Sandbox:Reddy: Difference between revisions
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''E. coli'' 0157:H7 | ''E. coli'' 0157:H7 | ||
''''C.difficile'''' | '<nowiki/>'''C.difficile'''' | ||
|'''Ciprofloxacin''' 500 mg PO BID | |'''Ciprofloxacin''' 500 mg PO BID | ||
OR | OR | ||
Line 77: | Line 77: | ||
|Mild, self-limited cases can be treated with fluid and electrolyte repletion and bismuth subsalicylate. | |Mild, self-limited cases can be treated with fluid and electrolyte repletion and bismuth subsalicylate. | ||
Prophylaxis generally not recommended. | Prophylaxis generally not recommended. | ||
|} | |||
{| class="wikitable" | |||
|'''Diverticulitis''' | |||
|Enterobacteriaceae | |||
''Bacteroides fragilis'' | |||
'<nowiki/>'''Enterococcus'''' | |||
|'''Amoxicillin/clavulanate''' | |||
875 mg/125 mg PO BID | |||
OR | |||
'''Moxifloxacin'''ID-R: SFGH 400 mg PO daily | |||
OR the combination of: | |||
'''Metronidazole''' 500 mg PO TID | |||
PLUS ONE OF: | |||
'''Ciprofloxacin''' 500 mg PO BID | |||
OR | |||
'''Levofloxacin'''ID-R: VASF 500 mg PO daily | |||
|Duration of treatment should be until patient is afebrile for 3-5 days. | |||
Surgical evaluation and follow up is advised. | |||
|} | |||
{| class="wikitable" | |||
|- | |||
|'<nowiki/>'''''Acute Bronchitis'''''' | |||
| ''Viral'' | |||
|No drug therapy required | |||
| | |||
|- | |||
|'''Acute bacterial exacerbation of chronic bronchitis (COPD)''' | |||
|''S. pneumoniae'' | |||
''H. influenzae'' | |||
''Moraxellacatarrhalis'' | |||
|'''Doxycycline''' 100 mg PO BID X 10 days | |||
|'''Azithromycin''' 500 mg PO daily X 1 day; then 250 mg PO daily X 4 days | |||
|- | |||
|'''Community-acquired Pneumonia (CAP)''' | |||
|''S. pneumoniae'' | |||
''M. pneumoniae'' | |||
''C. pneumoniae'' | |||
Respiratory viruses | |||
''Legionella'' spp. | |||
C. psittaci | |||
'<nowiki/>'''H. influenzae'' (if patient has co-morbidity)''''' | |||
|No recent antibiotic therapy: | |||
'''Doxycycline''' 100 mg PO BID X 7 days | |||
OR | |||
'''Azithromycin''' 500 mg PO daily X 1 day; then 250 mg PO daily X 4 days | |||
Recent antibiotic therapy or patients with co-morbidities: | |||
'''Levofloxacin''' 750 mg PO daily X 5 days | |||
OR | |||
'''Moxifloxacin'''ID-R: SFGH 400 mg PO daily X 7 days | |||
|'''Previous antibiotic therapy within last 3 month''' should be elicited from patient. A course of antibiotics is a risk factor for drug resistance. Recent use of a fluoroquinolone should dictate selection of a non-fluoroquinolone regimen, and vice versa. | |||
Careful follow-up highly recommended. | |||
|- | |||
|Anerobic infection | |||
| | |||
|'''Amoxicillin/clavulanate''' 875 mg/125 mg PO BID | |||
OR | |||
'''Clindamycin''' 300 mg PO TID | |||
| | |||
|- | |||
|'''Acute otitis media''' | |||
OR | |||
'<nowiki/>'''''Otitis media with effusion'<nowiki/>'' '''(OME)''' with signs or symptoms of acute infection''' | |||
|''S. pneumoniae'' | |||
''H. influenzae'' | |||
''M. catarrhalis'' | |||
''Group A Strep.'' | |||
|'''Amoxicillin''' | |||
1 g PO BID x 5-7 days | |||
OR | |||
500 mg PO TID x 5-7 days | |||
|For severe PCN allergy: | |||
'''Azithromycin''' 500 mg PO daily x 1 day; then 250 mg PO daily x 4 days | |||
OR | |||
'''Doxycycline''' 100 mg PO BID for 5-7 days | |||
* Amoxicillin/clavulanic acid not indicated as initial therapy of acute otitis. | |||
* High dose amoxicillin 1 g PO TID should be used over low dose in the treatment of patients at risk for drug resistant ''S. pneumoniae''. | |||
* OME in the absence of acute signs and symptom of infection does not require antibiotics. | |||
