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2025 PACUPrep BCCCP Preparatory Course

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  1. Pulmonary

    ARDS
    4 Topics
    |
    1 Quiz
  2. Asthma Exacerbation
    4 Topics
    |
    1 Quiz
  3. COPD Exacerbation
    4 Topics
    |
    1 Quiz
  4. Cystic Fibrosis
    6 Topics
    |
    1 Quiz
  5. Drug-Induced Pulmonary Diseases
    3 Topics
    |
    1 Quiz
  6. Mechanical Ventilation Pharmacotherapy
    5 Topics
    |
    1 Quiz
  7. Pleural Disorders
    5 Topics
    |
    1 Quiz
  8. Pulmonary Hypertension (Acute and Chronic severe pulmonary hypertension)
    5 Topics
    |
    1 Quiz
  9. Cardiology
    Acute Coronary Syndromes
    6 Topics
    |
    1 Quiz
  10. Atrial Fibrillation and Flutter
    6 Topics
    |
    1 Quiz
  11. Cardiogenic Shock
    4 Topics
    |
    1 Quiz
  12. Heart Failure
    7 Topics
    |
    1 Quiz
  13. Hypertensive Crises
    5 Topics
    |
    1 Quiz
  14. Ventricular Arrhythmias and Sudden Cardiac Death Prevention
    5 Topics
    |
    1 Quiz
  15. NEPHROLOGY
    Acute Kidney Injury (AKI)
    5 Topics
    |
    1 Quiz
  16. Contrast‐Induced Nephropathy
    5 Topics
    |
    1 Quiz
  17. Drug‐Induced Kidney Diseases
    5 Topics
    |
    1 Quiz
  18. Rhabdomyolysis
    5 Topics
    |
    1 Quiz
  19. Syndrome of Inappropriate Antidiuretic Hormone (SIADH)
    5 Topics
    |
    1 Quiz
  20. Renal Replacement Therapies (RRT)
    5 Topics
    |
    1 Quiz
  21. Neurology
    Status Epilepticus
    5 Topics
    |
    1 Quiz
  22. Acute Ischemic Stroke
    5 Topics
    |
    1 Quiz
  23. Subarachnoid Hemorrhage
    5 Topics
    |
    1 Quiz
  24. Spontaneous Intracerebral Hemorrhage
    5 Topics
    |
    1 Quiz
  25. Neuromonitoring Techniques
    5 Topics
    |
    1 Quiz
  26. Gastroenterology
    Acute Upper Gastrointestinal Bleeding
    5 Topics
    |
    1 Quiz
  27. Acute Lower Gastrointestinal Bleeding
    5 Topics
    |
    1 Quiz
  28. Acute Pancreatitis
    5 Topics
    |
    1 Quiz
  29. Enterocutaneous and Enteroatmospheric Fistulas
    5 Topics
    |
    1 Quiz
  30. Ileus and Acute Intestinal Pseudo-obstruction
    5 Topics
    |
    1 Quiz
  31. Abdominal Compartment Syndrome
    5 Topics
    |
    1 Quiz
  32. Hepatology
    Acute Liver Failure
    5 Topics
    |
    1 Quiz
  33. Portal Hypertension & Variceal Hemorrhage
    5 Topics
    |
    1 Quiz
  34. Hepatic Encephalopathy
    5 Topics
    |
    1 Quiz
  35. Ascites & Spontaneous Bacterial Peritonitis
    5 Topics
    |
    1 Quiz
  36. Hepatorenal Syndrome
    5 Topics
    |
    1 Quiz
  37. Drug-Induced Liver Injury
    5 Topics
    |
    1 Quiz
  38. Dermatology
    Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis
    5 Topics
    |
    1 Quiz
  39. Erythema multiforme
    5 Topics
    |
    1 Quiz
  40. Drug Reaction (or Rash) with Eosinophilia and Systemic Symptoms (DRESS)
    5 Topics
    |
    1 Quiz
  41. Immunology
    Transplant Immunology & Acute Rejection
    5 Topics
    |
    1 Quiz
  42. Solid Organ & Hematopoietic Transplant Pharmacotherapy
    5 Topics
    |
    1 Quiz
  43. Graft-Versus-Host Disease (GVHD)
    5 Topics
    |
    1 Quiz
  44. Hypersensitivity Reactions & Desensitization
    5 Topics
    |
    1 Quiz
  45. Biologic Immunotherapies & Cytokine Release Syndrome
    5 Topics
    |
    1 Quiz
  46. Endocrinology
    Relative Adrenal Insufficiency and Stress-Dose Steroid Therapy
    5 Topics
    |
    1 Quiz
  47. Hyperglycemic Crisis (DKA & HHS)
    5 Topics
    |
    1 Quiz
  48. Glycemic Control in the ICU
    5 Topics
    |
    1 Quiz
  49. Thyroid Emergencies: Thyroid Storm & Myxedema Coma
    5 Topics
    |
    1 Quiz
  50. Hematology
    Acute Venous Thromboembolism
    5 Topics
    |
    1 Quiz
