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Published byMargaretMargaret Carpenter Modified over 9 years ago
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Failure to Thrive Dr Usha Mallinath Dr Richard Mones
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Definition Wt below 3 rd centile Wt drops 2 major centiles Wt for length below 3 rd centile Wt < 80% ideal wt for age
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Historic classification Organic: those for which there is a clear genetic, medical, or anatomic etiology, a very large differential Nonorganic: insufficient emotional or physical nurturing without pathophysiological abnormality
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Calories, Calories Root of growth failure stems from inadequate calories Inadequate intake Increased demands Poor absorption Infants require approximately110- 120 kcal/kg/day At age 1 year, 100 kcal/kg/day
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Normal Weight Gain AgeMean Daily weight gain 0-3 m26-31g 3-6 m17-18g 6-9 m12-13 g 9-12 m9 g 1-3 yr7-9g 4-6yr6g
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Epidemiology 1-5% tertiary hospital referrals 5% in 2006 in USA, CDC High incidence poverty, low socio- economic status 50% not identified by health care professions Non organic FTT common in females
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Pathogenesis Insufficient food intake Increase Energy Requirement Malabsorption
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Pathogenesis Insufficient food intake Inadequate amount of food provided or available Structural causes of poor feeding e.g. cleft palate, Treacher-Collins Anorexia of chronic disease
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Pathogenesis Malabsorption /Steatorrhea Celiac disease Chronic Liver disease Cystic Fibrosis Chronic diarrhea
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Pathogenesis Increase Energy Requirement HIV Congenital Heart disease Hyperthyroidism
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Etiology system based GI RS CVS Renal ID Genetic Heme/Onc Endocrine
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GI Causes Feeding disorders Diarrhea Cleft palate Infectious Dentition Malabsorption oro-motor Vomiting Hepatic Biliary atresia GERD Chronic Hepatitis Stricture Cirrhosis
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Pulmonary CF BPD Tonsilar/ Adenoidal hypertrophy
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Endocrine Hypothyroid Rickets DM GH deficiency Adrenal insufficiency
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Cardiac Causes Congenital cardiac disease/CHF POOR INTAKE ? Increased metabolic demands Possible fluid restrictions Early interventions which may interfere with development of normal suck/swallow coordination
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ID HIV TB Parasites
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Heme/Onc Classic B-symptoms include weight loss anorexia
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Genetic Chromosomal abnormalities Trisomy 13, 18, 21 Deletion of chromosome 22 Gonadal dysgenesis (45,X), etc Evaluate for dysmorphisms
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Renal Renal Tubular Acidosis Disorder of HCO3 and H+ reabsorption in renal tubules Urine pH >5.5 in light of systemic acidosis
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Diagnostic Classification of causes: inadequate Nutrition Intake Not enough food offered –Food insecurity –Poor knowledge of child's needs Poor transition to table food Avoidance of high-calorie foods –Formula dilution –Excessive juice –Breastfeeding difficulties –Neglect Child not taking enough food –Oromotor dysfunction –Developmental delay –Behavioral feeding problem Altered oromotor sensitivity Pain and conditioned aversion Emesis –Gastroesophageal reflux –Malrotation with intermittent volvulus –Increased intracranial pressure
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Malabsorption Cystic fibrosis Celiac disease Food protein insensitivity or intolerance
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Increase Metabolic demands Insulin resistance (eg, intrauterine growth restriction) Congenital infections (eg, human immunodeficiency virus, TORCH) Syndromes (eg, Russell-Silver, Turner, Down) Chronic disease (eg, cardiac, renal, endocrine)
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Evaluation Clinical History Complete Physical Examination Judicious Lab tests and other inv
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History Birth : IUGR,LBW,Prematurity, prenatal exposure alcohol, drugs Chronic diseases Recurrent infections Frequent injuries Review of systems
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Feeding history Kind, amount of formula Preparation of formula Excessive low calorie liquid/fruit Stool pattern, vomiting with feeding Special diet, vegetarian Breast feeding techniques CALORIE COUNT
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Feeding history Feeding environment Feeding behaviour/interactions
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Family history Family members’ heights and weights History of illness Developmental delay MID-PARENTAL HEIGHT FAMILY GROWTH TREE
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Psychosocial History Financial & Employment status Parental depression Substance abuse Family discordance /stress Maladaptive parental styles
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Physical Examination Begin with measurements – if all parameters are <5th percentile, 70%chance of organic etiology Need to follow pattern of growth (i.e.,isolated points are meaningless) Dysmorphism Palate intact Hypotonia or spasticiy Signs of neglect (diaper rashes, impetigo, poor hygiene, protuberant abdomen)
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Laboratory evaluation Guided by clinical evaluation No evidence extensive screening lab tests Sever malnutrition: albumin, alkaline phosphatase, calcium, phosphorous Diagnostic imaging studies based on clinical evaluation
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Diagnosis FTT
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Treatment Nutrition Repletion Treatment of underlying disease Assessment oromotor function Food intake 110-120% recommended intake
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Treatment Increased food intake; high calorie formula Enrichment of food: supplementation with minerals and protein Tube feeding/parentral feeding
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Treatment Addressing psychosocial stresses Development and behavioral assessment Child protection services
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Hospitalization Severe malnutrition Significant dehydration Serious intercurrent illness or significant medical problems Psychosocial circumstances that put the child at risk for harm Failure to respond to several months of outpatient management Precise documentation of energy intake Extreme parental impairment or anxiety Extremely problematic parent-child interaction Practicality of distance, transportation, or family psychosocial problems preclude outpatient management
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Refeeding syndrome Unknown pathology Post nutrition rehabilitation in severe malnourishment Changes in electrolytes( low phosphate, Mg,K) Disruption fluid balance, edema Impaired Heart function, hypoglycemia Prevention by increased K, Phos,Mg during repletion Montiore blood sugar,electrolytes,blood gases, wt,U/A
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Sequelae Early onset FTT, persistent reduction in Wt, Ht Long term adverse effects cognition, learning, behavior
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