This is the current release of the guideline.

This guideline updates a previous version: Kauffman CA, Hajjeh R, Chapman SW. Practice guidelines for the management of patients with sporotrichosis. For the Mycoses Study Group. Infectious Diseases Society of America. Clin Infect Dis 2000 Apr;30(4):684-7.

Definitions of the levels of evidence (I-III) and grades of recommendation (A-C) are provided at the end of the "Major Recommendations" field.

What Is the Treatment for Lymphocutaneous and Cutaneous Sporotrichosis?

• For cutaneous and lymphocutaneous sporotrichosis, itraconazole 200 mg orally daily is recommended to be given for 2 to 4 weeks after all lesions have resolved, usually a total of 3 to 6 months (AII).
• Patients who do not respond should be given a higher dosage of itraconazole, 200 mg twice daily (AII), terbinafine at a dosage of 500 mg orally twice daily (AII), or saturated solution of potassium iodide (SSKI) initiated at a dosage of 5 drops (using a standard eye-dropper) 3 times daily, increasing as tolerated to 40 to 50 drops 3 times daily (AII).
• Fluconazole at a dosage of 400 to 800 mg daily should be used only if the patient cannot tolerate these other agents (BII).
• Local hyperthermia can be used for treating patients, such as pregnant and nursing women, who have fixed cutaneous sporotrichosis and who cannot safely take any of the previous regimens (BIII).

What Is the Treatment for Osteoarticular Sporotrichosis?

• Itraconazole 200 mg orally twice daily for at least 12 months is recommended (AII).
• Amphotericin B, given as a lipid formulation at 3 to 5 mg/kg daily, or amphotericin B deoxycholate, 0.7 to 1.0 mg/kg daily, can be used for initial therapy (BIII). After the patient has shown a favorable response, therapy can be changed to itraconazole, 200 mg orally twice daily to complete a total of at least 12 months of therapy (BIII).
• Serum levels of itraconazole should be obtained after the patient has been on this agent for at least two weeks to ensure adequate drug exposure (AIII).

What is the Treatment for Pulmonary Sporotrichosis?

• For severe or life-threatening pulmonary sporotrichosis, amphotericin B, given as a lipid formulation at 3 to 5 mg/kg daily, is recommended (BIII). Amphotericin B deoxycholate, 0.7 to 1.0 mg/kg daily, could also be used (BIII).
• After the patient has shown a favorable response to amphotericin B, therapy can be changed to itraconazole, 200 mg orally twice daily to complete a total of at least 12 months of therapy (BIII).
• For less severe disease, itraconazole 200 mg orally twice daily for at least 12 months is recommended (AIII).
• Serum levels of itraconazole should be obtained after the patient has been on this agent for at least two weeks to ensure adequate drug exposure (AIII).
• Surgery combined with amphotericin B is recommended for localized pulmonary disease (BIII).

What is the Treatment for Meningeal Sporotrichosis?

• Amphotericin B, given as a lipid formulation at a dosage of 5 mg/kg daily for 4 to 6 weeks, is recommended for initial treatment of meningeal sporotrichosis (BIII). Amphotericin B deoxycholate, 0.7 to 1.0 mg/kg daily, could also be used but was not preferred by the panel (BIII).
• Itraconazole, 200 mg twice daily, is recommended as step-down therapy after the patient responds to initial treatment with amphotericin B and should be given to complete a total of at least 12 months of therapy (BIII).
• Serum levels of itraconazole should be obtained after the patient has been on this agent for at least two weeks to ensure adequate drug exposure (AIII).
• For patients with acquired immunodeficiency syndrome (AIDS) and other immunosuppressed patients, suppressive therapy with itraconazole, 200 mg daily, is recommended to prevent relapse (BIII)

What is the Treatment for Disseminated (Systemic) Sporotrichosis?

• Amphotericin B, given as a lipid formulation at a dosage of 3 to 5 mg/kg daily, is recommended for disseminated sporotrichosis (BIII). Amphotericin B deoxycholate, 0.7 to 1.0 mg/kg daily, could also be used but was not preferred by the panel (BIII).
• Itraconazole, 200 mg twice daily, is recommended as step-down therapy after the patient responds to initial treatment with amphotericin B and should be given to complete a total of at least 12 months of therapy (BIII).
• Serum levels of itraconazole should be obtained after the patient has been on this agent for at least two weeks to ensure adequate drug exposure (AIII).
• Lifelong suppressive therapy with itraconazole, 200 mg daily may be required in patients with AIDS and other immunosuppressed patients if immunosuppression cannot be reversed (BIII).

