Pulmonary embolism lastest guidelines
"pulmonary embolism"[MeSH Terms] AND "guideline"[pt]
pulmonary embolism guidelines 2024 2025 ESC AHA latest recommendations
PMID: 41712677
PMID: 40587333
2026 AHA ACC pulmonary embolism guideline key recommendations clinical categories treatment
PMID: 41193046
Key highlight: Introduces a new AHA/ACC Acute PE Clinical Classification System to replace the older massive/submassive/low-risk terminology, improving precision for risk stratification and therapeutic decision-making.
| Category | Hemodynamics | RV Dysfunction | Biomarkers |
|---|---|---|---|
| High-risk (obstructive shock) | SBP <90 mmHg or shock | Yes | Elevated troponin/BNP |
| Intermediate-high risk | Normotensive | Yes | Elevated |
| Intermediate-low risk | Normotensive | Yes or borderline | Normal or mildly elevated |
| Low-risk | Normal | No | Normal |
| Agent | Notes |
|---|---|
| DOACs (apixaban, rivaroxaban) | Preferred first-line — 2026 guideline strongly favors DOACs over VKA; rivaroxaban and apixaban are approved as monotherapy without parenteral bridge |
| LMWH (enoxaparin) | Preferred parenterally; better than UFH for most patients; preferred in pregnancy |
| UFH (IV unfractionated heparin) | Reserve for patients requiring thrombolysis/surgery (short half-life allows easy reversal) |
| Fondaparinux / Argatroban | For HIT (heparin-induced thrombocytopenia) |
| Scenario | Duration |
|---|---|
| Provoked PE (major transient risk factor) | 3 months |
| Unprovoked PE | ≥3 months; reassess for extended therapy |
| Recurrent PE or persistent risk factor | Indefinite |
| Cancer-associated | Until cancer resolved/remission |
| Guideline | Year | Scope |
|---|---|---|
| 2026 AHA/ACC et al. Guideline | 2026 | Comprehensive acute PE evaluation & management (first AHA/ACC) |
| 2025 ESVM Interventional VTE Guidelines | 2025 | Catheter-based therapy for DVT and PE |
| ACR Appropriateness Criteria – PE Management | 2025 | Imaging and interventional guidance by risk category |
| 2019 ESC PE Guidelines | 2019 | Still widely used in Europe; update expected |
Bottom line: The 2026 AHA/ACC guideline is the most current and comprehensive reference. Key shifts include a refined clinical classification system, strong preference for DOACs as first-line anticoagulation, expanded role for catheter-based interventions in intermediate-high risk PE, and structured PERT team approach for complex cases.
Sepsis
"sepsis"[MeSH Terms] AND "guideline"[pt]
sepsis surviving sepsis campaign guidelines 2024 2025 latest recommendations
"surviving sepsis campaign" AND "guidelines" AND "management"
Surviving Sepsis Campaign 2026 guidelines key changes recommendations antibiotics fluids vasopressors
PMID: 40163133
site:guidelinecentral.com OR site:infectiousdiseaseadvisor.com 2026 surviving sepsis campaign new statements vasopressors steroids fluids antibiotics
Key theme: More individualized, stratified care — moving away from one-size-fits-all protocols toward clinical phenotyping and dynamic assessment.
| Term | Definition |
|---|---|
| Sepsis | Life-threatening organ dysfunction caused by a dysregulated host response to infection. Operationalized as SOFA score increase ≥2 |
| Septic shock | Sepsis with vasopressor requirement to maintain MAP ≥65 mmHg AND serum lactate >2 mmol/L despite adequate fluid resuscitation |
| qSOFA | 2026 SSC now explicitly recommends against qSOFA for screening (low sensitivity); NEWS2 is preferred |
| Clinical Scenario | Recommendation |
|---|---|
| Septic shock (or probable/definite sepsis) | Administer antibiotics immediately, ideally within 1 hour of recognition |
| Possible sepsis, no shock | Time-limited rapid investigation first; administer within 3 hours if infection concern persists |
| Low suspicion for sepsis | Defer antibiotics — avoid unnecessary treatment |
This replaces the previous blanket "give antibiotics within 1 hour" for all suspected sepsis, reducing antibiotic overuse.
