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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 15, Topic 5
In Progress

Optimizing Pharmacotherapy and Management in Acute Kidney Injury

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Recovery Strategies and Care Transitions after AKI

Recovery Strategies and Care Transitions after AKI

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

Objective

Develop a plan to promote recovery, prevent long-term issues, and ensure safe care transitions after acute kidney injury (AKI).

I. Introduction

The recovery phase after AKI is a critical window to restore renal function, prevent progression to chronic kidney disease (CKD), reduce readmissions, and optimize patient outcomes through structured protocols.

Goals of Recovery:

  • Preserve native kidney function.
  • Minimize iatrogenic harm.
  • Facilitate community reintegration.

Impact of AKI:

AKI survivors have elevated risks of:

  • CKD progression.
  • Cardiovascular events.
  • Hospital readmissions.
  • Mortality.
Key Point Icon A lightbulb icon, indicating a key point. Key Point: Structured Recovery Pathways Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

Structured, multidisciplinary recovery pathways—including pharmacist-led transitions of care—reduce adverse events and readmissions and improve long-term renal outcomes.

II. Weaning and De-escalation Protocols

Protocolized assessment of renal recovery markers guides safe discontinuation of renal replacement therapy (RRT) and tapering of supportive measures.

1. Criteria for Renal Recovery

  • Serum creatinine: Down-trending toward baseline or stable off RRT.
  • Urine output: Sustained >0.5 mL/kg/h (approximately 400 – 500 mL/day) for 6 – 12 hours without diuretics.
  • Hemodynamic stability: Minimal or no vasopressors, euvolemia on dynamic monitoring (pulse pressure variation, stroke volume variation).
  • Absence of ongoing RRT indications: No refractory hyperkalemia, severe acidosis, or fluid overload.

2. RRT Discontinuation Algorithm

1. Confirm Clinical Stability & Resolution of RRT Triggers

2. Verify Recovery Markers:

  • Cr trend ↓, UO >0.5 mL/kg/h (6-12h no diuretics)
  • Hemodynamic stability (min/no vasopressors)
  • No ongoing RRT indications (K+, acidosis, fluid)

3. Initiate Trial-Off RRT (12–24 hours)

4. Monitor Serum Labs q6-12h
(Creatinine, BUN, Electrolytes, Acid-Base)

5. Clinically Stable?

Yes

Continue Supportive Care

No

Resume RRT
(Metabolic derangements recur or oliguria returns)

Figure: RRT Discontinuation Algorithm. Close monitoring is key during trial-off periods.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Vigilance During Trial-Off RRT Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

Trial-off periods reveal true renal capacity but require vigilant lab checks (every 6-12 hours) to prevent rebound azotemia or electrolyte disturbances.

3. Hemodynamic and Fluid Support Tapering

  • Avoid abrupt diuretic withdrawal or vasopressor discontinuation; de-escalate based on volume status and perfusion metrics.
  • Use dynamic assessments (e.g., echocardiographic IVC variability, pulse pressure variation/stroke volume variation) to guide fluid removal and prevent hypovolemia.

4. Monitoring for Rebound Azotemia

  • First 24–72 hours post-RRT: Check creatinine, BUN, potassium, and acid-base status every 8–12 hours.
  • Intervene early if BUN/creatinine rise >20% from post-trial baseline or if potassium rises >5.5 mEq/L.

III. Medication Route Transition

Converting from intravenous (IV) to enteral therapy enhances comfort and reduces complications but demands careful pharmacokinetic (PK) and pharmacodynamic (PD) adjustments in the context of a recovering kidney.

1. Assessment Criteria for Enteral Conversion

  • Return of gastrointestinal (GI) function: presence of bowel sounds, tolerance of small volumes of enteral intake, absence of ileus or significant emesis.
  • Secure enteral access: nasogastric, orogastric, or other feeding tube position verified and functional.

