30M from Indiana w/ peptic ulcer disease presents w/ abdominal pain & hematemesis. He reports taking ibuprofen 4000mg daily for the past 3 weeks. T 38.5C, HR 120, BP 100/60, RR 18, O2 93% on RA. Labs notable for WBC 11,000, Hb 4, plt 155,000
2/
Over the next 2 days, the patient receives 10 units of blood products. On day 3, the patient has a fever. A serum beta-d-glucan is ordered and results at 90 (positive > 80). What is the likely cause of the beta-d-glucan elevation?
1/11
Answer: Positive from blood products
🍎Patient developed an upper GI bleed from excess ibuprofen, requiring 10 units of blood products
🍊Blood products can contain glucans, and once infused into patients, it may cause a positive serum BDG. Plasma and IVIg can also do this
2/ Ibuprofen itself does not cause +BDG
⭐️Although aspergillus can cause a positive BDG, the question does not suggest any signal for aspergillus (no host factors or clinical picture consistent with aspergillosis)
3/ As we have reviewed in the past, typically blasto does not result in a positive BDG. We see in our Venn diagram that Blasto is on the perimeter of the BDG circle
4/ The reason that Blasto is called a dimorphic fungus is because in the environment at lower temperatures, it is found as a mold. At higher temperatures (in humans), it is found as a yeast.
5/ Blasto cell wall as a mold (environment) has a 60/40 ratio of 1,3-α glucan/1,3-B glucan (BDG)
🌈When it transitions from mold to yeast in humans, the amount of 1,3-α glucan in the cell wall increases from 60 to 95%, while BDG decreases from 40 to 5%!
6/ This is why on the Venn diagram, blasto is found on the BDG perimeter, as the Blasto yeast phase (what we find in humans), can produce very little BDG
7/ In the case of blood products, the filtration of blood plasma through cellulosic filters can result in leached plant BDG, which is then transfused in patients and can cause elevated serum BDG results
This elevation in BDG is transient
8/ Although I do not know of studies that show the transient rise and fall of serum BDG levels with packed red blood cells, we have some data with IVIg
9/ This study looked at BDG levels in patients that received IVIg (pre and post) and compared to those who did not receive IVIg
🌝IVIg led to positive BDG results in a majority of patients, all of which cleared 3 weeks after the infusion
10/ BDG can help in diagnosing invasive fungal infections (IFI) while considering host factors, clinical presentation, & prevalence of the fungal infection in your pt population
If +BDG doesn't fit w/ an IFI, ask these Qs to evaluate other causes of +BDG
11/ For a review of test characteristics of serum BDG and GM, which pathogens test positive for both biomarkers, and the causes of “false positive”, I refer you to this wonderful table by @febrilepodcast and @swinndong
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50F w/ EtOH cirrhosis & DM presents to ED w/ AMS & decreased UOP. She is febrile & hypotensive
She is started on vasopressors & CVVHD via central lines in the ICU
Due to concern for SBP, she is started on ceftriaxone
2/ Initial blood & ascites cultures show no growth. She remains critically ill for 7 days and still having fevers
In addition to blood cultures, which of the following is the next best test to order?
1/13
Answer: Serum BDG
You have suspicion for invasive candidiasis given the RF of cirrhosis, critical illness in ICU w/ central lines, dialysis, & broad-spectrum antibiotics (see other RF in table)
60M w/ asthma from China presents w/ SOB secondary to an asthma exacerbation. He has never smoked cigarettes. A CT chest shows a 7mm right upper lobe nodule
Which of the following tests should be ordered for further evaluation of the nodule?
1/14
Answer: AFB sputum culture
Without knowing much about the patient, other than age, geographic risk, smoking status, & normal immune status, most common infectious cause of a solitary pulmonary nodule (SPN) is TB.
2/ It’s possible that the SPN may be latent TB, but we need to rule out active TB first (AFB sputum cultures x3) before considering latent TB
Fungal causes are less likely. If we want to work it up, it would be pathogen specific (e.g., Cocci Ab) & not broad antigen testing (BDG)
75F w/ lupus, HTN, recent diagnosis of HIV (viral load 30,000, CD4- 57), presents to ED in winter w/ 4 weeks of shortness of breath & cough. T 38.5C, HR 105, BP 105/80, RR 20, O2 94% on 3L. Exam is notable for crackles & rhonchi in both lungs
2/ Labs: WBC 2,600, Hb 7.5 g/dL, platelet 70,000. CXR shows diffuse opacities. You have suspicion for Pneumocystis jirovecii pneumonia
Which of the following is the best non-invasive test to order to help confirm the diagnosis?
1/11
Answer: Serum BDG
⭐️LDH elevation is nonspecific and can be elevated in many diffuse pulm processes
Serum GM is not helpful in diagnosing PJP since its cell wall does not contain GM
BDG is a cell wall polysaccharide present in many pathogenic fungi including P. jirovecii