ESPNIC Children’s Intensive Care Textbook
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This textbook provides the fundamental of children’s critical care from a European perspective. It offers a valuable guide for beginners as well as for clinicians working in Intensive Care and allied professionals including the role of an ICU in a modern children’s hospital, specific situations and clinical practice achievements including techniques and the more appropriate therapies to be applied in different conditions.
A section is devoted to specific organs – lung, heart and circulation, kidney and RRT, gut, brain, liver and pancreas, inflammation, immunity and sepsis, metabolism and metabolic diseases in ICU – whilst other to Cardiac Critical Care and Neuro Critical Care. Edited and written by renowned key opinion leaders in the field, all chapters use a learning-oriented style, with practical examples, key points and take-home messages, so that readers can easily learn the content and, at the same time, apply what they have learned in the clinical setting.
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- Springer Nature
- 9783031647628
- 9783031647611
- ePub
- 0
- English
- 2025-07-01
- 100
- 2
- 2
Kaflar
- ESPNIC Children’s Intensive Care Textbook
- Introduction
- Contents
- Contributors
- I: Introduction
- 1. Paediatric and Neonatal Intensive Care: Quo Vadis
- 1.1 Introduction
- 1.2 Cell-Based and Genetic Therapy
- 1.3 Extracorporeal Support Devices
- 1.4 Brain and Critical Illness
- 1.5 Evidence Base Pharmacotherapy
- 1.6 Long-Term Outcome
- 1.7 Reflection
- II: Why Do Children Need Critical Care
- 2. Elective Admission to Critical Care
- 2.1 Introduction
- Case Study 1
- Questions to Consider
- Case Study 2
- 2.2 Preparing the Child and Family Psychologically for an Elective Critical Care Unit (CCU) Admission
- 2.3 Optimising the Physical Condition of the Child Prior to Surgery and Critical Care Unit Admission
- III: Mortality Predictions and Severity of Illness Scores
- 3. Severity of Illness and Organ Dysfunction Scoring in Pediatric Intensive Care Units: Developments in 2020
- 3.1 Introduction
- 3.1.1 Which Severity Scores Are Available for Use in Pediatric Intensive Care?
- 3.1.2 What Organ Dysfunction Scores Are Currently Available?
- 3.1.3 Probabilities of Death
- 3.1.4 ICU Score Quality
- 3.2 Performance and Adaptation of the Scores
- 3.2.1 Score Performance: What Is Evaluated and How to Measure Performance?
- 3.2.2 Adaptation of the Scores
- 3.2.3 Why Use a Severity or Organ Dysfunction Score in Pediatric Intensive Care?
- 3.2.3.1 Objective Assessment of the Severity and Organ Dysfunctions for Each Patient
- 3.2.3.2 Use in Studies
- Description of Tools Used
- Study Inclusion Criteria
- Comparing Illness Severity in Randomized Trials
- 3.3 Evaluation of the Recruitment and Performance of a Service
- 3.4 Future Considerations
- 3.4.1 Health Quality of Life Scores
- 3.4.2 Evaluation of Practices in Pediatric Intensive Care Units
- 3.5 Conclusion
- 4. Paediatric Early Warning Scores
- 4.1 Introduction
- 4.2 What Is a Paediatric Early Warning Score?
- 4.3 Why Might We Need a PEWS?
- 4.4 Types of PEWS
- 4.4.1 Score-Based System
- 4.4.2 Trigger-Based Systems
- 4.4.3 Which Type of PEWS Is Best?
- 4.5 What Is the Evidence for PEWS?
- 4.5.1 A Landmark Study: The EPOCH Trial
- 4.6 How Might We Assess the Quality of a PEWS?
- 4.7 PEWS as Part of a Wider System Response
- 4.8 What’s the Future for PEWS?
- 4.9 Practical Tips for Maximising the Effectiveness of PEWS
- IV: ICU Structure
- 5. ICU: Gas, Humidity, Power and Airflow
- 5.1 Introduction
- 5.2 Single Family Rooms Versus Open-Bay Units
- 5.3 NICU/PICU Location Within the Hospital
- 5.4 Support Areas
- 5.5 Specialized Procedure Spaces
- 5.6 Noise, Light, Temperature and Humidity
- 5.7 Electrical, Gas Supply and Mechanical Needs
- 5.8 Handwashing Facilities
- 5.9 Airborne Infection Isolation Room
- 5.10 Access to Nature and Other Positive Distraction
- 5.11 Ceiling Finishes, Wall Surface and Floor Surface
- 6. Basic Patient Safety and Quality in PICU
- 6.1 Introduction
- 6.2 Culture
- 6.3 Data, Data, Data!
- 7. Handover from Operating Theatre
- 7.1 Why Are Effective Handovers So Important for the Patient’s Safety?
- 7.2 Team Performance and Commons Errors
- 7.2.1 Communication Team Performance
- 7.2.2 Inputs
- 7.2.3 Processes
- 7.2.4 Outcomes
- 7.2.5 Mains Parameters of Ineffective Handover
- 7.3 How to Manage an Effective Handover?
- 8. Infection Prevention and Control in the Paediatric Intensive Care Unit
- 8.1 Introduction
- 8.2 Prevention of Infection in PICU
- 8.3 Modes of Transmission of Infectious Agents
- 8.4 Prevention for Transmission of Infectious Agents
- 8.4.1 Standard Infection Control Precautions (SICPs)
- 8.4.1.1 Hand Hygiene
- 8.4.1.2 Personal Protective Equipment (PPE)
- 8.4.1.3 Prevention of Invasive Device-Associated Infections
- 8.4.2 Care Bundles
- 8.4.2.1 VAP Care Bundle in Children
- 8.4.2.2 Central Line Care Bundle (Insertion and Care and Maintenance)
- 8.5 Aseptic Technique
- 8.6 Aseptic Non-Touch Technique (ANTT)
- 8.7 Environment Build, Materials and Equipment for IPC in PICU
- Case Study: IPC for SARS CoV-2 in PICU
- 8.8 Cleaning Standards
- 9. Information Technology in PICU
- 9.1 Introduction
- 9.2 Electronic Health Records
- 9.2.1 Clinical Documentation
- 9.2.2 Electronic Charting
- 9.3 Computerised Physician Order Entry (CPOE) Systems
- 9.4 Clinical Decision Support Systems (CDSS)
- 9.5 Automated Alerting Systems and Early Warning Scores
- 9.6 Telemedicine
- 9.7 Machine Learning, Big Data and Artificial Intelligence
- 9.8 Human–Technology Interface
- 9.9 Conclusion
- V: The Lung and Mechanical Ventilation in ICU
- 10. Basic Respiratory Physiology
- 10.1 Foetal and Postnatal Development
- 10.2 Surfactant and Foetal Lung Fluid
- 10.3 Transition from Foetal to Postnatal Cardiorespiratory Function