2. PK/PD Considerations

  • Renal clearance may remain impaired or fluctuate during recovery; adjust dosing accordingly based on estimated glomerular filtration rate (eGFR) and drug-specific recommendations.
  • Altered volume of distribution and protein binding due to fluid shifts and critical illness can affect drug levels.
  • First-pass metabolism and gut motility can be unpredictable in critically ill patients, potentially affecting bioavailability of oral medications.

3. Common Drug Classes and Enteral Options

Table: Enteral Conversion for Common Drug Classes in AKI Recovery
Drug Class Enteral Agents Approx. Bioavailability Renal Adjustment Notes Monitoring
Fluoroquinolones Levofloxacin, Moxifloxacin >90% Levofloxacin requires dose reduction for eGFR <50 mL/min. Moxifloxacin generally no adjustment. QT interval, mental status, tendon toxicity signs.
Linezolid Linezolid ~100% No dosage adjustment typically needed in renal impairment. CBC (thrombocytopenia), serotonin syndrome signs if concurrent serotonergic agents.
Antiepileptics Levetiracetam, Valproate Levetiracetam ~100%, Valproate >90% Levetiracetam dose reduction required for eGFR <80 mL/min. Valproate generally no adjustment for renal function but monitor for toxicity. Serum levels (if indicated), seizure activity, LFTs (valproate), mental status.
Antihypertensives (Beta-blockers, ACE-I) Metoprolol, Lisinopril Metoprolol 40–50% (tartrate), Lisinopril ~25% Titrate to blood pressure. Lisinopril initiate at lower doses if eGFR <30 mL/min; monitor K+ and renal function closely. Blood pressure, heart rate, renal function (eGFR, K+ for ACE-I).
Analgesics (Opioids, Non-opioids) Acetaminophen, Oxycodone Acetaminophen 80–90%, Oxycodone 60–87% Acetaminophen generally safe. Oxycodone use with caution, consider dose reduction/interval extension for eGFR <60 mL/min due to active metabolite accumulation. Pain scores, LFTs (acetaminophen), sedation scale, respiratory rate (oxycodone).
Pitfall IconAn exclamation mark in a triangle, indicating a pitfall. Clinical Pitfall: Enteral Feed Interactions Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

Enteral feeds can chelate certain medications, significantly reducing their absorption. For drugs like fluoroquinolones and phenytoin, it is crucial to hold tube feeds for 1–2 hours before and after drug administration to ensure adequate bioavailability.

IV. Mitigation of Post-ICU Syndrome (PICS)

AKI survivors, particularly those requiring RRT or with prolonged ICU stays, are at high risk for Post-ICU Syndrome (PICS)—a constellation of new or worsened physical, cognitive, and psychological impairments that benefit from early prevention and intervention strategies.

1. Identification of High-Risk Patients

  • Risk factors include: Age >65 years, prolonged ICU stay (>7 days), pre-existing CKD, diabetes, heart failure, severity of AKI (especially if RRT was required), delirium duration, and immobility.
  • Utilize multidisciplinary screening tools and clinical judgment to stratify patients for targeted PICS prevention and rehabilitation interventions.

2. ABCDEF Bundle Implementation

Figure: The ABCDEF Bundle for ICU Liberation and PICS Mitigation
  • Assess, Prevent, and Manage Pain: Regular pain assessment using validated scales (e.g., CPOT, BPS), multimodal analgesia strategies to minimize opioids.
  • Both Spontaneous Awakening Trials (SATs) and Spontaneous Breathing Trials (SBTs): Daily interruption of continuous sedation (SAT) and coordinated ventilator weaning trials (SBT) for eligible patients.
  • Choice of Analgesia and Sedation: Prioritize non-benzodiazepine sedatives (e.g., propofol, dexmedetomidine) when sedation is needed. Use targeted, light sedation.
  • Delirium: Assess, Prevent, and Manage: Routine delirium screening (e.g., CAM-ICU, ICDSC), non-pharmacological interventions (reorientation, sleep promotion, early mobility).
  • Early Mobility and Exercise: Progressive mobility protocols, from passive range of motion in bed to active ambulation, initiated as soon as feasible.
  • Family Engagement and Empowerment: Involve family in care planning, provide education about AKI and PICS, and support their role in the patient’s recovery.

