Morning report 11/14/22

Elderly man with history of coronary disease and heart failure presenting with respiratory failure and moderate large bilateral effusions. On lifelong DAPT.

1) Will thoracentesis help?

Dyspnea from altered respiratory mechanics (pushing down on diaphragm and against chest wall) and impaired gas exchange, hypoxemia through pulmonary shunt v/q mismatch, and thoracentesis often doesn’t have immediate effect on gas exchange.

Small study – shows improves respiratory mechanics and oxygenation.

2) What should we do about AC?

Old guidelines from 2010 recommend against, practice patterns are all over the place.  Papers with small numbers all had pretty low bleeding outcomes, especially in the hands of an experienced provider with ultrasound use.

More recently, Patel et al reported 451/8951 thoracentesis done on NOAC/antiplatelets, and there were ZERO bleeding complications. Done by IP.

Interestingly, draining one side led to less fluid on the other wise. Suspected to be Buffalo chest – plero-pleural communication – refers to life-threatening condition in which a simultaneous bilateral pneumothorax occurs due to this communication. Can be seen post-op thoracic surgery too.

Thanks for the case, Dr. Rowe!

Timothy Rowe, MD, Pulmonary and Critical Care

Morning report 10/31/22

Middle aged man with Crohn’s disease referred for cough, mucus production.

CT scan showed diffuse bronchiectasis and narrowed BI.

Bronchiectasis is associated with Crohn’s disease, see Review of pulmonary involvement of Crohn’s – often with suppurative mucus. Unclear if treatment of Crohn’s improves pulmonary features.

Focusing on tracheobronchial stenosis – malignancy, chronic infections, inflammatory (GPA, relapsing polychondritis, associated with IBD, amyloid)

Underwent dilation with IP -> path showing chronic inflammation, cultures negative for infectious organisms -> significant symptomatic improvement.

Thanks, Dr. Ludwig! Happy Halloween!

Amy Ludwig, MD, Pulmonary & Critical Care Medicine

 

Morning Report 10/24/22

Dr. Lawrence presented a case today of a patient with a 50+ pack-year smoking history with concern for bowel obstruction and need for surgery – imaging showed very significant bulla.

What might you recommend before the surgical procedure?

  • Optimization of medication (referred to COPD clinic)
  • Smoking cessation
  • PFTs (points were brought up about not using DLCO/VA, though might be helpful to compare to TLC; and N2 washout suboptimal in patient with obstruction)

Bullous emphysema – giant bulla is >1cm in diameter and giant bulla occupies at least 30% of hemothorax

Example from online:

Management varies – bullectomy sometimes but practices varies across institution.

Thanks for sharing, Dr. Lawrence!

Morning report 10/17/22

Thanks to our fearless leader Dr. Schroedl for presenting an interesting case of pulmonary MALT lymphoma!

Young woman with chest pain and dyspnea – left upper lobe lesion that didn’t respond to empiric treatment for CAP or even an empirical treatment for fungal pneumonia (unknown exact regimen). Bloodwork and noninvasive infectious workup were unrevealing. Initial bronchoscopy and biopsy were unrevealing. Repeat imaging six months later showed persistence of left upper lobe mass.

The patient got a repeat CT-guided biopsy that showed MALT lymphoma! This is a rare disease, and an extranodal low-grade B-cell lymphoma.

Treatment: ritxumab

The patient had good imaging response but persistent dyspnea, which is thought to be asthma that upon further probing, seemed present even prior to these.

Nice review article here: https://erj.ersjournals.com/content/34/6/1408

Thanks, Dr. Schroedl!

Clara Schroedl, MD, MSc, Medicine – Pulmonary/Critical Care

Welcome, visitors from Med Ed Day!

We are so excited that Med Ed Day is here!

Northwestern Medical Education (@NU_MedEd) / TwitterJoin us at 8:30 – Short Presentations – Session One – Baldwin Auditorium – as Dr. Rowe presents our preliminary data from the blog and highlights our experiences.

9:00 – Dr. Rowe will present at Eco-Normalization – Searle room

1:45 – Discussing Interactive Asynchronous Learning session – Baldwin Auditorium – a range of experiences with the modern digital age of medical education, including a piece about medical education blogging! Featuring also Dr. Angarone of our friend blog, bit.ly/nuidblog

We’re so glad you’re here, and are always excited to chat about our experience, hear your suggestions, or collaborate!

