-
What is the cell wall of prokaryotes (like bacteria) made of?
proteins, lipids, peptidoglycans
-
What is the cell wall of eukaryotes (such as fungi) made of?
- Chitin
- mannans, glucans (polysaccharides)
-
Which type of organisms have ergosterol, where is it, and what is its purpose?
- eukaryotes
- in the cell membrane
- it is a target or binding site for many antifungals
-
What is the difference between the cell walls of G(+) and G(-) bacteria?
- G(+) have a thick layer of peptidoglycan with many cross links
- G(-) have a thinner layer of peptidoglycan with fewer cross links
-
What is a gram stain used for?
- to classify bacteria as (+) or (-) on the basis of stain retention of the cell's peptidoglycan layer
- G(+) stain purple
- G(-) stain red
-
Name the 2 different types of media used to identify or differentiate between bacteria ad some examples of each.
- Differential - Identity of an organism - e.g. Macconkey inhibits growth of G(+) and supports G(-) growth, especially GIT orgs; CHROM differentiates betw Candida spp
- Selective - select specific bacteria from mixed cultures - e.g. Thayer-Martin allows Neisseria to grow
-
Name the 2 types of biochemical tests and what the results tell us.
- 1. Coagulase - if (+) the org is S. aureus; if (-) the org is other Staph spp
- 2. Catalase - if (+) the org is staphylococci; if (-) the org is streptococci
-
What is the purpose of the Lancefield serogroup test?
To group Strep spp. It can tell us where the infx came from.
-
What do respiration/fermentation tests tell us?
- if a bacteria has the ability to use lactose or glucose to produce acid or alcohol
- e.g. of non-fermenters - Pseudomonas, Acinetobacter
-
What does a hemolysis test on blood agar tell us about a bacteria?
- If alpha, they are partially hemolytic - a small zone is cleared. e.g. S. pneumoniae
- If beta, they are completely hemolytic - a large zone is cleared. e.g. S.pyogenes
- If gamma, they are not hemolytic.
-
What do serologic tests detect?
- Nonspecific or specific antibodies
- Presence and quantity can aid in identification of pathogen
-
If an unknown bacteria is a cluster of G+ cocci, what test might be used to determine the identity?
- A coagulase test.
- If (+) they'd probably be Staph aureus
- If (-) they'd probably be Staph epidermidis
-
If an unknown G+ bacteria is cocci in pairs or chains, what is its likely identity?
- Streptococci or Enterococcus
- If they are Streptococci, they could be Alpha or Beta hemolytic.
- If Alpha, likely identity is S. pneumoniae or Viridans group
- If Beta, Group A may be S pyogenes, Group B may be S. agalactiae, Group D may be S. bovis, or others
-
Gram + bacilli are unusual, but what are some of the more likely of this type of bacteria we may encounter?
- Bacillus anthracis
- Corynebacterium diptheriae
- Gardnerella vaginalis
- Listeria monocytogenes
-
Gram negative bacilli are usually what type of bacteria?
Enterobacteriaceae
-
Examples of coliform enterobacteriaceae
- E. coli
- Klebsiella spp
- Enterobacter
- Serratia
-
Examples of non-coliform enterobacteriaecae
- Proteus spp
- Salmonella spp
-
Are enterobacteriaceae fermentors or non-fermentors?
Fermentors
-
Name some non-fermentors
- P. aeruginosa
- Acinetobacter
-
Is Neisseria G(+) or (-)? Aerobic or anaerobic? Cocci or Bacilli?
Aerobic G(-) cocci
-
Name 3 G(+) anaerobes
- Clostridium
- Peptostreptococcus
- Propionibacterium acnes
-
Name one G(-) anaerobe and why it is a concern
- Bacteroides fragilis
- Concerning because it is inherently resistant to Abx
-
Name 3 atypical bacteria and the reason they're considered atypical
- Chlamydia spp - cell wall similar to G- but lack peptidoglycan
- Mycoplasma spp - lack a cell wall
- Legionella spp - G- but difficult to stain; difficult to grow on standard media; use serologic testing to identify
-
What is MIC? What is MBC?
