New Guideline for Scoring Pulmonary Embolism Severity: What to Know
Grading the new grades for PE risk
In February 2026, the American Heart Association and American College of Cardiology issued a new guideline on the evaluation and management of acute pulmonary embolism, with many other societies’ endorsements. PulmCCM is not affiliated with any specialty society.
New Guideline: Pulmonary Embolism Evaluation and Management
The American College of Chest Physicians (ACCP) has traditionally provided the most influential clinical guidance on pulmonary embolism treatment through its comprehensive flagship guidelines addressing all aspects of venous thromboembolism.
The guidance included a novel severity scoring or staging system that grades pulmonary embolism from “A” (nearly benign) to “E” (probably lethal).
The AHA’s model proposes to help triage more low-risk patients to outpatient management and guide the use of invasive or risky therapies like systemic thrombolytics and catheter-based interventions.
Of course, anyone proposing a new scoring system for any medical condition would do well to have read the oncologist researcher Florian Markowetz’s landmark 2024 monograph in Precision Oncology on the subject:
Markowetz delivers on his sardonic title with an unsparing takedown of most prediction models (including his own) and the researchers who produce them (including himself), arguing that such rubrics usually benefit their creators more than patients or their doctors.
But this isn’t some CV-padding manuscript in a third-rate journal by junior faculty struggling to publish or perish; it’s the AHA with nine other societies, publishing in Circulation! Let’s suspend our skepticism, examine the new AHA scoring system for PE on its own terms, and ask: Is this useful?
Grade “A” and “B” PE: Send Them Home?
Pulmonary embolism’s wide spectrum of possible outcomes—ranging from asymptomatic and probably benign to rapidly lethal—makes it an unsettling diagnosis for patients and physicians alike.
Research suggests clinical conservatism spawned by this variability has led to many thousands of unnecessary or overly long hospitalizations for patients with asymptomatic and otherwise low-risk pulmonary embolism.
The new guideline classifies asymptomatic PE as category “A”, and advises that they can “safely be discharged home from the emergency room and do not need to be hospitalized.”
This was one of the top-line “Take Home Messages” of the document—but in the actual guideline text, the authors weaken that statement.
There (p. e20), they lump category A together with category “B” PEs, which are symptomatic but with low clinical risk scores (either PESI I-II, simplified PESI = 0, or Hestia = 0; Bova < 4 is also mentioned).
It’s “reasonable” to manage “select” patients with category “A” or “B” on an outpatient basis, the authors advise, if they have low risk scores “and it aligns with patient goals.”
All discharged patients must have anticoagulation medication access (preferably a DOAC) and “rapid, reliable, expert follow-up in place,” the latter of which may not be arranged by the end of the average ED visit.
Grade “C” PEs, Sliced Thinly
Grade “C” PEs have both symptoms and elevated risk scores (PESI III-IV, simplified PESI ≥1, or Bova >4 ), but have preserved blood pressure and no shock.
They should be hospitalized, receive low molecular weight heparin, and undergo measurement of the right ventricle (by CT and/or echo), troponin, and brain natriuretic peptide, along with lactate.
Category C PE is further subdivided into 3 subcategories:
C1: with normal RV function and biomarkers
C2: Either an abnormal RV or elevated biomarker(s)
C3: With both an elevated RV and biomarker(s)
The panel did not address the clinical uncertainty regarding the indications for invasive catheter-based therapies (catheter-directed thrombolysis or mechanical thrombectomy) in the “C” category, which includes patients categorized in earlier European schemes as “intermediate-risk” (RV dysfunction without biomarker elevations) and “intermediate-high risk” (RV dysfunction plus biomarker elevations).
For “C1” patients, catheter-based treatments were discouraged as “No Benefit,” but this was already uncontroversial.
For “C2” and “C3” patients, the benefits of invasive therapies were described as “unclear,” but the panel left the door open for routine intervention by also giving a weak 2b recommendation (“Benefit ≥ Risk”) to both CDT and MT.
Grade “D” PEs: Things Get Dicey
Category “D” PEs are those with incipient cardiopulmonary failure: either transient hypotension (“D1”) or normotensive shock (“D2”).
