- •Abbreviations
- •1 Overview of Antimicrobial Therapy
- •Factors in Antibiotic Selection
- •Factors in Antibiotic Dosing
- •Microbiology and Susceptibility Testing
- •PK/PD and Other Considerations in Antimicrobial Therapy
- •Antibiotic Failure
- •Pitfalls in Antibiotic Prescribing
- •References and Suggested Readings
- •2 Empiric Therapy Based on Clinical Syndrome
- •Empiric Therapy of CNS Infections
- •Empiric Therapy of HEENT Infections
- •Empiric Therapy of Lower Respiratory Tract Infections
- •Empiric Therapy of GI Tract Infections
- •Empiric Therapy of Genitourinary Tract Infections
- •Empiric Therapy of Sexually Transmitted Diseases
- •Empiric Therapy of Bone and Joint Infections
- •Empiric Therapy of Skin and Soft Tissue Infections
- •Sepsis/Septic Shock
- •Febrile Neutropenia
- •Transplant Infections
- •Toxin-Mediated Infectious Diseases
- •Bioterrorist Agents
- •References and Suggested Readings
- •Gram Stain Characteristics of Isolates
- •Parasites, Fungi, Unusual Organisms in Blood
- •Parasites, Fungi, Unusual Organisms in CSF/Brain
- •Parasites, Fungi, Unusual Organisms in Lungs
- •Parasites, Fungi, Unusual Organisms in Heart
- •Parasites, Fungi, Unusual Organisms in the Liver
- •References and Suggested Readings
- •5 HIV Infection
- •HIV Infection Overview
- •Stages of HIV Infection
- •Acute (Primary) HIV Infection
- •Initial Assessment of HIV Infection
- •Indications for Treatment of HIV Infection
- •Antiretroviral Treatment
- •Treatment of Other Opportunistic Infections in HIV
- •HIV Coinfections (HBV/HCV)
- •References and Suggested Readings
- •6 Prophylaxis and Immunizations
- •Surgical Prophylaxis
- •Post-Exposure Prophylaxis
- •Chronic Medical Prophylaxis
- •Endocarditis Prophylaxis
- •Travel Prophylaxis
- •Tetanus Prophylaxis
- •Immunizations
- •References and Suggested Readings
- •Empiric Therapy of CNS Infections
- •Empiric Therapy of HEENT Infections
- •Empiric Therapy of Lower Respiratory Tract Infections
- •Empiric Therapy of Vascular Infections
- •Empiric Therapy of Gastrointestinal Infections
- •Empiric Therapy of Bone and Joint Infections
- •Empiric Therapy of Skin and Soft Tissue Infections
- •Common Pediatric Antimicrobial Drugs
- •References and Suggested Readings
- •8 Chest X-Ray Atlas
- •References and Suggested Readings
- •9 Infectious Disease Differential Diagnosis
- •11 Antimicrobial Drug Summaries
- •Appendix
- •Malaria in Adults (United States)
- •Malaria in Children (United States)
- •Index
364 |
A n t i b i o t i c E s s e n t i a l s |
CHRONIC MEDICAL PROPHYLAXIS
Some infectious diseases are prone to recurrence/relapse and may benefit from intermittent or chronic suppressive therapy.. The goal of suppressive therapy is to minimize the frequency/severity of recurrent infectious episodes..
