Cellulitis medical therapy: Difference between revisions
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==Overview== | ==Overview== | ||
Typically a combination of intravenous and oral [[antibiotics]] are administered for the treatment of [[cellulitis]]. Bed rest and elevation of the affected limbs are recommended to accompany the antibiotic treatment. In patients with [[edema]] of the extremities, compressive stockings may really aid in treating the fluid accumulation. Small [[abscess]] surrounding the affected tissue can be treated with a simple incision and drainage of the fluid. It is advised to drink plenty of fluids during your treatment and recovery. | Cellulitis is an acute spreading infection of the skin, characterized by spreading areas of edema, redness, and heat, sometimes accompanied by lymphangitis and inflammation of the regional lymph nodes. Typically a combination of intravenous and oral [[antibiotics]] are administered for the treatment of [[cellulitis]]. Bed rest and elevation of the affected limbs are recommended to accompany the antibiotic treatment. In patients with [[edema]] of the extremities, compressive stockings may really aid in treating the fluid accumulation. Small [[abscess]] surrounding the affected tissue can be treated with a simple incision and drainage of the fluid. It is advised to drink plenty of fluids during your treatment and recovery. | ||
==Non-Antibiotic Therapy== | ==Non-Antibiotic Therapy== | ||
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==Medical Therapy== | ==Medical Therapy== | ||
* Mostly the causative agent is streptococci (often group A, but also from other groups, such as B, C, or G) and rarely [[staphylococcus aureus]] that is associated with penetrating trauma, illicit drug use. | |||
* Cultures of needle aspirations from inflammed skin, blood or punch biopsies are variable and not useful in the setting of mild infection and hence performed in patients with systemic toxicity, underlying comorbidities ([[immunodeficiency]], [[diabetes]] etc) and special exposures (animal bites). | |||
* The antibiotic selection for treatment of [[cellulitis]] depends on whether the clinical presentation is purulent or nonpurulent, as purulent cellulitis is potentially attributable to [[staphylococcus aureus]], which should be empirically treated with Beta-lactam antibiotics.<ref name="pmid21208910">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= e18-55 | pmid=21208910 | doi=10.1093/cid/ciq146 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21208910 }} </ref> Latest reports suggest that this bacterium has acquired resistance ([[MRSA]]) and newer drugs are to be used to kill off the pathogen. Reports from the laboratory regarding the sensitivity of the pathogen is a key factor in deciding the therapy. | * The antibiotic selection for treatment of [[cellulitis]] depends on whether the clinical presentation is purulent or nonpurulent, as purulent cellulitis is potentially attributable to [[staphylococcus aureus]], which should be empirically treated with Beta-lactam antibiotics.<ref name="pmid21208910">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= e18-55 | pmid=21208910 | doi=10.1093/cid/ciq146 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21208910 }} </ref> Latest reports suggest that this bacterium has acquired resistance ([[MRSA]]) and newer drugs are to be used to kill off the pathogen. Reports from the laboratory regarding the sensitivity of the pathogen is a key factor in deciding the therapy. | ||
* Choice of the antibiotic therapy for [[cellulitis]] depends on the following factors: | |||
* Choice of the antibiotic therapy for [[cellulitis]] depends on the | |||
** Age of the individual: Early hospitalization and parenteral therapy are required for treatment of cellulitis in neonates, except for the mildest of cases. | ** Age of the individual: Early hospitalization and parenteral therapy are required for treatment of cellulitis in neonates, except for the mildest of cases. | ||
** Co-morbid conditions | ** Co-morbid conditions | ||
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** Pathogen involved (gram positive or negative and aerobic or anaerobic) | ** Pathogen involved (gram positive or negative and aerobic or anaerobic) | ||