| Source | First-Line Empiric Options |
|---|---|
| CAP | β-lactam (ceftriaxone/cefotaxime) + macrolide, OR respiratory fluoroquinolone |
| HAP/VAP | Vancomycin or linezolid + antipseudomonal β-lactam (piperacillin-tazobactam, cefepime, meropenem) |
| Undifferentiated sepsis, no Pseudomonas risk | 3rd-gen cephalosporin (ceftriaxone/cefotaxime) |
| Pseudomonas risk | Cefepime, pip-tazo, or carbapenem |
| MRSA risk (healthcare exposure, hospital-onset) | Add vancomycin or linezolid |
| Highly resistant GNR | Two empiric gram-negative agents from different classes |
| Fungal risk (abdominal surgery, TPN, Candida colonization) | Add empiric echinocandin |
| Priority | Agent | Notes |
|---|---|---|
| First-line | Norepinephrine | Preferred over vasopressin or angiotensin II (downgraded to conditional in 2026 — reflects new evidence) |
| Second-line | Vasopressin (0.03–0.04 U/min) | Add to norepinephrine for refractory shock or to spare norepinephrine dose |
| Adjunct | Angiotensin II | Option in catecholamine-refractory shock |
| Refractory shock | Epinephrine | Add if MAP target not achieved |
| Cardiogenic component | Dobutamine | For reduced cardiac output / impaired myocardial function |
2026 change: Peripheral vasopressor use is now supported as an acceptable alternative to central venous access in the early resuscitation phase — reducing delays to treatment.
2026 change: Concurrent early vasopressor initiation alongside fluid resuscitation is endorsed for unstable shock — no longer strictly "fluids first."
| Intervention | Recommendation |
|---|---|
| Blood glucose | Target 140–180 mg/dL; avoid hypoglycemia; use validated protocols |
| Renal replacement therapy (RRT) | Initiate for AKI with life-threatening indications (refractory hyperkalemia, acidosis, fluid overload, uremia); no benefit to early initiation without indications |
| DVT prophylaxis | LMWH preferred over UFH unless contraindicated |
| Stress ulcer prophylaxis | Proton pump inhibitor for patients with risk factors (coagulopathy, prior GI bleed, mechanical ventilation) |
| Nutrition | Early enteral nutrition within 48 hours when tolerated; avoid early parenteral nutrition if enteral route available |
| Transfusion | Restrictive strategy: Hb threshold 7 g/dL (9 g/dL if active cardiac ischemia) |
| Domain | 2021 | 2026 |
|---|---|---|
| Screening tool | qSOFA (discouraged but used) | NEWS2 preferred; qSOFA explicitly NOT recommended |
| Antibiotic timing | Within 1 hr for all suspected sepsis | Stratified: immediate for shock, ≤3 hrs for possible sepsis, defer if low suspicion |
| Vasopressor initiation | Fluids first, then vasopressors | Early concurrent vasopressor acceptable in unstable shock |
| Vasopressor route | Central line preferred | Peripheral vasopressors now endorsed for initial use |
| Blood pressure target | MAP ≥65 mmHg | MAP ≥65 mmHg; higher target for older adults with hypertension |
| Fluid removal | Not addressed | De-resuscitation after acute phase — new statement |
| Post-discharge care | Minimal guidance | New: rehabilitation, PICS screening, follow-up clinics |
| Guideline | Year |
|---|---|
| Surviving Sepsis Campaign 2026 – SCCM/ESICM | 2026 |
| SSC 2026 Pediatric Guidelines (PMID 41869844) | 2026 |
| ESICM Fluid Therapy Guideline Part 2 – Volume of Resuscitation (PMID 40163133) | 2025 |
| German S3 Sepsis Guideline Update (PMID 40824313) | 2025 |
| Sepsis-3 Definitions — Singer et al., JAMA 2016 | Still current |
Bottom line: The 2026 SSC guideline is the current gold standard. The biggest paradigm shifts are stratified antibiotic timing (not all suspected sepsis needs immediate antibiotics), NEWS2 over qSOFA for screening, peripheral vasopressors as an acceptable early route, and a new focus on de-resuscitation and post-sepsis rehabilitation.