Table 6.4. Chronic Medical Prophylaxis
|
Usual |
Preferred |
Alternate |
|
Disorder |
Organisms |
Prophylaxis |
Prophylaxis |
Comments |
|
|
|
|
|
Asplenia/ |
S.. pneumoniae |
Amoxicillin |
Respiratory |
Long-term prophylaxis |
impaired |
H.. influenzae |
1 gm (PO) q24h |
quinolone* (PO) |
effective. Vaccines may |
splenic function |
N.. meningitidis |
indefinitely |
q24h indefinitely |
be given but are not |
|
|
|
|
always protective.. Use |
|
|
|
|
amoxicillin in children.. |
UTIs (recurrent) |
Gram-negative |
Nitrofurantoin |
Amoxicillin |
Prophylaxis for |
|
bacilli Enterococci |
100 mg (PO) |
500 mg (PO) |
reinfection UTIs (≥ 3 |
|
|
q24h × 6 months |
q24h × 6 mos or |
per year).. Relapse UTIs |
|
|
|
TMP–SMX 1 SS |
should be investigated |
|
|
|
tablet (PO) q24h × |
for stones, abscesses, or |
|
|
|
6 months |
structural problems.. |
Asymptomatic |
Gram-negative |
Nitrofurantoin |
Amoxicillin 1 gm |
Prophylaxis prevents |
bacteriuria in |
bacilli |
100 mg (PO) |
(PO) q24h × 1 |
symptomatic |
pregnancy |
|
q24h × 1 week |
week |
infections.. |
Prophylaxis |
Candida albicans |
Posaconazole |
|
Prophylaxis given until |
of fungal |
Non-albicans |
200 mg (PO) |
|
neutropenia resolves |
infections in |
Candida |
q8h or |
|
(absolute neutrophil |
neutropenic |
Aspergillus |
Itraconazole 200 |
|
count ≥ 500 cells/mm3).. |
patients† |
|
mg (PO) q12h |
|
|
Recurrent |
H.. simplex (HSV-2) |
Famciclovir |
Acyclovir 200 mg |
Begin therapy as soon |
genital herpes |
|
125 mg (PO) |
(PO) 5x/day × 5 |
as lesions appear.. (For |
(< 6 episodes/ |
|
q12h × 5 days or |
days |
HIV disease, see Ch.. 5..) |
year) |
|
Valacyclovir 500 |
|
Famciclovir 1 gm (PO) |
|
|
mg (PO) q24h × |
|
q12h ×1 day ↓lesion |
|
|
5 days |
|
progression by 2 days.. |
Recurrent |
H.. simplex (HSV-2) |
Famciclovir |
Acyclovir 400 mg |
Suppressive therapy is |
genital herpes |
|
250 mg (PO) |
(PO) q12h × 1 year |
indicated for frequent |
(> 6 episodes/ |
|
q12h × 1 year |
|
recurrences.. (For HIV |
year) |
|
or Valacyclovir |
|
disease, see Ch.. 5..) |
|
|
1 gm (PO) q24h |
|
|
|
|
× 1 year |
|
|
|
Chapter 6. Prophylaxis and Immunizations |
365 |
||
Table 6.4. Chronic Medical Prophylaxis (cont’d) |
|
|
||
|
|
|
|
|
|
Usual |
Preferred |
Alternate |
|
Disorder |
Organisms |
Prophylaxis |
Prophylaxis |
Comments |
|
|
|
|
|
Acute |
S.. pneumoniae H.. |
Moxifloxacin 400 mg or levofloxacin |
Treat each episode |
|
exacerbation |
influenzae |
500 mg or gatifloxacin 400 mg or |
individually.. |
|
of chronic |
M.. catarrhalis |
gemifloxacin 320 mg (PO) q24h × 5 |
|
|
bronchitis |
|
days or Amoxicillin/clavulanic acid |
|
|
(AECB) |
|
XR 2 tablets (PO) q12h × 5 days or |
|
|
|
|
Clarithromycin XL 1 gm (PO) q24h × |
|
|
|
|
5 days or Doxycycline 100 mg (PO) |
|
|
|
|
q12h × 5 days or Azithromycin 500 |
|
|
|
|
mg (PO) × 3 days |
|
|
Acute |
Group A |
Benzathine |
Amoxicillin 500 mg |
Group A streptococcal |
rheumatic fever |
streptococci |
penicillin 1..2 mu |
(PO) q24h or |
pharyngitis and acute |
(ARF) |
|
(IM) monthly |
Azithromycin |
rheumatic fever are |
|
|
until age 30 |
500 mg (PO) q72h |
uncommon after |
|
|
|
until age 30 |
age 30.. |
Neonatal Group |
Group B |
Ampicillin 2 gm |
Clindamycin |
Indications: previous |
B streptococcal |
streptococci |
(IV) q4h at onset |
600 mg (IV) q8h |
infant with GBS |
(GBS) infection |
|
of labor until |
at onset of labor |
infection, maternal GBS |
(primary |
|
delivery |
until delivery |
colonization/infection |
prevention) |
|
|
or |
during pregnancy, |
|
|
|
Vancomycin 1 gm |
vaginal/rectal culture |
|
|
|
(IV) q12h at onset |
of GBS after week 35 |
|
|
|
of labor until |
of gestation, delivery ≤ |
|
|
|
delivery |
week 37 of gestation |
|
|
|
|
without labor/ruptured |
|
|
|
|
membranes, ruptured |
|
|
|
|
membranes ≥12 hrs, |
|
|
|
|
or intrapartum temp ≥ |
|
|
|
|
100..4°F.. |
*Levofloxacin 500 mg (PO) or gatifloxacin 400 mg (PO) q24h or moxifloxacin 400 mg (PO)..
