Dysentery medical therapy: Difference between revisions
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==Overview== | ==Overview== |
Revision as of 19:21, 3 December 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Kalsang Dolma, M.B.B.S.[2]
Overview
Medical Therapy
Dysentery is initially managed by maintaining fluid intake using oral rehydration therapy. If this treatment cannot be adequately maintained due to vomiting or the profuseness of diarrhea, hospital admission may be required for intravenous fluid replacement. In ideal situations, no antimicrobial therapy should be administered until microbiological microscopy and culture studies have established the specific infection involved. When laboratory services are not available, it may be necessary to administer a combination of drugs, including an amoebicidal drug to kill the parasite and an antibiotic to treat any associated bacterial infection.
If shigella is suspected and it is not too severe, the doctor may recommend letting it run its course — usually less than a week. The patient will be advised to replace fluids lost from diarrhea. If the shigella is severe, the doctor may prescribe antibiotics, such as ciprofloxacin or TMP-SMX (Bactrim). However, many strains of shigella are becoming resistant to common antibiotics, and effective medications are often in short supply in developing countries. If necessary, a doctor may have to reserve antibiotics for those at highest risk for death, including young children, people over 50, and anyone suffering from dehydration or malnutrition.
Amoebic dysentery usually calls for a two-pronged attack. Treatment should start with a 10-day course of the antimicrobial drug metronidazole (Flagyl). To finish off the parasite, the doctor can prescribe a course of diloxanide furoate (available only through the Centers for Disease Control and Prevention), paromomycin (Humatin), or iodoquinol (Yodoxin).
- Shown below is a table summarizing the preferred and alternative empiric treatment for Dysentery.[1]
Possible Pathogens | Characteristics of the Patient | Preferred Treatment | Duration of Treatment |
Shigella species |
|
TMP-SMZ, 160 and 800 mg, respectively (pediatric dose, 5 and 25 mg/kg, respectively) b.i.d. (if susceptible)
OR Fuoroquinolone (e.g., 300 mg ofloxacin, 400 mg norfloxacin, or 500 mg ciprofloxacin b.i.d.); nalidixic acid, 55 mg/kg/d (pediatric) or 1 g/d (adults) OR Ceftriaxone OR Azithromycin |
TMP-SMZ for 3 days
OR Flouroquinolones [( ofloxacin,norfloxacin and ciprofloxacin for 3 days ) and (nalidixic acid for 5 days )] |
Shigella species |
|
Same as above | Same as above except that duration of antibiotics is for 7- 10 days |
Non-typhi species of Salmonella | Immunocompetent patient
Not recommended routinely, but if
|
TMP-SMZ (if susceptible) or fluoroquinoloneas above, b.i.d;
OR Ceftriaxone, 100 mg/kg/d in 1 or 2 divided doses |
TMP-SMZ (if susceptible) or fluoroquinolone for 5 - 7 days |
Non-typhi species of Salmonella |
|
Same as above | Same as above except that duration of antibiotics is for 14 days (or longer if relapsing) |
Campylobacter species |
|
Erythromycin 500 mg b.i.d. | Erythromycin for 5 days |
Campylobacter species |
|
Same as above | Same as above but may require prolonged treatment |
Enterohemorrhagic E Coli |
|
Avoid antimotility drugs ; role of antibiotics unclear,and administration should be avoided | Avoid antimotility drugs ; role of antibiotics unclear,and administration should be avoided |
Yersina species |
|
TMP-SMZ, 160 and 800 mg, respectively (pediatric dose, 5 and 25 mg/kg, respectively) b.i.d. (if susceptible)
OR ciprofloxacin 500 mg b.i.d. OR Doxycycline 100 mg PO b.i.d. |
TMP-SMZ for 3 - 5 days
OR Ciprofloxacin for 3 days OR Doxycycline for 3 days |
Entamoeba histolytica |
|
Metronidazole, 750 mg t.i.d.
+ Diiodohydroxyquin, 650 mg t.i.d. OR Paromomycin, 500 mg t.i.d. |
Metronidazole for 5 - 10 days
+ Diiodohydroxyquin for 20 days OR Paromomycin for 7 days |
References
- ↑ IDSA Guidelines for Management of Infectious Diarrhoea; Clin Infect Dis 2001; 32:331-50. Infectious diarrhea in developed countries:J Clin Gastroenterol 2005:39:757-773