Last semester Flashcards

(92 cards)

1
Q
Newborn
Infant
Toddler
Young Children
Older Children
Adolescents
A
Newborn --> birth to 1 month
Infant --> 1 month to 1 year
Toddler --> 1 year to 2 years
Young Children --> 2 years to 5 years
Older Children --> 5 years to 12 years
Adolescents
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2
Q
Normal gestation
Pre term infants
Post term infants
Low birth weight
Very low birth weight
A
Normal gestation --> 38 to 42 weeks
Pre term infants --> before the end of 37th week
Post term infants --> 42 weeks
Low birth weight --> under 2500g
Very low birth weight --> under 1500g
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3
Q

Gross motor physical development of a child

When does child understand name?

A
Newborn: flexed posture
7 mo: sits without support
1 year: stands independently 
15-18 months: walks independently and steadily
2 1/2 years: rund and jumps

Child understands name at 1 year

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4
Q

3 endocrine levels

A

Primary: gonads, thyroid gland
Secondary: anterior pituitary
Tertiary: Hypothalamus

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5
Q

Goitre - causes

A

Non-toxic:
- dietary deficiency, hashimotos, neoplasm, genetics

Toxic:
- graves, hashimotos, neoplasm, TSH-secreting pituitary gland tumor

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6
Q

In hyperthyroidism, TSH levels are…

A

…decreased

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7
Q

Calcium daily balance

A
  • 1 g Ca per day!
  • Total calcium is twice as high as ionic calcium
  • decreased ca levels –> PTH released
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8
Q

Growth hormone - IGF-1 axis

A
  • produced at anterior pituitary
  • released into blood stream
  • action via its mediator IGF-1
  • directly on traget tissue
  • ghrelin is secreted in stomach and increases the release of growth hormone
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9
Q

Puberty

  • hormones involved
  • Stages
A
  • Anterior pituitary: LH and FSH
  • LH: stimulates testes –> testosterone
  • FSH: stimulates ovaries
  • puberty starts at 11 in boys, 10 in girls (LH is a good marker for beginning)

1- Adrenarche: implement of adrenal androgen which could give some pubic/ axillary hair –> not conencted to gonadarche
2- Gonadarche: maturation of gonads

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10
Q

Window of opportunity

A
  • mini-puberty at 3-6 months of age

- increased LH and FSH levels

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11
Q

What should we ask in history taking of urinary tract?

A

ANTENATAL HISTORY:

  • amniotic fluid volume
  • alpha-fetoprotein level
  • presence of fetal distress
  • maternal drug history and diabetes

BIRTH HISTORY:

  • delivery, apgar, weight…
  • low weight –> low nephron number; high weight –> Beckwith-Wiedemann syndrome
  • number of umbilical vessels
  • weight of placenta
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12
Q

Kidneys are enlarged/ palpable with…(7)

A
  • autosomal recessive polycystic kidney disease
  • autosomal dominant polycystic kidney disease
  • tuberous sclerosis
  • multicystic dysplastic kidney
  • severly obstructed kidneys
  • renal venous thrombosis
  • renal tumor
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13
Q

Evidence of renal osteodystophy

A
  • thickened wrists
  • ricekty rosary
  • lower limb deformities
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14
Q

Red Urine can be due to:

A
  • macroscopic hematuria: the longer the contact and the more acidic the urine, the darker the color
  • certain foods (beetroot)
  • Hemoglobinuria
  • myoglobinuria
  • urate crystals
  • drugs
  • inborn errors of metabolism
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15
Q

Causes of cloudy urine

A

secondary to the presence of:

  • pyuria (white blood cells)
  • Calcium phosphate crystals
  • combination of calcium salts, uric acid, cysteine or struvite
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16
Q

What does a dipstick urine test look for: (6)

A
  • pH
  • Blood
  • Protein
  • Glucose
  • Leukocytes
  • nitrites
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17
Q

Urine pH

A
  • from 5 to 8
  • important in diagnosing renal tubular acidosis
  • important in treating and preventing urinary stones
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18
Q

Specific gravity

A
  • 1.001 to 1.035
  • reflects concentrating and diluting ability of kidney
  • reflets persons hydration status
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19
Q

Causes of false positive and false negative proteinuria

A

FALSE POSITIVE:

  • concentrated urine
  • alkaline urine
  • gross hematuria
  • dipstick was left in too long
  • contamination with secretions from urinary tract or vagina
  • contamination with antiseptics, chlorhexidine, benzalkonium

FALSE NEGATIVE:

  • diluted urine
  • acidic urine
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20
Q