†During induction chemotherapy for acute myelogenous leukemia (AML) or myelodysplastic syndrome (MDS)..
Table 6.5. HIV Pre-Exposure Prophylaxis (PrEP)
|
Usual |
Preferred |
Alternate |
|
Disorder |
Organisms |
Prophylaxis |
Prophylaxis |
Comments |
|
|
|
|
|
Repeated |
HIV |
Truvada 1 tablet |
|
Avoid if CrCl < 60 ml/ |
potential HIV |
|
(PO) q24h × 90 |
|
min.. Avoid if breast |
exposures |
|
days (recheck |
|
feeding.. |
|
|
HIV status) |
|
|
|
|
|
|
|
366 |
|
|
|
|
A n t i b i o t i c E s s e n t i a l s |
|
|||||
Table 6.6. HIV Post-Exposure Prophylaxis (PEP) |
|
|
|
|
|||||||
|
|
|
|
|
|
|
|
||||
|
|
Preferred |
|
Recommended |
Alternate recommended |
|
|||||
Exposure |
regimen |
|
|
|
regimen |
|
|
regimen |
Comments |
||
|
|
|
|
|
|
||||||
HIV |
Truvada |
|
Truvada 1 tablet (PO) |
Truvada 1 tablet (PO) q24h |
… |
||||||
|
|
1 tablet |
|
q24h [tenofovir (TDF) |
[tenofovir (TDF) 300 mg |
|
|||||
|
|
(PO) q24h |
|
300 mg (PO) q24h + |
(PO) q24h +emtricitabine |
|
|||||
|
|
[tenofovir |
|
emtricitabine (FTC) |
(FTC) 200 mg (PO) q24h] × |
|
|||||
|
|
(TDF) 300 mg |
|
200 mg (PO) q24h] × 4 |
4 weeks |
|
|||||
|
|
(PO) q24h + |
|
weeks |
plus |
|
|
plus |
|
||
|
|
emtricitabine |
|
|
|
|
Zidovudine (ZDV) 300 mg |
|
|||
|
|
(FTC) 200 mg |
|
(one of the following) |
(PO) q12h × 4 weeks |
|
|||||
|
|
(PO) q24h] × |
|
Darunavir (DRV) 800 mg |
|
|
or |
|
|||
|
|
4 weeks |
|
(PO) q24h × 4 weeks |
Truvada 1 tablet (PO) |
|
|||||
|
|
plus either |
|
|
|
|
or |
q24h [tenofovir (TDF) 300 |
|
||
|
|
Raltegravir |
|
Atazanavir (ATZ) 300 mg |
mg (PO) q24h + |
|
|||||
|
|
(RAL) 400 mg |
|
(PO) q24h × 4 weeks |
emtricitabine (FTC) 200 mg |
|
|||||
|
|
(PO) q12h × |
|
|
|
|
or |
(PO) q24h] × 4 weeks |
|
||
|
|
4 weeks |
|
Fosamprenavir (FPV)1400 |
|
|
plus |
|
|||
|
|
or |
|
mg (PO) q24h ×4 weeks |
Kaletra 2 tablets (PO) |
|
|||||
|
|
Dolutegravir |
|
|
|
|
plus |
q12h [lopinavir (LPV) |
|
||
|
|
(DTG) 50 mg |
|
Ritonavir (RTV) 100 mg |
200 mg (PO) q12h |
|
|||||
|
|
(PO) q24h × |
|
(PO) q24h × 4 weeks |
+ritonavir (RTV) 50 mg (PO) |
|
|||||
|
|
4 weeks |
|
|
|
|
|
q12h] × 4 weeks |
|
||
|
|
|
|
|
|
||||||
Table 6.7. HIV: Prophylaxis of Opportunistic Infections |
|
|
|||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Indication for |
|
|
|
|
Disorder |
Usual organism |
|
|
|
Prophylaxis |
|
|
Intervention |
|||
|
|
|
|
|
|
|
|
|
|
|
|
HIV |
|
PCP |
|
CD |
4 |
< 200/mm3 |
|
|
TMP-SMX: 1 SS tablet or 1 DS |
||
|
|
|
|
|
|
|
|
|
tablet (PO) q24h or Atovaquone 1500 |
||
|
|
|
|
|
|
|
|
|
|
||
|
|
|
|
|
|
|
|
|
|
mg (PO) q24h |