- Minimum Inhibitory Concentration - the lowest conc of an agt that inhibits the visible growth of an organism
- Minimum Bactericidal Concentration - the lowest conc of an agt that results in a 99.9% reduction in colony forming units (kills the bacteria)
-
What does a bimodal susceptibility distribution indicate?
resistance
-
If the MBC is ______ times the MIC, the organism is tolerant
4-8
-
What are breakpoint values?
- they help evaluate MIC results and guide clinical decisions
- based on pkin and pdyn of drug, MIC distribution in the bacteria population, clinical efficacy
- tell if bacteria is susceptible, intermediate, or resistant to particular drugs
-
What is an antibiogram?
a table telling the bug, drug, % susceptibility to various drugs
-
Is the true MIC ever determined?
Rarely
-
Define virulence and virulence factors
- Virulence is a quantitative measurement of pathogenicity - the likelihood a pathogen will cause a disease
- Virulence factors are factors that allow a microbe to establish itself on or in a host and enhance its potential to cause disease
-
What are the 5 steps of pathogenesis?
- 1. Colonize the host
- 2. Gain access to the host
- 3. find a niche within the host
- 4. Evade host defenses
- 5. Multiply within the host
-
What are adhesions? Name 4.
- Microbial structures that mediate adherence of binding of a microbe to the host. Susceptible hosts have receptors for the adhesions.
- 1. fimbriae/pili
- 2. lectins
- 3. lipids
- 4. mechanical
-
Why might microbes produce biofilms? What are 2 pathogens that commonly produce biofilms?
- to facilitate binding to target cells
- to elude host defenses and Abx
-
How does a microbe maintain viability once inside a host?
- Must evade host defenses by:
- Producing antiphagocytic capsule
- Producing toxins or destructive enzymes
- Stealth
-
What are exotoxins? What are endotoxins?
- Exotoxins - bacterial proteins that the bacterium releases during exponential growth that are toxic for target cells
- Endotoxins - intracellular and cell-associated toxic components of G(-) microbes - lipopolysaccharides
-
List 3 factors that have contributed to the emergence of antimicrobial resistance
- 1. Inappropriate antibiotic use by clinicians
- 2. lack of pt education or ineffective education
- 3. widespread antimicrobial use in the food production industry
-
Difference between primary and secondary resistance
- Primary is naturally occurring and no exposure to antimicrobials is required; secondary follows exposure to antimicrobials
- Primary is predictable; secondary is not
- Primary is also known as inherent, intrinsic, or native; secondary is also known as acquired
-
How does secondary resistance come about?
- Selection of resistant subpopulations
- Genetic alterations - spontaneous mutations or acquisition of new genetic material
-
List 3 common mechanisms of antimicrobial resistance
- 1. antibiotic inactivating enzymes
- 2. alteration of antimicrobial target or active site
- 3. alterations in bacterial cellular membranes
-
how do beta-lactamases work?
inactivate beta-lactam antibiotics by splitting the beta-lactam ring at the amide bond
-
What are ESBLs and what are they active against?
- Extended-spectrum beta-lactamases
- Active vs. all beta lactams except cephamycins, cefepime, carbapenems
- Inhibited by beta-lactamase inhibitors such as sulbactam, clavulanate, and tazobactam
-
Are AmpC-type beta-lactamases inhibited by beta-lactamase inhibitors?
no
-
Examples of resistance by alteration of the antimicrobial target or active site
- penicillin binding proteins (PBPs)
- ribosomal binding sites
- cell wall precursors
- DNA gyrase
-
Examples of resistance by alterations in bacterial cellular membranes
- porin channels (change in # or size)
- transport proteins
- efflux pumps
-
What is MRSA's resistance secondary to? What is the treatment of choice?
- altered PBP
- vancomycin (linezolid and daptomycin may also be used)
-
What may be a good treatment option for VISA?
TMP/SMX
-
What therapy is necessary for a cidal effect in enterococcus? Name 3 treatment strategies.
- combo therapy with an aminoglycoside (with penicillin or vanco - these are static alone)
- 1. vanco, linezolid, daptomycin, and streptogramins
- 2. intermittent vs. continuous infusions of beta-lactams and vanco
- 3. traditional vs once-daily dosing of AGs
-
List 6 strategies to prevent the spread of antibiotic resistance
- 1. patient education
- 2. knowledge of local susceptibility patterns
- 3. prescriber education
- 4. develop guidelines for appropriate antimicrobial usage
- 5. vaccination
- 6. hand washing
-
Can penicillins still work in pen-resistant S. pneumoniae?
yes
-
Do AGs exhibit time-dependent or concentration-dependent bactericidal activity?
concentration-dependent
-
What are the 2 major toxicities assoc with AGs? What factor is best correlated to toxicity?