#NUPCCM Blog Team

Update – thanks to all who came out to support us, and for all of you visiting the blog for the first time after our presentation. We had a great time with the discussion and can’t wait to see the community continue to grow!

From left:
Mike Angarone, Mac Walter, Brianna Valdes, Tim Rowe, Tricia Pendergrast

 

 

Morning Report – 9/26/22

Thanks to Dr. Rowe for a great morning report case – a middle aged man with well-controlled HIV, ESRD on HD, referred to clinic for an abnormal CT as part of pre-transplant workup.

CT with some moderate subcarinal and right paratracheal lymphadenopathy, minimal parenchymal findings.

What next?

Differential:

  • Sarcoidosis
  • Infection (TB, endemic fungi, anything really)
  • Malignancy
  • Reactive

EBUS to the rescue! – REMEDY: AJRCCM 2012 study showed that EBUS mediastinoscopies in 87% of cases – 67/77 cases were diagnosed with EBUS; of the 10 undiagnosed, only 6 got diagnoses in mediastinoscopy

Thanks, Tim!

Timothy Rowe, MD, Pulmonary and Critical Care

Morning Report: spontaneous pneumothorax

Thanks to Ale for sharing a case of a young man without any significant PMH who had chest pain and cough and abnormal imaging. Sent to ED with left upper lobe pneumothorax that improved with a small bore chest tube.

What’s the differential for spontaneous pneumothorax in this kind of case? What is the long-term management?

https://www.nejm.org/doi/full/10.1056/nejmoa1910775 – RCT of 316 patients randomized to intervention vs conservative management for spontaneous pneumothorax; conservative management was noninferior.

There was significant family history of pneumothoraces. A review of genetic causes of pneumothorax: https://pubmed.ncbi.nlm.nih.gov/30681372/.

A CT showed some cysts – we reviewed the wide range of causes of this:

Key points in the chat during this asked about skin findings as suspicion climbed for Birt Hogg Dube syndrome.

  • skin lesions develop in 80% of patients in 30s-40s, fibrofolliuclomas in mid face
  • 7x increased risk of malignancy especially renal cancer > annual surveillance with US
  • genetic testing (refer to Center for Genetics), counseling, screening of family members (autosomal dominance inheritance)
  • consider early ipsilateral VATS pleurodesis after pneumothorax

Bonus: case report by Dr. Kalhan and Dr. Jain 

Thanks, Ale!

Alexandra Hanrahan, MD, Pulmonary and Critical Care

 

HFNC review

Case

A 55 y/o male with a h/o EtOH abuse is intubated and admitted to the MICU for hypoxemic respiratory failure secondary to aspiration PNA.  Three days later, his vital signs have normalized, he is awake and able to follow commands, minimal secretions are noted with suctioning of his ET tube, and his SpO2 is >95% on 40% FiO2 and 5 PEEP.  He passes a 30 minute trial of spontaneous breathing with a T-piece.

Question

Following extubation, should he be given high-flow nasal oxygen to help prevent the need for reintubation?

