BOOK
Fracture Management for Primary Care and Emergency Medicine E-Book
M. Patrice Eiff | Robert L. Hatch
(2018)
Additional Information
Book Details
Abstract
Fracture Management for Primary Care and Emergency Medicine E-Book
Table of Contents
Section Title | Page | Action | Price |
---|---|---|---|
Front Cover | Cover | ||
IBC | ES1 | ||
Neonatology Questions and Controversies | i | ||
Series Page | ii | ||
Neonatology Questions and Controversies | iii | ||
Copyright | iv | ||
Contributors | v | ||
Preface | ix | ||
Series Foreword | xi | ||
Contents | xiii | ||
1 - Cerebral Circulation and Hypotension in the Premature Infant: Diagnosis and Treatment | 1 | ||
Definition of Hypotension | 2 | ||
Pathogenesis and Diagnosis of Pathologic Cerebral Blood Flow | 7 | ||
Monitoring of Blood Pressure, Systemic and Organ Blood Flow, and Cerebral Function | 11 | ||
Doppler Ultrasound | 11 | ||
Impedance Electrical Cardiometry | 12 | ||
Near-Infrared Spectroscopy | 12 | ||
Amplitude-Integrated EEG (Cerebral Function Monitoring) | 13 | ||
Summary of the Monitoring Methods Discussed | 14 | ||
Treatment Strategies | 14 | ||
Systemic Hypotension | 15 | ||
Treatment of Hypotension Associated With PDA | 16 | ||
Treatment of Hypotension Associated With Other Causes Such as Sepsis, Adrenal Insufficiency, and Hypovolemia | 17 | ||
The Impact of Provision of Intensive Care on Systemic and Cerebral Hemodynamics | 18 | ||
Summary and Recommendations | 19 | ||
Diagnosis of Hypotension | 19 | ||
Treatment of Hypotension | 20 | ||
REFERENCES | 22 | ||
2 - Intraventricular Hemorrhage and White Matter Injury in the Preterm Infant | 27 | ||
Background | 28 | ||
Neuropathology: Relevance to Clinical Findings | 28 | ||
Pathogenesis | 28 | ||
Periventricular White Matter Injury Associated With IVH | 29 | ||
Clinical Features | 30 | ||
Complications | 30 | ||
Prevention | 30 | ||
Perinatal Strategies | 30 | ||
Antenatal Steroids | 30 | ||
Pregnancy-Induced Hypertension | 31 | ||
Magnesium Sulfate | 31 | ||
Route of Delivery | 31 | ||
Delayed Cord Clamping | 32 | ||
Postnatal Strategies | 32 | ||
Postnatal Factors Associated With an Increased Risk | 32 | ||
Postnatal Administration of Medications to Reduce Severe IVH | 33 | ||
White Matter Injury in the Absence of Hemorrhage | 33 | ||
Periventricular Leukomalacia | 35 | ||
Pathogenesis | 35 | ||
Vascular Factors | 35 | ||
Intrinsic Vulnerability of the Differentiating Oligodendrocyte | 36 | ||
Free Radical Injury | 36 | ||
Excitotoxic Injury (Glutamate) | 36 | ||
Cytokines | 37 | ||
Maternal Fetal Infection and/or Inflammation and White Matter Injury | 37 | ||
Clinical Factors Associated With PVL | 38 | ||
Prevention | 38 | ||
Outcome | 39 | ||
Intraventricular Hemorrhage | 39 | ||
White Matter Injury | 39 | ||
Gaps in Knowledge | 40 | ||
Conclusions | 40 | ||
REFERENCES | 40 | ||
3 - Posthemorrhagic Hydrocephalus Management Strategies | 47 | ||
Question 1: What Measurements of Ventricular Size Are Used in Diagnosis of PHVD? | 49 | ||
Question 2: How Can Ventricular Dilation Driven By Cerebrospinal Fluid Under Pressure Be Distinguished From Ventricular Dilation Caused By Loss of Periventricular White Matter? | 51 | ||
Question 3: How Is Excessive Head Enlargement Defined? | 51 | ||
Question 4: How Is Raised Intracranial Pressure Recognized? | 51 | ||
Question 5: What Is Infant A’s Prognosis? | 52 | ||
Question 6: What Is the Mechanism of PHVD? | 53 | ||
Question 7: How Can PHVD Injure White Matter? | 53 | ||