* For recurrent prolonged otitis consider ENT referral. | |||
|- | |||
|'''Pharyngitis''' | |||
|Viral (EBV, rhinovirus, coronavirus, adenovirus etc) | |||
''Group A Streptococcus'' | |||
(5-20%) | |||
|'''Penicillin VK''' 250 mg PO TID-QID x 10 days | |||
|For severe PCN allergy: | |||
'''Clindamycin'''300 mg PO TID x 7-10 days | |||
* Most pharyngitis is viral thus antibiotics should not be used. | |||
* Treatment with PCN prevents rheumatic fever. | |||
* Treat documented Group A streptococcal infection confirmed by rapid strep. antigen test or culture or if 3 out 4 clinical criteria present. | |||
* Clinical Criteria: history of fever, tender anterior cervical adenopathy, absence of cough, tonsillar exudates. | |||
|- | |||
|'''Acute Sinusitis''' | |||
|Viruses | |||
''S. pneumoniae'' | |||
''H. influenzae'' | |||
''M. catarrhalis'' | |||
|'''Amoxicillin''' 500 mg PO TID X 5-7 days | |||
|For severe PCN allergy: | |||
'''Doxycycline''' 100 mg PO BID X 5-7 days | |||
Consider treatment only in presence of fever, purulence or bloody discharge following an upper respiratory infection if symptoms persist for 7-10 days suggesting bacterial etiology. | |||
|- | |||
|'''Chronic Sinusitis''' | |||
|Viruses | |||
''S. pneumoniae'' | |||
''H. influenzae'' | |||
''M. catarrhalis'' | |||
Anaerobes | |||
''Staph. aureus'' | |||
''Enterobacteriacae'' | |||
|'''Amoxicillin/clavulanate''' | |||
875 mg/125 mg PO BID X 10-14 days | |||
OR | |||
'''Amoxicillin/clavulanate''' CR 2 g BID X 10-14 days if drug-resistant ''Streptococcus pneumonia'' | |||
|For severe PCN allergy: | |||
'''Ciprofloxacin''' 500 mg PO BID | |||
OR | |||
'''Levofloxacin''' 500 mg PO daily x 10-14 days | |||
EITHER OF ABOVE WITH OR WITHOUT*: | |||
'''Clindamycin''' 300 mg PO TID | |||
* Consider otolaryngology consult to rule out anatomic abnormality. | |||
* If acute exacerbation, treat as acute sinusitis. | |||
* HIV positive patients may need a 2-3 week course. | |||
|- | |||
|'''Treatment of active tuberculosis''' | |||
| | |||
|'''Isoniazid''' 300 mg PO daily x 6 months | |||
PLUS | |||
'''Rifampin''' 600 mg PO daily x 6 months | |||
PLUS | |||
'''Pyrazinamide''' 25 mg/kg PO daily x 2 months | |||
PLUS | |||
'''Ethambutol''' 15 mg/kg PO daily until Isoniazid or Rifampin sensitivity established | |||
PLUS: | |||
'''Pyridoxine''' (Vitamin B-6) 50 mg PO daily for 6 months | |||
| | |||
|- | |||
|'''Latent TB''' | |||
| | |||
|'<nowiki/>'''''Isoniazid'''''' 300 mg PO daily x 9 months | |||
|'''Rifampin''' 600 mg PO daily x 4 months | |||
|} | |||
{| class="wikitable" | |||
|'''Abscess''' | |||
|'<nowiki/>'''S. aureus'''' | |||
| | |||
* Uncomplicated: Incision and drainage, no antibiotics needed | |||
* Complicated: Incision and drainage PLUS '''TMP/SMX''' 1-2 DS tablets PO BID OR '''Doxycycline''' 100 mg PO BID | |||
|Give antibiotics for complicated abscess | |||
* Abscess is large (> 5 cm) or incompletely drained | |||
* There is significant surrounding cellulitis | |||
* Systemic signs and symptoms of infection are present | |||
* Patient is immunocompromised | |||
7-10 days of therapy is generally adequate | |||
|- | |||
|'''Bites''' | |||
Dog and Cat | |||
|Streptococci | |||
''Pasteurella'' spp.* | |||
Staphylococci | |||
Oral anaerobes | |||
|'''Amoxicillin/clavulanate''' | |||
875 mg/125 mg PO BID | |||
Prophylaxis – x 5 days | |||
Treatment – x 10 days | |||
|For severe PCN allergy | |||
'''Clindamycin''' 300 mg PO TID | |||
PLUS ONE OF: | |||
'''Ciprofloxacin''' 500 mg PO BID | |||
OR | |||
'''Levofloxacin''' 500 mg PO daily | |||
* Only 5% of dog bites become infected, whereas 30-50% of cat bites become infected. | |||