GLUCOSE on urine dipstick

A
  • lower limit of detection is 4-5 mmol/l

- appears when serum glucose is >8.910 mmol/l

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21
Q

Nitrites of urine dipstick

A
  • majority of pathogenic bacteria produce nitrite

- high specificity and low sensitivity for UTI

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22
Q

Casts in urine

A
  • Hyaline casts –> in proteinuria
  • Cellular casts
  • ->RBCs (in glomerular bleeding) –> >5 RBC/mcl
  • ->WBCs (renal inflammation) –> > 10 WBC/mcl
  • ->epithelial cells
  • can be a normal finding
  • centrifugation can damage casts
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23
Q

Diagnostic tools in urinary system

A
  • Ultrasound
  • Intravenous urogram
  • voiding cysturethrogram (to detect VUR)
  • DMSA scan
  • Dynamic renography (to asses renal blood flow)
  • CT
  • MRI
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24
Q

Hematopoiesis in children

A
  • by birth, all bone marrow cavities are actively hematopoietic
  • in childhood, hematopoiesis moves to central bones
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25
Causes of an increase and decrease in WBCs Normal levels
Normal: 5.0-10 INCREASE: infection, tissue necrosis, bone marrow malignancies, inflammation DECREASE: - infection, conditions that suppress immune system or exhaust bone marrow
26
WBCs precentages of different types
prcentages of total WBC count - Neutrophils 40-60% (elevated in bacterial infection) - Monocytes 2-10% (viral infectio) - Lymphocytes 20-40% (viral infection) - Eosinophils 0-5% (allergic and parasitic disorder) - Basophils 0-1% (systemic allergic reaction)
27
Physiologic WBC changes
- newborn has high WBC count (falls within 2 weeks) | - until 8 years, lymphocytes are more dominant than neutrophils
28
Causes of increase and decrease of RBC
INCREASE - congenital heart disease, chronic hypoxia, high altitudes, polycythemia vera DECREASE - renal disease, RBC destruction, iron deficiency, vit. B12 deficiency, blood loss, bone marrow depression
29
MCV MCH MCHC RDW
- Mean corpuscular volume: average size of RBCs - Mean corpuscular hemoglobin: average weight of Hb per RBC - Mean corpuscular hemoglobin concentration: average concentration of Hb (normo-, hyper- and hypochromic) - Red Cell Distribution Width: uniformity of RBDs
30
Hemoglobin Causes for increase and decrease
- 115-145 g/l) - Hgb F (fetal hemoglobin) - Hgb A (adult hemoglobin) INCREASE: - congenital heart disease, chronic hypoxia, high altitudes, polycythemia vera, fluid loss DECREASE - decreased production(anemia, renal disease, iron deficiency, bone marrow depression) - Increased destruction (sickel cell, shperocytosis) - blood loss - fluid volume overload
31
Reticulocytes | causes of increase and decrease
- immature RBC (0.5%-1.5%) INCREASE - anemia, chronic hemolytic anemia DECREASE - bone marriw failure syndrome, iron deficiency anemia, vit. B 12 anemia, folate deficiency anemia
32
Physiologic anemia of the newborn
at one week postnatal --> all RBC indices begin declinign to a minimum
33
Platelets causes of increase and decrease
- 150-450 INCREASE - acute blood loss, myeloproliferative disease, polycythemia vera DECREASE - decreased production (leukemias, bone marrow failure syndromes) - increased destruction (ITP, certain drugs) - Abnormal pooling (splenic sequestration, splenomegaly)
34
Lymph node exam
- size: insignificant if 2cm or less - consistency: soft (hard --> malignancy, rubber --> lymphoma) - tender: no - Mobility: yes, should not be fused together - Patient's age: 2-12 years -> always palpable head and neck
35
Examination of fontanelles
- anterior fontanel closes until 1-2 y - posteiror fontanel closes into 2 months - anterior fontanel is felt for bulging (raised intracranial pressure) or depression (dehydration)
36
Macrocephaly and Microcephaly
Macrocephaly: OFC > 2 standard devations (SD) above the mean Microcephaly: OFC > 2 SD below the mean Severe Microcephaly: OFC > 5 SG below the mean
37
Meningeal signs
1. Neck muscle (Nuchal) rigidity 2. Kernig sign: pain or resistance to straightening leg from flexed position 3. Brudzinsky signs: involuntary flexion of knees when lyign supine 4. Lasegue sign: pain or resistance to lift extended leg
38
Munich functional Deelopmental Diagnostics | --> 8 most important psychomotor functions