Raised Intracranial Pressure, Parenchymal Compression, and Ischemia | 53 | ||
Free Radical‒Mediated Injury | 54 | ||
Proinflammatory Cytokines | 55 | ||
Loss of White Matter and Gray Matter | 55 | ||
Question 8: What Interventions Have Been Used in PHVD, and Is There Any Evidence That They Improve Outcome? | 55 | ||
Ventriculoperitoneal Shunt Surgery | 55 | ||
Objectives in Treating PHVD | 55 | ||
Repeated Lumbar Punctures or Ventricular Taps | 56 | ||
Drug Treatment to Reduce CSF Production | 56 | ||
Intraventricular Fibrinolytic Therapy | 56 | ||
External Ventricular Drain | 56 | ||
Tapping Via an Ommaya Reservoir | 57 | ||
Ventriculosubgaleal Shunt | 57 | ||
Third Ventriculostomy | 58 | ||
Choroid Plexus Coagulation | 58 | ||
Drainage, Irrigation, and Fibrinolytic Therapy | 58 | ||
Stem Cell Therapy | 60 | ||
Conclusions | 60 | ||
Gaps in Knowledge | 60 | ||
REFERENCES | 60 | ||
4 - Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy: Different Cooling Regimens and Infants Not Included in Prior Trials | 63 | ||
Rationale for Further Investigations of Therapeutic Hypothermia | 64 | ||
What Is the Optimal Temperature and Duration for Therapeutic Hypothermia? | 64 | ||
How Late Can Hypothermia be Initiated? | 66 | ||
Should Infants With Mild HIE Receive Hypothermia Therapy? | 68 | ||
Should Hypothermia Be Used in Preterm Infants With HIE? | 70 | ||
How Should Cooling on Transport Be Conducted? | 71 | ||
Is Therapeutic Hypothermia Neuroprotective When Used in Low- and Middle-Income Countries? | 72 | ||
Conclusions | 73 | ||
REFERENCES | 74 | ||
5 - General Supportive Management of the Term Infant With Neonatal Encephalopathy Following Intrapartum Hypoxia-Ischemia | 77 | ||
Introduction | 79 | ||
Delivery Room Management | 79 | ||
Early Identification of Infants at Highest Risk for Development of Hypoxic-Ischemic Brain Injury | 80 | ||
Supportive Care | 81 | ||
Ventilation | 81 | ||
Maintenance of Adequate Perfusion | 82 | ||
Fluid Status | 82 | ||
Control of Blood Glucose Concentration | 82 | ||
Temperature | 83 | ||
Seizures | 84 | ||
Prophylactic Barbiturates | 84 | ||
Potential Neuroprotective Strategies Aimed at Ameliorating Secondary Brain Injury | 85 | ||
Oxygen Free Radical Inhibitors and Scavengers | 85 | ||
Excitatory Amino Acid Antagonists | 86 | ||
Magnesium | 86 | ||
Xenon | 87 | ||
Erythropoietin | 87 | ||
Gaps in Knowledge | 88 | ||
REFERENCES | 88 | ||
6 - Focal Cerebral Infarction | 93 | ||
Perinatal Arterial Ischemic Stroke | 94 | ||
Epidemiology | 94 | ||
Risk Factors | 94 | ||
Maternal Risk Factors | 94 | ||
Antepartum and Intrapartum Risk Factors | 95 | ||
Placental Risk Factors | 95 | ||
Infant Factors | 95 | ||
Clinical Manifestations | 96 | ||
Fetal Ischemic Stroke | 96 | ||
Neonatal Arterial Stroke | 96 | ||
Ischemic Stroke in the Preterm Infant | 96 | ||
Presumed Perinatal Ischemic Stroke | 97 | ||
Imaging Arterial Ischemic Stroke | 97 | ||
Management of Perinatal Arterial Ischemic Stroke | 98 | ||
Cerebral Sinovenous Thrombosis | 99 | ||
Epidemiology | 99 | ||
Risk Factors for CSVT | 99 | ||
Clinical Manifestations | 100 | ||
Imaging CSVT | 100 | ||
Management of CSVT | 100 | ||
Hemorrhagic Stroke | 101 | ||
Clinical Features | 101 | ||
Hemorrhagic Stroke in Preterm Infants | 102 | ||
Imaging Hemorrhagic Stroke | 102 | ||
Management of Perinatal Hemorrhagic Stroke | 102 | ||
Evaluation of Newborns With Suspected Stroke | 102 | ||
History and Physical Examination | 102 | ||
Differential Diagnosis | 103 | ||
Approach to Investigations (Table 6.2) | 103 | ||