* '''Prophylaxis''' in high risk patients or in high risk bite only: | |||
* ''High risk patient'' = post splenectomy, immunocompromised | |||
* ''High risk bite'' = hand or foot | |||
* ''P.multocida'' is resistant to cephalexin & clindamycin; many strains are resistant to erythromycin but sensitive to fluoroquinolones, doxycycline and penicillin | |||
|- | |||
|'''Bites''' | |||
Human | |||
|Viridans streptococci | |||
''Eikenella''* | |||
Oral anaerobes | |||
|'''Amoxicillin/clavulanate''' 875 mg/125 mg PO BID | |||
Prophylaxis – x 5 days | |||
Treatment – x 10 days | |||
|For severe PCN allergy: | |||
'''Clindamycin''' 300 mg PO TID | |||
PLUS ONE OF: | |||
'''Ciprofloxacin''' 500 mg PO BID | |||
OR | |||
'''Levofloxacin'''500 mg PO daily | |||
OR | |||
'''TMP/SMX''' One DS tablet PO BID | |||
|} | |||
{| class="wikitable" | |||
|'''Cellulitis''' | |||
|β-hemolytic streptococci (most common) | |||
''S. aureus'' (less common) | |||
|'''Cephalexin'''500 mg PO QID | |||
OR | |||
'''Amoxicillin'''500 mg PO TID | |||
OR | |||
'''Clindamycin'''300 mg PO TID | |||
| | |||
* If the patient does not respond to beta-lactam-based therapy consider adding TMP/SMX or doxycycline for MRSA coverage. | |||
* Clindamycin monotherapy provides reasonable coverage for both Group A strep and community-acquired MRSA however some isolates may be resistant. Please refer to hospital-specific antibiogram. | |||
* For cellulitis associated with an abscess treat for complicated abscess (see below). | |||
* 7-10 days of therapy is generally adequate | |||
|- | |||
|'''Diabetic Foot Ulcer''' | |||
Localized cellulitis without systemic signs or symptoms, no osteomyelitis | |||
|''S. aureus'' | |||
''Streptococci'' | |||
''Enterobacteriaceae'' | |||
|'''Clindamycin''' 300 mg PO TID | |||
If patient has been treated with antibiotics within the past month ADD: | |||
'''Levofloxacin'''ID-R: VASF 750 mg PO daily | |||
OR | |||
'''Ciprofloxacin''' 500 mg PO BID | |||
| | |||
* While infections may be polymicrobial, they frequently respond to Gram-positive coverage alone. | |||
* Increasing rates of MRSA in the community may be a cause for failure to respond to initial therapy. | |||
* Consider osteomyelitis especially if there is a failure to respond to therapy. | |||
* 7-14 days of treatment is generally sufficient, duration should be based on clinical response. | |||
|- | |||
|Herpes Zoster | |||
|'''Immunocompetent''' | |||
(Shingles/Zoster) | |||
'''Immunocompromised''' | |||
(Lymphoma, HIV infection, etc) and not severe (one dermatome) | |||
|'''Acyclovir''' 800 mg PO 5x/day x 7-10 days | |||
OR | |||
'''Valacyclovir''' 1 g PO TID x 7 days | |||
| | |||
* Treatment effective only if initiated within 48-72 hours of onset of lesions. May shorten duration of illness in immunocompetent patients. | |||
* In patients > 65 years old administration of concomitant corticosteroids may improve quality of life. | |||
|- | |||
|'''Primary Infection in Adults''' (Chicken Pox) | |||
|'''Acyclovir''' 800 mg PO 5x/day x 5 days | |||
OR | |||
'<nowiki/>'''''Valacyclovir'''''' 1 g PO TID x 5 days | |||
| | |||
| | |||
* Initiate therapy within 24 hours of onset of rash. | |||
* Vaccination of non-immune close contacts recommended. Acyclovir treatment may also be effective for prophylaxis of at-risk individuals. | |||
|- | |||
|'''Mastitis''' | |||
Postpartum | |||
|''S. aureus'' | |||
''Including MRSA becoming more frequent'' | |||
|'''Dicloxacillin''' 500 mg PO QID x 10-14 days | |||
OR | |||
'''Cephalexin''' 500 mg PO QID x 10 -14 days | |||
If patient with risk factors for MRSA: | |||