|
|
|
TB |
|
PPD > 5 mm (current or |
|
|
INH: 300 mg (PO) q24h × 9 months |
||||
|
|
|
|
|
past) or contact with active |
|
Rifabutin: Dose based on concomitant |
||||
|
|
|
|
|
case |
|
|
ART × 4 months |
|
||
|
|
Toxoplasmosis |
|
IgG (+) and CD < 100/mm3 |
|
TMP-SMX: 1 DS tablet (PO) q24h |
|||||
|
|
|
|
|
|
|
4 |
|
|
|
|
|
|
MAI |
|
CD |
4 |
< 50/mm3 |
|
|
Azithromycin: 1200 mg (PO) q week |
||
|
|
S..pneumoniae |
|
CD |
4 |
> 200/mm3 |
|
|
Pneumococcal vaccine |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hepatitis B (HBV) |
|
Susceptible patients |
|
|
Hepatitis B vaccine |
|
|||
|
|
|
|
|
|
|
|
|
|
||
|
|
Hepatitis A (HAV) |
|
Susceptible patients |
|
|
Hepatitis A vaccine |
|
|||
|
|
|
|
|
|
|
|
|
|
||
|
|
Influenza |
|
All patients |
|
|
Annual influenza vaccine |
||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
VZV |
|
CD |
4 |
> 200/mm3, VZV |
|
|
VZV vaccine |
|
|
|
|
|
|
|
antibody negative |
|
|
|
|
||
|
|
|
|
|
|
|
|
|
|
|
|
|
Chapter 6. Prophylaxis and Immunizations |
367 |
|||||
Table 6.8. Transplant Prophylaxis (BMT/SOT) |
|
|
|
||||
|
|
|
|
|
|
|
|
|
Usual |
Preferred |
Alternate |
|
|
||
Exposure |
organism |
prophylaxis |
prophylaxis |
Comments |
|
||
|
|
|
|
|
|
|
|
Herpes simplex |
Herpes |
HSV →< 6 |
|
Acute prophylaxis |
|
||
|
|
|
|
|
|
|
|
(HSV) |
simplex |
recurrences/year |
|
Nearly all post-tranplant HSV |
|||
|
|
Valacyclovir 500 |
Acyclovir |
infections occur < 1 month.. |
|
||
|
|
mg (PO) q24h × |
400 mg (PO) |
Transplants receiving CMV |
|
||
|
|
30 days |
q8h × |
prophylaxis with ganciclovir, |
|
||
|
|
|
or |
30 days post- |
or valganciclovir are protected |
||
|
|
Famciclovir 1 g |
BMT |
against HSV (see CMV |
|
||
|
|
(PO) q12 × 30 |
|
prophylaxis).. |
|
||
|
|
days |
|
|
|
||
|
|
HSV → > 6 |
|
Chronic prophylaxis |
|
||
|
|
|
|
|
|
|
|
|
|
recurrences/year |
|
Valacyclovir 500 mg (PO) q12h |
|||
|
|
Valacyclovir 1 gm |
Acyclovir 400 |
or |
|
||
|
|
(PO) q24h × 90 |
mg (PO) q8h |
Famciclovir 500 mg (PO) q12h |
|||
|
|
days |
× 90 days |
or |
|
||
|
|
|
or |
post-BMT |
Acyclovir 400 mg (PO) q8h |
|
|
|
|
Famciclovir 250 |
|
|
|
||
|
|
mg (PO) q12 × |
|
|
|
||
|
|
30 days |
|
|
|
||
|
|
|
|
|
|
|
|
Varicella zoster |
Varicella |
VZV seropositive |
Acyclovir |
Post-transplant VZV infections |
|||
virus (VZV) |
zoster virus |
recipient |
400 mg (PO) |
occur later than HSV.. |
|
||
|
|
Valacyclovir 500 |
q8h post- |
> 95% of adults are VZV |
|
||
|
|
mg (PO) q12h |
transplant x |
seropositive.. In transplants, |
|
||
|
|
post-transplant x |
4–24 months |
