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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
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    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 94, Topic 4
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Supportive Care, Complication Prevention, and Goals of Care in Parenteral Nutrition Support

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Supportive Care in Parenteral Nutrition

Supportive Care, Complication Prevention, and Goals of Care in Parenteral Nutrition Support

Objectives Icon A checkmark inside a circle, symbolizing achieved goals.

Lesson Objective

Recommend supportive care measures and complication‐prevention strategies for ICU patients receiving parenteral nutrition (PN), and facilitate multidisciplinary goals‐of‐care discussions when PN becomes burdensome.

1. Supportive Care Integration with Parenteral Nutrition

Effective parenteral nutrition is not delivered in a vacuum. Respiratory and circulatory support must be carefully tailored to preserve gastrointestinal (splanchnic) blood flow, which is essential for preventing gut ischemia and facilitating nutrient utilization by the body.

Mechanical Ventilation Considerations

  • Lung-Protective Strategy: Utilize low tidal volumes (4–8 mL/kg of predicted body weight) and maintain a plateau pressure of ≤30 cm H₂O to prevent barotrauma.
  • PEEP Optimization: A PEEP of 5–10 cm H₂O can balance alveolar recruitment against potential reductions in venous return and cardiac output.
  • Patient Positioning: Elevate the head of the bed to 30–45° to minimize the risk of ventilator-associated pneumonia and aspiration.
  • Sedation Management: Coordinate sedation levels to ensure patient-ventilator synchrony while avoiding deep sedation, which can impair gut motility.
Pearl IconA shield with an exclamation mark. Key Pearl: Monitoring for Splanchnic Hypoperfusion

The gut is highly vulnerable to ischemia during shock states. Closely monitor global markers of tissue oxygenation, such as a mixed-venous O₂ saturation (ScvO₂) >65% and a serum lactate <2 mmol/L, as indirect but crucial indicators of adequate splanchnic perfusion.

Hemodynamic Support and Fluid Management

  • First-Line Vasopressor: Norepinephrine (0.01–0.3 µg/kg/min) is preferred to maintain a MAP ≥65 mm Hg, as it has minimal vasoconstrictive effects on the mesenteric artery compared to other agents.
  • Adjunctive Vasopressor: Low-dose vasopressin (≤0.04 U/min) can be added to norepinephrine as a splanchnic-sparing adjunct to raise MAP.
  • Fluid Choice: Use balanced crystalloids for fluid resuscitation. Avoid large-volume boluses of normal saline, which can worsen metabolic acidosis and exacerbate electrolyte shifts common in patients on PN.
Pitfall IconA warning triangle with an exclamation mark. Pitfall: Vasopressor Selection

Avoid high-dose phenylephrine if possible. Its pure alpha-agonist activity can significantly compromise mesenteric blood flow, potentially leading to gut ischemia and negating the benefits of nutritional support. Always reassess intravascular volume status before reflexively escalating vasopressor doses.

2. Pharmacotherapy: Prophylactic and Supportive Agents

Prophylactic pharmacotherapy is critical for reducing the incidence of major ICU complications, such as VTE and stress ulcers, in vulnerable patients dependent on PN.

Prophylactic Therapies in PN-Dependent ICU Patients
Intervention Agent & Dose Key Indications Clinical Considerations
VTE Prophylaxis Enoxaparin 40 mg SC daily OR
Heparin 5,000 U SC TID
All ICU patients unless contraindicated (e.g., active bleed, platelets <50 × 10⁹/L). Use heparin in severe renal dysfunction (CrCl <30 mL/min). Consider anti-Xa monitoring in obesity or renal impairment.
Stress Ulcer Prophylaxis Pantoprazole 40 mg IV daily OR
Ranitidine 50 mg IV q8h
Mechanical ventilation >48h, coagulopathy, or shock requiring vasopressors. Reassess need daily. H₂RAs may have a lower risk of C. difficile and pneumonia than PPIs. Discontinue when risk factors resolve.

