Well Child Flashcards

1
Q

Lead Screening

A

Risk assess at 6 mo, 9 mo, 18 mo, 3, 4, 5, 6 yr.

If in high risk area or Medicaid, lead test at 1 and 2 yrs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

TB test

A

Risk assess: by 1 mo, 6 mo annually 1-21 y

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

dyslipidemia

A

Risk assess at 2,4,6,8, 12-17 annually

Screen at 10, 20

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

STI/HIV

A

If sexually active 11-21, chlamydia screen.

Screen once between 16-18

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

cervical dysplasia

A

once at 21

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Oral health

A

Risk assess or screen at 12 mo, 18 mo, 24 mo, 30 mos.

Screen at 3 yr, 6 yr.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Rh incompatibility

A

When mom is Rh neg and fetus is Rh pos, fetal RBC enter mom’s blood and she forms antibodies. This can attack the fetus during birth or during a subsequent pregnancy –> hemolytic anemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Tx for Rh incompatibility

A

Screen initially, repeat again at 28 weeks. If Rh-, give RhoGAM between 28-30 weeks, and again w/in 72 hrs of delivery. RhoGAM prevents mom from developing anti Rh antibodies.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Aplastic Anemia

A

Congeintal (Fanconi) or Acquired (NSAIDs, meds, vial infections)
SSx: Thrombocytopenia, Neutropenia, macrocytic Anemia
Dx: CBC, bone marrow bx
Tx: HSCT –> 80% survival, increased CA risk

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Thalassemia

A

Eti: African, Middle E, Asia. Abnormal Hgb –> RBC destruction. Alpha or Beta.
SSx: trait: mild microcytic anemia. mild B: homozygous chronic hemolytic anemia. major: develops transfusion, folic acid, splenectomy, HSCT.
Dx: Hgb electrophoresis, blood smear

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Sickle Cell

A

Eti: AA
SSx: bone pain, chest pain, tibial ulcers, poor healing
Dx: howell-jolly bodies, target cells
Tx: Folic acid, hydroxyurea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Iron Def Anemia

A

Eti: Microcytic,
Sx: pallor, fatigue, Pica,
Tx: give Iron supplements

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

G6PD

A

Eti: hemolysis –> heinz bodies during stress
Dx: Bite cells, blister cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Idiopathic Thrombocytopenic Purpura

A

Eti: Age 2-5, most common childhood bleeding disorder; post infection
Sx: acute, petechiae, ecchymoses, epistaxis
Dx: low platelets, increased megakaryocytes, normal PT and PTT
Tx: self-limiting. Transfusion if severe

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Hemophilia

A

Eti: missing either Factor VIII or IX. (8 or 9). X-link recessive - seen in boys.
Sx: hemarthrosis, bleeding
Dx: prolonged PTT, low factors
Tx: give factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

VWD

A

Eti: inherited, caucasian
Sx: menorrhagia, prolonged bleeding
Dx: VWF assay; possible prolonged PTT
Tx: Desmopressin; VWF replacement

17
Q

Salmon patches

A

Nevus simplex, “stork bite”, angel kiss;

dilated capillaries; fade w/in 1 yr

18
Q

Erythema Toxicum

A

full term, begin 24-48 hrs from birth; blotchy red macules 2-3 cm w/ central vesicle/pustule.
Chest, back, face, proximal extremities (spares palms, soles).
Eosinophils in lesions.
Lasts 1 week.

19
Q

Acne Neonatorum

A

2-4 weeks old
Tx: topical erythromycin or benzoyl peroxide.
Resolves 6 mo-1 yr spontaneously.