- 10.4 Postnatal Development
- 10.5 How Structure Serves Function
- 10.6 Ventilation and Lung Volumes
- 10.7 Diffusion
- 10.8 Pulmonary Perfusion
- 10.9 Ventilation–Perfusion Relationships
- 10.10 Mechanics of Breathing
- 10.11 Control of Respiration
- 10.12 Ventilator Waveform Monitoring
- Summary
- Take-Home Messages
- 11. Basics of Mechanical Ventilation
- 11.1 The Mechanical Behaviour of the Respiratory System (in the Ventilated Patient)
- 12. Oxygen Therapy and Acute Noninvasive Ventilation in Children
- 12.1 Noninvasive Ventilation
- 12.1.1 Introduction
- 12.1.2 Indications
- 12.1.2.1 Long-Term Ventilatory Support
- 12.1.2.2 Short-Term Ventilatory Support
- Hypoxemic Respiratory Failure (Type I)
- Hypercapnic Respiratory Failure (Type II)
- 12.1.3 Contraindications
- 12.1.4 Equipment
- 12.1.4.1 Types of NIV Ventilators
- 12.1.4.2 Circuits (◘ Fig. 12.1)
- 12.1.4.3 Humidification
- 12.1.4.4 Exhalation Port (◘ Fig. 12.2)
- 12.1.4.5 Anti-Asphyxia Valve (◘ Fig. 12.3)
- 12.1.4.6 Interfaces (◘ Table 12.3)
- 12.1.5 Ventilation Modes
- 12.1.5.1 Volume-Controlled Modes
- 12.1.5.2 Pressure-Controlled Modes (◘ Table 12.4)
- 12.1.5.3 Initial Settings
- 12.1.6 Installation
- 12.1.7 Analysis
- 12.1.7.1 Efficiency
- 12.1.7.2 Tolerance
- 12.1.8 Next Steps
- 12.2 HFNC
- 12.2.1 Introduction
- 12.2.2 Mechanism of Action
- 12.2.2.1 Gas Mixture Conditioning
- 12.2.2.2 High Flow
- 12.2.2.3 Generated Pressures
- 12.2.3 Side Effects and Monitoring
- 12.2.4 HFNC Initiation in Practice (◘ Fig. 12.5)
- 12.2.4.1 Where to Initiate HFNC
- 12.2.4.2 Cannula
- 12.2.4.3 Generator
- 12.2.4.4 Settings (◘ Table 12.7)
- 12.2.5 Indications for HFNC
- 12.2.5.1 Acute Viral Bronchiolitis
- 12.2.5.2 Withdrawal of Invasive Ventilation
- 12.2.5.3 Asthma
- 12.2.5.4 ARDS
- 12.2.5.5 Preoxygenation and Intubation
- 12.2.6 Conclusion
- 13. Paediatric Acute Respiratory Distress Syndrome (pARDS)
- 13.1 Introduction
- 13.2 Definition of Paediatric ARDS (pARDS) (◘ Table 13.1)
- 13.3 Epidemiology
- 13.4 Pathophysiology
- 13.5 Monitoring
- 13.5.1 General
- 13.5.2 Respiratory System Mechanics
- 13.5.3 Oxygenation and CO2 Monitoring
- 13.5.4 Chest Imaging
- 13.5.5 Hemodynamic Monitoring
- 13.6 Treatment
- 13.6.1 Non-Invasive Respiratory Support (NRS)
- 13.6.1.1 High Flow Nasal Cannula (HFNC)
- 13.6.1.2 Non-Invasive Ventilation (NIV): Continuous Positive Airway Pressure (CPAP) and Bilevel Positive Airway Pressure (BiPAP)
- 13.6.1.3 NRS in Resource-Limited Settings (RLS)
- 13.6.2 Invasive Mechanical Ventilation (IMV)
- 13.6.2.1 VT
- 13.6.2.2 Pressures
- 13.6.2.3 PEEP
- 13.6.2.4 Lung-Protective Ventilation (LPV) Bundles
- 13.6.2.5 Oxygenation Target
- 13.6.2.6 Ventilation Target
- 13.6.2.7 Mode of Ventilation
- 13.6.2.8 Recruitment Manoeuvres (RMs)
- 13.6.3 Ancillary Treatments [16, 17]
- 13.6.3.1 Prone Positioning
- 13.6.3.2 Inhaled Nitric Oxide (iNO)
- 13.6.3.3 Surfactant
- 13.6.3.4 Corticosteroids
- 13.6.3.5 Neuromuscular Blockade (NMB)
- 13.6.4 Other Ancillary Treatments [17]
- 13.6.4.1 Fluid Management
- 13.6.4.2 Nutrition
- 13.6.4.3 Transfusion
- 13.7 ECMO
- 13.7.1 Indications/Initiation
- 13.7.2 Ventilation Management
- 13.8 Outcomes
- 14. Physiology of Modes of Ventilation in Severe Acute Lung Injury (ALI)
- 14.1 Introduction
- 14.2 Taxonomy of Mechanical Ventilation
- 14.3 Conventional Mechanical Ventilation Approaches During Acute Lung Injury
- 14.4 High-Frequency Oscillatory Ventilation
- 14.4.1 What Is HFOV?
- 14.4.2 Clinical Evidence in Children
- 14.4.3 Clinical Evidence in Adults
- 14.4.4 Indications for and Timing of HFOV
- 14.4.5 Lung Volume Optimization Manoeuvres
- 14.4.6 Achieving the Lowest Stroke Volume
- 14.4.7 HFOV Titration Weaning
- 14.5 Airway Pressure Release Ventilation
- 14.5.1 Description of APRV
- 14.5.2 Physiologic Benefits
- 14.5.3 Clinical Evidence in Children
- 14.6 Liquid Ventilation
- 14.7 Conclusions
- 15. Paediatric Ventilator Liberation
- 15.1 Introduction
- 15.2 Operational Definitions: A Common Language
- 15.2.1 Respiratory Support
- 15.2.2 Liberation from Invasive MV
- 15.2.3 Assessment for Liberation from Invasive MV
- 15.2.4 Post-extubation NRS
- 15.3 The Liberation Process
- 15.3.1 Gradual Adjustment of Respiratory Support
- 15.3.2 Protocol-Based Screening
- 15.3.2.1 Clinical Criteria
- 15.3.2.2 Respiratory Support
- 15.3.3 Extubation Readiness
- 15.3.3.1 Anticipate and Prevent Post-extubation UAO
- 15.3.3.2 Airway Protection
- 15.3.3.3 Anticipate Post-extubation Non-invasive Respiratory Support
- 15.3.4 Spontaneous Breathing Test (SBT)
- 16. Ventilation of the Infant
- 16.1 Introduction
- 16.2 Indications
- 16.3 Ancillary Therapies During Infant Ventilation
- 16.4 Monitoring During Infant Ventilation
- VI: Fluids and Hemodynamics
- 17. Hemodynamic Physiology
- 17.1 Introduction
- Case Study 1
- 17.2 The Heart
- 17.2.1 Preload
- 17.2.2 Afterload
- 17.2.3 Contractility
- 17.2.4 Other Aspects
- 17.3 Venous Return
- 17.4 Arterial Pressure
- 17.5 Venous Pressure
- Case Study 2
- 17.6 Oxygen Transport
- 17.7 Microcirculation
- 17.8 Specific Aspects of Young Children
- Summary
- 18. Hemodynamic Monitoring in the PICU
- 18.1 Introduction
- 18.2 Cardiovascular Instability Is Common in Critically Ill Children
- 18.3 Basic Bedside Assessment
- 18.4 Blood Pressure
- 18.4.1 Central Venous Pressure (CVP)
- 18.4.2 Central Venous Oxygen Saturation Measurement
- 18.4.3 Cardiac Output Monitoring and Transpulmonary Indicator Dilution
- 18.4.4 Pulmonary Artery Pressure
- 18.4.5 Serum Lactate Measurement
- 18.4.6 Near-Infrared Spectroscopy
- 18.4.7 Microcirculation
- 18.4.8 Echocardiography/Ultrasonography
- 18.4.9 Prediction of Volume Resuscitation and Fluid Responsiveness
- 19. Fluids on PICU (Paediatric Intensive Care Unit)
- 19.1 Introduction
- 19.2 History of Intravenous Fluids
- 19.3 The Body Fluid Compartments
- 19.3.1 What Is the Total Body Water Content of a Child?