'''TMP/SMX''' One DS tablet PO BID x 10-14 days | |||
OR | |||
'''Clindamycin''' 300mg PO TID x 10-14 days | |||
|For mild PCN allergy: | |||
'''Cephalexin''' 500 mg PO QID x 10-14 days | |||
For severe PCN allergy: | |||
'''Clindamycin''' 300 mg PO TID x 10-14 days | |||
* If no abscess, increased frequency of nursing may hasten response. | |||
* If abscess, I & D required; discontinue nursing. | |||
* Doxycycline is active against MRSA but should not be used if patient is breastfeeding. | |||
|} | |||
{| class="wikitable" | |||
|'''Uncomplicated Cystitis''' | |||
Women | |||
|Enterobacteriaceae ''(E. coli)'' | |||
''S. saprophyticus'' (Coagulase negative staphylococcus) (4%) | |||
|'''Nitrofurantoin''' 100 mg PO BID x 5-7 days – contraindicated in renal insufficiency (CrCl < 60 ml/min) | |||
OR | |||
'''TMP/SMX''' 1 DS tablet PO BID x 3 days (if no previous antibiotic therapy) | |||
OR | |||
'''Fosfomycin''' 3 g PO x1 dose | |||
|Reserve for patients at highest risk of failure (selection for resistant isolates): | |||
'''Ciprofloxacin''' 500 mg PO BID x 3 days | |||
OR | |||
'''Levofloxacin''' 500 mg PO daily x 3 days | |||
Reserve for patients with history of resistant organisms or therapeutic failure (less effective): | |||
'''Cephalexin''' 500 mg PO QID x 7 days | |||
OR | |||
'''Cefpodoxime''' 200 mg PO BID x 7 days | |||
* IDSA guidelines state Trimethoprim/ Sulfamethoxazole is appropriate if resistance rates do not exceed 20%. | |||
* Nitrofurantoin is contraindicated in renal insufficiency (CrCl <60 ml/min). | |||
|- | |||
|'''Recurrent Cystitis''' | |||
|Enterobacteriaceae (''E. coli'') | |||
''S. saprophyticus''(Coagulase negative staphylococcus) (4%) | |||
|Prophylaxis: | |||
Either self administration if symptoms occur or prophylactic post-coital antibiotics | |||
Post menopausal: topical estrogen | |||
| | |||
|- | |||
|'''Asymptomatic bacteriuria''' | |||
|''E.coli'' | |||
''Klebsiella'' | |||
''Enterococcus'' | |||
|No treatment required | |||
| | |||
|- | |||
|'''Pyelonephritis''' | |||
|Enterobacteriaceae ''(E. coli)'' | |||
Enterococci | |||
|'''Ciprofloxacin''' 500 mg PO BID X 7-14 days | |||
OR | |||
'''Levofloxacin'''ID-R: VASF 500 mg PO daily X 7-14 days | |||
OR | |||
'''Trimethoprim/ Sulfamethoxazole''' 1 DS tablet PO BID X 14 days | |||
PLUS | |||
'''Ceftriaxone''' 1 g IV X 1 dose | |||
|'''Cephalexin''' 500 mg PO QID X 10-14 days | |||
OR | |||
'''Cefpodoxime'''200 mg PO BID X 10-14 days | |||
EITHER OF ABOVE PLUS: | |||
'''Ceftriaxone''' 1 g IV X 1 dose | |||
* Urine analysis and urine culture should be performed and therapy adjusted based on culture and sensitivity. | |||
* Trimethoprim-sulfamethoxazole is preferred if organism is susceptible. | |||
* Consider a single intravenous dose of ceftriaxone prior to fluoroquinolone therapy if patient is at high risk for fluoroquinolone-resistant organisms. | |||
|- | |||
|'''Prostatitis''' | |||
Acute | |||
|Enterobacteriaceae''(E. coli)'' | |||
|'''Cephalexin''' 500 mg PO QID x 21 days | |||
OR | |||
'''Ciprofloxacin''' 500 mg PO BIDX 2-4 weeks* | |||
OR | |||
'''Levofloxacin'''ID-R: VASF 500 mg PO daily x 2-4 weeks* | |||
|'''Trimethoprim/ Sulfamethoxazole''' 1 DS tablet PO BID | |||
* Antibiotic penetration in the acute inflammatory state is adequate for most antibiotics. | |||
* Consider sexually transmitted disease treatment (Gonococcus or ''C. trachomatis'') for appropriate patient populations. | |||
* Cultures should be obtained and definitive therapy should be based on sensitivities. | |||
|- | |||
|'''Prostatitis''' | |||
Chronic | |||
|Enterobacteriaceae''(E. coli)'' | |||
