Hi #IDFellows and #IDTwitter, back with another case: 63F h/o ESRD on HD p/w fever. Blood cx positive for MSSA x 4 days. Blood cx clear on day 5 with Rx Cefazolin. TTE on HD2 without vegetations. What is the best next step?
1/ Let’s talk about when to get a TEE for Staph aureus bacteremia (SAB) to identify infective endocarditis (IE)!
2/ For background, SAB has a high mortality (~20%); determining the presence of IE changes the duration of treatment to 6+ weeks.
The sensitivity of TTE for IE is ~60-65% compared to ~95% for TEE. But TEE has associated costs & procedural risks (sedation, esophageal perf, etc)
3/ A review of SAB literature in 2014 found 9 very low to low quality studies assessing the role of echocardiography for SAB. TTE poorly predicted presence of TEE results (15-19% of negative TTEs had IE on TEE). pubmed.ncbi.nlm.nih.gov/25268440
4/ In this study, these criteria identified patients at low risk for IE from SAB (NPV 93-100% in 5 studies):
1) No permanent intracardiac devices 2) Follow-up BCx negative within 4 days 3) Not on HD 4) Nosocomial SAB 5) No secondary foci of infection or clinical signs of IE
5/ Using a high quality TTE in a lower risk patient could preclude use of TEE using “strict negative criteria” for TTE interpretation. Using this criteria, a strict neg TTE has a NPV of 97.1%. However, only 26% of patients in this study had SAB. ncbi.nlm.nih.gov/pmc/articles/P…
6/ A series of prediction tools using retrospective data have been developed, namely the PREDICT score from @MayoClinicINFD & the VIRSTA score from France
10/ A negative VIRSTA score had a sensitivity of 96.7% with NPV of 99.5%.
Comparatively, a negative day 5 PREDICT score was only 51.6% sensitive with NPV of 95.1% & missed 4.8% of cases of IE (vs 0.44%).
A negative VIRSTA avoided 49.2% of TEEs.
11/ Neither PREDICT or VIRSTA have a high specificity or PPV at assigned cut-offs, but they have utility in determining low-risk patients to avoid invasive TEE testing.
Further studies are needed & defined utility of other modalities (e.g., PET-CT) still need to be elucidated.
12/ How do YOU make the decision about which patients get TEE in SAB? Do you prefer one of the scoring systems to the other?
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We know is subjective & expect feedback/future improvements 👇
1. Clinical management of Staphylococcus aureus bacteremia: a review. pubmed.ncbi.nlm.nih.gov/25268440/
👉 A must read written by Holland et al. where they review the evidence of the management of SAB.
2. Impact of Infectious Disease Consultation on Quality of Care, Mortality, and Length of Stay in Staphylococcus aureus Bacteremia: Results From a Large Multicenter Cohort Study. pubmed.ncbi.nlm.nih.gov/25701854/
👉ID consult associated with reduced inpatient mortality.
1/ #IDTwitter and #IDFellows, here is another #IDboardreview question: 20F p/w pharyngitis w/fever. There is no cough. Exam: Cervical adenopathy; tonsillar exudate. Rapid Strep antigen test pos. You start to prescribe her Amoxicillin but there is an allergy alert.
2/ She reports an allergic reaction to penicillin around age 8 or 9. She had a rash but no other symptoms. It resolved following discontinuation of med. She did not receive any treatment. Which of the following would you do next?
3/ Today we are going to talk about everyone’s favorite – #penicillin#allergy!
1/ Follow up for our #IDFellows and #IDTwitter on an #IDCase - 25 year old female with behcet's disease and chronic pain who presents for positive T Spot done for screening. Started on Rifampin for latent TB Infection. She calls 3 days later with diffuse pain.
2/ Great job, #IDTwitter, honing in on the issue! This was intentionally vague to stimulate discussion. As you alluded to, the key lies in what else she was taking. But first, what might we worry about as adverse effects Rifampin?
3/ Allergic reactions to rifampin are relatively rare though they have been described. However, patients may experience flushing, rash and itching that is unrelated to hypersensitivity. Rifampin can often be continued in these patients. PMID: 10575418
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2/ A case of 70F with ring-enhancing brain/lung lesions was presented. Here is how @MDdreamchaser walked thru the case:
1⃣Define pt risk of infection (e.g. splenectomy, steroid use)
2⃣Take presenting clinical syndrome
3⃣Tempo of illness: abrupt? gradual?
3/ In this case, co-occurrence of brain-lung nodules was helpful clue
Background:
Up to 50% pts with solid tumors & >80% pts with hem malignancy will develop fever during chemo cycle assoc’d with neutropenia
Only 20-30% of these identify clinical infection
Only 10-25% bacteremia
3/ The very basics:
🔹Here is the classic article from 1966 that demonstrated ⬆️susc to infection as neutrophils<500
🔹Freq and severity of infection inversely proportional to neutrophil count
🔹Risk of severe infection and BSI greatest at ANC <100 pubmed.ncbi.nlm.nih.gov/5216294/