Neuroimaging | 103 | ||
Laboratory Investigations | 103 | ||
Electroencephalography | 104 | ||
Placental Pathology | 105 | ||
Neurologic Outcome | 105 | ||
Neuromotor Outcome | 105 | ||
Neonatal Seizures and Epilepsy | 105 | ||
Neurobehavioral Outcome | 105 | ||
Visual Function | 106 | ||
Stroke Recurrence | 106 | ||
Controversies in Neonatal Stroke | 106 | ||
Hematologic Investigations | 106 | ||
Therapeutic Hypothermia for Neonatal Stroke | 106 | ||
Anticoagulation for CSVT | 107 | ||
REFERENCES | 107 | ||
7 - Diagnosis and Management of Acute Seizures in Neonates | 111 | ||
Diagnosis | 111 | ||
Classifications | 111 | ||
Focal Clonic Seizures | 111 | ||
Focal Tonic Seizures | 114 | ||
Myoclonic Jerks | 114 | ||
Autonomic Signs | 114 | ||
Spasms | 114 | ||
Subclinical Seizures | 114 | ||
Definition of Seizures | 114 | ||
Definition of Neonatal Status Epilepticus | 115 | ||
Controversies in Definition and Classification of Seizures | 115 | ||
Differential Diagnosis | 115 | ||
Diagnostic Tools and Monitoring | 116 | ||
EEG Characteristics of Neonatal Seizures | 117 | ||
Standard EEG Versus Long-Term or Continuous Monitoring | 117 | ||
Controversies in Monitoring | 117 | ||
Management | 118 | ||
Therapy | 120 | ||
Efficacy and Safety of Antiseizure Medications for Seizures | 121 | ||
Phenobarbital and Phenytoin | 121 | ||
Midazolam | 122 | ||
Lidocaine | 122 | ||
Levetiracetam | 122 | ||
Topiramate | 122 | ||
Antiepileptic Drug Treatment Duration and Discontinuation | 122 | ||
Hypothermia | 123 | ||
Controversies in Therapy | 123 | ||
“Newborn-Tailored” Pharmacotherapy | 123 | ||
Age-Appropriate Antiseizure Therapies | 124 | ||
Timing of Therapy Administration | 124 | ||
Predictors of Response to Antiseizure Medications | 124 | ||
Electrographic-Only Seizures | 124 | ||
Synergistic Effects of Hypothermia and Anticonvulsant Medications | 124 | ||
Conclusions | 124 | ||
REFERENCES | 125 | ||
8 - Neonatal-Onset Epilepsies: Early Diagnosis and Targeted Treatment | 131 | ||
The New Chapter of Neonatal Epilepsies | 132 | ||
Landscape of the Neonatal Epilepsies | 132 | ||
KCNQ2/3-Associated Neonatal Epilepsies | 133 | ||
Epilepsy of Infancy With Migrating Focal Seizures Associated With KCNT1 | 137 | ||
SCN2A-Associated Neonatal Epilepsies | 138 | ||
The Promise and the Challenge of Precision Medicine in the Nursery | 138 | ||
REFERENCES | 139 | ||
9 - Glucose and Perinatal Brain Injury—Questions and Controversies | 141 | ||
Glucose Metabolism in the Fetus and Newborn | 142 | ||
Preterm Infants | 142 | ||
Intrauterine Growth Restriction | 142 | ||
Cerebral Metabolism of Glucose | 143 | ||
Alternate Substrates to Glucose | 143 | ||
Glucose Transporters | 144 | ||
Definitions | 144 | ||
Controversy and Question | 145 | ||
Symptomatic Versus Asymptomatic Hypoglycemia | 145 | ||
Duration of Hypoglycemia | 146 | ||
Causes of Hypoglycemia | 148 | ||
Incidence | 148 | ||
Pathophysiology of Hypoglycemia | 149 | ||
Cerebral Blood Flow, Glucose Utilization, and Cerebral Energy Metabolism | 149 | ||
Cerebral Biochemical Alterations During Hypoglycemia | 149 | ||
Hypoglycemia and Brain Damage | 150 | ||
Neuroimaging Abnormalities | 151 | ||
Controversy and Question | 153 | ||
Hypoglycemia and Hypoxia-Ischemia, Seizures | 153 | ||
Case History | 154 | ||
Outcome | 155 | ||
Treatment | 156 | ||
Conclusions | 157 | ||
REFERENCES | 157 | ||
10 - Hyperbilirubinemia and the Risk for Brain Injury | 163 | ||
Definition and Epidemiology | 164 | ||
History of KSD Prevalence | 165 | ||
