empyema, however, the above data may indicate a more aggressive approach in these patients.

Antibiotics

  • 1. Empiric antimicrobial therapy or culture negative therapy
  • Causative pathogens:
  • Streptococcus milleri
  • Streptococcus pneumoniae
  • Streptococcus intermedius
  • Staphylococcus aureus
  • Enterobacteriaceae
  • Escherichia coli
  • Fusobacterium spp.
  • Bacteroides spp.
  • Peptostreptococcus spp.
  • 2. Pathogen-based therapy
  • 2.1 Acute empyema
  • 2.1.1 Streptococcus pneumoniae, Group A streptrococcus
  • 2.1.2 Staphylococcus aureus
  • 2.1.2.1 MSSA
  • 2.1.2.2 MRSA
  • 2.1.3 Hemophilus influenzae
  • 2.2 Subacute/chronic empyema
  • 2.2.1 Anaerobic streptococcus, Streptococcus milleri, Bacteroides species, Enterobacteriaceae, Mycobacterium tuberculosis

References

  1. LastName, FirstName (2007). Sanford guide to antimicrobial therapy. Place of publication not identified: Antimicrobial Therapy. ISBN 9781930808386.