** Strain and resistance of the pathogen | ** Strain and resistance of the pathogen | ||
* Parenteral therapy is indicated for severely ill patients or for those unable to tolerate oral medications. | |||
* The duration of antibiotic therapy in immunocompetent individuals is until 3 days after acute inflammation disappears. | * The duration of antibiotic therapy in immunocompetent individuals is until 3 days after acute inflammation disappears. | ||
===Uncomplicated Cellulitis=== | ===Uncomplicated Cellulitis=== | ||
* Simple infection without [[abscesses]] or drainage should be managed with empiric therapy for infection due to beta-hemolytic [[streptococci]] and [[methicillin]] sensitive [[staphylococcus aureus]] (MSSA). | * Simple infection without [[abscesses]] or drainage should be managed with empiric therapy for infection due to beta-hemolytic [[streptococci]] and [[methicillin]] sensitive [[staphylococcus aureus]] (MSSA). | ||
* Patients allergic to penicillin drugs can be given macrolide antibiotics like [[azithromycin]]. | * Patients allergic to penicillin drugs can be given macrolide antibiotics like [[azithromycin]]. | ||
* According to the 2011 [[clinical practice guideline]]s, if both [[methicillin resistant staphylococcus aureus]] and [[Streptococcus pyogenes]] are possible causes, then "options include the following: [[clindamycin]] alone (A-II) or [[TMP-SMX]] or a [[tetracycline]] in combination with a β-lactam (eg, [[amoxicillin]]) (A-II) or [[linezolid]] alone (A-II)."<ref name="pmid21217178">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= 285-92 | pmid=21217178 | doi=10.1093/cid/cir034 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21217178 }} </ref> [[MRSA]] is commonly the causative agent of cellulitis in cases presenting with abscesses.<ref name="pmid16914702">{{cite journal |author=Moran GJ, Krishnadasan A, Gorwitz RJ, ''et al.'' |title=Methicillin-resistant S. aureus infections among patients in the emergency department |journal=N. Engl. J. Med. |volume=355 |issue=7 |pages=666–74 |year=2006 |month=August |pmid=16914702 |doi=10.1056/NEJMoa055356 |url=}}</ref> In mild cases, treatment will be [[TMP-SMX]] with [[doxycycline]] and in severe cases, the most cost effective therapy will be [[vancomycin]].<ref name="pmid18462092">{{cite journal |author=Stryjewski ME, Chambers HF |title=Skin and soft-tissue infections caused by community-acquired methicillin-resistant Staphylococcus aureus |journal=Clin. Infect. Dis. |volume=46 Suppl 5 |issue= |pages=S368–77 |year=2008 |month=June |pmid=18462092 |doi=10.1086/533593 |url=}}</ref> | * According to the 2011 [[clinical practice guideline]]s, if both [[methicillin resistant staphylococcus aureus]] and [[Streptococcus pyogenes]] are possible causes, then "options include the following: [[clindamycin]] alone (A-II) or [[TMP-SMX]] or a [[tetracycline]] in combination with a β-lactam (eg, [[amoxicillin]]) (A-II) or [[linezolid]] alone (A-II)."<ref name="pmid21217178">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= 285-92 | pmid=21217178 | doi=10.1093/cid/cir034 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21217178 }} </ref> [[MRSA]] is commonly the causative agent of cellulitis in cases presenting with abscesses.<ref name="pmid16914702">{{cite journal |author=Moran GJ, Krishnadasan A, Gorwitz RJ, ''et al.'' |title=Methicillin-resistant S. aureus infections among patients in the emergency department |journal=N. Engl. J. Med. |volume=355 |issue=7 |pages=666–74 |year=2006 |month=August |pmid=16914702 |doi=10.1056/NEJMoa055356 |url=}}</ref> In mild cases, treatment will be [[TMP-SMX]] with [[doxycycline]] and in severe cases, the most cost effective therapy will be [[vancomycin]].<ref name="pmid18462092">{{cite journal |author=Stryjewski ME, Chambers HF |title=Skin and soft-tissue infections caused by community-acquired methicillin-resistant Staphylococcus aureus |journal=Clin. Infect. Dis. |volume=46 Suppl 5 |issue= |pages=S368–77 |year=2008 |month=June |pmid=18462092 |doi=10.1086/533593 |url=}}</ref> | ||
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===Severe Cellulitis=== | ===Severe Cellulitis=== | ||
* In severe cases of the disease, parenteral therapy is advocated. | * In severe cases of the disease, parenteral therapy is advocated. | ||