  51. Drug-Induced Thrombocytopenia
    5 Topics
    |
    1 Quiz
  52. Anemia of Critical Illness
    5 Topics
    |
    1 Quiz
  53. Drug-Induced Hematologic Disorders
    5 Topics
    |
    1 Quiz
  54. Sickle Cell Crisis in the ICU
    5 Topics
    |
    1 Quiz
  55. Methemoglobinemia & Dyshemoglobinemias
    5 Topics
    |
    1 Quiz
  56. Toxicology
    Toxidrome Recognition and Initial Management
    5 Topics
    |
    1 Quiz
  57. Management of Acute Overdoses – Non-Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  58. Management of Acute Overdoses – Cardiovascular Agents
    5 Topics
    |
    1 Quiz
  59. Toxic Alcohols and Small-Molecule Poisons
    5 Topics
    |
    1 Quiz
  60. Antidotes and Gastrointestinal Decontamination
    5 Topics
    |
    1 Quiz
  61. Extracorporeal Removal Techniques
    5 Topics
    |
    1 Quiz
  62. Withdrawal Syndromes in the ICU
    5 Topics
    |
    1 Quiz
  63. Infectious Diseases
    Sepsis and Septic Shock
    5 Topics
    |
    1 Quiz
  64. Pneumonia (CAP, HAP, VAP)
    5 Topics
    |
    1 Quiz
  65. Endocarditis
    5 Topics
    |
    1 Quiz
  66. CNS Infections
    5 Topics
    |
    1 Quiz
  67. Complicated Intra-abdominal Infections
    5 Topics
    |
    1 Quiz
  68. Antibiotic Stewardship & PK/PD
    5 Topics
    |
    1 Quiz
  69. Clostridioides difficile Infection
    5 Topics
    |
    1 Quiz
  70. Febrile Neutropenia & Immunocompromised Hosts
    5 Topics
    |
    1 Quiz
  71. Skin & Soft-Tissue Infections / Acute Osteomyelitis
    5 Topics
    |
    1 Quiz
  72. Urinary Tract and Catheter-related Infections
    5 Topics
    |
    1 Quiz
  73. Pandemic & Emerging Viral Infections
    5 Topics
    |
    1 Quiz
  74. Supportive Care (Pain, Agitation, Delirium, Immobility, Sleep)
    Pain Assessment and Analgesic Management
    5 Topics
    |
    1 Quiz
  75. Sedation and Agitation Management
    5 Topics
    |
    1 Quiz
  76. Delirium Prevention and Treatment
    5 Topics
    |
    1 Quiz
  77. Sleep Disturbance Management
    5 Topics
    |
    1 Quiz
  78. Immobility and Early Mobilization
    5 Topics
    |
    1 Quiz
  79. Oncologic Emergencies
    5 Topics
    |
    1 Quiz
  80. End-of-Life Care & Palliative Care
    Goals of Care & Advance Care Planning
    5 Topics
    |
    1 Quiz
  81. Pain Management & Opioid Therapy
    5 Topics
    |
    1 Quiz
  82. Dyspnea & Respiratory Symptom Management
    5 Topics
    |
    1 Quiz
  83. Sedation & Palliative Sedation
    5 Topics
    |
    1 Quiz
  84. Delirium Agitation & Anxiety
    5 Topics
    |
    1 Quiz
  85. Nausea, Vomiting & Gastrointestinal Symptoms
    5 Topics
    |
    1 Quiz
  86. Management of Secretions (Death Rattle)
    5 Topics
    |
    1 Quiz
  87. Fluids, Electrolytes, and Nutrition Management
    Intravenous Fluid Therapy and Resuscitation
    5 Topics
    |
    1 Quiz
  88. Acid–Base Disorders
    5 Topics
    |
    1 Quiz
  89. Sodium Homeostasis and Dysnatremias
    5 Topics
    |
    1 Quiz
  90. Potassium Disorders
    5 Topics
    |
    1 Quiz
  91. Calcium and Magnesium Abnormalities
    5 Topics
    |
    1 Quiz
  92. Phosphate and Trace Electrolyte Management
    5 Topics
    |
    1 Quiz
  93. Enteral Nutrition Support
    5 Topics
    |
    1 Quiz
  94. Parenteral Nutrition Support
    5 Topics
    |
    1 Quiz
  95. Refeeding Syndrome and Specialized Nutrition
    5 Topics
    |
    1 Quiz
  96. Trauma and Burns
    Initial Resuscitation and Fluid Management in Trauma
    5 Topics
    |
    1 Quiz
  97. Hemorrhagic Shock, Massive Transfusion, and Trauma‐Induced Coagulopathy
    5 Topics
    |
    1 Quiz
  98. Burns Pharmacotherapy
    5 Topics
    |
    1 Quiz
  99. Burn Wound Care
    5 Topics
    |
    1 Quiz
  100. Open Fracture Antibiotics
    5 Topics
    |
    1 Quiz