- crawling - sitting down - walking - gripping - perception - speaking - understanding speech (from 10 mo) - social skills
39
Iron deficiency anemia
- Hb < 110g/l in children younger than 2 | - Hb < 120 g/l in children older than 2
40
Fe metabolism after birth
- mothers Fe keeps Fe level of infant until 1 year - postnatal high Hb - high iron storage - during first 4 months Fe storage increases only 10% - 4-12 months: Fe storage increases 50%
41
Impaired absorption of Iron
- Malabsorption syndrome - Celiac disease - Prolonged diarrhea - Anatomic gut lesions - Allergic gastroenteropathy - intestinla parasites - colonisation of H. pylori
42
Stages of Iron Deficiency
1- Prelatent Stage: decrease in ferritin, no symtpoms 2. Latent stage: decrease of MCV, MCH, reticulocytes, ferritin 3. Iron deficiency anemia: decrease of Hb
43
Consequences of IDA in pregnant women and children
PREGNANT WOMEN - pre-eclampsia - abortion - peripartal bleeding complications - Premature delivery - low birth weight CHILDREN - impaired motor development - impaired language development - psychological and behavioural effects - decreased physical activity - mild to moderate mental retardation
44
Stages of IDA and their treatment
- mild: Hb 110-90 g/l (1-3 mg/kg/day to normal Hb + 1-2mo) - moderate: 90-70 (3-5 mg(kg/day to normal Hb + 2-3 mo) - severe: < 70 (5-7 mg/kg/day), tapering 5-6 mo give premature babies 1-4mg of Fe/kg to prevent
45
four baby miracles after birth
1. Physical growth 2. Cognitive development 3. Immature maturation 4. Digestive maturation
46
Celiac disease oral manifestations
``` Enamel defects Delayed eruption recurrent aphthous ulcers Cheilosis Oral lichen planus Atrophic glossitis ```
47
Etiology of halithosis
1. mouth (gingivitis, aphta, ulcer) 2. Nasopharynx (tonsils, adenoids) 3. Esophagus (GERD) 4. Stomach (gastritis, peptic ulcer disease) 5. Liver 6. Other: lungs, renal, metabolic disease
48
Peutz-Jager syndrome
- autosomal dominant disorder characterized by the development of benign hamartomatous polyps in the GI tract and hyperpigmented macules on the lips and oromucosa
49
What does parotid gland produce?
- amylase - growth hormone - lipase
50
Stomach functions
- Chief cells: pepsinogen - lipase - Parietal cells: HCl - G cells: gastrin - D cells: somatostatine - horomones: ghrelin - mucous production less acidic the younger the child
51
Importane of HCL
1. Activation of pepsinogens 1-5 2. Protein digestion 3. Food sterilization
52
Stomach pH and pepsin relation
the higher the pH, the lower the pepsin activity
53
Maturing of digestive system
- enzyme activities develop throughout the digestive system during the first year of life - first 4-6 mo: infants gut is more open and antibodies from breast milk can enter - 6 mo: gut barrier is closed, infant produces antibodies
54
Human pancreatic exocrine enzymes
PROTEASES LIPASES (low during first months of life) GLYCOSIDASES (amylase; is low at birth) NUCLEASES
55
Protein digestion
1. Stomach: pepsin | 2. Intestine: pancreatic proteases
56
Exocrine pancreas secreted enzymes during:
- fasting - interdigestive period - after eating
57
Clinical symtpoms of exocrine pancreatic insufficiency
- poor growth - diarrhea - lipid soluble vitamins deficiency
58
Development of skeletal system
- 3rd week: formation of notochord - 4th week: first signs of arms and legs - 5th to 8th week: limbs begin to extend - ossification of most bony nuclei of long and rouhnd bones does not complete until after birth
59
Bone formation
1. Intramembranous ossification: flat bones of the skull and mandible 2. Endochondral ossification: replacement of cartilage by bone, most bones of the body
60
Factors affecting bone growth
- lack of calcium, protein and other nutrients - vitamin D needed to absorption of calcium(lack --> ricketts in childhood and osteomalacia in adults) - vitamin C needed for collagen synthesis (lack --> scurvy, teeth fall out, wounds do not heal)
61
Gait in children
- Toddler who begins to walk: wide and unstable gait - 18 mo: wide base narrows and more stable - 4 years: child can hop on one foot and arm swing occurs - 6 years: gait and arm swing similar to adult
62
Joint hypermobility is assessed by the ...
Beighton score - one point for each thumb - one point for each finger + 90° - one point for each elbow + 10° - one point for each knee + 10° - one point with straight legs
