Jaypee Brothers
In Current Chapter
In All Chapters
X
Clear
X
GO
Normal
Sepia
Dark
Default Style
Font Style 1
Font Style 2
Font Style 3
Less
Normal
More
Recent Advances in Pediatrics (Volume 22): Hot Topics
Suraj Gupte
PART 1: INFECTIOUS DISEASES AND IMMUNOLOGY
1:
Dengue Fever
INTRODUCTION
EPIDEMIOLOGY
ETIOLOGY
PATHOPHYSIOLOGY
SYMPTOMS
Dengue Hemorrhagic Fever (DHF) and Dengue Shock Syndrome (DSS)
Role of Tourniquet Test
NEW (2009) DENGUE CASE CLASSIFICATION17
LABORATORY INVESTIGATIONS
TREATMENT17,18
MONITORING
PROGNOSIS
PREVENTION20–23
2:
Complicated Malaria
INTRODUCTION
CLINICAL MANIFESTATIONS
DIFFERENTIAL DIAGNOSIS
LABORATORY DIAGNOSIS
MANAGEMENT
Role of Primaquine
Important Points
PREVENTION
RECENT STUDIES
3:
Tuberculosis: Current Concepts in Diagnosis and Management
INTRODUCTION
DIAGNOSIS
Recommended Approach to Diagnose TB in Children
INVESTIGATIONS
Drug Resistance
TREATMENT
Standard Regimen
Treatment Regimens
Risk Factors for MDR TB31–33
Fixed Dose Combinations
Monitoring of Treatment31,32
Management of Adverse Events31,32
Alternative Drugs
Role of Steroids
4:
Influenza: What is Special in Children?
INTRODUCTION
SPECIAL FEATURES IN A NUTSHELL
HIGH-RISK CHILDREN
ETIOLOGIC VIRUS1,6–8
EPIDEMIOLOGIC CHARACTERISTICS9,10
PATHOGENESIS
CLINICAL MANIFESTATIONS11–14
DIAGNOSIS1,15,16
Clinical
Routine
Specific
PREVENTION
Vaccines16–18
Additional (Nonpharmaceutical) Measures
Role of Chemoprophylaxis
MANAGEMENT1,5,19
Supportive Care
Antiviral Drugs
Treatment of Avian Influenza
COMPLICATIONS19–21
PROGNOSIS
5:
Approach to a Child with Primary Immunodeficiency Disorders
INTRODUCTION
BASICS OF IMMUNOLOGY
CLINICAL PRESENTATION
T-cell Defects and Combined B-cell and T-cell Defects
B-cell Immunodeficiencies
Innate Immunodeficiencies
Disorders of Immune Regulation
APPROACH TO DIAGNOSIS
CLINICAL EVALUATION
LABORATORY EVALUATION
Complete Blood Counts
Screening for B Cells Deficiency
Screening for T Cells Deficiency
TREATMENT
SCID/CID
B-cell Immunodeficiencies
Innate Disorders
PRENATAL DIAGNOSIS
PROGNOSIS
PART 2: NEUROLOGY
6:
Cerebral Palsy
INTRODUCTION
EPIDEMIOLOGY AND ETIOLOGY
CLINICAL MANIFESTATIONS
COMORBIDITIES12 (TABLE 6.2)
CLASSIFICATIONS
DIAGNOSIS
MANAGEMENT
What's New in the Management of CP?
PREVENTION
7:
The Ketogenic Diet
INTRODUCTION
HISTORY
WHAT IS KETOGENIC DIET?