- 19.3.2 Fluid Input and Output
- 19.3.2.1 Definitions
- 19.3.3 Isotonic, Hypotonic, and Hypertonic Fluids
- 19.4 Regulation of Extracellular Fluid Osmolarity and Sodium
- 19.5 Intravenous Fluids Commonly Used on PICU
- 19.5.1 Crystalloid
- 19.5.2 Colloid
- 19.5.2.1 5% Human Albumin Solution
- 19.5.2.2 Gelatin-Based Solutions
- 19.5.2.3 Starch-Based Solutions
- 19.5.3 What Happens During Rapid Infusion 10–20 mL/kg 0.9% Saline into a Patient?
- 19.5.3.1 Distribution
- 19.5.3.2 Changes to Plasma Oncotic Pressure
- 19.5.3.3 Excretion
- 19.5.3.4 Acid–Base Effects
- 19.5.3.5 Possible Deleterious Effects
- 19.5.3.6 Rationale for Intravenous Fluids
- 19.6 Fluid Resuscitation in Shock
- 19.6.1 What Is a Fluid Bolus? How Much to Give?
- 19.6.2 Haemodynamic Targets of Fluid Bolus Therapy
- 19.6.3 What Fluid to Use for Acute Resuscitation?
- 19.6.4 What Are the Potential Harms of Fluid Bolus Therapy?
- 19.7 Intravenous Fluid Maintenance in PICU
- 19.7.1 Paediatric Fluid Requirements
- 19.7.2 Neonatal Fluid Requirements
- 19.7.3 Dealing with Fluid Losses
- 19.7.4 What Maintenance Fluid to Use?
- 19.7.5 Glucose Requirements
- 19.7.6 What Maintenance Fluid to Use Postoperatively?
- 19.7.7 How Is Fluid Balance Assessed?
- 19.8 Phases of Fluid Therapy: The “ROSE” Concept
- 19.8.1 What Is Fluid Overload and Is It Important?
- 19.8.2 How Do I Deresuscitate My Patient?
- 20. Vasoactive Agents
- 20.1 Introduction
- 20.2 What Are Inotropes?
- 20.3 Some Terms
- 20.4 Cardiovascular System
- 20.4.1 Recognition and Assessment of Shock
- 20.4.2 Targets
- 20.4.3 How Do Inotropes Work
- 20.4.3.1 Polymorphisms
- 20.4.3.2 Receptor Downregulation
- 20.4.4 Physiologic Mechanisms of Vasoconstriction
- 20.5 Endogenous Inotropes and Vasoactive Agents: Sympathomimetic Amines
- 20.5.1 Adrenaline
- 20.5.2 Noradrenaline
- 20.5.3 Vasopressin
- 20.5.4 Dopamine
- 20.6 Exogenous Inotropes and Vasoactive Agents
- 20.6.1 Dobutamine
- 20.6.2 Phenylephrine
- 20.6.3 Phosphodiesterase Inhibitors
- 20.6.4 Levosimendan
- 20.7 Selection of Inotropic and Vasoactive Agents in Shock
- 20.7.1 Septic Shock
- 20.7.2 Cardiogenic Shock
- 20.7.3 Neurogenic Shock
- 20.8 Failure of Shock Reversal
- 20.9 Conclusion
- VII: Specific Organ System Failure
- 21. The Lung
- 21.1 Introduction
- 21.2 Basics of Respiratory Physiology and Mechanics in the Neonate and the Growing Child
- 21.3 Gas Exchange and Its Measures
- 21.4 Respiratory Physiology, Mechanics and Gas Exchange Disturbances in Disease
- 21.5 Cardiopulmonary Interactions
- 22. Acute Kidney Injury in the PICU
- 22.1 Introduction
- 22.2 pAKI Definition
- 22.3 Epidemiology
- Box 22.1: Most Common AKI-Inducing Nephrotoxins
- 22.4 Specific Aspects of pAKI Diagnosis
- 22.5 Prevention
- 22.6 Pharmacological Treatment
- Box 22.2: Fluid Overload
- 22.7 Follow-Up of Patients Surviving AKI
- 23. The Gut
- 23.1 Introduction
- 23.2 The Gut: A Key Organ of Nutrition Physiology
- 23.3 Gut Dysfunction in Critically Ill Children
- 23.4 Main Symptoms of GI Dysfunction in Critically Ill Children: Prevalence, Causes, Prevention and Treatments
- 23.5 Enteral Feeding Intolerance as a Result of GI Dysfunction
- 23.6 Gut Damages in Case of Critical Illness
- 23.7 Children with History of Intestinal Condition
- 23.8 The Gut Microbiota
- 23.8.1 The Role of Gut Microbiota
- 23.8.2 Impact of Critical Illness on Gut Microbiota
- 23.8.3 The Promising Effect of Nutrition and Probiotics in Critical Care
- 24. Acute Liver Failure in PICU
- 24.1 Introduction
- 24.2 Definition of Paediatric Acute Liver Failure
- 24.3 Aetiology
- 24.4 Clinical Manifestation
- 24.5 Hepatic Encephalopathy
- 24.6 Management
- 24.6.1 General Supportive Care
- 24.6.2 Ventilation Strategies
- 24.6.3 Neuroprotective Measures
- 24.6.4 Ammonia Scavenging Strategy
- 24.6.5 Hemodynamic Monitoring
- 24.6.6 Fluid Requirement and Nutritional Support
- 24.6.6.1 Role of N-Acetyl Cysteine in Management of Non-acetaminophen (Non-APAP) ALF
- 24.6.6.2 Antibiotics in PALF
- 24.6.7 Neuro-Critical Care Monitoring and Management of Intracranial Hypertension and Cerebral Oedema
- 24.6.8 Indications
- 24.7 Medical Management of ICP
- 24.7.1 Hypertonic Saline
- 24.7.2 Mannitol
- 24.7.3 Thiopentone Sodium
- 24.7.4 Therapeutic Hypothermia
- 24.7.5 Hyperventilation
- 24.7.6 Coagulation
- 24.7.7 Acute Kidney Injury
- 24.7.8 Indication for Starting CKRT in Patients with PALF
- 24.7.9 Liver Support Devices
- 24.7.10 Liver Transplant in ALF
- 24.7.10.1 Models to Predict LT
- 24.7.10.2 Post-Liver Transplant Management
- 24.7.10.3 Long-Term Outcome
- 25. Immunology in Paediatric Intensive Care
- 25.1 Introduction
- 25.2 Mucosal Immunity
- 25.3 Inflammation and Innate Immunity
- 25.3.1 Cell Autonomous Immunity
- 25.3.2 Circulating Mediators of Infection
- 25.4 Innate Immune Cells
- 25.5 Adaptive Immunity
- 25.5.1 T-Cell-Mediated Immunity
- 25.5.2 B Cell-Mediated Immunity
- 25.5.3 T Cell-Independent B Cell Immunity
- 25.5.4 T Cell-Dependent B Cell Immunity
- 25.6 Sepsis
- 25.6.1 Personalised Immunomodulation in Sepsis?
