Acute and Chronic Sinusitis Flashcards
What are risk factors for Antibiotic resistance in Acute bacterial rhinosisusitis
- Age <2 and >65
- Prior ABs in the last month
- Prior hospitalization in past 5 days
- Comorbidities
- Immunocompromised.
What are the 3 clinical presentations for identifying patients with acute bacterial vs. Viral rhinosinusitis? Any of these three count
- Onset with persistent symptoms or signs compatible with acute rhinosinusitis, lasting for ≥10 days without any evidence of clinical improvement (strong, low-moderate);
- Onset with severe symptoms or signs of high fever (≥39°C [102°F]) and purulent nasal discharge or facial pain lasting for at least 3–4 consecutive days at the beginning of illness (strong, low-moderate); or
- Onset with worsening symptoms or signs characterized by the new onset of fever, headache, or increase in nasal discharge following a typical viral upper respiratory infection (URI) that lasted 5–6 days and were initially improving (“double-sickening”)
Should Amoxicillin or Amox/clav be used for initial emperic therapy of ABRS in adults and children?
Amoxicillin-clavulanate rather than amoxicillin alone is recommended as empiric antimicrobial therapy for ABRS in adults (weak, low).
The recommendation that amoxicillin-clavulanate rather than amoxicillin alone be considered as first-line therapy for ABRS is based on 2 observations: (1) the increasing prevalence of H. influenzae among other upper respiratory tract infections of children, particularly AOM, since the introduction of conjugated pneumococcal vaccines [84]; and (2) the high prevalence of β-lactamase–producing respiratory pathogens in ABRS (particularly H. influenzae and Moraxella catarrhalis) among recent respiratory tract isolates
When is high dose Amox/clav recommended during initial Emperic antimicrobial therapy for ARBS in Children or adults?
“High-dose” (2 g orally twice daily or 90 mg/kg/day orally twice daily) amoxicillin-clavulanate is recommended for children and adults with ABRS:
1. from geographic regions with high endemic rates (≥10%) of invasive penicillin-nonsusceptible (PNS) S. pneumoniae,
2. those with severe infection (eg, evidence of systemic toxicity with fever of 39°C [102°F] or higher,
3. and threat of suppurative complications), attendance at daycare, age <2 or >65 years, recent hospitalization, antibiotic use within the past month, or who are immunocompromised (weak, moderate).
Should a respiratory FQ vs. a B-lactam agent be used as first line agents for the initial Emperic therapy for ARBS?
Betalactam (Amox/clav) is preferred over FQs
Besides a Respiratory Fluoroquinolone, Should a Macrolide, Trimethoprim-Sulfamethoxazole, Doxycycline, or a Second- or Third-Generation Oral Cephalosporin Be Used as Second-line Therapy for ABRS in Children or Adults?
- Macrolides (clarithromycin and azithromycin) are not recommended for empiric therapy due to high rates of resistance among S. pneumoniae (∼30%) (strong, moderate).
- Trimethoprim-sulfamethoxazole (TMP/SMX) is not recommended for empiric therapy because of high rates of resistance among both S. pneumoniae and Haemophilus influenzae (∼30%–40%) (strong, moderate).
- Doxycycline may be used as an alternative regimen to amoxicillin-clavulanate for initial empiric antimicrobial therapy of ABRS in adults because it remains highly active against respiratory pathogens and has excellent pharmacokinetic/pharmacodynamic (PK/PD) properties (weak, low).
- Second-and third-generation oral cephalosporins are no longer recommended for empiric monotherapy of ABRS due to variable rates of resistance among S. pneumoniae. Combination therapy with a third-generation oral cephalosporin (cefixime or cefpodoxime) plus clindamycin may be used as second-line therapy for children with non–type I penicillin allergy or from geographic regions with high endemic rates of PNS S. pneumoniae
Surveillance data from the TRUST (Tracking Resistance in the United States Today) and PROTEKT (Prospective Resistant Organism Tracking and Epidemiology of the Ketolide Telithromycin) studies reveal that whereas only 5% of S. pneumoniae clinical isolates in the United States were resistant to macrolides in 1993, >30% had become resistant by 2006 [117].