|'''Ciprofloxacin''' x 2 months* | |||
OR | |||
'''Levofloxacin'''ID-R: VASF x 2 months* | |||
|'''Trimethoprim/ Sulfamethoxazole''' 1 DS tablet PO BID | |||
* Few drugs penetrate non-inflamed prostate. Fluoroquinolones and trimethoprim/sulfamethoxazole adequately penetrate in non-inflamed state. | |||
* Consider sexually transmitted disease treatment (Gonococcus or ''C. trachomatis'') for appropriate patient populations. | |||
|} | |||
{| class="wikitable" | |||
|'''Chlamydia''' | |||
'''Genital/Rectal''' | |||
'<nowiki/>'''''Pharyngeal'''''' | |||
|'<nowiki/>'''Chlamydia trachomatis'''' | |||
|'''Azithromycin''' 1 g PO once | |||
OR | |||
'<nowiki/>'''''Doxycycline'''''' 100 mg PO BID X 7 days | |||
| | |||
|- | |||
|'''First Clinical Episode or Anogenital Herpes''' | |||
|HSV 2 = 70-90% | |||
HSV 1 = 10-30% | |||
|'''Acyclovir''' 400 mg PO TID x 7-10 days | |||
|'''Valacyclovir''' 1 g PO BID x 7-10 days | |||
In HIV patients with documented acyclovir resistance, use foscarnet. | |||
|- | |||
|'''Episodic Therapy for Recurrent Episodes''' | |||
| | |||
|'''Acyclovir''' 400 mg PO TID x 5 days | |||
OR | |||
'''Acyclovir''' 800 mg PO BID x 5 days | |||
OR | |||
'''Acyclovir''' 800 mg PO TID x 2 days | |||
|'''Valacyclovir''' 1 g PO daily x 5 days | |||
* HIV patients: | |||
'''Acyclovir''' 400 mg PO TID x 5-10 days | |||
OR | |||
'''Valacyclovir''' 1 g PO BID x 5-10 days | |||
|- | |||
|'''Suppression for Frequent Recurrence''' | |||
|HSV 2 = 70-90% | |||
HSV 1 = 10-30% | |||
|'''Acyclovir''' 400 mg PO BID | |||
HIV patients: | |||
'''Acyclovir''' 400-800 mg BID or TID | |||
OR | |||
'''Valacyclovir''' 500 mg PO BID | |||
|'''Valacyclovir''' 500-1000 mg PO daily | |||
Consider suppressive therapy for patients experiencing greater than 3-4 episodes in 12 months. | |||
|} | |||
{| class="wikitable" | |||
|'''Pelvic inflammatory diseases (PID''' | |||
|''N.gonorrhoeae'' | |||
''C.trachomatis'' anaerobes | |||
Gram-negative facultative bacteria streptococci | |||
|'''Ceftriaxone''' 250 mg IM X 1 | |||
PLUS | |||
'''Doxycycline''' 100 mg PO BID X 14 days | |||
PLUS | |||
'''Metronidazole''' 500 mg PO BID x 14 days if BV is present or cannot be ruled out | |||
| | |||
* Follow-up examination should be performed within 72 hours when PID is treated with these regimens. | |||
* Fluoroquinolones should not be used due to increasing resistance and treatment failures. | |||
|- | |||
|'''Syphilis''' | |||
'''Primary, Secondary, Early Latent''' | |||
|'<nowiki/>'''T. pallidum'''' | |||
|'''Benzathine penicillin G'''2.4 MU IM X 1 dose | |||
|'''Doxycycline'''100 mg PO BID X 2 weeks | |||
|- | |||
|'''Syphilis''' | |||
'''Late Latent and Latent of Unknown Duration''' | |||
|'<nowiki/>'''T. pallidum'''' | |||
|'''Benzathine penicillin G'''2.4 MU IM Q week X 3 doses | |||
|'''Doxycycline'''100 mg PO BID X 4 weeks | |||
Sexual partners must be treated. | |||
* Alternatives should only be used for penicillin-allergic patients because efficacy of these therapies has not been established. Compliance with some of these regimens is difficult, and close follow-up is essential. | |||
|} | |||
{| class="wikitable" | |||
|'''Candidal Vaginitis''' | |||
|''''''Fluconazole'''''' 150 mg PO x 1 dose | |||
|'''Miconazole''' 2% cream 5 g intravaginally x 3 days | |||
OR | |||
'''Miconazole''' 100 mg suppository, one suppository daily x 7 days | |||
OR | |||
'''Clotrimazole''' 1% cream 5 g intravaginally x 7-14 days | |||
|- | |||
|'''Protazoan Vaginitis''' | |||
|'''Metronidazole''' 2 g PO x 1 dose | |||
|'''Metronidazole''' 500 mg PO BID x 7 days | |||
