Loefflers syndrome medical therapy: Difference between revisions
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The majority of cases of Löffler syndrome are self-limited and require only supportive care. Nevertheless, pharmacologic medical therapy is recommended among patients with parasitic infections and hence, appropriate use of [[Anthelmintic|anthelmintic drugs]] is warranted. Additionally, patients with sever symptoms are treated with [[Corticosteroid|corticosteroids]]. [[Anti inflammatory medications|Anti-inflammatory]] effects of [[Corticosteroid|corticosteroids]], reverse increased capillary permeability and suppress [[Neutrophil|PMN]] activity. [[Corticosteroid]]<nowiki/>s such as [[prednisone]] decrease [[Interleukin 5|interleukin-5]], and [[granulocyte macrophage colony stimulating factor]], and hence decrease eosinophil survival. | The majority of cases of Löffler syndrome are self-limited and require only supportive care. Nevertheless, pharmacologic medical therapy is recommended among patients with parasitic infections and hence, appropriate use of [[Anthelmintic|anthelmintic drugs]] is warranted. Additionally, patients with sever symptoms are treated with [[Corticosteroid|corticosteroids]]. [[Anti inflammatory medications|Anti-inflammatory]] effects of [[Corticosteroid|corticosteroids]], reverse increased capillary permeability and suppress [[Neutrophil|PMN]] activity. [[Corticosteroid]]<nowiki/>s such as [[prednisone]] decrease [[Interleukin 5|interleukin-5]], and [[granulocyte macrophage colony stimulating factor]], and hence decrease eosinophil survival. | ||
==Medical Therapy== | ==Medical Therapy== | ||
*The majority of cases of Löffler syndrome are self-limited and require only supportive care. Nevertheless, pharmacologic medical therapy is recommended among patients with parasitic infections and hence, appropriate use of [[Anthelmintic|anthelmintic drugs]] is warranted. Additionally, patients with sever symptoms are treated with [[Corticosteroid|corticosteroids]]. [[Anti inflammatory medications|Anti-inflammatory]] effects of [[Corticosteroid|corticosteroids]], reverse increased capillary permeability and suppress [[Neutrophil|PMN]] activity. [[Corticosteroid]]<nowiki/>s such as [[prednisone]] decrease [[Interleukin 5|interleukin-5]], and [[granulocyte macrophage colony stimulating factor]], and hence decrease eosinophil survival. | |||
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*'''Strongyloidiasis''' | |||
** Preferred regimen (1): [[Ivermectin]] 200 μg/kg/day PO q24h for 2 days. | |||
*** Note: For [[immunocompromised]] patients, several treatment courses at 2-week intervals is recommended. | |||
** Alternative regimen (1): [[Thiabendazole]] 1.5 g PO q24h for 2 consecutive days. | |||
*** Note: The maximum dosage is 3 g/d every 2 days (this dosage is likely to be toxic and needs to be reduced) | |||
*** Note: Cure rates are as high as 87% to 94%, but the drug may not be effective in the disease that is disseminated beyond the [[gastrointestinal tract]]. | |||
*** Note: Many patients have [[gastrointestinal]] adverse effects, it is used rarely in the U.S. because of adverse effects | |||
** Alternative regimen (2): [[Albendazole]] 400 mg PO bid for 3 days | |||
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*Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3]. | *Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3]. | ||
*Pharmacologic medical therapies for Löffler syndrome include (either) [therapy 1], [therapy 2], and/or [therapy 3]. | *Pharmacologic medical therapies for Löffler syndrome include (either) [therapy 1], [therapy 2], and/or [therapy 3]. |
Revision as of 19:30, 6 June 2019
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Soroush Seifirad, M.D.[2]
Overview
The majority of cases of Löffler syndrome are self-limited and require only supportive care. Nevertheless, pharmacologic medical therapy is recommended among patients with parasitic infections and hence, appropriate use of anthelmintic drugs is warranted. Additionally, patients with sever symptoms are treated with corticosteroids. Anti-inflammatory effects of corticosteroids, reverse increased capillary permeability and suppress PMN activity. Corticosteroids such as prednisone decrease interleukin-5, and granulocyte macrophage colony stimulating factor, and hence decrease eosinophil survival.
Medical Therapy
- The majority of cases of Löffler syndrome are self-limited and require only supportive care. Nevertheless, pharmacologic medical therapy is recommended among patients with parasitic infections and hence, appropriate use of anthelmintic drugs is warranted. Additionally, patients with sever symptoms are treated with corticosteroids. Anti-inflammatory effects of corticosteroids, reverse increased capillary permeability and suppress PMN activity. Corticosteroids such as prednisone decrease interleukin-5, and granulocyte macrophage colony stimulating factor, and hence decrease eosinophil survival.
- Strongyloidiasis
- Preferred regimen (1): Ivermectin 200 μg/kg/day PO q24h for 2 days.
- Note: For immunocompromised patients, several treatment courses at 2-week intervals is recommended.
- Alternative regimen (1): Thiabendazole 1.5 g PO q24h for 2 consecutive days.
- Note: The maximum dosage is 3 g/d every 2 days (this dosage is likely to be toxic and needs to be reduced)
- Note: Cure rates are as high as 87% to 94%, but the drug may not be effective in the disease that is disseminated beyond the gastrointestinal tract.
- Note: Many patients have gastrointestinal adverse effects, it is used rarely in the U.S. because of adverse effects
- Alternative regimen (2): Albendazole 400 mg PO bid for 3 days
- Preferred regimen (1): Ivermectin 200 μg/kg/day PO q24h for 2 days.
- Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3].
- Pharmacologic medical therapies for Löffler syndrome include (either) [therapy 1], [therapy 2], and/or [therapy 3].