Participants 432

  • Allison Clemens
  • April
  • ababaabhay
  • achoi2392
  • adhoward1
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Lesson 50, Topic 5
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Recovery, De-escalation, and Transition of Care in VTE

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VTE: Recovery, De-escalation, and Transition of Care

Recovery, De-escalation, and Transition of Care in VTE

Objective Icon A target symbol, representing the chapter’s main goal.

Learning Objective

Facilitate patient recovery, mitigate long-term sequelae, and ensure a safe transition of care after acute VTE stabilization.

1. De-escalation of Anticoagulation Intensity

After achieving hemodynamic and thrombotic stability, the intensity of anticoagulation must be carefully stepped down to balance the ongoing risks of bleeding and thrombosis. This process requires clear clinical criteria and structured monitoring.

Criteria for Transition to Prophylactic Dosing

  • Isolated distal deep vein thrombosis (DVT) with no extension on serial imaging (e.g., at days 7 and 14).
  • Stable submassive pulmonary embolism (PE) with evidence of normalized right ventricular (RV) function and cardiac biomarkers.
  • Development of a new or evolving bleeding risk (e.g., platelet count <50 × 10⁹/L, upcoming invasive procedure).
  • Sustained clinical stability for at least 48–72 hours without any signs of thrombus propagation or clinical worsening.
Case Vignette IconA clipboard icon representing a patient case. Case Vignette +

A 65-year-old patient, post-operative day 5 from a total knee arthroplasty, developed a new isolated calf DVT. The patient was started on a therapeutic unfractionated heparin (UFH) infusion. Serial compression ultrasounds on day 7 and day 14 showed the thrombus was stable with no proximal extension. Given the provoked nature and stability, the patient was successfully transitioned from the UFH infusion to prophylactic enoxaparin 40 mg subcutaneously once daily.

