
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Suppurative thrombophlebitis medical therapy
Introduction
Overview
Overview
The mainstay of therapy for suppurative thrombophlebitis is antimicrobial therapy. Empiric therapy includes anti-staphylococcal antibiotics plus antibiotics with coverage against enterobacteriaceae. The benefit of pharmacologic anticoagulation is uncertain in suppurative thrombophlebitis and is not routinely recommended.
Medical Therapy
Medical Therapy
- The mainstay of therapy for suppurative thrombophlebitis is a prolonged course of targeted antibiotic therapy.
- Duration of therapy is at least 4 weeks for all cases regardless of the causative organism. Patients may need 6 weeks of therapy to clear the infection.
- Any long-term catheters should be removed from patients with suppurative thrombophlebitis. It is recommended that no long-term catheters are inserted before clearing of blood cultures.
- All recommendations are based on observational data. There is no randomized data to determine the optimal duration of antibiotics, use of anticoagulants, thrombolytic agents, or excision of the involved vessel.
- The use of anticoagulants remains controversial, but anticoagulation with heparin should be considered in refractory cases.[1]
Antimicrobial Regimens
- Treatment of suppurative thrombophlebitis[1]
- 1. Bacterial pathogens
- 1.1 Gram-positive bacilli
- 1.1.1 Staphylococcus aureus
- 1.1.1.1 Methicillin-sensitive
- Preferred regimen: Nafcillin 2 g IV q4h OR Oxacillin 2 g IV q4h
- Alternative regimen: Cefazolin 2 g IV q8h OR Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- 1.1.1.2 Methicillin-resistant
- Preferred regimen: Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- Alternative regimen (1): Daptomycin 6-8 mg/kg/day IV q24h OR Linezolid 600 mg IV q12h
- Alternative regimen (2): Trimethoprim-sulfamethoxazole 3–5 mg/kg PO/IV q8h
- 1.1.2 Coagulase-negative staphylococci
- 1.1.2.1 Methicillin-sensitive
- Preferred regimen: Nafcillin 2 g IV q4h OR Oxacillin 2 g IV q4h
- Alternative regimen: Cefazolin 2 g IV q8h OR Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- 1.1.2.2 Methicillin-resistant
- Preferred regimen: Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- Alternative regimen: Daptomycin 6-8 mg/kg/day IV q24h OR Linezolid 600 mg IV q12h OR Quinupristin/Dalfopristin 7.5 mg/kg IV q8h
- Note: Linezolid-resistant strains have been reported
- 1.1.3 Enterococcus faecalis & Enterococcus faecium
- 1.1.3.1 Ampicillin-sensitive
- Preferred regimen: Ampicillin 2 g IV q4-6h ± Gentamicin 1 mg/kg IV q8h
- Alternative regimen: Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- 1.1.3.2 Ampicillin-resistant & Vancomycin-sensitive
- Preferred regimen: Ampicillin 2 g IV q4-6h AND Gentamicin 1 mg/kg IV q8h
- Alternative regimen: Daptomycin 6-8 mg/kg/day IV q24h OR Linezolid 600 mg IV q12h
- 1.1.3.3 Ampicillin-resistant & Vancomycin-resistant
- Preferred regimen: Daptomycin 6-8 mg/kg/day IV q24h OR Linezolid 600 mg IV q12h
- Alternative regimen: Quinupristin/Dalfopristin 7.5 mg/kg IV q8h
- Note: Quinupristin/Dalfopristin is not effective against E. faecalis
- 1.2 Gram-negative bacilli
- 1.2.1 Escherichia coli & Klebsiella spp.
- 1.2.1.1 ESBL negative
- Preferred regimen: Ceftriaxone 1-2 g IV q24h
- Alternative regimen: Ciprofloxacin 400 mg IV q8-12h OR Aztreonam 1-2 g IV q6-12h (maximum dose 8 g/day)
- 1.2.1.2 ESBL positive
- 1.2.2 Enterobacter spp. & Serratia marcescens
- Preferred regimen: Ertapenem 1 g IV/IM q24h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h
- Alternative regimen: Cefepime 1-2 g IV q8-12h OR Ciprofloxacin 400 mg IV q8-12h
- 1.2.3 Acinetobacter spp.
- Preferred regimen: Ampicillin-Sulbactam 1.5-3 g IV/IM q6h OR Ertapenem 1 g IV/IM q24h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h OR Doripenem 500 mg IV q8h
- 1.2.4 Stenotrophomonas maltophilia
- Preferred regimen: Trimethoprim-Sulfamethoxazole 3–5 mg/kg PO/IV q8h
- Alternative regimen: Ticarcillin-Clavulanate 3.1 g IV q4-6h
- 1.2.5 Pseudomonas aeruginosa
- Preferred regimen: Cefepime 1-2 g IV q8-12h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h OR Amikacin 15 mg/kg IV q24h or Tobramycin 5–7 mg/kg IV q24h
- 1.2.6 Burkholderia cepacia
- Preferred regimen: Trimethoprim-Sulfamethoxazole 3–5 mg/kg PO/IV q8h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h
- 2. Fungal pathogens
- 2.1 Candida spp.
- Preferred regimen (1): Caspofungin 70 mg IV single dose THEN 50 mg IV q24h
- Preferred regimen (2): Micafungin 100 mg IV q24h
- Preferred regimen (3): Anidulafungin 200 mg IV single dose THEN 100 mg IV q24h
- Preferred regimen (4): Fluconazole 400–600 mg IV q24h
- Alternative regimen: Amphotericin B, Liposomal 3-5 mg/kg IV q24h
- 3. Uncommon pathogens
- 3.1 Corynebacterium jeikeium
- Preferred regimen: Vancomycin 15 mg/kg q12h (trough levels 15-20 mcg/ml)
- Alternative regimen: Linezolid 600 mg IV q12h
- Note: No clinical studies available for Linezolid. Recommendation based on in vitro activity.
- 3.2 Chryseobacterium (Flavobacterium) spp.
- Preferred regimen: Levofloxacin 750 mg IV q24h
- Alternative regimen: Trimethoprim-Sulfamethoxazole 3–5 mg/kg PO/IV q8h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h
- 3.3 Ochrobacterium anthropi
- Preferred regimen: Trimethoprim-Sulfamethoxazole 3–5 mg/kg PO/IV q8h OR Ciprofloxacin 400 mg IV q8-12h
- Alternative regimen: (Ertapenem 1 g IV/IM q24h OR Imipenem 500 mg IV q6h OR Meropenem 1 g IV q8h OR Doripenem 500 mg IV q8h) AND Gentamicin 1 mg/kg IV q8h
- 3.4 Malassezia furfur
- Preferred regimen: Amphotericin B, Liposomal 3-5 mg/kg IV q24h
- Alternative regimen: Voriconazole 6 mg/kg IV q12h for first 24h THEN 4 mg/kg IV q12h
References
References
- ↑ 1.0 1.1 Mermel LA, Allon M, Bouza E, Craven DE, Flynn P, O’Grady NP; et al. (2009). “Clinical practice guidelines for the diagnosis and management of intravascular catheter-related infection: 2009 Update by the Infectious Diseases Society of America”. Clin Infect Dis. 49 (1): 1–45. doi:10.1086/599376. PMC 4039170. PMID 19489710.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