- ototoxicity & nephrotoxicity
- prolonged course of AG tx
-
What are the main goals of high-dose, extended-interval (once daily) AG dosing? How is the dosing interval determined?
- Optimize bactericidal activity
- Minimize toxicity
- Dosing interval determined and evaluated using a nomogram
- (basically a LD is given every time and the conc goes down to 0 in between doses each time)
-
How many half-lives does it take to reach steady state?
approx 5 (assuming renal fxn is stable)
-
How do we empirically dose vanco?
- based on pt's weight (TBW) and CrCl
- using nomogram
-
Does Vanco exhibit concentration-dependent or concentration-independent killing?
concentration-independent (time-dependent) - time above MIC
-
What are the usual vanco target drug concentrations?
Trough: 5-20 mg/ml
-
What is "red man syndrome"? How can it be prevented?
- Hypotensive rxn assoc with rapid infusion of vancomycin. D/T a vanco-induced histamine release.
- Prevent by slowing the infusion and/or premedicating with an antihistamine
-
A pt has a sinus infx susceptible to both amoxicillin and ampicillin. Which do you choose and why?
Amoxicillin because it has better bioavailability, you can give it with or without food, there is less frequent dosing than with ampicillin (bid or tid as opposed to qid)
-
An MD wants to prescribe Augmentin 500 mg TID for a pt with recurrent sinusitis. The pt can't swallow Augmentin 500 mg tabs. He writes for Augmentin 250 mg 2 tabs TID. Is this a good idea? Why?
No. Too much clavulanic acid - leads to diarrhea.
-
A pt has a severe pen allergy. Can the pt receive azetreonam? A carbapenem?
- Aztreonam yes
- Carbapenem no
-
Which FQs inhibit DNA gyrase? Topoisomerase IV? What is the advantage of inhibiting Topo IV?
- All FQs inhibit DNA gyrase
- 3rd and 4th Generation FQs inhibit Topo IV
- Advantage - less resistance and enhanced G(+) activity
-
Why shouldn't pediatric pts generally receive FQs? Which pediatric pts sometimes receive FQs?
- Because they can cause cartilage malformations
- CF patients
-
A pt develops a sternal wound infx following bypass surgery after an acute MI. He is placed on vanco. The pt is now complaining of severe itching on his face and neck. The nurse just hung the vanco bag on this pt about 10 minutes ago. He has been receiving vanco for about 7 days. What is the most plausible explanation for this event? How can you treat/prevent this rxn?
- Red Man Syndrome
- slow rate of infusion, give diphenhydramine, give fluids, dilute, change Abx
-
What is the difference in indications for vanco PO and IV?
- PO is for C. diff
- IV is for G(+) resistant infx like MRSA and MRSE
-
Describe the ototoxicity and nephrotoxicity that can occur with AGs
- Ototoxicity - Cochlear and Vestibular - May or may not be reversible.
- Nephrotoxicity - selectively toxic to proximal tubule - can cause acute tubular necrosis and glomerular nephrotoxicity
- Related to prolonged duration of therapy or concurrent ototoxic or nephrotoxic drugs
-
Which macrolide would you not use for bacteremia because of its extensive tissue penetration?
Azithromycin
-
Why should you drink a full glass of water with TCs and not take any doses at bedtime?
to prevent esophageal ulcerations
-
Which of the following Abx can be used to treat CAP in a pt on antiarrhythmics? moxifloxacin, azithromycin, doxycycline
no, no, yes
-
You have a pt on clindamycin who developed severe diarrhea and is C difficile (+) by toxin assay. How would you manage the diarrhea? List abx that can be used to treat AAD.
- Stop the clindamycin
- Give metronidazole 1st line PO x 10 days
- Vanco is 2nd line x 10 days
-
List unique SEs of metronidazole. What drug intx would you caution a pt about?
- furry tongue feeling, abnormal taste, peripheral neuropathy
- counsel about dirulfiram-like rxn with alcohol
-
What are rifampin's indications for use? Why isn't rifampin ever used alone to treat an infection?