Pathogenesis of Bilirubin Neurotoxicity | 165 | ||
Active Transport of Bilirubin | 166 | ||
Mechanisms of Bilirubin Damage | 166 | ||
Bilirubin and Calcium Homeostasis | 166 | ||
Mechanisms of Auditory Dysfunction | 167 | ||
Neuroprotective Action of Bilirubin | 167 | ||
Molecular Response to Hyperbilirubinemia | 167 | ||
Developmental Susceptibility | 168 | ||
Diagnosis: Acute Bilirubin Encephalopathy and Kernicterus Spectrum Disorders | 168 | ||
Suggested Improvements to the AAP Guidelines for the Treatment of Hyperbilirubinemia | 168 | ||
Acute Bilirubin Encephalopathy | 169 | ||
ABE and Auditory Nervous System | 169 | ||
ABE and Neuroimaging | 171 | ||
New Strategies in the Diagnosis of ABE | 172 | ||
Kernicterus Spectrum Disorders | 172 | ||
Diagnosis of Kernicterus Spectrum Disorders | 172 | ||
Recommendations for Prevention and Treatment | 174 | ||
Recommendation for the Prevention and Treatment of ABE | 174 | ||
Recommendation for the Diagnosis of KSD and Treatment of Its Clinical Manifestations | 178 | ||
Expanding the Idea of Kernicterus as a Spectrum of Disorders | 179 | ||
Bilirubin Neurotoxicity in the Very Premature Infant | 179 | ||
Difficulties in Assessing Kernicterus in Preterm Infants | 180 | ||
Genetics of KSDs and Susceptibility to Bilirubin Neurotoxicity | 181 | ||
Gaps in Knowledge | 182 | ||
Conclusion | 182 | ||
REFERENCES | 183 | ||
11 - Neonatal Meningitis: Current Treatment Options | 187 | ||
Question 1: What Risk Factors Predispose This Infant to Have Early-Onset Bacterial Meningitis? | 188 | ||
Question 2: Do Infants With Meningitis Have Positive Blood Cultures? | 189 | ||
Question 3: What Is the Optimal Evaluation for Possible Late-Onset Sepsis in Preterm Infants in the NICU? | 191 | ||
Question 4: What Is the Empirical Antimicrobial Choice for Possible Late-Onset Sepsis in the NICU? | 192 | ||
Question 5: What Is the Treatment of Meningitis in Neonates, Particularly That Caused by Gram-Negative Bacilli? | 193 | ||
Question 6: Should Other Therapies Be Considered? | 195 | ||
Question 7: What Is the Duration of Treatment for Meningitis in Neonates? | 197 | ||
Question 8: When Should Neuroimaging Be Considered, and What Type of Examination Is Recommended? | 197 | ||
Question 9: Should Other Adjunctive Therapies Be Provided to an Infant With Meningitis? | 199 | ||
Question 10: What If the Infant’s CSF Is Abnormal but Routine Bacterial Cultures of CSF and Blood Are Sterile? | 199 | ||
Question 11: What Is the Outcome of Meningitis in Neonates? | 200 | ||
Conclusion | 200 | ||
REFERENCES | 200 | ||
12 - Neonatal Herpes Simplex Virus, Congenital Cytomegalovirus, and Congenital Zika Virus Infections | 207 | ||
Question 1: When Does Infection Occur? | 207 | ||
Neonatal HSV Disease | 207 | ||
Congenital CMV Infection | 208 | ||
Congenital Zika Infection | 208 | ||
Question 2: What Are the Risk Factors for Neonatal Infection? | 208 | ||
Neonatal HSV Disease | 208 | ||
Congenital CMV Infection | 209 | ||
Congenital Zika Infection | 209 | ||
Question 3: What Are the Clinical Manifestations of Neonatal Infection and Disease? | 210 | ||
Neonatal HSV Disease | 210 | ||
Congenital CMV Infection | 210 | ||
Congenital Zika Infection | 211 | ||
Question 4: What Are the Treatments and Outcomes for HSV, CMV, and Zika Virus Infections in Neonates? | 212 | ||
Neonatal HSV Disease | 212 | ||
13 - Neonatal Hypotonia | 223 | ||
Clinical History Collection | 223 | ||
Clinical Evaluation | 224 | ||
Neurologic Examination of the Hypotonic Infant | 225 | ||