* | * Patients who do not respond to initial therapy, or with signs of systemic illness, or with recurrent infection in the setting of underlying predisposing conditions, or with risk factors for [[MRSA]], or in communities where the prevalence of [[MRSA]] is greater, additional empiric coverage for [[MRSA]] is considered.<ref name="pmid21217178">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= 285-92 | pmid=21217178 | doi=10.1093/cid/cir034 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21217178 }} </ref> | ||
* Patients with a penicillin allergy can be given [[vancomycin]] and [[clindamycin]]. | * Patients with a penicillin allergy can be given [[vancomycin]] and [[clindamycin]]. | ||
* In diabetic individuals, broad coverage antibiotics are used. Carbapenams, beta-lactam antibiotics with [[Beta-lactamase]] inhibitors are given in a combined regimen for antibiotic coverage. | * In diabetic individuals, broad coverage antibiotics are used. Carbapenams, beta-lactam antibiotics with [[Beta-lactamase]] inhibitors are given in a combined regimen for antibiotic coverage. |
Revision as of 20:17, 19 May 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mugilan Poongkunran M.B.B.S [2]
Cellulitis Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Cellulitis medical therapy On the Web |
American Roentgen Ray Society Images of Cellulitis medical therapy |
Risk calculators and risk factors for Cellulitis medical therapy |
Overview
Cellulitis is an acute spreading infection of the skin, characterized by spreading areas of edema, redness, and heat, sometimes accompanied by lymphangitis and inflammation of the regional lymph nodes. Typically a combination of intravenous and oral antibiotics are administered for the treatment of cellulitis. Bed rest and elevation of the affected limbs are recommended to accompany the antibiotic treatment. In patients with edema of the extremities, compressive stockings may really aid in treating the fluid accumulation. Small abscess surrounding the affected tissue can be treated with a simple incision and drainage of the fluid. It is advised to drink plenty of fluids during your treatment and recovery.
Non-Antibiotic Therapy
- Elevation of the affected area facilitates gravity drainage of edema and inflammatory substances. The skin should be sufficiently hydrated to avoid dryness and cracking without interdigital maceration.
- Treat underlying conditions such as tinea pedis, lymphedema, and chronic venous insufficiency, that predispose them to developing recurrent cellulitis.
- Compressive stockings and diuretic therapy may help patients with edema.
Medical Therapy
- Mostly the causative agent is streptococci (often group A, but also from other groups, such as B, C, or G) and rarely staphylococcus aureus that is associated with penetrating trauma, illicit drug use.
- Cultures of needle aspirations from inflammed skin, blood or punch biopsies are variable and not useful in the setting of mild infection and hence performed in patients with systemic toxicity, underlying comorbidities (immunodeficiency, diabetes etc) and special exposures (animal bites).
- The antibiotic selection for treatment of cellulitis depends on whether the clinical presentation is purulent or nonpurulent, as purulent cellulitis is potentially attributable to staphylococcus aureus, which should be empirically treated with Beta-lactam antibiotics.[1] Latest reports suggest that this bacterium has acquired resistance (MRSA) and newer drugs are to be used to kill off the pathogen. Reports from the laboratory regarding the sensitivity of the pathogen is a key factor in deciding the therapy.
- Choice of the antibiotic therapy for cellulitis depends on the following factors:
- Age of the individual: Early hospitalization and parenteral therapy are required for treatment of cellulitis in neonates, except for the mildest of cases.
- Co-morbid conditions
- Site of lesion
- Severity of lesion
- Pathogen involved (gram positive or negative and aerobic or anaerobic)
- Strain and resistance of the pathogen
- Parenteral therapy is indicated for severely ill patients or for those unable to tolerate oral medications.
- The duration of antibiotic therapy in immunocompetent individuals is until 3 days after acute inflammation disappears.