- Indicated for TB, and for asymptomatic carriers of N. meningidites, in combo for synergy in G(+) infx
- Combo with vanco or penicillin for endocarditis or osteomyelitis
- Increased chance of resistance
-
If a pt is allergic to Bactrim what other non-abx drugs may they also be allergic to?
diuretics, celecoxib, sulfonylureas
-
Statins should be stopped for pts on which abx because of the risk on increased CPK/myopathy
Daptomycin
-
Which abx has an increased risk of serotonin syndrome if given concomitantly with SSRIs or MAOIs?
linezolid
-
Which abx is available PO for the treatment of hospital-acquired MRSA/MRSE?
linezolid
-
Which abx are assoc with dysglycemia?
FQs
-
Which abx exhibit concentration-dependent killing?
- AGs
- FQs
- Metronidazole
- Amphotericin B
- Daptomycin
-
Which abx exhibit concentration-independent killing?
- Beta-lactams
- Glycopeptides (e.g. Vanco, teicoplanin)
- Clindamycin
- Macrolides
- Fluconazole
-
What DI should you warn young women about with all antibiotics?
- Decreased efficacy of OCs
- Especially with rifampin
- Use backup for duration of abx therapy plus add'l 7 days
-
Which antibiotics interact with warfarin most significantly?
bactrim and flagyl
-
Which antibiotics can discolor urine?
- nitrofurantoin
- rifampin
- metronidazole
-
Which Abx cause photosensitivity?
-
Which Abx require therapeutic drug level monitoring?
- AGs
- Vanco IV
- chloramphenicol
-
Which abx is telithromycin related to? Which abx is tigecycline related to? Which abx is tinidazole related to?
- telithromycin - macrolides
- tigecycline - tetracyclines
- tinidazole - metronidazole
-
Which abx inhibit bacterial cell wall synthesis?
-
Which abx inhibit protein synthesis?
- AGs
- TCs
- glycocyclines, chloramphenicol
- macrolides
- synercid
- etc.
-
Which abx are pregnancy category B?
- beta-lactams
- nitrofurantoin
- macrolides (but not clarithromycin)
- dlindamycin
- metronidazole (but not in the 1st trimester)
- sulfonamides (except in the 3rd trimester)
- daptomycin
-
Are beta-lactams BS or BC? What is their MOA?
- Bactericidal
- Inhibit cell wall synthesis by binding to PBPs leading to the bacteria having a weak cell wall which becomes leaky and then bursts
-
What penicillin combos are antipseudomonal?
- ticarcillin/potassium clavulanate
- piperacillin/tazobactam sodium
-
What is the monobactam used in combo with AGs to fight pseudomonas?
aztreonam
-
Which carbapenems are antipseudomonal?
- imipenem/cilastatin
- meropenem
-
Which PCN is the DOC for otitis media and acute sinusitis?
amoxicillin
-
What abx are the DOC in pregnancy?
beta-lactams
-
How do penicillins produce a DI with warfarin?
they suppress the gut bacteria that produce Vitamin K
-
Which cephalosporin is ok to use in neonates?
cefotaxime
-
Which cephs are antipseudomonal?
- ceftazidime (3rd Gen)
- cefepime (4th Gen)
-
What is the purpose of cilastatin in combo with imipenem?
- It has no antibacterial activity
- Its role is to prevent renal tubular damage from imipenem
-
What is the MOA of aminoglycosides?
- Bactericidal
- Inhibits bacterial protein synthesis
- Has long PAE vs. G(-) organisms
-
For G(+) aerobes gentamicin has synergy with which abx?
vanco or a penicillin
-
What is the MOA of fluoroquinolones?
- Bactericidal
- Inhibits DNA gyrase (Topo II)
- 3rd and 4th Gen also inhibit Topo IV
- Possess PAE for all bacteria
-
What is the BBW for FQs?
Tendonitis and tendon rupture
-
Which class of Abx can cause crystalluria, QT prolongation and dysglycemia?