Diagnostic Investigation | 225 | ||
Most Common Neuromuscular Disorders Presenting With Congenital Hypotonia | 227 | ||
Spinal Muscular Atrophies | 227 | ||
Myopathies | 228 | ||
Congenital Muscular Dystrophies | 228 | ||
Congenital Myopathies | 230 | ||
Pompe Disease | 230 | ||
Congenital Myotonic Dystrophy | 231 | ||
Neuromuscular Junction Defects | 231 | ||
REFERENCES | 232 | ||
14 - Amplitude-Integrated EEG and Its Potential Role in Augmenting Management Within the NICU | 235 | ||
Amplitude-Integrated EEG | 235 | ||
Assessment of aEEG Background Pattern | 236 | ||
Comparison With Standard EEG | 237 | ||
Background Pattern | 237 | ||
Prognostic Value of aEEG in HIE: Noncooled Situation | 237 | ||
Prognostic Value of aEEG in HIE: Cooled Situation | 238 | ||
aEEG and Seizures | 240 | ||
Seizure Detection | 240 | ||
Should We Treat Subclinical Seizures? | 242 | ||
aEEG in Preterm Infants | 243 | ||
Pitfalls and Artifacts | 246 | ||
Seizure-Like Artifacts | 247 | ||
aEEG in Other Clinical Conditions | 247 | ||
Gaps in Knowledge | 248 | ||
Conclusion | 252 | ||
REFERENCES | 252 | ||
15 - Congenital Heart Disease: An Important Cause of Brain Injury and Dysmaturation | 257 | ||
Fetal Brain Injury and Maturation | 258 | ||
Prenatal Diagnosis | 258 | ||
Postnatal Diagnosis | 258 | ||
Malformation Grouping | 260 | ||
Transposition of Great Vessels | 260 | ||
Hypoplastic Left Heart Syndrome | 262 | ||
Brain Injury and Brain Maturation | 262 | ||
Cranial Ultrasound Versus MRI | 262 | ||
Cerebral Ischemia and Stroke | 264 | ||
White Matter Injury | 265 | ||
Cerebral Sinovenous Thrombosis | 266 | ||
Subdural Hemorrhage | 266 | ||
Brain Dysmaturation | 266 | ||
Neuromonitoring | 267 | ||
Intraoperative Monitoring | 267 | ||
Near-Infrared Spectroscopy | 267 | ||
Amplitude-Integrated Electroencephalography | 268 | ||
Continuous Electroencephalography | 268 | ||
Advanced Magnetic Resonance Imaging Techniques in Congenital Heart Disease | 269 | ||
MR Diffusion Tensor Imaging | 269 | ||
Magnetic Resonance Spectroscopy | 269 | ||
Functional MRI | 269 | ||
Other Techniques | 270 | ||
Neurodevelopment of the Infant With CHD | 270 | ||
Predictors of Outcomes | 270 | ||
Preoperative Factors | 272 | ||
Intraoperative Factors | 272 | ||
Postoperative Factors | 272 | ||
New Interventions and Neuroprotection | 273 | ||
Gaps in Knowledge | 273 | ||
REFERENCES | 273 | ||
16 - Long-Term Follow-Up of the Very Preterm Graduate | 281 | ||
The Major Sequelae of Very Preterm Birth | 282 | ||
Cerebral Palsy | 282 | ||
Cognitive Impairment in Infancy | 283 | ||
Sensory Outcomes | 283 | ||
Behavior | 283 | ||
Classification of Impairment | 284 | ||
Learning Points | 284 | ||
Transition to School | 285 | ||
Starting School | 285 | ||
Emerging Impairments at Early School Age | 285 | ||
Cognitive Function | 285 | ||
School Attainment | 286 | ||
Behavior | 286 | ||
Motor Problems | 286 | ||
Changes Over Time for Individual Children | 287 | ||
Learning Points | 287 | ||
Transition to Young Adult Life | 288 | ||
Learning Points | 289 | ||
Components of a Follow-Up Program | 289 | ||
Gaps in Knowledge | 290 | ||
Conclusions | 290 | ||
REFERENCES | 290 | ||
Index | 293 | ||
A | 293 | ||
B | 294 | ||
C | 294 | ||
D | 295 | ||
E | 296 | ||
F | 296 | ||
G | 296 | ||
H | 297 | ||
I | 298 | ||
K | 299 | ||
L | 299 | ||
M | 299 | ||
N | 300 | ||
O | 301 | ||
P | 301 | ||
Q | 302 | ||
R | 302 | ||
S | 302 | ||
T | 303 | ||
U | 304 | ||
V | 304 | ||
W | 304 | ||
X | 304 | ||
Y | 304 | ||
Z | 304 | ||
IFC | ES2 |