- 26. Metabolic Emergencies in the Paediatric Intensive Care Setting
- 26.1 Introduction
- 26.2 Clinical History and Examination
- 26.3 Biochemical Investigations
- 26.4 Management Principles
- 26.5 Specific Scenarios
- 26.5.1 Hyperammonaemia
- 26.5.2 Metabolic Acidosis
- 26.5.3 Glycaemic Control
- 26.6 Peri-Mortem Considerations
- Appendix: Other Key Drug Doses in the Intensive Care Setting
- VIII: Cardiac Critical Care
- 27. Basics in Cardiac Intensive Care
- 27.1 Introduction
- 27.2 Hemodynamic Monitoring
- 27.2.1 Basic Hemodynamic Monitoring
- 27.2.2 Assessment of Cardiac Output
- 27.3 Preoperative Care of Pediatric Cardiac Surgical Patients
- 27.3.1 Assessment of Patient Status and Predominant Physiology [1, 14]
- 27.3.1.1 Defects with Left-to-Right Shunts
- 27.3.1.2 Cyanotic Congenital Heart Defects
- 27.3.1.3 Obstructive Congenital Heart Defects
- 27.3.2 Other General Considerations
- 27.4 Post-operative Care of Pediatric Cardiac Patients
- 27.4.1 Preoperative and Intra-Operative Course Evaluation [6]
- 27.4.2 General Principles of Post-Operative Care [6, 7, 14]
- 27.4.3 Post-operative Complications
- 27.4.4 Discharge from CICU
- Case Study
- 27.4.4.1 Proposed Evaluation
- 28. Pre-operative Management of Neonates with Congenital Heart Disease
- 28.1 Lesion-Specific Management
- 28.2 Duct Dependent Systemic Lesions
- 28.2.1 Coarctation of Aorta
- 28.2.1.1 Pathophysiology
- 28.2.1.2 Clinical Signs
- 28.2.1.3 Pre-operative Management
- 28.2.2 Critical Aortic Stenosis
- 28.2.2.1 Pre-operative Management
- 28.2.3 Hypoplastic Left Heart Syndrome (HLHS)
- 28.2.3.1 Pathophysiology
- 28.2.3.2 Main risk Factors for Postnatal Survival in HLHS Include
- 28.2.3.3 Clinical Signs
- 28.2.3.4 Pre-operative Management
- 28.3 Duct Dependent Pulmonary Lesions
- 28.3.1 Critical Pulmonary Stenosis
- 28.3.1.1 Pathophysiology and Clinical Signs
- 28.3.1.2 Pre-operative Management
- 28.3.2 Pulmonary Atresia with Intact Ventricular Septum
- 28.3.2.1 Pathophysiology and Clinical Signs
- 28.3.2.2 Pre-operative Management
- 28.3.3 Tetralogy of Fallot
- 28.3.3.1 Pathophysiology and Clinical Signs
- 28.3.3.2 Pre-operative Management
- 28.4 Common Mixing Lesion
- 28.4.1 Transposition of Great Arteries
- 28.4.1.1 Pathophysiology
- 28.4.1.2 Pre-operative Management
- 28.4.2 Total Anomalous Pulmonary Venous Connection
- 28.4.2.1 Pathophysiology and Clinical Signs
- 29. Principles of Postoperative Management in the Paediatric Cardiac Intensive Care: Low Cardiac Output State (LCOS) and Lesion-Specific Management
- 29.1 Introduction
- 29.2 Low Cardiac Output State (LCOS)
- 29.2.1 Definition
- 29.2.2 Pathophysiology and Aetiology
- 29.2.3 Diagnosis
- 29.2.4 Prevention
- 29.2.5 Treatment
- 29.2.5.1 Optimising Preload
- 29.2.5.2 Improving Myocardial Function
- 29.2.5.3 Manipulating Afterload
- Vasodilators
- SVR Reduction
- PVR Reduction
- 29.2.6 Vasoconstrictors
- 29.2.6.1 The Role of Positive Pressure Ventilation (PPV)
- 29.2.6.2 The Role of Corticosteroids
- 29.2.6.3 Mechanical Circulatory Support (MCS)
- 29.3 Lesion-Specific Postoperative Management
- 30. ECMO in Children with Cardiac Failure
- 30.1 History of Cardiac ECMO
- 30.2 Cardiac ECMO: Description and Indications
- 30.3 Use and Strategy
- 30.4 Contraindications
- 30.5 Cannulation and ECMO Circuit
- 30.5.1 Cannulation Technique
- 30.5.2 Site of Cannulation
- 30.5.3 Additional Cannulas
- 30.5.4 Circuit
- 30.6 ECMO Run: Management, Monitoring and Complications
- 30.6.1 Goals and Principles of Cardiac ECMO
- 30.6.2 Myocardial Stun
- 30.6.3 Ventricular Decompression
- 30.6.4 Residual Lesions
- 30.6.5 Single Ventricle Physiology
- 30.7 Cardiovascular Management and Monitoring
- 30.7.1 Inotropes and Vasoactive Drugs
- 30.7.2 Respiratory Management and Monitoring
- 30.7.3 Anticoagulation
- 30.7.4 Bleeding Management
- 30.7.5 Blood Product Administration
- 30.7.6 Renal Function
- 30.7.7 Neurology and Sedation
- 30.7.8 Infection
- 30.8 Weaning and Decannulation
- 30.9 Outcomes
- 30.10 Future of Cardiac ECMO
- 31. Extracorporeal Cardiopulmonary Resuscitation in Pediatric Age
- 31.1 Introduction
- 31.2 Definition of ECPR, Objective, and Indications
- 31.3 Epidemiology of ECPR
- 31.4 Outcomes
- 31.4.1 Neurologic Outcomes
- 31.4.2 Medium and Long-Term Outcomes
- 31.5 ECPR Peculiarities in Specific Populations
- 31.5.1 ECPR in Children with Cardiac Disease
- 31.5.2 ECPR in Children with Noncardiac Disease
- 31.5.3 Out-of-Hospital ECPR and ECPR for Deep Hypothermia
- 31.6 Patient Selection and Factors Influencing EPCR Decision
- 31.7 Team and Algorithm
- 31.8 Cannulation Strategies and Equipment
- 31.9 Post-ECPR Care
- 32. Mechanical Circulatory Support in Paediatric Heart Failure
- 32.1 Introduction
- 32.2 Part 1: VAD Support
- 32.2.1 Choice of Support Strategy: ECMO versus VAD
- 32.2.2 Types of VAD
- 32.2.3 Selecting the Right Type of VAD
- 32.3 Part 2: Devices/Strategies LVAD, BiVAD and UVAD
- 32.3.1 Strategies and Applications
- 32.3.2 Right Ventricular Dysfunction
- 32.3.3 Single-Ventricle Anatomy
- 32.3.4 Recovery and Explant
- 32.3.5 Destination Therapy
- 32.4 Part 3: Anticoagulation
- 32.4.1 Detection of Thrombosis
- 32.5 Part 4: Patient Management and Outcomes
- 32.5.1 Thrombotic and Bleeding Complications
- 32.5.2 Optimising Haemodynamics
- 32.5.3 Nursing and Multi-professional Care
- 32.5.4 Outcomes
- Case Studies
- Case 1
- Case 2
- Case 3
- Case 4
- Summary
- 32.6 Part 5: Palliative and Holistic Care
- 32.6.1 Home Discharge
- 33. Cardiac Arrhythmias: Diagnosis and Management for the Paediatric Intensivist
- 33.1 Normal Cardiac Conduction
- 33.1.1 Electrical Anatomy of the Heart
- 33.1.2 ECG Recording in PICU
- 33.2 Mechanism of Cardiac Arrhythmias
- 33.3 Management
- 33.3.1 General Considerations
- 33.3.2 Antiarrhythmics
- 33.3.3 Cardioversion and Defibrillation
- 33.3.4 Temporary Cardiac Pacing
- 33.4 Individual Arrhythmias
- 33.4.1 Premature Atrial and Ventricular Complexes
- 33.4.2 Tachyarrhythmias
- 33.4.2.1 Junctional Ectopic Tachycardia (JET)
- 33.4.2.2 Atrial Ectopic Tachycardia (AET)
- 33.4.2.3 Supraventricular Tachycardia (SVT)
- 33.4.2.4 Atrial Flutter and Intra-atrial Re-entry Tachycardia (IART)
- 33.4.2.5 Ventricular Tachycardia (VT)
- 33.4.3 Bradyarrhythmias
- 33.4.3.1 Sinus Node Dysfunction
- 33.4.3.2 Atrioventricular (AV) Block
- 34. Outcomes of Paediatric Cardiac Intensive Care
- 34.1 Introduction
- 34.2 Outcome Measures
- 34.3 Outcome Evaluation
- 34.3.1 Registries and Multi-Institutional Collaborations
- 34.3.2 Relationship Between Case Mix Complexity and Outcomes
- 34.4 Solutions and Future Directions
- IX: Neurocritical Care
- 35. Paediatric Major Trauma in Context for the PICU Clinician
- 35.1 What Is Major Trauma?