Uncomplicated Cellulitis
- Simple infection without abscesses or drainage should be managed with empiric therapy for infection due to beta-hemolytic streptococci and methicillin sensitive staphylococcus aureus (MSSA).
- Patients allergic to penicillin drugs can be given macrolide antibiotics like azithromycin.
- According to the 2011 clinical practice guidelines, if both methicillin resistant staphylococcus aureus and Streptococcus pyogenes are possible causes, then "options include the following: clindamycin alone (A-II) or TMP-SMX or a tetracycline in combination with a β-lactam (eg, amoxicillin) (A-II) or linezolid alone (A-II)."[2] MRSA is commonly the causative agent of cellulitis in cases presenting with abscesses.[3] In mild cases, treatment will be TMP-SMX with doxycycline and in severe cases, the most cost effective therapy will be vancomycin.[4]
- According to the 2005 clinical practice guidelines, which state that staphylococcus aureus is very uncommon: "Suitable agents include dicloxacillin, cephalexin, clindamycin, or erythromycin, unless streptococci or staphylococci resistant to these agents are common in the community."[5] Another trial confirms that if purulence or diabetes are not present then coverage for staphylococcus aureus is not needed.[6]
- A study of failed treatment concluded that failure is reduced if higher dose antibiotics are used:
- Vancomycin at least 30 mg/kg/day
- Clindamycin at least 10 mg/kg/day (450 mg every 8 hours)
- TMP-SMX at least 5 mg/kg/day of trimethoprim (a single strength pill has 80 mg trimethoprim) (two double strength pills every 12 hours)[7]
- If levofloxacin is used for treatment, 5 days is as effective as 10 days.[8] However, levofloxacin is ineffective against methicillin-resistant Staphylococcus aureus.
Severe Cellulitis
- In severe cases of the disease, parenteral therapy is advocated.
- Patients who do not respond to initial therapy, or with signs of systemic illness, or with recurrent infection in the setting of underlying predisposing conditions, or with risk factors for MRSA, or in communities where the prevalence of MRSA is greater, additional empiric coverage for MRSA is considered.[2]
- Patients with a penicillin allergy can be given vancomycin and clindamycin.
- In diabetic individuals, broad coverage antibiotics are used. Carbapenams, beta-lactam antibiotics with Beta-lactamase inhibitors are given in a combined regimen for antibiotic coverage.
- The duration of therapy should be individualized depending on clinical response; 5 to 10 days is usually appropriate (7 to 10 days in neonates); longer duration of therapy may be warranted in patients with severe disease.
Empiric Therapy
▸ Click on the following categories to expand treatment regimens.
Cellulitis ▸ Infants 0-4 weeks of age ▸ Infants <1 week of age ▸ Infants ≥1 week of age Non-purulent Cellulitis ▸ Adults ▸ Children age >28 days Purulent Cellulitis ▸ Adults ▸ Children age >28 days |
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Note:
- Treatment of cellulitis in neonates usually requires hospitalization and parenteral therapy. Oral therapy is given for completion of the treatment when the patogen is unknown.
- Optimal dose should be based on determination of serum concentrations.
- The above antibiotic regimen is NOT for initial empirical treatment of infections involving the face.
- Dose alteration for renal insufficiency may be needed in case of cephalosporins.
- Clindamycin is an alternate therapy for patients at risk of severe hypersensitivity reaction to penicillins and cephalosporins.
- Doxycycline is NOT recommended for children <8 years of age.
- Studies have shown an increase in treatment failure with TMP-SMX compared to other agents for cellulitis in children, reflecting TMP-SMX less action against Group A streptococcus.[9]
Special Cases
Orbital Cellulitis
- Treatment regimens are usually empiric and designed to address the usual pathogens like Streptococcus pneumoniae, Hemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus, anaerobes (when intracranial extension is suspected), group A streptococci, and sometimes gram negative bacilli because, in the absence of surgical intervention, reliable culture results are difficult to obtain.
▸ Click on the following categories to expand treatment regimens.