What is the Treatment for Sporotrichosis in Pregnant Women and in Children?

• Amphotericin B, given as a lipid formulation at a dosage of 3 to 5 mg/kg daily, or amphotericin B deoxycholate, given as 0.7 to 1 mg/kg daily, is recommended for severe sporotrichosis that must be treated during pregnancy (BIII); azoles should be avoided.
• Local hyperthermia can be used for cutaneous sporotrichosis in pregnant women (BIII).
• Itraconazole, at a dosage of 6 to 10 mg/kg to a maximum of 400 mg orally daily, is recommended for children with cutaneous or lymphocutaneous sporotrichosis (BIII).
• An alternative for children is SSKI initiated at a dosage of 1 drop (using a standard eye-dropper) 3 times daily, increasing as tolerated up to a maximum of 1 drop/kg or 40 to 50 drops 3 times daily, whichever is lowest (BIII).
• For children with disseminated sporotrichosis, amphotericin B, 0.7 mg/kg daily should be the initial therapy followed by itraconazole, 6 to 10 mg/kg up to 400 mg daily maximum as step-down therapy (BIII).

Performance Measures

1. Lymphocutaneous sporotrichosis should be treated with itraconazole or SSKI in countries in which the latter is the standard of care. When other azole agents are used, the medical record should document the specific reasons that they were chosen over itraconazole or SSKI.
2. Patients with disseminated or severe pulmonary sporotrichosis should be treated with an amphotericin B formulation initially. When amphotericin B is used, the patient's electrolytes, renal function, and blood counts should be monitored several times a week and documented in the medical record.

Definitions:

Quality of Evidence

1. Evidence from ≥1 properly randomized, controlled trial.
2. Evidence from ≥1 well-designed clinical trial, without randomization; from cohort or case-controlled analytic studies (preferably from >1 center); from multiple time-series; or from dramatic results from uncontrolled experiments.
3. Evidence from opinions of respected authorities, based on clinical experience, descriptive studies, or reports of expert committees.

Strength of Recommendation

1. Good evidence to support a recommendation for use.
2. Moderate evidence to support a recommendation for use.
3. Poor evidence to support a recommendation

None provided

The recommendations for the treatment of sporotrichosis were derived primarily from case reports and nonrandomized treatment trials.

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

Not applicable: The guideline was not adapted from another source.

2000 Apr (revised 2007)

Infectious Diseases Society of America - Medical Specialty Society

Infectious Diseases Society of America (IDSA)

Infectious Diseases Society of America (IDSA) Standards and Practice Guidelines Committee

Authors: Carol A. Kauffman, University of Michigan, VA Medical Center, Ann Arbor, MI; Beatriz Bustamante, Universidad Peruana Cayetano Heredia, Lima - Perú; Stanley W. Chapman, University of Mississippi Medical Center, Jackson, MS; Peter G. Pappas, University of Alabama at Birmingham, Birmingham, AL

C.A.K. Has research grants with Merck, Astellas and Schering-Plough and is on the Speaker's Bureau for Merck, Pfizer, Astellas and Schering-Plough

B.B. has a research grant from Schering-Plough

P.G.P. has research grants from Merck, Astellas, Pfizer and Schering-Plough and is on the speaker's bureau of Merck, Pfizer, Astellas and Schering-Plough

S.W.C. No conflicts

This is the current release of the guideline.

This guideline updates a previous version: Kauffman CA, Hajjeh R, Chapman SW. Practice guidelines for the management of patients with sporotrichosis. For the Mycoses Study Group. Infectious Diseases Society of America. Clin Infect Dis 2000 Apr;30(4):684-7.

None available

This summary was completed by ECRI on May 1, 2001. The information was verified by the guideline developer as of June 29, 2001. This NGC summary was updated by ECRI Institute on October 24, 2007. The updated information was verified by the guideline developer on November 8, 2007.

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.