FQs
-
DIs with FQs
- Warfarin
- multivalent cations
- calcium
- antiarrhythmics
- sulfonylureas
-
MOA of vancomycin
- BC and BS (depending on the organism)
- Inhibits bacterial cell wall synthesis
-
What rate should infusion of vanco be limited to in order to avoid redman syndrome?
give 1 gram no faster than over 1 hour
-
What toxicities can vanco cause?
nephro and oto
-
MOA of macrolides/azalides and ketolides
inhibit protein synthesis
-
Which antibiotic classes are good for covering atypical organisms such as mycoplasma, legionella, chlamydiae, and protozoa?
-
clarithromycin is the DOC for which organisms?
-
DOC for CAP
macrolides/azalides
-
Which abx can cause QT prolongation?
-
MOA of tetracyclines
- inhibit protein synthesis
- bacteriostatic
-
What class of abx is the DOC for lyme disease and rocky mountain spotted fever?
TCs
-
Which abx have the SE of discoloration of teeth/depression of bone and teeth development?
TCs
-
MOA of sulfonamides
- competitive antagonism of PABA synthesis so bacteria cannot make folic acid
- bacteriostatic
-
DIs with sulfonamides
- diuretics
- celecoxib
- sulfonylureas
-
What is kernicterus and what abx can cause it?
- a yellow staining of parts of the brain d/t increased unbound drug in the neonate because of neonate's inability to conjugate bilirubin
- sulfonamides - they displace bilirubin from protein, resulting in increased free bilirubin
-
Sulfas inhibit 2C9 which can lead to significant intx with what drug? What must be monitored?
- warfarin
- monitor INR carefully
-
MOA of trimethoprim
inhibits dihydrofolate reductase
-
Only indication for trimethoprim
UTIs
-
MOA of lincosamides
Inhibit bacterial protein synthesis
-
What is the BBW on clindamycin?
severe and possibly fatal colitis
-
MOA of metronidazole
- toxic to bacterial RNA and DNA
- bactericidal to anaerobes (no activity vs. aerobes)
-
What is the BBW on metronidazole?
possible carcinogenicity
-
MOA of rifampin
- inhibits DNA-dependent RNA polymerase
- never used alone d/t rapid development of resistance
-
What is a unique SE of rifampin?
reddish-orange discoloration of urine, stool, saliva, tears (permanent discoloration of contacts), sweat, sputum
-
What abx is non-systemic and a derivative of rifamycin?
rifaximin
-
Indications for nitrofurantoin
UTIs
-
SEs of nitrofurantoin
- discolors urine brown
- pulmonary toxicity
- G6P deficiency hemolytic anemia
-
BBW for chloramphenicol
bone marrow suppression
-
Which abx can cause gray baby syndrome?
chloramphenicol
-
What 4 elements make up the basis of pharmacokinetics?
- absorption
- distribution
- metabolism
- elimination
-
How does concentration-dependent bactericidal activity work? What is the goal?
- The rate and/or extent of activity increases with increasing concentration of the antimicrobial
- Goal is to optimize the peak:MIC ratio
- These agents have a shallow dose-response curve
-
How does non-concentration-dependent bactericidal activity work? What is the goal?
- the rate and extent of bacterial killing is not significantly influenced by increasing antimicrobial concentrations - it is increased by the length of drug exposure (time-dependent killing)
- Goal is to optimize the time above the MIC (time > MIC)
-
Four factors that influence the PAE
- microorganism
- antimicrobial
- length of antimicrobial exposure
- antimicrobial concentration
-
Agents that exhibit concentration-dependent bactericidal activity and have relatively long PAEs should be administered as ________________ doses to optimize the peak:MIC ratio
large infrequent doses
-
If a peak:MIC ratio of 10-20:1 cannot be reached, which parameter best correlates with outcome?
- AUC:MIC
- want it to be >100:1
-
How should agents with concentration-independent killing and relatively short or no PAEs be dosed?
- in order to maximize the amount of time at or above the MIC
- small frequent doses or continuous infusion
-
Define PAE
post antibiotic effect - a persistent suppression of bacterial growth following a brief exposure to an antimicrobial
-
7 patient risk factors for pneumonia
- 1. altered consciousness (stroke, intoxication, seizure, sleep)
- 2. cigarette smoking
- 3. advanced age
- 4. underlying medical conditions
- 5. intubation
- 6. recent viral respiratory tract infx
- 7. HIV/AIDS
-
S/S of pneumonia
- fever or hypothermia
- rigors
- sweats
- new cough with or without sputum production
- chest discomfort
- dyspnea
-
Can pneumonia be diagnosed based on symptoms?
no
-
According to PORT scores, which risk classes treat pts as inpatients, and which treat as outpatients?