Orbital Cellulitis ▸ Usual pathogens ▸ MRSA |
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- Bite Wounds (Mammalian).
- Bite wounds suffered from a mammal often contain polymicrobial sources that are anaerobic in nature.[10]
- Mild cases can be treated with amoxicillin and clavulanate, and in cases of penicillin allergy cotrimoxazole along with metronidazole is used.
- In severe cases, piperacillin and tazobactum are used.
- Acquatic punctures and lacerations.[11]
- This is seen mainly in professional swimmers and divers both in freshwater and in brackish water.
- Failure to recognize these wounds and delay treatment may cause a larger morbidity.
- Wounds in fresh water are treated with doxycycline and ceftazidime (or fluroquinolones).
- Wounds in brackish water are treated with ceftazidime and levofloxacin.
References
- ↑ Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ; et al. (2011). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children". Clin Infect Dis. 52 (3): e18–55. doi:10.1093/cid/ciq146. PMID 21208910.
- ↑ 2.0 2.1 2.2 Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ; et al. (2011). "Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary". Clin Infect Dis. 52 (3): 285–92. doi:10.1093/cid/cir034. PMID 21217178.
- ↑ Moran GJ, Krishnadasan A, Gorwitz RJ; et al. (2006). "Methicillin-resistant S. aureus infections among patients in the emergency department". N. Engl. J. Med. 355 (7): 666–74. doi:10.1056/NEJMoa055356. PMID 16914702. Unknown parameter
|month=
ignored (help) - ↑ Stryjewski ME, Chambers HF (2008). "Skin and soft-tissue infections caused by community-acquired methicillin-resistant Staphylococcus aureus". Clin. Infect. Dis. 46 Suppl 5: S368–77. doi:10.1086/533593. PMID 18462092. Unknown parameter
|month=
ignored (help) - ↑ 5.0 5.1 Stevens DL, Bisno AL, Chambers HF; et al. (2005). "Practice guidelines for the diagnosis and management of skin and soft-tissue infections". Clin. Infect. Dis. 41 (10): 1373–406. doi:10.1086/497143. PMID 16231249. Unknown parameter
|month=
ignored (help) - ↑ Pallin DJ, Binder WD, Allen MB, Lederman M, Parmar S, Filbin MR; et al. (2013). "Clinical Trial: Comparative effectiveness of cephalexin plus trimethoprim-sulfamethoxazole vs. cephalexin alone for treatment of uncomplicated cellulitis: A randomized controlled trial". Clin Infect Dis. doi:10.1093/cid/cit122. PMID 23457080.
- ↑ Halilovic J, Heintz BH, Brown J (2012). "Risk factors for clinical failure in patients hospitalized with cellulitis and cutaneous abscess". J Infect. doi:10.1016/j.jinf.2012.03.013. PMID 22445732.
- ↑ Hepburn, Matthew J (2004-08-09). "Comparison of short-course (5 days) and standard (10 days) treatment for uncomplicated cellulitis". Archives of Internal Medicine. 164 (15): 1669–1674. doi:10.1001/archinte.164.15.1669. ISSN 0003-9926. PMID 15302637. Retrieved 2009-09-01. Unknown parameter
|coauthors=
ignored (help) - ↑ Elliott DJ, Zaoutis TE, Troxel AB, Loh A, Keren R (2009). "Empiric antimicrobial therapy for pediatric skin and soft-tissue infections in the era of methicillin-resistant Staphylococcus aureus". Pediatrics. 123 (6): e959–66. doi:10.1542/peds.2008-2428. PMID 19470525.
- ↑ Abrahamian FM, Goldstein EJ (2011). "Microbiology of animal bite wound infections". Clin. Microbiol. Rev. 24 (2): 231–46. doi:10.1128/CMR.00041-10. PMC 3122494. PMID 21482724. Unknown parameter
|month=
ignored (help) - ↑ Noonburg GE (2005). "Management of extremity trauma and related infections occurring in the aquatic environment". J Am Acad Orthop Surg. 13 (4): 243–53. PMID 16112981.