Besides anticoagulation with low molecular weight heparin and vasopressors when needed, the AHA guidelines now endorse either systemic thrombolysis or catheter-based therapies (CDT or MT), each with a 2b (weak, “may be considered”) recommendation in this category of patients.
Grade “E” PEs: Extreme Risk
Category “E” represents PEs with persistent hypotension, either without (E1) or with (E2) refractory shock or cardiac arrest.
In line with usual practice, the panel suggests systemic thrombolysis for either “E1” or “E2”—but interestingly, with only a moderate 2a (“we suggest”) recommendation.
For the first time, both mechanical thrombectomy and catheter-directed thrombolysis were indirectly endorsed as reasonable alternatives to systemic thrombolysis for patients with PE and hypotension (“E1”). Although the panel did not compare CDT / MT to systemic thrombolysis, it gave both invasive therapies a 2a recommendation—the same as for systemic thrombolysis for category “E1” PE.
“R” For Respiratory Complications
Patients with more severe PE (“C”, “D”, and “E”) with respiratory symptoms and signs crossing a certain threshold tailored to each category receive an “R+” (or “R-” for lacking that degree of respiratory failure):
C: O₂ <90% and/or RR ≥30 and/or need supplemental O₂
D: >6 L nasal cannula or NRB mask
E: hypoxemic respiratory failure or ventilatory failure
Grading the New PE Grading System
Pulmonary embolism presents with a very wide spectrum of hemodynamic involvement, symptoms, and risk.
From a practical standpoint the new system will help triage patients more effectively and enable clearer communication among clinicians by creating an objectively describable “shared reality”.
For low risk patients, it will likely enable more discharges from the ED and shorter hospitalizations (i.e., next-day or even same-day discharge) for those who are admitted.
(By the way, regarding category “A”, how does an asymptomatic patient end up in the ED and undergo a CT angiogram of the chest that happens to diagnose an incidental PE?)
Among more severely affected patients, the refinement of categories “C” through “E” will permit the collection and analysis of more detailed and granular observational data, and help standardized randomized trial enrollment.
But the new system’s most immediate and far reaching effect will be its tacit endorsement of invasive procedures in all but the mildest PEs requiring hospitalization (“C1”).
So, to answer our original question: is it useful? Yes: the new severity scoring system will help standardize management and care coordination for acute PE, especially among less-experienced clinicians.
And it will be extremely useful if you happen to be an interventionalist performing catheter-based treatments.
References
Creager MA, Barnes GD, Giri J, et al. 2026 AHA/ACC/ACCP/ACEP/CHEST/SCAI/SHM/SIR/SVM/SVN Guideline for the Evaluation and Management of Acute Pulmonary Embolism in Adults: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. Published online February 19, 2026. doi:https://doi.org/10.1161/cir.0000000000001415
Watson NW, Carroll BJ, Krawisz A, Schmaier A, Secemsky EA. Trends in Discharge Rates for Acute Pulmonary Embolism in U.S. Emergency Departments. Annals of Internal Medicine. Published online January 30, 2024. doi:https://doi.org/10.7326/m23-2442






As usual, it’s great that you’re casting a concerned gaze over this new schema. But it's not exactly Plato's philospher-kings offering this schema.
Am actually very conservative medically (though liberal politically!) and when I dug into this, the big theme for me was: how did device-makers and interventional types become so widely accepted in this space despite the absence of well-run, large-scale RCTs that clearly inform patients what they’re getting — and what might happen if they don’t? (C1 indeed!)
Loved your point about the uselessness of category A.
No trial really answers this yet. PE-TRACT is enrolling. Until then, we are… aspirational.
But AHA/ACCP is just one set of institutions where (somewhat self-appointed) “thought leaders” gather and attempt to influence what it is we should do.
And here’s who they asked:
General cardiologists.
Interventional cardiologists.
Cardiac imaging experts.