Serial Imaging and Management Protocol for Distal DVT

Distal DVT Imaging Flowchart A flowchart showing the decision-making process for managing isolated distal DVT. It starts with diagnosis, proceeds to serial ultrasound at days 7-14. If there is no extension, the patient continues prophylactic anticoagulation or surveillance. If there is extension, the patient resumes full-dose anticoagulation. Isolated Distal DVT Serial Ultrasound (Days 7 & 14) Resume Full-Dose AC Extension Continue Prophylaxis No Extension
Figure 1. Decision algorithm for managing isolated distal DVT with serial imaging.

Discontinuation of IVC Filters and Thrombolytics

Retrievable inferior vena cava (IVC) filters should be removed as soon as therapeutic anticoagulation is safely established, ideally within 4–6 weeks of placement. Catheter-directed thrombolysis is generally reserved for select cases of extensive, limb-threatening DVT (phlegmasia cerulea dolens).

Clinical Pearl IconA lightbulb icon representing a clinical pearl or key insight. Clinical Pearl: IVC Filter Retrieval +

Prompt retrieval of IVC filters is critical. Prolonged dwell time significantly increases the risk of complications, including caval thrombosis, filter fracture, and device migration. A dedicated tracking system and protocol for scheduling removal are essential quality improvement measures.

2. Conversion from Intravenous to Oral Anticoagulants

Transitioning from intravenous (IV) to enteral anticoagulants is a key step toward discharge. The choice of agent and timing depends on clinical stability, renal function, and the ability to absorb oral medications.

Transitioning to Direct Oral Anticoagulants (DOACs)

DOACs are now the preferred oral agents for most patients with VTE. The transition strategy varies by agent.

DOAC Transition and Dosing Summary
Agent Initial Dosing (Acute Phase) Maintenance Dosing Key Transition Considerations
Apixaban 10 mg BID × 7 days 5 mg BID Can be started immediately after stopping UFH infusion. No parenteral lead-in required.
Rivaroxaban 15 mg BID × 21 days 20 mg QD with food Can be started immediately after stopping UFH. No parenteral lead-in. Must be taken with food.
Edoxaban N/A 60 mg QD Requires 5-10 days of parenteral anticoagulation (e.g., LMWH) before starting.
Dabigatran N/A 150 mg BID Requires 5-10 days of parenteral anticoagulation before starting. Capsule must not be opened.

PK/PD Considerations with Enteral Nutrition

  • Administration: Administer DOACs as intact tablets if possible. If crushing is unavoidable (off-label), flush the feeding tube with at least 30 mL of water before and after administration.
  • Feeding Interruption: For continuous tube feeds, consider holding feeds for 1 hour before and 1 hour after the DOAC dose to maximize absorption, though clinical evidence is limited.
  • Interactions: High-calcium or high-protein enteral formulations may chelate or bind to anticoagulants, potentially altering absorption. Monitor closely for signs of bleeding or thrombosis.
Clinical Pearl IconA lightbulb icon representing a clinical pearl or key insight. Clinical Pearl: DOACs and Feeding Tubes +

Crushing DOAC tablets for feeding tube administration is an off-label use and alters their pharmacokinetics. This practice should only be considered when no alternative exists and requires institutional protocol. Confirming tube placement and ensuring adequate flushing are paramount to prevent dose loss and tube occlusion.

3. Post-ICU Syndrome (PICS) Mitigation

A severe VTE requiring an ICU stay places patients at high risk for Post-ICU Syndrome (PICS)—a constellation of new or worsened physical, cognitive, and psychological impairments. Proactive mitigation is essential.

Risk Identification and the ABCDEF Bundle

Key risk factors for PICS include advanced age (>65 years), mechanical ventilation for more than 48 hours, prolonged ICU stay (>7 days), and documented delirium. The ABCDEF Bundle is a proven, evidence-based strategy to reduce these risks.