POSSIBLE MECHANISMS OF ACTION
INDICATIONS
CONTRAINDICATIONS
EXECUTION OF THE DIET
COMPLICATIONS
EFFICACY
VARIANTS OF THE KETOGENIC DIET
POSITIVE EFFECTS OTHER THAN SEIZURE CONTROL
INDIAN DATA
CONTROVERSIES AND FUTURE TRENDS
PART 3: GASTROENTEROLOGY AND HEPATOLOGY
8:
Celiac Disease: Issues and Concerns
INTRODUCTION
SEMENTICS/DEFINITIONS
EPIDEMIOLOGY
Risk in Relatives
Risk in Autoimmune Conditions8
Risk in Syndromes8
ETHNICITY
PATHOPHYSIOLOGY
1. Enviornmental Factors
2. Genetic Factors
3. Immune Factors
CLINICAL FEATURES
Atypical Celiac Disease (Manifestations)
DIAGNOSIS
DIFFERENTIAL DIAGNOSIS
COMPLICATIONS
MANAGEMENT
Recommendations after Diagnosis
Grains not Permitted in CD
Gluten-free Grains Allowed in a Gluten-free Diet
Other Foods for a Basic Gluten-free Diet
Monitoring
Refractory Celiac Disease
NEWER MANAGEMENT STRATEGIES
9:
Revisiting Hepatitis B
INTRODUCTION
HISTORICAL ASPECTS
GLOBAL BURDEN
BURDEN IN INDIA
ETIOLOGIC VIRUS
TRANSMISSION AND SPREAD
NATURAL HISTORY AND COURSE7
Acute HBV Infection
Fulminant Hepatitis B
Chronic HBV Infection
FACTORS AFFECTING THE NATURAL COURSE
PATHOPHYSIOLOGY
SEROLOGICAL MARKERS8–11
CLINICAL MANIFESTATIONS
Prodromal Phase
Symptomatic Phase
Convalescent Phase
COMPLICATIONS
DIAGNOSIS
DIFFERENTIAL DIAGNOSIS
MANAGEMENT
Interferon
Polyethylene Glycol (PEG) Interferon
Lamivudine (LMV)
Adefovir
Famciclovir
Entecavir
PREVENTION
Vaccine
Postexposure Prophylaxis
PROGNOSIS
10:
Hepatocyte Transplantation
INTRODUCTION
ADVANTAGES
INDICATIONS
ISOLATION OF HUMAN HEPATOCYTES
EVALUATION OF HEPATOCYTE QUALITY
CRYOPRESERVATION
SITES OF HEPATOCYTE ENGRAFTMENT AND CLINICAL TRANSPLANTATION
Intraportal Injection
Spleen
Peritoneal Cavity
CELL LOSS IMMEDIATELY AFTER TRANSPLANTATION
IMMUNOSUPPRESION
ALTERNATIVE CELL SOURCES
TECHNIQUES TO IMPROVE LIVER ENGRAFTMENT
Partial Embolization of PV
Liver Irradiation
11:
Nonalcoholic Fatty Liver and Steatohepatitis
INTRODUCTION
EPIDEMIOLOGY
ETIOLOGY
PATHOGENESIS
The ‘2-hit Hypothesis’
Pathogenesis of NAFLD Different in Children and Adolescents
CLINICAL FEATURES
DIAGNOSIS
IMAGING
LIVER HISTOLOGY
NASH Type 1 (Adult NASH)
NASH Type 2 (Pediatric NASH)
NATURAL HISTORY
TREATMENT
Lifestyle Modification
Pharmacotherapy
Liver Transplantation
PART 4: NUTRITION-RELATED DISORDERS
12:
Pediatric Obesity
INTRODUCTION
DEFINITION
Limitations of BMI include–
CLASSIFICATION
EPIDEMIOLOGY
ETIOPATHOGENESIS
COMORBIDITY
ASSESSMENT AND EVALUATION
MANAGEMENT
Dietary Measures
Behavior Modification
Lifestyle Modification
Drugs
PREVENTION
13:
Severe Acute Malnutrition
INTRODUCTION
MAGNITUDE OF THE PROBLEM
ETIOLOGIC CONSIDERATIONS
HUMAN IMMUNODEFICIENCY VIRUS (HIV), TUBERCULOSIS AND SAM
SCREENING FOR SAM
TREATMENT
The Inpatient Treatment Model
Complications
Criteria for Admission
Laboratory Investigations
Treatment and Prevention of Hypoglycemia
Treatment and Prevention of Hypothermia
Treatment of Dehydration without Shock
Treatment of Shock
Treatment of Electrolyte Imbalance
Duration of Treatment
Supplementation of Micronutrients
Feeding
Feeding in Stabilization Phase
Feeding in Rehabilitation Phase
Treatment of SAM in HIV and Tuberculosis Children
Criteria for Discharge
Treatment Outcome
Community based Therapeutic Care (CTC)40,41
Ready to Use Therapeutic Food (RUTF)
PREVENTION
14:
Vitamin D Deficiency and Childhood Diseases
INTRODUCTION
BACKGROUND AND PHYSIOLOGY
SOURCES OF VITAMIN D
BLOOD LEVELS OF VITAMIN D
GLOBAL BURDEN OF VITAMIN D DEFICIENCY AND INSUFFICIENCY
VITAMIN D DEFICIENCY AND CHILDHOOD ILLNESSES
REVISED GUIDELINES FOR RECOMMENDED DIETARY ALLOWANCE OF VITAMIN D
PREVENTION OF NUTRITIONAL VITAMIN D DEFICIENCY
Exposure to Sunlight (Cutaneous Vitamin D Synthesis from Solar UV-B Exposure)
Fortification of Food with Vitamin D
Use of Supplements
PART 5: NEPHROLOGY
15:
Pediatric Acute Kidney Injury
INTRODUCTION
DEFINITION
ETIOLOGY
EPIDEMIOLOGY
NEONATAL ACUTE KIDNEY INJURY (AKI)
PATHOGENESIS -WHAT'S NEW?