- 35.1.1 Paediatric Major Trauma Networks
- 35.2 Paediatric ‘Trauma Call’
- 35.2.1 Pre-alerts
- 35.2.2 Role of the PICU Doctor in a Trauma Call
- 35.2.3 Team Preparation and ‘Crowd Control’
- 35.2.4 Parents
- 35.2.5 Handover
- 35.3 Assessing the Paediatric Trauma Patient aka ‘The Primary Survey’
- 35.3.1 Catastrophic Haemorrhage
- 35.3.2 Airway Issues
- 35.3.3 Breathing (Thoracic Injury)
- 35.3.3.1 Blunt Injuries
- 35.3.4 Penetrating Injuries
- 35.3.4.1 Thoracotomy
- 35.3.5 Circulation (Haemorrhage)
- 35.3.5.1 Challenge of the Bleeding Child
- 35.3.5.2 ‘One on the Floor and Four More’
- 35.3.5.3 Blood Products or Crystalloid
- 35.3.5.4 ‘Code Red’ Care in Children
- 35.3.6 Disability (Traumatic Brain Injury and Spinal Injury)
- 35.3.6.1 Potential Spinal Injury and Immobilisation
- 35.3.6.2 Confirmed Spinal Injury
- 35.3.7 Exposure
- 35.4 Decision-Making After the Primary Survey
- 35.5 Burns and Blasts
- 35.5.1 Electric Burns
- 35.5.2 Blast Injuries
- 35.6 Traumatic Cardiac Arrest
- 35.6.1 Which Children Survive TCA?
- 35.6.2 Logistics of Running the Arrest
- 35.6.3 H: Addressing Hypovolaemia
- 35.6.4 O: Addressing Hypoxia
- 35.6.5 T: Addressing Tension Pathology
- 35.6.6 Non Accidental Injury or Suspected Physical Abuse
- 35.6.7 Rational Prioritisation
- 35.6.8 Recognition of Futility
- 35.6.9 Debrief
- 35.7 Traumatic Asphyxia—Hanging and Drowning
- 35.7.1 Hanging and Near Hanging
- 35.7.2 Drowning
- 35.8 Deterioration in PICU
- 36. Traumatic Brain Injury
- 36.1 Introduction
- 36.2 Basic Concepts
- 36.2.1 Cerebral Blood Flow, Perfusion Pressure, Autoregulation
- 36.2.1.1 ICP Waveforms
- 36.2.1.2 The Pressure-Time Burden
- 36.2.2 Concepts Behind Brain Injury
- 36.2.2.1 Primary Brain Injury
- 36.2.2.2 Secondary Injury
- Ischaemia
- Excitotoxicity and Inflammation
- Oxidative Stress
- Cortical Spreading Depolarisation
- Impaired Glymphatic Drainage
- Energy Failure
- 36.2.2.3 Herniation Syndromes
- 36.3 Management
- 36.3.1 Pre-Hospital Management
- 36.3.2 Emergency Room
- 36.3.3 PICU Management
- 36.3.3.1 ICP Monitoring
- 36.3.4 Post-TBI Neuroprotection Bundle
- 36.3.4.1 Managing CPP
- 36.3.5 Multimodal Neuromonitoring
- 36.3.5.1 Quantitative EEG
- 36.3.5.2 Near-Infrared Spectroscopy (NIRS)
- 36.3.5.3 PbtO2 (Brain Tissue Oxygen Monitoring)
- 36.3.5.4 Transcranial Doppler (TCD)
- 36.3.5.5 Pressure Reactivity Index (PRx)
- 36.3.5.6 ICP Treatment Thresholds
- 36.3.6 ICP Reduction Strategies
- 36.3.6.1 Hyperosmolar Therapy
- 36.3.6.2 CSF Drainage
- 36.3.6.3 Tier 2 Therapies
- 36.3.6.4 Hyperventilation
- 36.3.6.5 Hypothermia
- 36.3.6.6 Barbiturate Infusion
- 36.3.6.7 Decompressive Craniectomy
- 36.3.7 The Lund Concept
- 36.4 Rehabilitation and Outcomes
- 36.4.1 Step-Down from PICU
- 36.4.2 Outcomes and Prognostication
- 36.4.3 Biomarkers
- 36.4.4 Late Effects of Paediatric TBI
- 36.5 Clinical Trials in Paediatric TBI
- 37. Monitoring the Brain
- 37.1 Introduction
- 37.2 Neuromonitoring Techniques
- 37.2.1 EEG
- 37.2.2 Imaging
- 37.2.3 Increased Intracranial Pressure (ICP) and Advanced Cerebral Monitoring
- 37.2.4 Brain Oxygenation and Metabolism
- 37.2.5 Transcranial Doppler (TCD)
- 37.2.6 Key Points
- 38. Management of Seizures and Refractory Status Epilepticus in Critically Ill Children
- 38.1 Introduction
- 38.1.1 Definitions
- 38.1.2 Epidemiology: Incidence of Each Including Morbidity and Mortality
- 38.1.3 Aetiology
- 38.1.4 Pathophysiology
- 38.2 Investigations and Diagnosis
- 38.3 Treatment
- 38.3.1 Stabilization
- 38.3.2 First-Line Therapy
- 38.3.3 Second-Line Therapy
- 38.3.4 Anaesthetic Drugs: Refractory and Super Refractory SE
- 38.3.4.1 Midazolam
- 38.3.4.2 Thiopental/Pentobarbital
- 38.3.4.3 Propofol
- 38.3.4.4 Ketamine
- 38.3.5 Special Considerations for Seizures in Critically Ill Children with Acute Neurological Conditions
- 38.3.5.1 Post-traumatic Seizures and Status Epilepticus
- 38.3.5.2 Post-anoxic Seizures
- 38.3.6 Other Agents to Consider
- 38.3.6.1 Anti-Seizure Medications
- 38.3.6.2 Pyridoxine, Pyridoxal-5-Phosphate, Folinic Acid, and Biotin
- 38.3.6.3 Steroids and Immunotherapy
- 38.3.6.4 Ketogenic Diet
- 38.3.6.5 Epilepsy Surgery
- X: Hematological Issues in PICU
- 39. Haemoglobinopathies and Haemostatic Disorders in the PICU
- 39.1 Introduction
- 39.2 Sickle Cell Disease
- 39.2.1 Multi-System Organ Failure
- 39.2.2 Acute Chest Syndrome
- 39.2.3 Stroke
- 39.2.4 Transfusions for Sickle Cell Disease
- 39.3 Haemophilia
- 39.3.1 Haemophilia A
- 39.3.2 Haemophilia B
- 39.4 Thalassaemia
- 39.5 Catastrophic Antiphospholipid Syndrome (CAPS)
- 39.6 Immune Thrombocytopenia
- 39.7 Thrombotic Thrombocytopenic Purpura
- 39.8 Disseminated Intravascular Coagulation
- 40. Transfusion Medicine in the Pediatric Intensive Care Unit
- 40.1 Introduction
- 40.2 Red Blood Cells
- 40.2.1 Anemia and O2 Delivery
- 40.2.2 When Should We Transfuse?