In treatment failures to metronidazole, retreat with metronidazole 500 mg PO BID x 7 days. | |||
|- | |||
|'''Bacterial Vaginitis''' | |||
|'''Metronidazole''' 500 mg BID PO x 7 days | |||
OR | |||
'''Metronidazole''' vaginal gel 0.75%, 5 g intravaginally daily x 5 days | |||
OR | |||
'''Clindamycin''' vaginal cream 2%, 5 g intravaginally daily x 7 days | |||
|'''Clindamycin''' 300 mg PO BID X 7 days | |||
OR | |||
'''Clindamycin''' ovules 100 mg intravaginally daily x 3 days | |||
|} | |} |
Latest revision as of 20:27, 29 June 2017
OUT Patient
Dysenteric Diarrhea
Frequent, sometimes bloody, small-volume diarrhea associated with abdominal pain and cramping. Patient may be febrile and toxic. |
Shigella
Salmonella Campylobacter Yersinia E. coli 0157:H7 'C.difficile' |
Ciprofloxacin 500 mg PO BID
OR Ciprofloxacin 750 mg daily x 3 days (avoid in cases of E. coli O157:H7 as it may increase the risk of hemolytic-uremic syndrome) Recent antibiotic exposure: consider C. difficile Antimotility drugs should not be used in C.difficile. C. difficile - Metronidazole 500 mg PO TID x 10-14 days. If no response at 5 days, switch to Vancomycin 125mg PO QID x10-14 days. See inpatient guidelines for severe or recurrent C. difficile infection and/or policy on C. difficile management. |
|
Nondysenteric Diarrhea
Large volume, nonbloody, watery diarrhea. Patient may have nausea, vomiting, and abdominal cramping but fever often absent. |
Viruses
Giardia Enterotoxigenic E. coli Enterotoxin-producing bacteria |
General Care: Observation
Oral rehydration Antimotility agents Giardia – especially if patient describes recent history of travel and/or ingestion of unfiltered water (e.g., camping), consider – Metronidazole 250 mg PO TID x 5 days. |
|
Traveler’s diarrhea
Empiric treatment while abroad |
Toxigenic E. coli
Salmonella Shigella Campylobacter Amebiasis |
Ciprofloxacin 500 mg PO BID x 1-3 days
Pregnancy or fluoroquinolone-resistant campylobacter: Azithromycin 1 g x 1 dose EITHER WITH or WITHOUT: Loperamide 4 mg PO x 1; then 2 mg after each loose stool, MAX 16 mg/day |
Mild, self-limited cases can be treated with fluid and electrolyte repletion and bismuth subsalicylate.
Prophylaxis generally not recommended. |
Diverticulitis | Enterobacteriaceae
Bacteroides fragilis 'Enterococcus' |
Amoxicillin/clavulanate
875 mg/125 mg PO BID OR MoxifloxacinID-R: SFGH 400 mg PO daily OR the combination of: Metronidazole 500 mg PO TID PLUS ONE OF: Ciprofloxacin 500 mg PO BID OR LevofloxacinID-R: VASF 500 mg PO daily |
Duration of treatment should be until patient is afebrile for 3-5 days.
Surgical evaluation and follow up is advised. |
'Acute Bronchitis' | Viral | No drug therapy required | |
Acute bacterial exacerbation of chronic bronchitis (COPD) | S. pneumoniae
H. influenzae Moraxellacatarrhalis |
Doxycycline 100 mg PO BID X 10 days | Azithromycin 500 mg PO daily X 1 day; then 250 mg PO daily X 4 days |
Community-acquired Pneumonia (CAP) | S. pneumoniae
M. pneumoniae C. pneumoniae Respiratory viruses Legionella spp. C. psittaci 'H. influenzae (if patient has co-morbidity) |
No recent antibiotic therapy:
Doxycycline 100 mg PO BID X 7 days OR Azithromycin 500 mg PO daily X 1 day; then 250 mg PO daily X 4 days Recent antibiotic therapy or patients with co-morbidities: Levofloxacin 750 mg PO daily X 5 days OR MoxifloxacinID-R: SFGH 400 mg PO daily X 7 days |
Previous antibiotic therapy within last 3 month should be elicited from patient. A course of antibiotics is a risk factor for drug resistance. Recent use of a fluoroquinolone should dictate selection of a non-fluoroquinolone regimen, and vice versa.