DIAGNOSIS — ROLE OF BIOMARKERS
MANAGEMENT
Investigations
TREATMENT
Dialysis
Continuous Renal Replacement Therapy
LONG TERM OUTCOMES
16:
Urinary Tract Infection
INTRODUCTION
DEFINITION
EPIDEMIOLOGY
ETIOLOGY
PATHOGENESIS
RISK FACTORS
CLASSIFICATION AND CLINICAL FEATURES
COMPLICATIONS
DIAGNOSIS
Urine Culture
DIFFERENTIAL DIAGNOSIS
TREATMENT
Surgical Intervention
Imaging Studies
Recommendations for Imaging in UTI
PREVENTION OF RECURRENT UTI
General Measures
Bowel Bladder Dysfunction
Vesicoureteral Reflex
PROGNOSIS
17:
Idiopathic Steroid-resistant Nephrotic Syndrome: Trends in Management
INTRODUCTION
DEFINITIONS
INVESTIGATIONS
TREATMENT
Specific Therapy
Management of Edema
Prophylaxis for Thromboembolism
Management of Hyperlipidemia
Immunization
SUMMARY AND CONCLUSION
PART 6: HEMATOLOGY
18:
Sickle Cell Disease
INTRODUCTION
PATHOPHYSIOLOGY
SICKLE CELL TRAIT (HBAS)
LABORATORY DIAGNOSIS
Complete Blood Counts
Peripheral Blood Film (PBF)
Sickling Test
Sickle Solubility Test
Specific Tests for Detection of HbS
Hb Electrophoresis
HPLC
Isoelectric Focusing
DNA Testing
NEWBORN SCREENING FOR SICKLE CELL DISEASE
CLINICAL FEATURES AND THEIR SPECIFIC MANAGEMENT
Infection
Acute Sickle Crises, Pain and Bone-related Issues
Acute Splenic Sequestration
Priapism
Acute Chest Syndrome
Cerebrovascular Issues
Renal Problems
Anemia and Related Issues
Pulmonary Hypertension
Growth
Ocular Issues
Other Problems
ROLE OF SPLENECTOMY
VACCINATIONS IN SCD
LONG-TERM FOLLOW UP
SURGERY IN CHILDREN WITH SCD
NEWER THERAPEUTIC MODALITIES
Hydroxyurea (Hydroxycarbamide)
Gamma-globin Gene Modulation
Other Agents
Hematopoietic Stem Cell Transplantation (HSCT)
Gene-based Therapies
FUTURE DIRECTIONS
19:
Thalassemia Syndromes
INTRODUCTION
HISTORY
STRUCTURE OF HUMAN HEMOGLOBIN
THE β THALASSEMIAS
Molecular Basis of β Thalassemias
Distribution
Pathophysiology
Clinical Presentation
Thalassemia Major
Anemia and Extramedullary Hematopoiesis Related Features
Iron Overload Features
Transfusion Related Complications
Thalassemia Intermedia
Thalassemia Minor
Laboratory Findings
OTHER β-THALASSEMIA VARIANTS
Sickle Cell β-thalassemia
Hemoglobin C Thalassemia
Hemoglobin E β Thalassemia
The δβ Thalassemias
Hereditary Persistence of Fetal Hemoglobin
THE α-THALASSEMIAS
Molecular Basis of α-thalassemia
Distribution
Pathophysiology
CLINICAL PRESENTATION
Hemoglobin Bart's Hydrops Fetalis Syndrome
Hemoglobin H Disease
Milder Forms of α-Thalassemia, Including the Traits
α-Thalassemia and Mental Retardation
Labaratory Diagnosis
Alpha Thalassemia Trait