Critical care physicians (see note below of how the one that I could find is like the PERT team publisher)
Hospitalists (not sure any in the cited authors)
Cardiothoracic surgeons
Advanced practice nurses. (!) -- who needs med school really.
Pharmacists.
Vascular medicine physicians.
Vascular interventionalists.
Hematologists. (the one that could find...google her and she's acting like STORM-PE a small RCT that showed an aspiration device was better than systemic AC (no TPA arm!) at 48hr RV/LV ratio was positive for its 2ndary outcomes too, research device backing)
Pulmonologists (guess ones not trained in crit?)
Emergency physicians (saw one in the cited authors which is sad because they usually make the diagnosis and call the consult)
Patient representatives (did they ask the families of the ones whose pulmonary arteries might have ruptured while mucking around or the ones who got pictures of the big clot that were removed?)
Representatives from ACC, AHA, SCAI, SIR, SVS.
Ok — they left out the hospital cafeteria worker.
At some point, if you fish in enough societies that are procedure-adjacent, you will successfully generate buy-in for your “suggestion” to EKOS a normotensive, non-hypoxic PE because the BNP is 350 (and it’s 2pm on Wednesday).
More seriously: MANY of the listed authors are vascular-trained and device-focused. RPVI, MSVM, etc. Even the cardiologists who didn’t alphabet-soup their credentials? Interventional cardiologists. (Guess after putting in tons of stents in stable angina patients that were likely not helpful or harmful new vascular horizons must await in the pulmonary artery).
The one critical care physician I came across is a PERT director. There’s a DNP in there — not disqualifying — but if you Google her she only gets mentioned in such guidelines. , Like I'd get it should it have been a DNP who was a PhD in medical devices or something prior.
This is not shocking. But it does shape perspective.
Other societies exist. The American Society of Hematology. The American Thoracic Society. The European Respiratory Society. They are not nearly as device-forward. For them, if no contraindication exists, systemic lytics >>> device.
From what I can tell of the cited authors, it's a lot American people who are friends and see each other at meetings and support research in devices. Moreover, exact conflict disclosures of the many authors are not exactly spotlighted in a way that inspires deep belief in the recommendations either.
My point is simple: why not ask pain-in-the-butt skeptics like me? Or, to be fair, much smarter and better scribes -- people like you? People with no RVUs tied to putting any device past the vena ceva. Physicians who simply care about patient outcomes. Ask the AZNICS crew.
I’ve seen IR/IC cases go spectacularly well. I’ve also seen them go very, very poorly. What I have not seen is RCT data robust enough to clarify which subgroup truly benefits. (Or which procedure. In my shop a different IR attending seems to have his favorite tool and sticks to it).
And that brings me to PERT.
In theory:
An erudite, multidisciplinary debate.
Go over prior echos.
Assess true acuity of RV strain.
Discuss clot anatomy most amenable to device therapy.
Weigh bleeding risk thoughtfully.
In practice (at many places):
“PE. BNP 400. RV strain (on CT!). Call IR. Call ICU."
IR: “We can EKOS or mechanically remove this one.” (It's 2pm on Wed!)
Patient goes to ICU for babysitting. If things go south, palliation.
These teams are not always built for spirited physiologic debate. I’m usually the annoying one saying: mild BNP/trop bump — we can lovenox this. Or if truly acute, maybe 15 mg TPA and see what happens. Never has a plugged-in cardiologist noted that the TR gradient of 52 mmHg suggests this situation might not be acute RV failure.
Like so much in conflict-flavored guideline making, we will likely chug along as long as profit and fee-for-service incentives exist — and C1 evidence is enough to “pass" like a good C is!
Is anyone in the US having PE treated as outpatient? We admit asymptomatic hypertensive patients here…
Also I would be curious what majority practice is around LMWH vs UFH. I practically see everyone C2 and beyond get IV UFH drips.
Functionally PERT team is deciding on if the schedule allows another EKOS catheter or if it can wait until regular office hours tomorrow. These guidelines really don’t give justice to the lack of real evidence of these modalities. I have seen a ton of bad outcomes including death from CDL.
I am excited though we seem to get more backing for low dose systemic TPA.