Insulin Therapy for Glycemic Control

Hyperglycemia is a common and serious complication of PN. A continuous intravenous insulin infusion is the standard of care for maintaining glycemic control.

  • Initiation and Titration: Start a continuous IV insulin infusion via a dedicated line at 0.05–0.1 U/kg/h when blood glucose exceeds 150 mg/dL. Adjust the rate based on a validated protocol.
  • Target Range: Aim for a blood glucose level of 110–150 mg/dL. This range balances the benefits of glycemic control (reduced infection risk) with the danger of hypoglycemia.
  • Hypoglycemia Management: If glucose drops below 80 mg/dL, hold the insulin infusion, administer 50 mL of D10W as a bolus, and recheck glucose in 15 minutes.
Pearl IconA shield with an exclamation mark. Key Pearl: Separate Infusion Lines

Always infuse insulin and PN through separate IV lines. This allows for rapid titration or cessation of the insulin drip without interrupting the continuous PN infusion, which can be crucial during episodes of hypoglycemia or hemodynamic instability.

Antimicrobial Lock Therapies

Antimicrobial lock therapies are a salvage strategy, not a routine preventive measure. They are considered for patients with a history of recurrent catheter-related bloodstream infections (CLABSIs) despite proper line care.

  • Agents: Common protocols involve instilling Taurolidine 2% or Ethanol 70% into the catheter lumen for a dwell time of 2-4 hours.
  • Indication: Reserved for patients with recurrent CLABSIs to salvage a long-term central line.
  • Safety: Always verify catheter material compatibility, as ethanol can damage certain types of polyurethane catheters.

3. Prevention of Catheter-Related Complications

The central venous catheter required for PN is a major source of morbidity. Strict adherence to evidence-based insertion and maintenance bundles is the cornerstone of preventing mechanical and infectious complications.

CLABSI Prevention Bundle A flowchart showing four key steps in preventing catheter-related bloodstream infections: hand hygiene, maximal barrier precautions, chlorhexidine skin prep, and daily review of line necessity. HandHygiene Maximal BarrierPrecautions ChlorhexidineSkin Prep DailyReview Key Elements of the CLABSI Prevention Bundle
Figure 1: Core Interventions for CLABSI Prevention. Adherence to a bundled set of practices during insertion and maintenance is more effective than any single intervention alone. Daily review of line necessity is crucial for timely removal.

Insertion Bundle

  • Asepsis: Perform meticulous hand hygiene before donning a cap, mask, sterile gown, and sterile gloves. Use a full-body sterile drape for the patient.
  • Antisepsis: Prep the insertion site with a >0.5% chlorhexidine with alcohol solution, allowing it to air dry completely.
  • Site Selection: Use real-time ultrasound guidance for all internal jugular and femoral insertions to reduce mechanical complications. Avoid the femoral site in adults when possible.

Maintenance Practices

  • Dressing Care: Use a transparent, semipermeable dressing. Change every 7 days or immediately if it becomes damp, loose, or visibly soiled. Chlorhexidine-impregnated dressings can further reduce risk.
  • Hub Care: Vigorously “scrub the hub” with an alcohol or chlorhexidine pad for at least 15 seconds before every access.
  • Line Necessity: Perform a daily, formal assessment of the need for the central line. Remove the catheter as soon as it is no longer essential.

4. Management of Metabolic Complications

Parenteral nutrition can cause significant metabolic derangements. Early risk stratification, vigilant monitoring, and proactive interventions are essential to prevent severe complications like refeeding syndrome and liver dysfunction.

Refeeding Syndrome

This is a life-threatening condition caused by rapid shifts in fluids and electrolytes when nutrition is reintroduced in a malnourished patient. Prevention is key.