- Risk Class I, II: outpatient
- Risk Class III: outpatient or brief inpatient
- Risk Class IV, V: inpatient
-
Explain the CURB-65 Index and what it is used for
- Used to determine need for hospitalization and need for ICU admission
- Score based on how many of the following a patient has:
- Confusion
- BUN > 20 mg/dL
- Resp Rate >/= 30 breaths/min
- Low BP (systolic < 90 or diastolic </= 60)
- Age >/= 65 years
- If the score is 0-1 treat as outpatient
- If the score is 2 admit to ward
- If the score is 3 or more admit to ICU
-
Risk factors for drug-resistant S.pneumoniae
- extremes of age (< 5 or > 65)
- antibiotic use within the past 3 months
- exposure to a child in daycare
- alcoholism
- immunosuppression
- recurrent otitis media
- recent hospitalization
- multiple medical comorbidities
-
Outpatient treatment for pneumonia
- If no recent Abx exposure, treat with macrolide (azithromycin or clarithromycin) or doxycycline
- If pt has comorbidities or Abx exposure within last 3 months, treat with macrolide plus high-dose amoxicillin (or amox/clav) OR a FQ (levo, moxi, gemi)
-
Inpatient treatment of pneumonia in the medical ward
- Same if pt has had recent abx exposure or not.
- Macrolide plus beta-lactam OR FQ
- Options for beta-lactams - cefotaxime, ceftriaxone, ampicillin/sulbactam, ertapenem
-
Inpatient treatment of pneumonia in the ICU
- If Pseudomonas infx is not an issue, give a beta lactam + either a macrolide or a FQ
- If Pseudomonas infx is an issue, give Anti-pseudomonal agt plus ciprofloxacin, OR an Antipseudomonal agt plus an AG + a FQ or macrolide Antipseudomonal agents are piperacillin/tazobactam, imipenem, meropenem, cefepime
-
Organisms likely to cause pneumonia
S. pneumoniae, M. pneumoniae, C. pneumoniae, H. influenzae
-
What is the minimum duration of therapy for pneumonia? How long should a pt be afebrile?
- Min 5 days
- afebrile for at least 48-72 hours
-
CAP assoc signs of clinical instability
- temp > 37.8
- pulse > 100 bpm
- resp rate > 24 breaths/min
- systolic bp < 90
- O2 sat < 90%
- inability to maintain oral intake
- mental status changes
-
What is HAP
hospital acquired pneumonia - it occurs 48 h or more after admission and was not incubating at the time of admission
-
What is VAP?
ventilator-associated pneumonia - it arises more than 48-72 hours after endotracheal intubation
-
What is HCAP?
Healthcare associated pneumonia
-
Risk factors for HCAP
- pt hospitalized in an acute care hospital for > 2 days within 90 days of infection
- pt resided in a nursing home or LTC facility
- Pt received recent IV Abx, chemotherapy, or wound care within the past 30 days
- pt attended a hospital or hemodialysis clinic
-
Empiric antibiotic therapy for nosocomial pneumonia
- if not late onset or no risk factors for MDR pathogens, treat with ceftriaxone, FQ, Amp/sulbactam, or ertapenem
- if late onset (>/= 5 days) or risk factors for MDR pathogens, give an anti-psa ceph, or an anti-psa carbapenem, or pip/tazo PLUS an anti-psa FQ or an AG (also give vanco or linezolid if MRSA is suspected)
-
What should be ordered in all pts with suspected pneumonia?
- a chest x-ray - helpful with diagnosis, assessing need for hospitalization, and possible etiology
- note: a CXR is not very valuable for monitoring pt response to therapy b/c it lags behind the clinical picture by about 3 days
-
What are the major antigenic determinants of influenza A viruses?
- hemagglutinin - mediates attachment and entry of virus into host cells
- neuraminidase - facilitates the spread of virons
-
3 steps in the pathogenesis of influenza
- 1. virus enters human via inhalation of virus-containing respiratory secretions
- 2. Virus is internalized in resp tract epithelial cells
- 3. Replicates within cells and is then released throughout the body
-
Clinical course of influenza
- 1-4 days of incubation
- abrupt onset of sx
- fever, chills, headache, myalgia, persist for about 3 days
- resp sx may persist 3-4 d after fever subsides
- convalescence 1-2 weeks
-
What is the duration of infectivity for influenza?
