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Clinical Methods in Paediatrics

Clinical Methods in Paediatrics. DEPARTMENT OF PAEDIATRICS CHINESE UNIVERSITY OF HONG KONG. Methods in Clinical medicine. History prenatal, natal, postnatal development social allergy and drugs family hx, enviromental hx F/E Physical examination + Investigations. An example.

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Clinical Methods in Paediatrics

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  1. Clinical Methodsin Paediatrics DEPARTMENT OF PAEDIATRICS CHINESE UNIVERSITY OF HONG KONG

  2. Methods in Clinical medicine • History • prenatal, natal, postnatal • development • social • allergy and drugs • family hx, enviromental hx • F/E • Physical examination + Investigations

  3. An example • Growth problem in paediatrics

  4. Why do we need to understand growth problems in Paediatrics? • Parental concerns • Almost all chronic childhood disorders can affect growth • Most children with “growth problems” actually DO NOT have problems and NEED NO investigations.

  5. Questions • What is normal growth? Pattern , charts - normal reference • Normal variations of growth

  6. Questions • What is normal growth? Pattern , charts - normal reference • Normal variations of growth? • What influences normal growth?

  7. Growth Disorders - Physiology NutritionDiseases HormonesNormal Growth GeneticsPuberty

  8. Normal Growth • Biological variations • Arbitrary: 3% - 97% = “Normal”

  9. Normal Growth * Biological variations * Arbitrary : 3rd% to 97%= normal • Trend of growth: Serial data : changes over time • Charts - for comparison of an individual to a reference population: assumption < 3% or > 97% = likely to be abnormal. i.e. disease

  10. Short stature • Definition • Children with heights below the 3%tile • MAJORITY • >90% due to familial short stature or constitutional growth delay • others -Pathological short stature • Familial short stature • Constitutional growth delay with delayed puberty

  11. Familial Short Stature • Family history - positive • a height within the target height defined by the parental size

  12. Target Heights Ht (boy) = Ht (mom) + Ht (dad) +12 2 Ht(girl) = Ht (mom) + Ht (dad) -12 2

  13. Familial Short Stature • Family history - positive • a height within the target height defined by the parental size • Normal growth velocity • Normal age of onset of puberty • Bone age consistent with chronological age

  14. Constitutional growth delay with delayed sexual maturation • Familial condition with hereditary delay in growth and maturation • Short stature during childhood • Delayed onset of puberty • Bone age - retarded for chronological age but appropriate for height age • Normal adult height

  15. Differential Diagnoses Short Stature Normal Abnormal -familial R/O Disproportionate -constitutional short stature *F Hx, Growth rate - Rickets :Vit. D, PO4 - Skeletal dysplasia (check upper , lower segments ) > 90% < 10% Proportionate short stature

  16. Proportionate Short Stature Prenatal onset Postnatal Onset -Syndromes::Down’s, Russell-silver -Chronic illness -Chromosome: Trisomies GI, CVS, Renal, Chest, Hema -IUGR Fetal: intrauterine infection -Endocrine: thyroid Maternal: toxemia G.H. Combined -severe malnutrition

  17. Skeletal Dysplasia • developmental defects of skeletal growth leading to disproportionate short stature and deformity > 200 types e.g. Achondroplasia, most common 1/ 25000

  18. CLINICAL APPROACH TO SHORT STATURE History 1. Onset: Since when ? 2. ? Growth arrest: e.g. no growth for the past 2 years 3. Prenatal history: Intrauterine growth retardation - drugs, smoke, alcohol, illness, rash, weight gain 4. Natal history - Birth weight, length 5. Postnatal history -Medical illness CNS - irradiation, Cardiac, Pulmonary, Renal, G.I.

  19. CLINICAL APPROACH TO SHORT STATURE History 6. GROWTH DATA FROM THE PAST - Plot the growth curve - Calculate the growth rate (normal = 4-6 cm/year 4 years to prepuberty) 7. Family history -Short stature, growth delay, menarche 8. Systemic enquiry: e.g.Symptoms of Hypothyroidism 9. Social history: assess impact of short stature

  20. SHORT STATURE - PHYSICAL EXAMINATION 1. Dysmorphic features suggesting syndromes: Turner, Noonan, Russell-Silver 2. Midline defects - Cleft lip/palate: Hypopituitarism 3. Visual field defects 4. MEASUREMENT- HT, WT, Arm-span, upper & lower segments, sitting height , proportions AGE U/L RATIO BIRTH 1.7 3 years 1.3 >7 years 1.1 5. ? Goitre and signs of hypothyroidism 6. Careful systemic examination:Heart, Lungs, Abdomen examination to detect possible organic cause 5. Pubertal status -BREAST, PUBIC HAIR, GENITAL STAGE, TESTES

  21. INVESTIGATIONS FOR SHORT STATURE 1. MAJORITY OF CASES- NONE- If Hx is compatible with normal variants i.e. Familial or constitutional - Growth rate -NORMAL 2. Recheck patient in 6 months to calculate the growth rate 3. INVESTIGATES IF - Very short: > 3 s.d. below mean(many cm below the 3rd%tile or history of growth arrest or history and physical abnormalities suggestive of endocrine disorders or other systemic disorders

  22. TESTS - FOR SHORT STATURE • BONE AGE: X-ray left hand and wrist • BLOOD COUNT, URINALYSIS, RFT • STSH, FT4 • KARYOTYPE FOR GIRLS (TURNER) • If patient has - Delayed bone age - Normal screening investigations - No other medical cause - abnormal growth rate THEN consider growth hormone testing

  23. As a GP, when to refer? • Height ‘way below’ 3rd % • Growth arrest • Obvious chronic problems-poorly controlled • Social reason: Unable to settle the extreme parental anxiety . DO NOT USE tests to reassure the parents

  24. Summary • Variations and control of normal growth • Approach to short stature (proportionate or disproportionate types) • DDx of short stature • History taking & physical examination • Investigations and follow-up

  25. Rickets • Clinical signs -stature, frontal bossing wrist, bow legs , ribs • Biochemical abnormalities: Bone profile: Ca, phosphate, ALP • Radiological signs of rickets

  26. Summary • Normal Growth • Approach to short stature • History, physical , investigations • DDx, Rickets • Examples of proportionate or disproportionate short stature

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