- 40.3 Plasma
- 40.3.1 When Should We Transfuse?
- 40.4 Platelets
- 40.4.1 When Should We Transfuse?
- 40.4.2 When Should We Not Transfuse?
- 40.5 Blood Product Modifications
- 40.5.1 Leukoreduction
- 40.5.2 Irradiated Blood Products
- 40.5.3 Pathogen Reduction
- 40.6 Transfusion Reactions and Complications
- 40.6.1 Early-Onset Reactions
- 40.6.2 Delayed Transfusion Reactions
- 40.6.3 Infectious Risks
- XI: Specific Situations
- 41. Sepsis and Septic Shock
- 41.1 Introduction
- 41.2 Evolving Definitions of Sepsis
- 41.3 Aetiology
- 41.4 Identifying the Child with Sepsis
- 41.5 Pathophysiology
- 41.6 Antimicrobial Therapy
- 41.7 Vascular Access and Fluid Therapy
- 41.8 Vasoactive Agents
- 41.9 Corticosteroids
- 41.10 Respiratory Support
- 41.11 Monitoring the Child with Septic Shock
- 41.12 Electrolytes and Metabolites
- 41.13 Blood and Blood Product Transfusion
- 41.14 Refractory Septic Shock
- 41.15 Renal Replacement Therapy
- 41.16 Therapeutic Plasma Exchange/Plasmapheresis
- 41.17 Immunoglobulin Therapy
- 41.18 Extracorporeal Membrane Oxygenation (ECMO)
- 41.19 Conclusion
- 42. Hemorrhagic Shock in Children
- 42.1 Introduction
- 42.2 Diagnosis of Hemorrhagic Shock
- 42.3 Management of Hemorrhagic Shock in Children
- 42.3.1 Context of Damage Control Resuscitation in Children
- 42.3.2 Stop the Bleed
- 42.3.3 Rapid Rewarming
- 42.3.4 Permissive Hypotension in Children
- 42.3.5 Fluids and Drugs Administration
- 42.4 Damage Control Hemostatic
- 42.5 Damage Control Surgery (DCS)
- 42.6 Assessment of the Effectiveness of Treatment
- 43. Abdominal Trauma
- 43.1 Introduction
- 43.2 Spleen
- 43.2.1 Frequency
- 43.2.2 Trauma Mechanism
- 43.2.3 Diagnosis
- 43.2.3.1 Clinical
- 43.2.3.2 Imaging and Biology
- 43.2.3.3 Grade Classification
- 43.2.4 Treatment
- 43.2.4.1 Non-operative Management
- 43.2.4.2 Arterial Embolization
- 43.2.4.3 Surgery
- 43.2.5 Monitoring
- 43.2.6 Follow-Up
- 43.2.6.1 Complications
- 43.2.6.2 Control Imaging
- 43.2.6.3 Vaccination
- 43.3 Liver
- 43.3.1 Frequency
- 43.3.2 Trauma Mechanism
- 43.3.3 Diagnosis
- 43.3.3.1 Clinical
- 43.3.3.2 Imaging and Biology
- 43.3.3.3 Grade Classification
- 43.3.4 Treatment
- 43.3.4.1 Non-operative Management
- 43.3.4.2 Arterial Embolization
- 43.3.4.3 Surgery
- 43.3.5 Monitoring
- 43.3.6 Complications
- 43.3.6.1 Vascular Complications
- 43.3.6.2 Biliary Peritonitis
- 43.3.6.3 Bilioma
- 43.3.7 Follow-Up
- 43.3.7.1 Control Imaging
- 43.4 Kidney
- 43.4.1 Frequency
- 43.4.2 Trauma Mechanism
- 43.4.3 Diagnosis
- 43.4.3.1 Clinical
- 43.4.3.2 Biology and Radiology
- 43.4.4 Treatment
- 43.4.4.1 Non-operative Management
- 43.4.4.2 Surgical Treatment
- 43.4.5 Complications
- 43.5 Pancreas
- 43.5.1 Frequency
- 43.5.2 Trauma Mechanism
- 43.5.3 Diagnosis
- 43.5.3.1 Clinical
- 43.5.3.2 Radiological and Biological
- 43.5.4 Treatment
- 43.5.4.1 Non-operative Management
- 43.5.4.2 Surgery
- 43.5.5 Follow-Up
- 44. Immunosuppressed Patients
- 44.1 Introduction
- 44.2 Primary Immunodeficiency (PID)
- 44.3 Hemophagocytic Lymphohistiocytosis (HLH)
- 44.3.1 Clinical Diagnosis
- 44.3.2 Treatment
- 44.4 Hematopoietic Stem Cell Transplantation (HSCT)
- 44.4.1 General Considerations
- Box 44.1: Key Information Upon Admission of a HSCT Patient on PICU
- 44.4.2 Approach to the HSCT Patient with Organ Failure
- 44.4.2.1 Respiratory Failure
- 44.4.2.2 Acute Kidney Injury (AKI)
- 44.4.2.3 Acute Encephalopathy
- Box 44.2: Immune Reconstitution and Infections
- Box 44.3: Early HSCT-Related Morbidity
- Acute Graft-Versus-Host Disease (aGVHD)
- Veno-Occlusive Disease (VOD)
- Transplant-Associated Thrombotic MicroAngiopathy (TA-TMA)
- 45. Paediatric Onco-Critical Care
- 45.1 Introduction
- 45.2 Tumour Lysis Syndrome
- 45.2.1 Pathophysiology
- 45.2.2 Diagnosis
- 45.2.3 Treatment
- 45.3 Hyperleukocytosis
- 45.3.1 Pathophysiology
- 45.3.2 Diagnosis
- 45.3.3 Treatment
- 45.4 Mediastinal Tumours
- 45.4.1 Symptoms
- 45.4.2 Treatment
- 45.5 Posterior Reversible Encephalopathy Syndrome (PRES)
- 45.5.1 Pathophysiology
- 45.5.2 Diagnosis
- 45.5.3 Treatment
- 45.6 Intracranial Hypertension
- 45.6.1 Pathophysiology
- 45.6.2 Symptoms and Clinical Signs of Intracranial Hypertension
- 45.6.3 Diagnostics
- 45.6.4 Therapy
- 45.6.4.1 Conservative Treatment Strategies
- 45.6.4.2 Surgical Treatment Strategies
- 45.7 Sepsis and Non-infectious Inflammatory Conditions
- 45.7.1 Sepsis Definition
- 45.7.2 Micro-organisms and Antibiotics
- 45.7.3 Septic Shock Management and Organ Support
- 45.7.4 Special Circumstances
- 46. End-of-Life Nursing for Children and Families in ICU
- 46.1 Introduction
- 46.2 Experiences and Care Needs of Families in the PICU
- 46.3 When a Child Dies in the PICU
- 46.3.1 Family Experiences of End-of-Life Care in the PICU
- 46.3.2 Supporting Families When Their Child Is Dying: Some Practical Suggestions
- 46.4 After a Child Has Died in the ICU
- 46.4.1 Family Experiences of Post-death and Bereavement Care in the ICU
- 46.4.2 Supporting Families After a Child’s Death: Some Practical Suggestions