Harrison et al [94] evaluated the susceptibility to common pediatric antibiotics among S. pneumoniae, nontypeable H. influenzae, and M. catarrhalis isolated from 2005 through 2007. TMP/SMX resistance rates according to CLSI breakpoints were 50% for S. pneumoniae (75% for serotype 19A), 27% for H. influenzae, and 2% for M. catarrhalis (73% according to PK/PD breakpoints). Resistance to TMP/SMX among S. pneumoniae isolates is due to mutations in the dihydrofolate reductase gene [121], and is strongly associated with prior exposure to TMP/SMX, macrolides, or penicillin [117]. Not surprisingly, TMP/SMX resistance rates are significantly higher (>80%) among macrolide- or penicillin-resistant S. pneumoniae [122]. Similarly, among H. influenzae isolates collected during 2001–2005 in the TRUST program, resistance rates to TMP/SMX was 25%
Which Antimicrobial Regimens Are Recommended for the Empiric Treatment of ABRS in Adults and Children With a History of Penicillin Allergy?
a. ADULTS: Either doxycycline (not suitable for children) or a respiratory fluoroquinolone (levofloxacin or moxifloxacin) is recommended as an alternative agent for empiric antimicrobial therapy in adults who are allergic to penicillin (strong, moderate).
b. Children: Levofloxacin is recommended for children with a history of type I hypersensitivity to penicillin; combination therapy with clindamycin plus a third-generation oral cephalosporin (cefixime or cefpodoxime) is recommended in children with a history of non–type I hypersensitivity to penicillin (weak, low).
Should Coverage for Staphylococcus aureus (Especially Methicillin-Resistant S. aureus) Be Provided Routinely During Initial Empiric Therapy of ABRS?
No, even though it is a potential pathogen.
How long do we treat for in adults and kids for ABRS
Adults - 5 to 7 days
Children - 10-14
Is Saline Irrigation of the Nasal Sinuses of Benefit as Adjunctive Therapy in Patients With ABRS?
Yes in adults
Should intranasal corticosteroids be adjunct treatment in ABRS?
Yes, primarily in patients with a history of allergic rhinitis.
Should Topical or Oral Decongestants or Antihistamines Be Used as Adjunctive Therapy in Patients With ABRS?
No
How Long Should Initial Empiric Antimicrobial Therapy in the Absence of Clinical Improvement Be Continued Before Considering Alternative Management Strategies?
An alternative management strategy is recommended if symptoms worsen after 48–72 hours of initial empiric antimicrobial therapy or fail to improve despite 3–5 days of initial empiric antimicrobial therapy (strong, moderate).
What Is the Recommended Management Strategy in Patients Who Clinically Worsen Despite 72 Hours or Fail to Improve After 3–5 Days of Initial Empiric Antimicrobial Therapy With a First-line Regimen?
Patients who clinically worsen despite 72 hours or fail to improve after 3–5 days of empiric antimicrobial therapy with a first-line agent should be evaluated for the possibility of resistant pathogens, a noninfectious etiology, structural abnormality, or other causes for treatment failure (strong, low).
How to get sinus cultures in patients who have failed to respond to empiric first line and second line agents?
- It is recommended that cultures be obtained by direct sinus aspiration rather than by nasopharyngeal swab in patients with suspected sinus infection who have failed to respond to empiric antimicrobial therapy (strong, moderate).
- Endoscopically guided cultures of the middle meatus may be considered as an alternative in adults, but their reliability in children has not been established (weak, moderate).
- Nasopharyngeal cultures are unreliable and are not recommended for the microbiologic diagnosis of ABRS (strong, high).