Careful follow-up highly recommended. |
Anerobic infection | Amoxicillin/clavulanate 875 mg/125 mg PO BID
OR Clindamycin 300 mg PO TID |
||
Acute otitis media
OR 'Otitis media with effusion' (OME) with signs or symptoms of acute infection |
S. pneumoniae
H. influenzae M. catarrhalis Group A Strep. |
Amoxicillin
1 g PO BID x 5-7 days OR 500 mg PO TID x 5-7 days |
For severe PCN allergy:
Azithromycin 500 mg PO daily x 1 day; then 250 mg PO daily x 4 days OR Doxycycline 100 mg PO BID for 5-7 days
|
Pharyngitis | Viral (EBV, rhinovirus, coronavirus, adenovirus etc)
Group A Streptococcus (5-20%) |
Penicillin VK 250 mg PO TID-QID x 10 days | For severe PCN allergy:
Clindamycin300 mg PO TID x 7-10 days
|
Acute Sinusitis | Viruses
S. pneumoniae H. influenzae M. catarrhalis |
Amoxicillin 500 mg PO TID X 5-7 days | For severe PCN allergy:
Doxycycline 100 mg PO BID X 5-7 days Consider treatment only in presence of fever, purulence or bloody discharge following an upper respiratory infection if symptoms persist for 7-10 days suggesting bacterial etiology. |
Chronic Sinusitis | Viruses
S. pneumoniae H. influenzae M. catarrhalis Anaerobes Staph. aureus Enterobacteriacae |
Amoxicillin/clavulanate
875 mg/125 mg PO BID X 10-14 days OR Amoxicillin/clavulanate CR 2 g BID X 10-14 days if drug-resistant Streptococcus pneumonia |
For severe PCN allergy:
Ciprofloxacin 500 mg PO BID OR Levofloxacin 500 mg PO daily x 10-14 days EITHER OF ABOVE WITH OR WITHOUT*: Clindamycin 300 mg PO TID
|
Treatment of active tuberculosis | Isoniazid 300 mg PO daily x 6 months
PLUS Rifampin 600 mg PO daily x 6 months PLUS Pyrazinamide 25 mg/kg PO daily x 2 months PLUS Ethambutol 15 mg/kg PO daily until Isoniazid or Rifampin sensitivity established PLUS: Pyridoxine (Vitamin B-6) 50 mg PO daily for 6 months |
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Latent TB | 'Isoniazid' 300 mg PO daily x 9 months | Rifampin 600 mg PO daily x 4 months |
Abscess | 'S. aureus' |
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Give antibiotics for complicated abscess
7-10 days of therapy is generally adequate |
Bites
Dog and Cat |
Streptococci
Pasteurella spp.* Staphylococci Oral anaerobes |
Amoxicillin/clavulanate
875 mg/125 mg PO BID Prophylaxis – x 5 days Treatment – x 10 days |
For severe PCN allergy
Clindamycin 300 mg PO TID PLUS ONE OF: Ciprofloxacin 500 mg PO BID OR Levofloxacin 500 mg PO daily
|
Bites
Human |
Viridans streptococci
Eikenella* Oral anaerobes |
Amoxicillin/clavulanate 875 mg/125 mg PO BID
Prophylaxis – x 5 days Treatment – x 10 days |
For severe PCN allergy:
Clindamycin 300 mg PO TID PLUS ONE OF: Ciprofloxacin 500 mg PO BID OR Levofloxacin500 mg PO daily OR TMP/SMX One DS tablet PO BID |
Cellulitis | β-hemolytic streptococci (most common)
S. aureus (less common) |
Cephalexin500 mg PO QID
OR Amoxicillin500 mg PO TID OR Clindamycin300 mg PO TID |
|
Diabetic Foot Ulcer
Localized cellulitis without systemic signs or symptoms, no osteomyelitis |
S. aureus
Streptococci Enterobacteriaceae |
Clindamycin 300 mg PO TID
If patient has been treated with antibiotics within the past month ADD: LevofloxacinID-R: VASF 750 mg PO daily OR Ciprofloxacin 500 mg PO BID |
|
Herpes Zoster | Immunocompetent
(Shingles/Zoster) Immunocompromised (Lymphoma, HIV infection, etc) and not severe (one dermatome) |
Acyclovir 800 mg PO 5x/day x 7-10 days
OR Valacyclovir 1 g PO TID x 7 days |
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Primary Infection in Adults (Chicken Pox) | Acyclovir 800 mg PO 5x/day x 5 days
OR 'Valacyclovir' 1 g PO TID x 5 days |
| |
Mastitis
Postpartum |
S. aureus
Including MRSA becoming more frequent |
Dicloxacillin 500 mg PO QID x 10-14 days
OR Cephalexin 500 mg PO QID x 10 -14 days If patient with risk factors for MRSA: TMP/SMX One DS tablet PO BID x 10-14 days OR Clindamycin 300mg PO TID x 10-14 days |
For mild PCN allergy:
Cephalexin 500 mg PO QID x 10-14 days For severe PCN allergy: Clindamycin 300 mg PO TID x 10-14 days
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Uncomplicated Cystitis
Women |
Enterobacteriaceae (E. coli)
S. saprophyticus (Coagulase negative staphylococcus) (4%) |