- 47. Paediatric Organ Donation
- 47.1 Introduction
- 47.1.1 Importance of Deceased Organ Donation
- 47.2 Paediatric Perspective
- 47.3 Ethics of Deceased Donation
- 47.3.1 What Makes Deceased Donation Ethical
- 47.3.1.1 Implicit or Presumed Consent
- 47.3.1.2 Explicit Consent
- 47.3.2 Ethical Framework
- 47.4 Understanding the Diagnosis of Death Using Circulatory and Neurological Criteria
- 47.4.1 All Human Death Is Death of the Brain
- 47.4.1.1 Somatic Criteria
- 47.4.1.2 Circulatory Criteria
- 47.4.1.3 Neurological Criteria
- 47.5 How to Diagnose Death Using Circulatory Criteria
- 47.6 How to Diagnose Death Using Neurological Criteria [13]
- 47.7 UK Procedure for Neurological Determination of Death [13]
- 47.7.1 Neurological Determination of Death in the Neonate
- 47.8 Donation Processes
- 47.8.1 UK Example
- 47.8.2 Donation After Circulatory (Cardiac) Death DCD
- 47.8.2.1 Warm Ischaemic Injury in DCD
- 47.8.3 Donation After Neurological Determination of Death DBD
- 47.8.4 Donor Identification and Referral
- 47.8.5 Organ Retrieval
- 47.9 International Perspectives
- 48. Toxicology in Pediatric ICU
- 48.1 Introduction
- 48.2 Clinical Presentation
- 48.3 Initial Management
- 48.4 Investigations
- 48.5 Criteria for PICU Admission
- 48.6 Specific Management
- 48.6.1 Whole Bowel Irrigation
- 48.6.2 Multi-dose Activated Charcoal
- 48.6.3 Urine Alkalinization
- 48.6.4 Extracorporeal Removal
- 48.6.5 Antidote Therapy
- 48.6.6 Lipid Emulsion Therapy
- 48.7 Ancillary Support and Prevention
- Summary
- Case Study
- Presenting Complaints and History
- Physical Examination
- Initial Treatment
- Details of Substance Ingested and Past Medical History
- Diagnostic Testing
- Hospital Course
- Ancillary Tests
- 49. Burns in Children
- 49.1 Introduction
- 49.2 Resuscitation and Stabilization
- 49.2.1 Airway and Lower Respiratory Tract
- 49.2.2 Fluid Resuscitation After Thermal Injuries
- 49.2.3 Transport to a Burn Service
- 49.2.4 Ongoing Management: Surgical
- 49.2.5 Ongoing Management: Medical
- 49.2.5.1 Cardiovascular
- 49.2.5.2 Hypermetabolic Response
- 49.2.5.3 Nutritional Support and Gastro-Intestinal Support
- 49.2.5.4 Infection and Sepsis
- 49.2.5.5 Lines and Thromboprophylaxis
- 49.2.5.6 Sedation and Pain Management
- 49.3 Conclusion
- Appendix
- 50. Surgical Neonates in PICU
- 50.1 Introduction
- 50.2 Preoperative Care of Surgical Neonates
- 50.3 Common Surgical Conditions
- 50.3.1 Tracheo-Oesophageal Fistula and Oesophageal Atresia
- 50.3.2 Congenital Diaphragmatic Hernia
- 50.3.3 Abdominal Wall Defects
- 50.3.3.1 Exomphalos
- 50.3.3.2 Gastroschisis
- 50.3.4 Intestinal Obstruction
- 50.3.5 Necrotising Enterocolitis
- 50.4 Postoperative Care of Surgical Neonates
- 51. Transport of the Critically Ill Child
- 51.1 Introduction
- 51.2 Referral to a PCCT
- Box 51.1: Suggested Structure for the Initial Referral Call
- 51.3 The Transport Process
- 51.3.1 Staffing and Equipment
- 51.3.2 Handover at Referring Centre
- 51.3.3 Patient Stabilisation
- Box 51.2: Suggested Emergency Equipment and Drugs for Transport
- 51.3.3.1 Airway
- 51.3.3.2 Breathing
- 51.3.3.3 Circulation
- 51.3.3.4 Disability
- 51.3.3.5 Exposure
- 51.3.4 Packaging for Transport
- Box 51.3: Oxygen Cylinder Capacities for Commonly Used Cylinder Types [14]
- 51.3.5 The Transport Phase
- 51.3.6 Handover at Receiving Centre
- 51.4 Time-Critical Transfers
- 51.5 Air Transport
- 51.6 Safety and Clinical Governance
- 52. Analgosedation in the Pediatric Intensive Care Unit
- 52.1 Introduction
- 52.2 Two Basic Concepts: Pain and Distress
- 52.2.1 Definition of Pain
- 52.2.2 Developmental Aspects of Pain
- 52.2.3 The Conceptual Model of Pain
- 52.2.4 Incidence of Pain
- 52.3 Pain Assessment
- 52.4 Treatment Interventions
- 52.4.1 Non-pharmacological Interventions
- 52.4.2 Pharmacological Interventions
- 52.5 Conclusion
- Supplementary Data
- Specific Pharmacology Data
- Analgesic Drugs
- Opioids
- Non-opioids
- Sedative Drugs
- Benzodiazepines
- Alfa (α-2)-Adrenergic Agonists
- Barbiturates
- Volatile Anesthetics
- Local Anesthetics
- XII: Vital Support
- 53. Clinical Pharmacology in the Paediatric Intensive Care Unit
- 53.1 Introduction
- 53.2 General Aspects of Clinical Pharmacology
- 53.2.1 PK Processes: Its Language and Parameters
- 53.2.2 Dose and Dosing Interval
- 53.2.3 Targeted Pharmacotherapy
- 53.2.4 Pharmacokinetic Models
- 53.2.5 General Factors
- 53.3 Specific Aspects of Clinical Pharmacology
- 53.3.1 Maturational Factors
- 53.3.2 Non-maturational Factors
- 53.4 Evidence-based Pharmacotherapy
- 53.4.1 Rational Use of Drugs
- 53.4.2 Therapeutic Drug Monitoring
- 53.4.3 Specific Drugs
- 53.5 Conclusion
- Appendix
- 54. Continuous Kidney Replacement Therapy in Children
- 54.1 Introduction
- 54.2 Early Development
- 54.3 Mechanisms of Solute Removal in KRT
- 54.4 Modalities of KRT
- 54.5 Indications of KRT
- 54.6 Timing of Initiation of KRT
- 54.7 CKRT Devices–CKRT Devices