most VZV infections are due |
|
||
|
|
4–24 months |
|
to reactivation rather than |
|
||
|
|
|
|
|
|
primary infection.. Patients |
|
|
|
|
|
|
|
may develop shingles after |
|
|
|
|
|
|
|
prophylaxis is discontinued.. |
|
|
|
|
|
|
|
|
|
|
|
VZV |
Acyclovir |
Transplant recipients on CMV |
|||
|
|
seronegative |
800mg (PO) |
prophylaxis with gangciclovir |
|||
|
|
recipient (VZV |
5x/day post- |
or valganciclovir do not |
|
||
|
|
seropositive |
transplant x |
require VZV prophylaxis.. |
|
||
|
|
graft) |
4–24 months |
|
|
||
|
|
Valacyclovir 1 g |
|
|
|
||
|
|
(PO) q8h post- |
|
|
|
||
|
|
transplant x |
|
|
|
||
|
|
4–24 months |
|
|
|
||
|
|
|
|
|
|
|
|
368 |
|
A n t i b i o t i c |
E s s e n t i a l s |
|
|
Table 6.8. Transplant Prophylaxis (BMT/SOT) (cont’d) |
|
||||
|
|
|
|
|
|
|
Usual |
Preferred |
|
Alternate |
|
Exposure |
organism |
prophylaxis |
|
prophylaxis |
Comments |
|
|
|
|
|
|
Cytomegalovirus |
Transplants |
Valganciclovir |
|
Ganciclovir |
Alternately, preemptive |
(CMV) |
(SOT) |
900 mg (PO) |
|
5 mg/kg (IV) |
therapy may be used.. When |
|
D+/R-, D+/ |
q24h × 3–6 |
|
q24h × 3–6 |
quantitative CMV PCR/pp 65 |
|
R+, D-/R+ |
months |
|
months |
antigenemia levels become |
|
|
|
|
|
+/↑. |
|
|
|
|
|
D-/R- patients should receive |
|
|
|
|
|
CMV negative blood and |
|
|
|
|
|
leukocyte depleted RBCs |
|
|
|
|
|
but do not require antiviral |
|
|
|
|
|
prophylaxis.. |
|
|
|
|
|
|
PCP |
SOT/BMT |
TMP-SMX |
|
TMP-SMX |
See Drug Summaries for drug- |
|
(with |
1 DS tablet (PO) |
|
1 SS tablet |
drug interactions.. |
|
GVHD) |
q week × 12 |
|
(PO) q24h × |
|
|
|
months |
|
12 months |
|
|
|
|
|
or |
|
|
|
|
|
Atovaquone |
|
|
|
|
|
1500 mg |
|
|
|
|
|
(PO) q24h × |
|
|
|
|
|
12 months |
|
|
|
|
|
(with a meal) |
|
|
|
|
|
|
|
Toxoplasmosis |
Heart |
TMP-SMX |
|
Atovaquone |
See Drug Summaries for drug- |
|
transplants |
1 DS tablet (PO) |
|
1500 mg |
drug interactions.. |
|
|
q24h |
|
(PO) q24h |
|
|
|
|
|
(take with |
|
|
|
|
|
a meal) |
|
|
|
|
|
|
|
Candida sp. |
Liver/ |
Fluconazole 400 |
|
Posacona |
See Drug Summaries for drug- |
|
pancreas |
mg (IV/PO) |
|
zole 200 mg |
drug interactions.. |
|
transplants |
q24h × 4 weeks |
|
(PO) q8h × 4 |
|
|
|
|
|
weeks |
|
|
|
|
|
|
|
Aspergillus sp. |
Allogeneic |
Voriconazole 200 |
|
Posacona |
Until engrafted (BMT); |
|
BMT/lung |
mg (PO) q12h |
|
zole 200 mg |
duration in lung transplants |
|
transplants |
|
|
(PO) q8h |
unclear.. |
|
|
|
|
|
See Drug Summaries for drug- |
|
|
|
|
|
drug interactions.. |
|
|
|
|
|
|
GVHD = graft vs.. host disease..