The ABCDEF Bundle for ICU Care A circular diagram showing the six components of the ABCDEF bundle: Assess, prevent & manage pain; Both SAT & SBT; Choice of analgesia & sedation; Delirium assessment; Early mobility & exercise; and Family engagement & empowerment. AAssess, Prevent & Manage Pain BBoth SAT & SBT CChoice of Sedation DDelirium Assessment EEarly Mobility FFamily Engagement
Figure 2. The ABCDEF bundle provides a structured approach to optimizing ICU patient care, reducing delirium, and mitigating the long-term consequences of critical illness.

Support Strategies

  • Early Mobilization: Begin passive range-of-motion exercises on ICU day 1. Progress systematically to sitting, standing, and ambulation as tolerated, guided by physical and occupational therapy.
  • Cognitive Support: Minimize sedation depth and duration. Use ICU diaries to help patients orient themselves and process their experience.
  • Psychological Support: Actively engage family and caregivers in the patient’s care. Refer patients with persistent symptoms of PTSD, anxiety, or cognitive deficits for formal neuropsychological evaluation post-discharge.

4. Medication Reconciliation and Discharge Counseling

A meticulous medication reconciliation process and comprehensive patient education are the cornerstones of a safe discharge, critical for preventing adverse drug events and hospital readmissions.

Comprehensive Reconciliation Steps

  1. Verify Pre-Admission List: Obtain the best possible medication history from the patient, family, or outpatient pharmacy.
  2. Review In-Hospital Changes: Account for all medications started, stopped, or adjusted during the hospital stay.
  3. Assess Final Plan: Confirm the final anticoagulant choice, dose, duration, and any necessary monitoring. Cross-reference with renal and hepatic function.
  4. Check for Interactions: Screen the final medication list for significant drug-drug interactions (e.g., amiodarone, certain antifungals with DOACs).

Patient and Caregiver Education

  • Dosing Clarity: Provide a written dosing calendar, especially for DOACs with initial step-down dosing. Clearly state what to do in case of a missed dose.
  • Bleeding Signs: Educate on recognizing both minor (gum bleeding, easy bruising) and major (hematuria, melena, severe headache) signs of bleeding and when to seek medical attention.
  • Adherence: Emphasize that consistent adherence is crucial for preventing recurrent VTE.
  • Family Involvement: Engage family members or caregivers in all teaching sessions, particularly if the patient has cognitive or physical limitations. Provide emergency contact numbers for the anticoagulation clinic or pharmacy.

5. Long-Term Anticoagulation Management

Decisions regarding the duration of anticoagulation must balance the risk of VTE recurrence against the patient-specific risk of major bleeding. This decision should be revisited over time.

Duration Decisions: Provoked vs. Unprovoked VTE

Recommended Duration of Anticoagulation by VTE Etiology
VTE Etiology Typical Duration Considerations for Extended Therapy
Provoked VTE (transient major risk factor, e.g., surgery, trauma) 3 months Extension is generally not recommended if the provoking factor has resolved.
Unprovoked VTE (no identifiable risk factor) At least 3-6 months Extended therapy should be considered, especially if bleeding risk is low. Re-evaluate risk/benefit annually.
Cancer-Associated VTE Minimum 6 months Continue anticoagulation as long as cancer is active or patient is receiving treatment. LMWH or DOACs are preferred.

Extended-Phase Prophylaxis

For patients with unprovoked VTE who have completed the initial treatment phase, extended prophylaxis can reduce recurrence risk. Options include:

  • Reduced-Dose DOACs: Apixaban 2.5 mg BID or rivaroxaban 10 mg QD are effective options with a lower bleeding risk than full treatment doses.
  • Aspirin: Offers a modest reduction in VTE recurrence but is less effective than anticoagulation. It may be an option for patients who decline or cannot tolerate anticoagulants.
Clinical Pearl IconA lightbulb icon representing a clinical pearl or key insight. Clinical Pearl: Annual Reassessment +

The decision to continue long-term anticoagulation is not permanent. An annual, structured reassessment of the patient’s VTE recurrence risk (e.g., using the HERDOO2 score for women) and bleeding risk (e.g., HAS-BLED score, new comorbidities) is essential to ensure the benefits continue to outweigh the harms.