- 54.8 CKRT Prescription (◘ Table 54.3)
- 54.9 Future Directions
- 54.10 Conclusions
- 55. Role of Dietitian and Nutrition in Paediatric Critical Care
- 55.1 Introduction
- 55.2 Organising Nutrition Care
- 55.3 Anthropometry (A)
- 55.3.1 Quality Assurance Framework for the Measurement of Anthropometry
- 55.4 Biochemistry (B)
- 55.4.1 Refeeding Syndrome
- 55.5 Clinical (C)
- 55.6 Dietary (D)
- 55.7 Evaluation (E)
- 56. Psychology
- 56.1 Introduction
- 56.2 Psychological Care of the Child
- Box 56.1. Post-traumatic Stress Disorder (ICD-11 Code 6B40)
- 56.3 Supporting Parents
- Box 56.2. Psychological First Aid [18]
- Box 56.3. Useful Online Resources
- 57. Ethics in Paediatric and Neonatal ICU
- 57.1 Introduction
- 57.2 Traditional Moral Theories
- 57.3 Ethics in Modern PICU
- 57.4 Death
- 57.5 Moral Injury
- 57.6 Pandemics
- 57.7 Consent
- 57.8 Research
- 57.9 Second Opinions
- 57.10 Ethics Support
- 58. Chaplains and Faith Support
- 58.1 Introduction
- 58.2 The Taxonomy
- 58.3 Setting
- 58.3.1 Intended Effect
- 58.3.2 Method
- 58.3.3 Intervention
- 58.4 Who Carries Out This Work?
- 58.5 How Does the Work Happen?
- 58.6 What Are the Processes?
- 58.7 Distinctions
- 58.8 Themes
- 58.9 Outcomes
- 58.10 Resourcing and Training
- 58.11 Conclusion
- XIII: Looking After People
- 59. Caring and Listening to Families in the ICU
- 59.1 Introduction
- 59.2 Family-Centred Care
- 59.2.1 The Parental Impact of Paediatric Intensive Care
- 59.2.2 Paediatric Intensive Care and Its Effect on Siblings
- 59.3 PIC Survivorship: Morbidity
- 59.4 Supporting the Parental Role
- 59.4.1 Visiting
- 59.4.2 Delivering Care
- 59.4.3 Ward Rounds, Decision-Making and Communication
- 59.4.4 Transitions
- 59.5 The Multidisciplinary Team
- 59.5.1 Family Liaison Service
- 59.5.2 Psychology
- 59.5.3 Religious and Spiritual Support
- 59.5.4 Play Specialists
- 59.6 Care of the Family at the End of Life
- 59.7 When Death is Expected or Imminent
- 59.8 Resuscitation
- 59.9 After Death
- 59.10 Bereavement Services
- 59.11 Mediation, Feedback and Liaison
- 59.12 Peer Support Services
- 59.13 Practical Matters
- Summary
- 60. Care of the Critical Care Team
- 60.1 Introduction
- 60.2 Burnout
- 60.3 Post-Traumatic Stress
- 60.4 Moral Distress
- 60.5 Special Situations
- 60.6 Self-Care and Organisational Level Interventions
- Box 60.1. Burnout
- Box 60.2. Post-traumatic Stress Disorder (ICD-11 code 6B40)
- Box 60.3. Moral Distress
- Box 60.4. Useful Online Resources
- 61. Management of Older Children in the ICU
- 61.1 Introduction
- 61.2 Definitions
- Box 61.1 Definitions Pertinent to Adolescent Medicine
- 61.3 Diagnostic Spectrum
- Box 61.2 The 6 Ps
- 61.4 Practical Issues
- 61.4.1 Physical Differences
- 61.4.2 Experiences on ICU
- 61.5 Privacy
- 61.6 Personal Life
- Box 61.3 HEADSSS Risk Assessment
- 61.7 Puberty
- 61.8 Prophylaxis
- Box 61.4 Risk Factors for VTE
- 61.9 Permission
- 61.9.1 Communication
- 61.9.2 Consent
- 61.9.3 Confidentiality
- XIV: Where Do Critically Ill Children Go?
- 62. Outcomes in PICU
- 62.1 Introduction
- 62.2 Case Reports
- 62.3 Physical Outcomes After Pediatric Critical Illness
- 62.4 Psychological Outcomes After Pediatric Critical Illness
- 62.4.1 The “New Normal”
- 62.4.2 Quality of Life
- 62.5 Post-traumatic Stress
- 62.6 Neurocognitive Outcome
- 62.7 Predictors: What Affects Outcome After a PICU Admission?
- 62.8 Challenges and Future Directions for Follow-Up
- XV: Research Needed in the ICU
- 63. What Do We Need to Find Out?
- 63.1 Introduction
- 63.2 So, What Do We Need to Find Out?
- Case Study
- 63.2.1 Consider Now: How Much of the Therapies, Practices, and Policies Above Do We Have Clear Evidence For?
- 63.2.1.1 Why We Need to Question the Evidence for Our Routine and Historical Practices
- XVI: Education
- 64. Online Education
- 64.1 Introduction
- 64.2 What Qualifies as “Online Education”?
- 64.3 Implementing Online Education: A Pragmatic Approach
- 64.3.1 Problem Identification
- 64.3.2 Needs Assessment
- 64.3.3 Describing Goals and Objectives
- 64.3.4 Selecting Educational Strategies
- 64.3.5 Implementation of the Intervention
- 64.3.6 Evaluation and Feedback
- 64.4 Evidence for Online Medical Education
- 64.5 Educational Features (◘ Table 64.2)
- 65. Simulation in Pediatric Critical Care
- 65.1 Introduction
- 65.1.1 Challenges in Pediatric Critical Care Education
- 65.2 Evolution of Paediatric Resuscitation Training
- 65.2.1 History of CPR Training
- 65.2.2 Quality CPR Training in Pediatrics
- 65.2.3 Basic Concept of Role-Play Simulated Scenarios
- 65.2.4 Importance of Simulation and Debriefing in CPR Training
- 65.3 Crisis Resource Management in Pediatric Resuscitation Teams
- 65.3.1 Leadership and Followership
- 65.3.2 Communication
- 65.3.3 Use of Resources
- 65.3.4 Situational Awareness
- 65.4 Future Perspectives
- 65.4.1 Rapid Cycle Deliberate Practice and Repeated Encounters
- 65.4.2 Gaming
- 65.4.3 Boot Camp
- 65.4.4 Coaching, Codes and Mock Codes
- 65.4.5 Telesimulation