3. Early Mobilization and Rehabilitation Coordination

  • Initiate physical and occupational therapy consultations as soon as the patient is hemodynamically stable, even during their ICU stay if appropriate.
  • Communicate rehabilitation progress and ongoing needs clearly to post-acute care teams and facilities during care transitions.

4. Tracking Functional Recovery and Mental Health

  • Use standardized functional assessment tools (e.g., Barthel Index, 6-minute walk test, Katz ADL) at discharge and during follow-up appointments.
  • Screen for common psychological sequelae such as depression, anxiety, and PTSD. Refer to mental health professionals or support groups as needed.
  • Assess for cognitive deficits and provide resources or referrals for cognitive rehabilitation if indicated.
Pearl IconA shield with an exclamation mark, indicating a clinical pearl. Clinical Pearl: Drug Exposure and Mobility Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

Minimizing cumulative exposure to sedative (especially benzodiazepines) and anticholinergic medications is a key strategy that supports early mobilization goals and reduces the incidence and duration of delirium, thereby mitigating PICS.

V. Medication Reconciliation and Discharge Counseling

Meticulous medication reconciliation and comprehensive patient education at discharge are crucial to ensure continuity of renal-safe pharmacotherapy, prevent adverse drug events, and empower patients in their ongoing recovery.

1. Structured Reconciliation with a Renal Focus

  • Systematically review all pre-admission, inpatient, and newly prescribed medications, including over-the-counter (OTC) drugs and herbal supplements.
  • Identify and explicitly discontinue any potentially nephrotoxic medications (e.g., NSAIDs, certain antimicrobials like aminoglycosides if alternatives exist) unless absolutely indicated with close monitoring.
  • Adjust doses of all renally cleared medications based on the patient’s estimated GFR at discharge. Document clear monitoring parameters and rationale for any deviations.

2. Patient and Caregiver Education

  • Employ the teach-back method to confirm understanding of:
    • Warning signs of AKI recurrence or worsening kidney function (e.g., decreased urine output, new swelling).
    • Specific medication changes, including new drugs, discontinued drugs, and dose adjustments.
    • Any fluid or dietary restrictions.
    • Importance of avoiding nephrotoxins like NSAIDs.
  • Provide clear, concise written instructions, including a reconciled medication list, schedule for follow-up laboratory tests, and clinic appointments.

3. Discharge Medication List Content

  • Clearly highlight any renal-dose adjustments made.
  • List medications to avoid or use with caution (especially NSAIDs).
  • Include contact information for the discharging physician, nephrology follow-up (if arranged), and a primary care provider. Pharmacy contact for questions can also be beneficial.

4. Coordination with Outpatient Providers

  • Communicate the patient’s AKI history, severity, presumed etiology, hospital course, and risk stratification for CKD progression to the primary care physician and any outpatient specialists (e.g., nephrologist).
  • Provide a clear follow-up schedule, including recommended timing for reassessment of renal function and proteinuria.
  • Recommend referral to a dedicated AKI follow-up clinic or nephrology consultation for high-risk patients (e.g., severe AKI, incomplete renal recovery, pre-existing CKD).
Key Point IconA lightbulb icon, indicating a key point. Key Point: Pharmacist-Led Discharge Impact Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

Pharmacist-led medication reconciliation and discharge counseling programs have been shown to significantly reduce medication errors (by up to 50%) and decrease 30-day hospital readmissions in AKI survivors.

VI. Quality Metrics, Controversies, and Future Directions

Tracking key outcomes such as readmissions, progression to CKD, and medication-related adverse events is essential for driving continuous quality improvement in post-AKI care. However, gaps persist in areas like standardized RRT weaning criteria and the optimal use of biomarkers to guide de-escalation strategies.