Hemoglobin H Disease
Hydrops Fetalis (alpha Thalassemia Major)
MANAGEMENT OF THALASSEMIAS
Prevention
Prenatal Diagnosis
Transfusion Therapy
Modifications to a Transfusion Regime
Volume and Rate of Transfusion
Post-transfusion Targets
Management of Iron Overload
Splenectomy
Supportive Care36,37
Pharmacologic Enhancement of Fetal Hemoglobin Synthesis
Hematopoietic Stem Cell Transplantation
Management of Thalassemia Intermedia
Gene Therapy
Follow up36
PART 7: CHILD-CENTRIC INITIATIVES
20:
National Child Health Programs
INTRODUCTION
HISTORICAL BACKGROUND OF HEALTH PROGRAMS2
LEGAL PROVISIONS BY THE STATE
Policies3
National Policy for Children
National Charter for Children
UN Convention on the Rights of the Child
Millennium Development Goals
National Plan of Action for Children (2005)
National Youth Policy (2003)5
National Nutritional Policy6
Constitutional Provisions3
Legislations3
DEVELOPMENTAL PROGRAMS
Integrated Child Protection Scheme (ICPS)7
Central Adoption Resource Agency (CARA)8
Balika Samridhi Yojana (BSY)9
Rajiv Gandhi National Crèche Scheme for the Children of Working Mothers10
Integrated Program for Juvenile Justice3
National Plan of Action to Combat Trafficking and Commercial Sexual Exploitation of Women and Children12, 1998
National Child Labor Project (NCLP)13
Scheme for Working Children in Need of Care and Protection15
NUTRITIONAL PROGRAMS
The Integrated Child Development Scheme (ICDS)16
HEALTH PROGRAMS
Integrated Management of Neonatal and Childhood Illness (IMNCI)2,22
Water Supply and Sanitation23
20 Point Program24
Reproductive and Child Health Program25,26
National Rural Health Mission (NRHM)—Child Health Component31
Thrust Area Under Child Health Program
National Rural Health Mission (NRHM)32 – Adolescent Health Component
Revised National TB Control Program33,34
Routine Immunization Program36
Pulse Polio Immunization Program 37
PART 8: CARDIOLOGY
21:
Rheumatic Fever and Rheumatic Heart Disease
INTRODUCTION
PATHOGENESIS
Host Factors
Agent Factors
DIAGNOSIS AND CLINICAL FEATURES
Arthritis
Chorea
Carditis
Subcutaneous Nodules
Erythema Marginatum
DIFFERENTIAL DIAGNOSIS
DIFFICULTIES IN DIAGNOSIS
ROLE OF ECHOCARDIOGRAPHY IN RESOLVING SOME ISSUES41,44–50
EPIDEMIOLOGY
TREATMENT
Symptomatic Treatment
Anti-inflammatory Treatment
Treatment of Carditis
PREVENTION
Primary Prevention
Secondary Prevention39,41,43
Vaccine: Is it the Answer?
Community-Based Measures for Prevention of RF/RHD
THE WAY OUT
PART 9: EMERGENCIES
22:
Neonatal Resuscitation Guidelines: What is New?