63
Causes of Rickets
- Vit D disorders - Calcium deficiency - Phosphorus deficiency
64
10 importatn clinical features in Rickets
- delayed closure of fontanelles - frontal bossing - dental hypoplasia - pectus carinatum - swelling in wrist and ankle - wide sutures (skull) - Craniotabes - Rachitic rosary - Harrison's sulcus - Bowing of legs
65
Spasmophilia
- in malnutrition of vit D - development of alkalosis and hypocalcemia - laryngospasm, convulsions, increased neuromuscular tone
66
Grading of heart murmurs
I°: only listening very carefully II°: audible, only in full contact of stetoscope with chest III°: audible at once without full contact IV°: audible thourgh the palm V°: audible through the forearm VI°: hear it without stetoscope
67
Innocent murmurs
- only systolic - mostly under II° - not audible from back - vertical position decreases intensity - temporary
68
Abnromal murmurs
- systolic and diastolic - Mostly above II° - audible from back and out of heart area - Vertical position increases intensity - permanent
69
Hypertension from 0-15 years (percentile)
over 95th percentile
70
CTI equation
(CD+DE)/AB (must be under 50%)
71
growth is controlled by
- genetics - nutrition - environment - hormones
72
Endocrine regulation of grwoth
- GH - growth factors (IGF-1) - thyroid hormones - insulin - sex steroids (during puberty)
73
Growth hormone - IGF-1 axis (more detailed)
GH --> Liver --> IGF-1 --> bone, cartilage and others
74
Physical growth components
Infancy component: mostly nutrition Childhood component: GH Pubertal component: sex steoids and GH
75
Target height
girls: Father height - 13 + mother hieght / 2 boys: mother height + 13 + father height /2
76
maturation of the hypothalamic-pituitary gonadal axis in puberty
- development of gonads | - increased secretion of sex steroids
77
Breast milk protective effect from
``` 1- Infections 2- Allergy 3- obesity 4- High blood pressure and total blood cholesterol 5- psychological and cognitive benefits 6- Higher intelligence 7- Crohns disease and ulcerative colitis ```
78
Recommendations on Breastfeeding
- 8-12 feedigns in 24 h - no supplements - begin daily vit D drops at hosptial discharge - avoid routine pacifier use (no earlier than 3-4 weeks)
79
Milk secretion
- prolactin and oxytocin are secreted and released into the circulation - prolactin stimulates milk synthesis - oxytocin stimulates the myoepithelial cells to contract domperidon could be given to induce mild secretion
80
Composition of human milk
- carbohydrates (lactose) - protein - lipids - vitamins (influenced by mothers diet) - Minerals - HMOs
81
HMOs
``` Glucose Galactose N-acetyl-glucosamine Fucose Sialic acid ```
82
HMOs protective factors
- healthy intestinal microbiota - support gut barrier - reduce harmful bacteria - promote the gut associated immune system
83
Contraindications of breast feeding
- baby has galactosemia - mother has active untreated tuberculosis - mother is receiving radioactive isotopes - mother is receiving antimetabolites, chemotherapeutic agents - mother is abusing drugs - mother is HIV positive - mother has herpes simplex lesions on breast
84
Fatty acids in formulas
- omega 6 and omega 3 is important for development of baby's eyes, brain, nerves and immune system
85
Weaning from bottle
- infants are introduced to a cup at 6 months - begin weaning from bottle around 1 year - should be fully weaned by 15 months
86
Complementary feeding guidelines
- 6 mo: pureed, mashed and semi-solid food - 8 mo: "finger food" - 12 mo: same types of food eated by the rest of the family
87
Daily nutritional needs from complementary foods
6-8 mo: 130 kcal 9-11 mo: 310 kcal 12-23 mo: 580 kcal
88
what not to give as complementary food
- no sugar/ salt - no whole nuts/ mushrooms - no juices and honey
89
Gluten and milk as complementary food
- gluten between 4-12 months, large quantities should be avoided - milk should not be used as the main drink before 11-12 months
90
When can the child eat what
``` Grain - porridge: 4-6 months Vegetables: 4-6 months Meat: 5-6 months Egg: 6-7 months Fish: 6-7 months Fruits: 6-7 months ```
91
Antenatal development of lungs
- embryonic - pseudovascular - canalicular - saccular
92
Postnatal development of lungs
- alveolar maturation (up to 2 years) - microvascular maturation (up to 3 years) - Late alveolarization (3 years tp to adulthood)