Refeeding Syndrome Prevention Protocol A flowchart outlining the steps to prevent refeeding syndrome: identify at-risk patients, administer thiamine, start nutrition slowly, monitor electrolytes closely, and replete as needed. Refeeding Syndrome Prevention Protocol 1. Identify At-Risk Patient 2. Give Thiamine 100mg IV Daily 3. Start PN at 40-50% Goal Calories 4. Monitor K, PO₄, Mg Q12h 5. Replete Electrolytes Aggressively
Figure 2: A Stepwise Approach to Preventing Refeeding Syndrome. Risk assessment is the first step, followed by proactive thiamine administration and a cautious, “start low, go slow” approach to nutrition initiation, coupled with intensive electrolyte monitoring.

Parenteral Nutrition-Associated Liver Dysfunction (PNALD)

This complication can range from simple steatosis to cholestasis and fibrosis. It is often multifactorial, but nutritional strategies can mitigate the risk.

  • Monitoring: Check liver function tests (ALT, AST, ALP, bilirubin) twice weekly.
  • Prevention: The most important step is to avoid overfeeding calories (target 20–25 kcal/kg/day) and dextrose (<5 mg/kg/min).
  • Intervention: If LFTs rise, consider switching from a pure soybean oil-based lipid emulsion to a mixed-oil or fish-oil-based formulation, which may have anti-inflammatory properties. Limit lipids to 1 g/kg administered 3 times per week.
Pearl IconA shield with an exclamation mark. Clinical Pearl: The Role of Lipid Emulsions

Newer generation mixed-oil lipid emulsions (e.g., containing soybean, MCT, olive, and fish oils) have been shown to attenuate inflammatory steatosis compared to pure soybean oil formulas, which are high in pro-inflammatory omega-6 fatty acids. This switch is a key strategy in managing PNALD.

5. Multidisciplinary Goals-of-Care and Ethical Considerations

Parenteral nutrition is a form of life support, and its application must align with the patient’s prognosis, quality of life, and expressed wishes. Open and recurrent communication is essential.

Initiation vs. Withholding

The decision to start PN requires a careful assessment of its potential benefits versus its burdens. In cases of refractory multi-organ failure, terminal illness, or when a patient’s prognosis is measured in days, PN may not offer meaningful benefit and can increase complications and suffering.

Shared Decision-Making

These complex decisions should not be made in isolation. Early involvement of a multidisciplinary team including palliative care specialists, ethics consultants, and most importantly, the patient or their surrogate decision-makers is crucial. All discussions, advance directives, and decisions regarding the goals and potential limitations of PN should be clearly documented.

Communication and De-escalation

The goals of care can change as a patient’s clinical condition evolves. Hold weekly interdisciplinary rounds to formally revisit the goals of PN. This creates a structured opportunity to discuss if the therapy is still meeting its intended purpose or if de-escalation or withdrawal is more appropriate.

Key Point IconA key icon symbolizing an important point.

Key Ethical Principle

Parenteral nutrition may be ethically and appropriately withheld or withdrawn when it is determined to be futile—that is, when it prolongs the dying process or imposes burdens that outweigh any potential benefits, in alignment with the patient’s values and goals.

References

  1. McClave SA, Taylor BE, Martindale RG, et al. Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.). JPEN J Parenter Enteral Nutr. 2016;40(2):159-211.
  2. Van den Berghe G, Wouters P, Weekers F, et al. Intensive insulin therapy in critically ill patients. N Engl J Med. 2001;345(19):1359-1367.
  3. da Silva JSV, Seres DS, Sabino K, et al. ASPEN consensus recommendations for refeeding syndrome. Nutr Clin Pract. 2020;35(2):178-195.
  4. O’Grady NP, Alexander M, Burns LA, et al. Guidelines for the prevention of intravascular catheter-related infections. Clin Infect Dis. 2011;52(9):e162-e193.
  5. Eriksen MK, Thomsen T, Nielsen K, et al. Effects of implementing a multidisciplinary nutrition support team on the use of parenteral nutrition in a university hospital. Aliment Pharmacol Ther. 2021;54(5):560-570.