INTRODUCTION
INITIAL RAPID ASSESSMENT
CONCEPT OF GOLDEN MINUTE
INITIAL STEPS
STATE OF OXYGENATION
POSITIVE-PRESSURE VENTILATION (PPV)
ENDOTRACHEAL TUBE PLACEMENT
Chest Compressions
MEDICATIONS
INDUCED THERAPEUTIC HYPOTHERMIA
GUIDELINES FOR WITHHOLDING AND DISCONTINUING RESUSCITATION
STRUCTURE OF EDUCATIONAL PROGRAMS TO TEACH NEONATAL RESUSCITATION
23:
Dermatological Emergencies
INTRODUCTION
STAPHYLOCOCCAL SCALDED SKIN SYNDROME (SSSS)2
Etiology
Presentation
Diagnosis
Treatment
Prognosis
STEVENS-JOHNSON SYNDROME (SJS) AND TOXIC EPIDERMAL NECROLYSIS (TEN)4
Etiology
Drugs Commonly Associated with SJS and TEN
Presentation
Diagnosis
Treatment5
Prognosis
Sequelae
NECROTIZING FASCIITIS7
Etiology
Presentation
Treatment8
PURPURA FULMINANS9
Neonatal Purpura Fulminans10
Idiopathic Purpura Fulminans
Acute Infectious Purpura Fulminans
Clinical Presentation and Treatment11
Neonatal Purpura Fulminans
Idiopathic Purpura Fulminans
Acute Infectious Purpura Fulminans
PEMPHIGUS VULGARIS13
Etiology
Presentation
Diagnosis
Treatment14
Prognosis15
24:
Status Epilepticus
INTRODUCTION
EPIDEMIOLOGY, ETIOLOGY, AND OUTCOME
CLASSIFICATION AND CLINICAL FEATURES
PATHOPHYSIOLOGY
CONSEQUENCES
Plasticity versus Vulnerability in the Developing Brain
Cognitive Sequelae
INVESTIGATIONS
TREATMENT
General Principles
Prehospital Treatment
Hospital Treatment
Initial Assessment and Management
Initial Treatment of Generalized Convulsive Status Epilepticus
Initial Treatment of Non-convulsive Status Epilepticus
Non-anesthetizing Anticonvulsants
Medications Used in the Treatment of RSE
Non-anesthetizing Anticonvulsants
Anesthetizing Anticonvulsants
Pharmacological Treatment for Refractory NCSE
Other Modalities in Treatment of SE
PROGNOSIS
FUTURE DIRECTIONS
25:
Intracranial Hypertension
INTRODUCTION
PHYSIOLOGY OF INTRACRANIAL PRESSURE
Cerebral Dynamics Overview2
Causes of Intracranial Hypertension3
NEUROIMAGING5
NEUROLOGIC INTENSIVE CARE MONITORING
Intracranial Pressure Monitoring6
Indications for Intracranial Pressure Monitoring7
Intracranial Pressure Treatment Measures: Brief Summary of Goals of Therapy
GENERAL CARE TO MINIMIZE INTRACRANIAL HYPERTENSION
Treatment of Intracranial Hypertension
ALGORITHM OF MANAGEMENT OF INCREASED INTRACRANIAL HYPERTENSION8
Management of ICP
Management Strategies to Decrease ICP and Increase CPP
Position of the Child
Sedation and Analgesia
Decreasing the Metabolic Rate
CSF Drainage
Osmotherapy9
Hyperventilation
Barbiturates
ROLE OF SURGERY10
26:
Intravenous Fluid Therapy for Critically-ill Children in Pediatric Intensive Care Unit
INTRODUCTION
PHYSIOLOGY OF FLUID BALANCE
Normal Regulation of Fluid Balance
Changes in Fluid Balance during Illness
INDICATIONS FOR FLUID THERAPY
TRADITIONAL APPROACH TO FLUID THERAPY AND ITS LIMITATIONS
CURRENT EVIDENCE ON FLUID THERAPY
Dextrose in Maintenance of Fluid Therapy
FLUID THERAPY IN SPECIAL SITUATIONS
Fluid Restriction
Hyperhydration or Liberal Fluid Therapy
PART 10: CHILD PSYCHIATRY
27:
Sleep Disorders in Children and Adolescents
INTRODUCTION
ELECTROPHYSIOLOGY OF SLEEP (FIG. 27.1)