1. Quality Metrics for Post-AKI Care

  • 30-day and 90-day hospital readmission rates: Overall and AKI-related readmissions.
  • Progression to CKD or end-stage kidney disease (ESKD): Incidence of new CKD diagnosis or worsening of pre-existing CKD stages within 6-12 months post-discharge.
  • Post-discharge adverse drug events (ADEs): Particularly those related to inappropriate dosing or use of nephrotoxic agents.
  • Follow-up rates: Percentage of patients attending scheduled nephrology or primary care follow-up appointments post-AKI.

2. Controversies and Evidence Gaps

  • There are no universally accepted, evidence-based thresholds for RRT discontinuation; practice often varies by institution and clinician experience.
  • The optimal timing and criteria for switching from IV to enteral medications in the context of recovering renal function lack robust trial data for many drugs.
  • Best strategies for long-term monitoring and management to prevent CKD progression after AKI are still evolving.

3. Emerging Biomarkers and Technologies

  • Novel kidney biomarkers: Urinary NGAL (Neutrophil Gelatinase-Associated Lipocalin), KIM-1 (Kidney Injury Molecule-1), and the [TIMP-2]*[IGFBP7] test (e.g., NephroCheck®) show promise for earlier detection of renal recovery or ongoing subclinical injury, potentially guiding RRT weaning or medication adjustments.
  • Electronic Health Record (EHR) alerts and clinical decision support tools: May facilitate timely medication adjustments, flag potential nephrotoxins, and prompt appropriate follow-up for AKI survivors.
Future Direction IconA trending up arrow, indicating future directions. Future Direction: Personalized Recovery Expand/Collapse IconA plus symbol that rotates to an X when the accordion is open.

The integration of novel biomarkers into routine clinical workflows, coupled with standardized recovery algorithms and enhanced clinical decision support, may personalize de-escalation strategies and improve long-term renal and patient-centered outcomes after AKI.

References

  1. Hoste EA, Kellum JA, Selby NM, et al. Global epidemiology and outcomes of acute kidney injury. Nat Rev Nephrol. 2018;14(10):607–625.
  2. Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group. KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int Suppl. 2012;2(1):1-138. (Note: While the prompt mentioned a 2023 update, the foundational AKI guideline is widely cited; specific content may draw from newer consensus or updates if available and relevant to recovery aspects.)
  3. Gameiro J, Agapito Fonseca J, Jorge S, Lopes JA. Acute kidney injury definition and diagnosis: a narrative review. J Clin Med. 2018;7(10):307.
  4. Kashani K, Rosner MH, Haase M, et al. Biomarkers of acute kidney injury: the pathway from discovery to clinical adoption. Clin Chem Lab Med. 2017;55(8):1074–1089.
  5. Hobson CE, Goldstein SL, Silver SA, et al. Applications for detection of AKI using electronic records: report of the 15th Acute Dialysis Quality Initiative (ADQI) consensus conference. Can J Kidney Health Dis. 2016;3:9.
  6. Chawla LS, Bellomo R, Bihorac A, et al. Acute kidney disease and renal recovery: consensus report of the Acute Disease Quality Initiative (ADQI) 16 Workgroup. Nat Rev Nephrol. 2017;13(4):241-257.
  7. Siew ED, Davenport A, Mehta RL, et al. The 21st International Consensus Conference of the ADQI (Acute Disease Quality Initiative) Group. Can J Kidney Health Dis. 2018;5:2054358118764680. (Illustrative of ongoing ADQI work relevant to AKI recovery).
  8. Silver SA, Goldstein SL, Horkan CM, et al. The RRT Weaning Workgroup of the 25th Acute Disease Quality Initiative. Renal recovery following acute kidney injury: a consensus report of the 25th Acute Disease Quality Initiative (ADQI) workgroup. Kidney Med. 2023;5(1):100578.