Evidence

  1. We previously reviewed the FLORALI trial, NEJM 2015 which looked at the up-front use of high-flow nasal cannula (HFNC) in patients with hypoxemic respiratory failure
  1. 313 patients randomized to HFNC vs NIV
    1. HFNC did not lower need for intubation at 28 days
    2. HFNC did lower ICU and 90-day mortality
  2. Interpretation of trial results complicated by significant cross-over in the use of HFNC and NIV between study arms
  1. There is a growing body of literature on the use of HFNC following extubation
    1. We previously reviewed a JAMA 2015 trial looking at the use of HFNC vs NIV in 830 patients at high-risk of reintubation following cardiac surgery
  1. No difference in treatment failure (defined as re-intubation, switch to other study treatment, or premature study discontinuation) between groups
  2. Roughly 14% required re-intubation in each group (no difference)
  • Similar dyspnea and comfort score between groups
    1. Nasal High-flow versus Venturi Mask Oxygen Therapy after Extubation, AJRCCM 2014, Italy
  1. 105 patients with a P/F < 300 following SBT randomized to oxygen via HFNC (flow 50 L/min) or venturi mask for 48 hrs or until ICU discharge (the low P/F perhaps indicative of a group at higher risk of post extubation hypoxemia and need for reintubation)
    1. P/F ratio at 24 hrs (primary end point) significantly higher in HFNC group (287 vs 247). P/F also higher at 36 and 48 hrs in HFNC group
    2. Patient comfort significantly higher in HFNC group
    3. Significantly fewer reintubations in HFNC group (4% vs 21%) although the study was not powered for this outcome
    1. A new trial was just published on the use of HFNC following extubation in patients felt to be at low-risk of post-extubation hypoxemia – Effect of Post-extubation HFNC vs Conventional Oxygen Therapy on Reintubation in Low-Risk Patients, JAMA 2016, Spain
  1. Methods
    1. Inclusion
      1. Pts on mechanical ventilation >12 hrs who passed an SBT and were defined as low risk of reintubation by having all of the following (few patients in our MICU would meet these criteria)
        1. Age <65
        2. Not initially intubated for CHF
  • Absence of mod-severe COPD
  1. APACHE II <12
  2. BMI <30
  3. No known airway problems and low risk of developing laryngeal edema
  • Adequate cough and requiring suctioning <2xs Q8hrs
  • Not difficult to wean
  1. Mechanical ventilation <7 days
  2. <2 co-morbidities
  1. Exclusions
    1. DNR
    2. Trach
    3. Hypercapnia during SBT
  2. Intervention
    1. Immediately following extubation, pts were randomized to either
      1. HFNC x 24 hrs
        1. set at 10L/min and titrated up at 5L/min intervals until pts experienced discomfort
        2. FiO2 titrated to SpO2 >92%.
      2. Conventional oxygen applied through facemask or nasal cannula titrated to SpO2 >92% x 24hrs
  • Primary outcome
    1. Need for reintubation at 72 hrs
  1. Results
    1. 1739 pts ready to be liberated from the vent  527 randomized (vast majority excluded as they were high risk for reintubation)
    2. Patient characteristics
      1. Age ≈51
      2. Neurologic co-morbidity 7.6% in HFNC group and 12.9% in conventional O2 group (only significant baseline difference between the two groups)
      3. Time on vent ≈ 1-2 days
      4. ≈30% admitted with primary neurologic diagnosis and ≈47% had either scheduled or urgent surgery at admission (not a typical MICU population)
    3. Outcomes
  HFNC (264) Coventional O2 (263) P value
All-cause Reintubation at 72hrs 13 (4.9%) 31 (12.2%) .004
Reintubation for respiratory failure 4 (1.5%) 23 (8.7%) .001
Time to reintubation (hrs) 19 (12-28) 15 (9-31) .99
ICU LOS (median) 6 (2-8) 6 (2-9) .29
Hospital mortality 10 (3.8%) 13 (5%) .94
  1. In multivariable analysis, HFNC was independently and inversely associated with all-cause reintubation.
  2. NNT to prevent 1 reintubation = 14
  1. Conclusion
    1. Among patients felt to be at low risk for reintubation, the use of HFNC following extubation vs conventional O2 reduced the need for reintubation at 72hrs with a NNT of 14

 

Faculty Feedback

I asked Dr. Ben Singer, Assistant Professor of Medicine in the Division of Pulmonary and Critical Care, whether he felt the JAMA trial was practice changing.  A summary of his comments:

  • Important to remember that supplemental O2 is not an entirely benign therapy.  In both animal models and studies of healthy controls, high levels of FiO2 have been found to promote lung injury.  Supplemental FiO2 after extubation should therefore be used thoughtfully.
  • With this in mind, it is important to note that the majority of the patients in the trial were placed on mechanical ventilation for surgical or neurologic diagnoses (only 16% had a primary respiratory reason for mechanical ventilation).  This population is likely at lower risk of lung injury from prolonged high levels of FiO2 than a patient recovering from PNA or ARDS.  This may have biased the trial toward a positive result.  Interestingly, more patients in the conventional O2 arm of the trial had ARDS (4.2% vs 1.5%) – perhaps contributing to the higher rates of reintubation seen in the control arm.
  • As noted above, the patient population in the trial is not representative of patients typically cared for in the MICU.  As a result, the positive results seen with post-extubation HFNC are not necessarily generalizable to MICU patients.
  • There were 7 cases of laryngeal edema necessitating reintubation in the control arm and 0 cases in the HFNC arm.  This is likely just an artifact of randomization as it is hard to imagine HFNC preventing severe laryngeal edema.  If 5 of the severe laryngeal edema patients had been randomized to the HFNC arm, the results of the trial would not have been significant.
  • The curves from Fig 2  look convincing as they immediately separate during the first 24 hrs (when HFNC is being used) and then become essentially parallel suggesting a real benefit from HFNC

  • Important for housestaff to recognize that this trial excluded hypercapnic patients, a group where the evidence supports the up-front use of NIV following extubation.
  • Overall this was a well performed and methodologically rigorous trial.  The results are provocative but limited by the unique patient population (largely healthy neurocritical care and surgical patients).  The trial highlights the need for a large randomized trial of HFNC following extubation in a more inclusive group of MICU patients

 

Take-home Points

  • The use of HFNC following extubation may reduce the risk of reintubation when compared to conventional O2.  Further trials are needed to clarify which patients stand to benefit most from this therapy.

 

LRP cycle open! Insight from Dr. Marc Sala on the process

The NIH LRP application cycle for this year has just opened, and I wanted to remind everyone of this amazing opportunity to help with those hundreds of thousands of dollars of debt you are burdened with. The NIH Loan Repayment Program helps to counteract that financial pressure by repaying $100,000/award period for research health professionals.

I had the opportunity to sit down with NIH LRP recipient, Dr. Marc Sala (@MarcSala_MD), to discuss the process.

Marc Sala, MD, Internal Medicine/Pulmonary

“Of course, the first step in getting an LRP is even knowing the program exists. Which means that by reading this, you’re already ahead of the curve,” Dr. Sala says, “The LRP is a very under-recognized source of debt relief for young academic faculty which helps reduce your monthly expenses and reduce your debt much faster than you would otherwise. I was successful at getting it, but only on my 3rd attempt. There was a lesson to be learned in that experience about calling the program officer every cycle for feedback because you don’t receive critiques as you would with other funding sources. After I got my feedback, I was able to achieve success by correcting the discrete deficiencies in the proposal.”

Tips for the process that he emphasized were, “to start the process, read and re-read the instructions on the LRP website and then it always behooves you to ask peers for their successful LRP proposals to mock-up the overall structure of your grant if you’re not used to writing grants. You need to collect a lot of loan servicer information, so start on that early (what is your current balance, where do you download your statements, what are your account numbers, etc).”

What about his mentors and project itself? “My mentor at the start of my LRP was Manu Jain when I was working on more cystic fibrosis related work and then changed to Ravi Kalhan as my focus shifted to Long COVID. The work in my proposal was derived from projects I had a good amount of preliminary data on, but your mentorship and institutional support and collaborators are probably far more important than the project aims and innovation of the idea for the LRP. Putting a grant together from scratch always takes a huge up front time investment, especially if you have multiple mentors who will be providing feedback. Things like equipment and institutional environment do not always need to be written from scratch if others have similar text blocks. Make sure for your letters of support that you give the courtesy of plenty advanced notice and usually scaffold basic text for them where appropriate to minimize resistance in getting them submitted on time.” It certainly feels like an overwhelming amount of paperwork at first, but dividing pieces up and tackling a small amount every day helps, and will also help with future grant applications!

To conclude, Dr. Sala said, “In the end, I only needed one cycle (2 years) of LRP to help pay off my debt and I used PSLF for the remainder, but you can renew for as long as you need to pay off your remaining loan balance (private and public loans are both eligible). It’s a wonderful program and can make or break one’s academic career if finances are tight, so I really encourage people in a such a situation to apply — you only can hit a ball if you take a swing…or three.”

Thanks to Dr. Sala for discussing the process with us! I was also fortunate enough to receive an LRP funded this last cycle. Both of us are happy to answer any questions you might have about the process, and encourage young investigators to take advantage of this great support opportunity!