- 5 days after illness onset for adults
- Children shed virus for several days before onset to > 10 days after onset of sx
-
What is ILI?
- influenza-like illness
- characterized by a fever AND a cough AND/OR a sore throat in the absence of a known cause
-
What drugs are approved for treatment and prophylaxis of influenza?
- Neuraminidase inhibitors (oseltamivir and zanamivir)
- must be administered within 48 h of symptom onset
-
Which influenza medication is safe in pregnancy?
oseltamivir (Tamiflu)
-
Which influenza med is CI'd in asthma pts?
zanamavir (Relenza)
-
who should receive the influenza vaccine?
- anyone who wants to reduce the risk of getting influenza
- kids 6 mo - 18 yr
- those > 50 years old
- pregnant women
- those with chronic medical conditions
- immunosuppressed pts
- residents of LTC facilities
- those with conditions that increase risk of aspiration
- persons who live with or care for high-risk persons (health care workers, household contacts of those < 5 and > 50 years, esp those < 6 mo, or with other high risk conditions)
-
What are the different ways to classify intraabdominal infx?
- 1. by location - can be localized (e.g. abscess, abdominal penetration trauma wound) or generalized (e.g. peritonitis)
- 2. by complexity - can be uncomplicated (involving single site/organ, not into peritoneal cavity - e.g. appendicitis, cholecystitis) or complicated (involving several sites/organs in add'n to source of infx; infx extends into peritoneal cavity - e.g. peritonitis, intra-abdominal abscess)
- 3. by acquisition locale - can be community-acquired or health-care associated (nosocomial)
-
Which type of IAIs usually require both source control and antimicrobial therapy?
complicated IAI
-
Community-onset health care-associated (IAI) infx include cases involving pts with at least one of the following health care risk factors. How is hospital-onset infx different?
- 1. presence of an invasive device at time of admission
- 2. hx of MRSA infx or colonization
- 3. hx of surgery, hospitalization, dialysis, or residence in a LTCF in the 12 mo preceding the culture date
Hospital-onset infx - pts have positive culture from a normally sterile site obtained more than 48 h after admission to hospital
-
Is appendicitis complicated or uncomplicated? How is it treated?
- usually uncomplicated
- managed by surgical intervention
-
What is cholecystitis?
sudden inflammation of gallbladder (often not infectious)
-
When does IAI result from diverticulitis?
When a perforation occurs and colonic contents move into the peritoneal cavity
-
How is peritonitis classified?
- Primary: aka SBP (spontaneous bacterial peritonitis) - no identified source - in adults with liver disease and/or ascites
- Secondary: most common form - almost always community-acquired - may affect anyone
- Tertiary: complication of improperly managed primary or secondary peritonitis or other abdominal medical procedures - healthcare facility-acquired - occurs in critically ill or immunocompromised pts
- Peritoneal-dialysis associated: only in pts who receive peritoneal dialysis
-
Common causes of peritonitis and abscess
- appendicitis
- diverticulitis
- IBD
- gastrointestinal cancer
-
Which classes of peritonitis require urgent medical attention?
- all of them require urgent medical attention
- pts with secondary and tertiary are usually in acute distress and their conditions deteriorate rapidly
- pts with primary or peritoneal dialysis-associated are not usually in acute distress
-
What is ileus?
the absence of peristalsis in the intestine
-
because primary peritonitis (SBP) has highly variable and non-specific presentation, how is it diagnosed? When do we initiate empiric antibiotic treatment?
- Must use paracentesis with lab testing of the ascites to confirm diagnosis
- PMN cell count of > 250/mm3 is diagnostic of SBP and warrants empiric antibiotic therapy
-
What can happen in severe cases of IAI?
- third-spacing
- abdominal distension
- ileus
- hypovolemia
- septic shock
- bacteremia
- if no intervention is performed, multi-organ failures, severe systemic inflammatory response (SIRS), death
-
What are the most common anaerobes involved in peritonitis?