Nitrofurantoin 100 mg PO BID x 5-7 days – contraindicated in renal insufficiency (CrCl < 60 ml/min)
OR TMP/SMX 1 DS tablet PO BID x 3 days (if no previous antibiotic therapy) OR Fosfomycin 3 g PO x1 dose |
Reserve for patients at highest risk of failure (selection for resistant isolates):
Ciprofloxacin 500 mg PO BID x 3 days OR Levofloxacin 500 mg PO daily x 3 days Reserve for patients with history of resistant organisms or therapeutic failure (less effective): Cephalexin 500 mg PO QID x 7 days OR Cefpodoxime 200 mg PO BID x 7 days
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Recurrent Cystitis | Enterobacteriaceae (E. coli)
S. saprophyticus(Coagulase negative staphylococcus) (4%) |
Prophylaxis:
Either self administration if symptoms occur or prophylactic post-coital antibiotics Post menopausal: topical estrogen |
|
Asymptomatic bacteriuria | E.coli
Klebsiella Enterococcus |
No treatment required | |
Pyelonephritis | Enterobacteriaceae (E. coli)
Enterococci |
Ciprofloxacin 500 mg PO BID X 7-14 days
OR LevofloxacinID-R: VASF 500 mg PO daily X 7-14 days OR Trimethoprim/ Sulfamethoxazole 1 DS tablet PO BID X 14 days PLUS Ceftriaxone 1 g IV X 1 dose |
Cephalexin 500 mg PO QID X 10-14 days
OR Cefpodoxime200 mg PO BID X 10-14 days EITHER OF ABOVE PLUS: Ceftriaxone 1 g IV X 1 dose
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Prostatitis
Acute |
Enterobacteriaceae(E. coli) | Cephalexin 500 mg PO QID x 21 days
OR Ciprofloxacin 500 mg PO BIDX 2-4 weeks* OR LevofloxacinID-R: VASF 500 mg PO daily x 2-4 weeks* |
Trimethoprim/ Sulfamethoxazole 1 DS tablet PO BID
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Prostatitis
Chronic |
Enterobacteriaceae(E. coli) | Ciprofloxacin x 2 months*
OR LevofloxacinID-R: VASF x 2 months* |
Trimethoprim/ Sulfamethoxazole 1 DS tablet PO BID
|
Chlamydia
Genital/Rectal 'Pharyngeal' |
'Chlamydia trachomatis' | Azithromycin 1 g PO once
OR 'Doxycycline' 100 mg PO BID X 7 days |
|
First Clinical Episode or Anogenital Herpes | HSV 2 = 70-90%
HSV 1 = 10-30% |
Acyclovir 400 mg PO TID x 7-10 days | Valacyclovir 1 g PO BID x 7-10 days
In HIV patients with documented acyclovir resistance, use foscarnet. |
Episodic Therapy for Recurrent Episodes | Acyclovir 400 mg PO TID x 5 days
OR Acyclovir 800 mg PO BID x 5 days OR Acyclovir 800 mg PO TID x 2 days |
Valacyclovir 1 g PO daily x 5 days
Acyclovir 400 mg PO TID x 5-10 days OR Valacyclovir 1 g PO BID x 5-10 days | |
Suppression for Frequent Recurrence | HSV 2 = 70-90%
HSV 1 = 10-30% |
Acyclovir 400 mg PO BID
HIV patients: Acyclovir 400-800 mg BID or TID OR Valacyclovir 500 mg PO BID |
Valacyclovir 500-1000 mg PO daily
Consider suppressive therapy for patients experiencing greater than 3-4 episodes in 12 months. |
Pelvic inflammatory diseases (PID | N.gonorrhoeae
C.trachomatis anaerobes Gram-negative facultative bacteria streptococci |
Ceftriaxone 250 mg IM X 1
PLUS Doxycycline 100 mg PO BID X 14 days PLUS Metronidazole 500 mg PO BID x 14 days if BV is present or cannot be ruled out |
|
Syphilis
Primary, Secondary, Early Latent |
'T. pallidum' | Benzathine penicillin G2.4 MU IM X 1 dose | Doxycycline100 mg PO BID X 2 weeks |
Syphilis
Late Latent and Latent of Unknown Duration |
'T. pallidum' | Benzathine penicillin G2.4 MU IM Q week X 3 doses | Doxycycline100 mg PO BID X 4 weeks
Sexual partners must be treated.
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Candidal Vaginitis | 'Fluconazole' 150 mg PO x 1 dose | Miconazole 2% cream 5 g intravaginally x 3 days
OR Miconazole 100 mg suppository, one suppository daily x 7 days OR Clotrimazole 1% cream 5 g intravaginally x 7-14 days |
Protazoan Vaginitis | Metronidazole 2 g PO x 1 dose | Metronidazole 500 mg PO BID x 7 days
In treatment failures to metronidazole, retreat with metronidazole 500 mg PO BID x 7 days. |
Bacterial Vaginitis | Metronidazole 500 mg BID PO x 7 days
OR Metronidazole vaginal gel 0.75%, 5 g intravaginally daily x 5 days OR Clindamycin vaginal cream 2%, 5 g intravaginally daily x 7 days |
Clindamycin 300 mg PO BID X 7 days
OR Clindamycin ovules 100 mg intravaginally daily x 3 days |