6. Handoff and Communication Tools

Safe transitions of care depend on clear, structured communication between inpatient and outpatient teams. Standardized tools minimize information loss and prevent errors.

Structured Handoff Templates

Using a standardized handoff tool like SBAR ensures all critical information is conveyed concisely and accurately. For VTE, this must include specific anticoagulant details.

SBAR Handoff Tool for VTE A diagram showing the four components of the SBAR handoff tool: Situation, Background, Assessment, and Recommendation, with VTE-specific examples for each. Situation Discharging Mr. Smith after treatment for unprovoked PE. Background 68M, CrCl 75 mL/min. No prior bleeding. Stable on apixaban. Assessment Low bleeding risk. High recurrence risk. Patient understands plan. Recommendation Continue apixaban 5mg BID. Follow-up with PCP in 7 days.
Figure 3. Application of the SBAR framework to a VTE patient discharge handoff.

Electronic Health Record (EHR) and Outpatient Coordination

  • EHR Best Practices: Implement standardized VTE discharge order sets that automatically populate the medication list, duration, and scheduled follow-up labs. Alerts can flag when the last inpatient dose was given to ensure seamless outpatient continuation.
  • Outpatient Coordination: Proactively schedule the first follow-up appointment (with primary care or an anticoagulation clinic) within 7 days of discharge. Ensure the complete discharge summary and medication plan are transmitted to the receiving provider before the visit.

References

  1. Ortel TL, Neumann I, Ageno W, et al. American Society of Hematology 2020 guidelines for management of venous thromboembolism: treatment of DVT and PE. Blood Advances. 2020;4(19):4693–4738.
  2. Stevens SM, Woller SC, Kreuziger LB, et al. Antithrombotic Therapy for VTE Disease: Second Update of the CHEST Guideline and Expert Panel Report. CHEST. 2021;160(6):e545–e608.
  3. Konstantinides SV, Meyer G, Becattini C, et al. 2019 ESC Guidelines for the diagnosis and management of acute pulmonary embolism. Eur Heart J. 2020;41(4):543–603.
  4. Vedantham S, Goldhaber SZ, Julian JA, et al; ATTRACT Trial Investigators. Pharmacomechanical catheter-directed thrombolysis for deep-vein thrombosis. N Engl J Med. 2017;377(23):2240–2252.
  5. Kahn SR, Shapiro S, Wells PS, et al; SOX trial investigators. Compression stockings to prevent post-thrombotic syndrome: a randomized placebo-controlled trial. Lancet. 2014;383(9920):880–888.
  6. Agnelli G, Buller HR, Cohen A, et al; AMPLIFY Investigators. Oral apixaban for the treatment of acute venous thromboembolism. N Engl J Med. 2013;369(9):799–808.
  7. Bauersachs R, Berkowitz SD, Brenner B, et al. Oral rivaroxaban for symptomatic venous thromboembolism. N Engl J Med. 2010;363(26):2499–2510.
  8. Schulman S, Kearon C, Kakkar AK, et al; RE-SONATE Trial Investigators. Extended use of dabigatran, warfarin, or placebo in venous thromboembolism. N Engl J Med. 2013;368(8):709–718.
  9. Agnelli G, Becattini C, Bauersachs R, et al; Caravaggio Investigators. Apixaban versus dalteparin for treatment of VTE associated with cancer. N Engl J Med. 2020;382(17):1599–1607.
  10. Raskob GE, van Es N, Verhamme P, et al; Hokusai VTE Cancer Investigators. Edoxaban for treatment of cancer-associated VTE. N Engl J Med. 2018;378(5):615–624.