NORMAL SLEEP REQUIREMENTS IN DIFFERENT AGE GROUPS
CLASSIFICATION OF THE SLEEP DISORDERS
Diagnostic and Statistical Manual of Mental Disorders (DSM-IV)
International Classification of Sleep Disorders (ICSD)
International Classification11
ICD-10
SLEEP DISORDERS COMMON IN CHILDREN AND ADOLESCENTS
Primary Sleep Disorders
Dyssomnias
Parasomnias
Sleep Disorders Related to Another Mental Disorder
Sleep Disorder Due to a General Medical Condition
Substance-Induced Sleep Disorder
EVALUATION OF SLEEP DISORDERS: A CONCLUDING NOTE
28:
Eating Disorders
INTRODUCTION
EATING DISORDERS IN CHILDREN AND ADOLESCENTS
SCREENING FOR EATING DISORDERS
Problems with Eating Disorder Subtypes
SPECIFIC EATING DISORDERS
Anorexia Nervosa
Epidemiology
Comorbidity
Etiology
Biological Factors
Social Factors
Psychological and Psychodynamic Factors
Clinical Features
Two Subtypes
Differential Diagnosis
Course and Prognosis
Bulimia Nervosa
Epidemiology
Etiology
Clinical Features
Subtypes
Pathology and Laboratory Examinations
Differential Diagnosis
Course and Prognosis
Avoidant/Restrictive Food Intake Disorder
Characteristic Features
Comorbidity
Diagnosis
Differential Diagnosis
Course and Prognosis
Binge Eating Disorder
ASSESSMENT
A. Basic Laboratory Assessment
B. Basic Psychiatric Assessment
MANAGEMENT
Anorexia Nervosa and Bulimia Nervosa
Management Plan
A. Psychotherapy
B. Pharmacotherapy
PART 11: PEDIATRIC PHARMACOTHERAPY
29:
Adverse Drug Reactions
INTRODUCTION
DEFINITIONS
ADVERSE DRUG REACTIONS IN CHILDREN/ADULTS: DIFFERENCES
RATIONALE
TYPES/CLASSIFICATION
MECHANISMS OF ADVERSE DRUG REACTIONS IN CHILDREN
EPIDEMIOLOGY
RISK FACTORS FOR ADVERSE DRUG REACTIONS
ADVERSE DRUG REACTIONS IN NEONATES
DETECTION OF ADVERSE DRUG REACTIONS/MONITORING
REPORTING
YELLOW CARD SYSTEM
CAUSALTY ASSESSMENT FOR ADVERSE DRUG REACTIONS
GENETICS OF ADVERSE DRUG REACTIONS
MANAGEMENT
ANTICANCER DRUGS AND ADVERSE DRUG REACTIONS
COMMONLY USED DRUGS AND ADVERSE DRUG REACTIONS
VACCINES AND ADVERSE REACTIONS
30:
Probiotics: Concepts, Concerns and Controversies
INTRODUCTION
BACKGROUND
Human Gut and Microbial Ecosystem
Factors Influencing Intestinal Colonization
HISTORICAL ASPECTS2
PROBIOTICS AND ALLIED ORGANISMS
SPECIFICITY OF PROBIOTICS IN DISEASE STATES
DOSAGE SCHEDULE
PROBIOTICS IN GASTROINTESTINAL DISORDERS
Diarrheal Diseases
Various Hypotheses on Modus Operandi
Pseudomembranous Colitis
Necrotizing Enterocolitis
Irritable Bowel Syndrome (IBD)
H. pylori Infection
Constipation
PROBIOTICS IN NONGASTROINTESTINAL DISORDERS
Allergy
Immunocompromised States and Immunologic Disorders
Obesity
Infections
Liver Disease
Neurologic Disorders
Wound Healing in Surgery
Cancer
RECOMMENDATIONS ON THERAPEUTIC EFFECTIVENESS
SAFETY ISSUES AND ADVERSE DRUG REACTIONS
CURRENT STATUS IN INDIA
31:
Newer Antibiotics for Vancomycin-resistant Staphylococcus aureus and Other Pathogens
INTRODUCTION
LINEZOLID (ZYVOX, ZYVOXID, LINOSPAN)6, 10
DALBAVANCIN (CUBICIN) AND ORITAVANCIN
TIGECYCLINE (TYGACIL)6, 13
TELITHROMYCIN (KETEK)6, 14
FIFTH-GENERATION CEPHALOSPORINS6,15,16
INDEX
TOC
Index
×
Chapter Notes
Save
Clear