- Empiric therapy for Löffler syndrome depends on [disease factor 1] and [disease factor 2].
- Patients with [disease subclass 1] are treated with [therapy 1], whereas patients with [disease subclass 2] are treated with [therapy 2].
Disease Name
- 1 Stage 1 - Name of stage
- 1.1 Specific Organ system involved 1
- 1.1.1 Adult
- Preferred regimen (1): drug name 100 mg PO q12h for 10-21 days (Contraindications/specific instructions)
- Preferred regimen (2): drug name 500 mg PO q8h for 14-21 days
- Preferred regimen (3): drug name 500 mg q12h for 14-21 days
- Alternative regimen (1): drug name 500 mg PO q6h for 7–10 days
- Alternative regimen (2): drug name 500 mg PO q12h for 14–21 days
- Alternative regimen (3): drug name 500 mg PO q6h for 14–21 days
- 1.1.2 Pediatric
- 1.1.2.1 (Specific population e.g. children < 8 years of age)
- Preferred regimen (1): drug name 50 mg/kg PO per day q8h (maximum, 500 mg per dose)
- Preferred regimen (2): drug name 30 mg/kg PO per day in 2 divided doses (maximum, 500 mg per dose)
- Alternative regimen (1): drug name10 mg/kg PO q6h (maximum, 500 mg per day)
- Alternative regimen (2): drug name 7.5 mg/kg PO q12h (maximum, 500 mg per dose)
- Alternative regimen (3): drug name 12.5 mg/kg PO q6h (maximum, 500 mg per dose)
- 1.1.2.2 (Specific population e.g. 'children < 8 years of age')
- Preferred regimen (1): drug name 4 mg/kg/day PO q12h(maximum, 100 mg per dose)
- Alternative regimen (1): drug name 10 mg/kg PO q6h (maximum, 500 mg per day)
- Alternative regimen (2): drug name 7.5 mg/kg PO q12h (maximum, 500 mg per dose)
- Alternative regimen (3): drug name 12.5 mg/kg PO q6h (maximum, 500 mg per dose)
- 1.1.2.1 (Specific population e.g. children < 8 years of age)
- 1.1.1 Adult
- 1.2 Specific Organ system involved 2
- 1.1 Specific Organ system involved 1
- 2 Stage 2 - Name of stage
- 2.1 Specific Organ system involved 1
- Note (1):
- Note (2):
- Note (3):
- 2.1.1 Adult
- Parenteral regimen
- Oral regimen
- Preferred regimen (1): drug name 500 mg PO q8h for 14 (14–21) days
- Preferred regimen (2): drug name 100 mg PO q12h for 14 (14–21) days
- Preferred regimen (3): drug name 500 mg PO q12h for 14 (14–21) days
- Alternative regimen (1): drug name 500 mg PO q6h for 7–10 days
- Alternative regimen (2): drug name 500 mg PO q12h for 14–21 days
- Alternative regimen (3):drug name 500 mg PO q6h for 14–21 days
- 2.1.2 Pediatric
- Parenteral regimen
- Preferred regimen (1): drug name 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
- Alternative regimen (1): drug name 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
- Alternative regimen (2): drug name 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day) '(Contraindications/specific instructions)'
- Oral regimen
- Preferred regimen (1): drug name 50 mg/kg/day PO q8h for 14 (14–21) days (maximum, 500 mg per dose)
- Preferred regimen (2): drug name (for children aged ≥ 8 years) 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
- Preferred regimen (3): drug name 30 mg/kg/day PO q12h for 14 (14–21) days (maximum, 500 mg per dose)
- Alternative regimen (1): drug name 10 mg/kg PO q6h 7–10 days (maximum, 500 mg per day)
- Alternative regimen (2): drug name 7.5 mg/kg PO q12h for 14–21 days (maximum, 500 mg per dose)
- Alternative regimen (3): drug name 12.5 mg/kg PO q6h for 14–21 days (maximum,500 mg per dose)
- Parenteral regimen
- 2.2 'Other Organ system involved 2'
- Note (1):
- Note (2):
- Note (3):
- 2.2.1 Adult
- Parenteral regimen
- Oral regimen
- Preferred regimen (1): drug name 500 mg PO q8h for 14 (14–21) days
- Preferred regimen (2): drug name 100 mg PO q12h for 14 (14–21) days
- Preferred regimen (3): drug name 500 mg PO q12h for 14 (14–21) days
- Alternative regimen (1): drug name 500 mg PO q6h for 7–10 days
- Alternative regimen (2): drug name 500 mg PO q12h for 14–21 days
- Alternative regimen (3):drug name 500 mg PO q6h for 14–21 days
- 2.2.2 Pediatric
- Parenteral regimen
- Preferred regimen (1): drug name 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
- Alternative regimen (1): drug name 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
- Alternative regimen (2): drug name 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day)
- Oral regimen
- Preferred regimen (1): drug name 50 mg/kg/day PO q8h for 14 (14–21) days (maximum, 500 mg per dose)
- Preferred regimen (2): drug name 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
- Preferred regimen (3): drug name 30 mg/kg/day PO q12h for 14 (14–21) days (maximum, 500 mg per dose)
- Alternative regimen (1): drug name 10 mg/kg PO q6h 7–10 days (maximum, 500 mg per day)
- Alternative regimen (2): drug name 7.5 mg/kg PO q12h for 14–21 days (maximum, 500 mg per dose)
- Alternative regimen (3): drug name 12.5 mg/kg PO q6h for 14–21 days (maximum,500 mg per dose)
- Parenteral regimen
- 2.1 Specific Organ system involved 1