Bacteroides spp
-
Describe the microbiology of IAI
- Primary (SBP): usually monomicrobial, common orgs are Streptococci spp, E. coli, and Klebsiella spp
- Secondary: usually polymicrobial with a mix of aerobic and anaerobic bacteria
- Tertiary: associated with nosocomial microbes such as MRSA, VRE, Pseudomonas, coagulase-negative staph, candida (fungi), and those assoc with secondary
- Peritoneal dialysis-associated: often involves enteric organisms and those found on the skin such as staph
- Abscess: anaerobes commonly
-
What is the typical treatment for uncomplicated IAIs?
- surgical source control only
- antimicrobials not required unless there is anticipated complication
- For appendicitis only prophylactic and perioperative abx for the surgery are required - no full course of routine abx is necessary
- For bowel injuries d/t penetrating or blunt trauma that are repaired within 12 hours and with no complications, antibiotics should be used for less than 24 hours post surgery (and prophylactic and perioperative abx)
-
Treatment for abscess
- surgical drainage
- abx therapy is just an adjuvant
-
Treatment for secondary or tertiary peritonitis
- IV fluids
- Infx source control
- Empiric IV abx ASAP
- 4-7 day course of abx therapy
-
Treatment for SBP
- May need IV fluids and/or surgical source control
- If fluid from ascites confirms diagnosis of SBP (PMN > 250) abx therapy is needed
- DOC is IV cefotaxime
- beta lactam/beta lactamase inhibitor combos and carbapenems would work but are too broad spectrum, so are inappropriate as empiric tx. Also avoid AGs.
- Optimal duration of therapy is 5 days minimum
-
What is the treatment for peritoneal dialysis-assoc peritonitis?
- may need IV fluids and surgical source control
- culture the dialysate to id the orgs, then determine abx susceptibilities
- empiric IV abx - followed by monotx with vanco, or a 1st gen ceph (e.g. cefazolin) given IP (would use vanco if pt is allergic to pens or if MRSA is suspected or confirmed)If more severe, can add AG given IP to the ceph
- Can admin the abx QD (intermittent dosing), and the dwell time must exceed 6 hours each time
- Duration of tx is usually 10-14 days
-
For IP abx therapy which abx are ok to mix in the same dialysis solution? Which should not and why?
- vanco, AGs, cephs can all be mixed in same dialysis sol'n
- AGs should not be mixed with pens because of chemical incompatibility (acid/base rxn)
-
What is the duration of therapy for community-acquired peritonitis?
4-7 days
-
What abx is the main component in combo therapy for community-acquired IAI? Which agents should not be used?
- metronidazole is main component (mostly used with a ceph or levo)
- Don't use amp/sulbactam d/t E.coli resistance, cefotetan and clindamycin d/t Bacteroides resistance, AGs b/c other agents are less toxic and equally or more effective
- Empiric antifungal tx is not necessary
- Don't use oral agents initially
-
Appropriate options for healthcare-acquired complicated IAI (tertiary peritonitis)
- should have broad coverage, including Pseudomonas
- Anti-psa B-lactam/B-lactamase inhibitor combo: piperacillin/tazobactam
- Anti-psa carbapenems: imipenem/cilastatin, meropenem, doripenem
- Anti-psa ceph + metronidazole: cefepime or ceftazidime
- Anti-psa FQ + metronidazole: cipro or levo
- Add vanco @ institutions with high incidence of MRSA/MRSE or if pt has hx of colonization
-
When would anti-fungal therapy be indicated in healthcare-acquired complicated IAI? Which agents?
- if pt is immunocompromised, has recurrent IAI, or failure to respond to appropriate initial therapy
- echinocandins or azole antifungals
-
Which type of peritonitis usually does not require culturing, speciation, and determination of antibiotic susceptibility?
Community-acquired (secondary peritonitis) - the empiric therapy is often maintained for the full course of abx treatment unless there is intolerance or complications
-
What is the duration of therapy for each type of peritonitis?
- primary - 5 d minimum
- secondary - 4-7 d
- tertiary - 4-7 d
- dialysis-assoc - 10-14 d
- abscess - abx are only adjuvant
-
What type of pneumococcal test is warranted for all pts admitted to the ICU?
pneumococcal urinary antigen test
-
What type of peritonitis might require prophylactic abx?
primary (SBP)
|
|