Obstetrics and gynecology Flashcards
Hemodilution during pregnancy
With normal pregnancy, blood volume increases, which results in a concomitant hemodilution. Although red blood cell (RBC) mass increases 17 % during pregnancy, plasma volume increases more 45%, resulting in a relative anemia. This results in a physiologically lowered hemoglobin (Hb) level, hematocrit (Hct) value, and RBC count, but it has no effect on the mean corpuscular volume (Mcv).
anemia defined as a value less than the fifth percentile is a hemoglobin level of 11 g/dL or less in the first trimester, 10.5 g/dL or less in the second trimester, and 11 g/dL or less in the third trimester.
Normal hb is 12 for women
What murmur is ok to hear in a pregnant woman?
Systolic murmur; diastolic murmur is NOT ok
What does increased minute ventilation during pregnancy cause?
a compensated respiratory alkalosis (pco2 decrease and hco3 decrease and ph normal)
PFT in normal pregnancy?
Inspiratory capacity increases by 15% during the third trimester because of increases in tidal volume and inspiratory reserve volume. The respiratory rate does not change during pregnancy, but the TV is increased which increases the minute ventilation, which is responsible for the respiratory alkalosis in pregnancy. Functional residual capacity (erv +rv) is reduced to 80% of the non-pregnant volume by term. These combined lead to subjective shortness of breath during pregnancy.
Pulmonary edema in pregnancy
What drug can cause it?
Plasma osmolality is decreased during pregnancy which increases the susceptibility to pulmonary edema. Common causes of acute pulmonary edema in pregnancy include tocolytic use, cardiac disease, fluid overload and preeclampsia.
Magnesium sulfate (used as a tocolytic to stop uterine contractions)
Cardiovascular changes in pregnancy
The cardiac output increases up to 33% due to increases in both the heart rate and stroke volume. The SVR falls during pregnancy. Up to 95% of women will have a systolic murmur due to the increased volume.
Right hydronephrosis (distention of the renal calyces and pelvis with urine as a result of obstruction of the outflow of urine distal to the renal pelvis)
Some degree of dilation in the ureters and renal pelvis occurs in the majority of pregnant women. The dilation is unequal (R > L) due to cushioning provided by the sigmoid colon to the left ureter and from greater compression of the right ureter due to dextrorotation (clockwise) of the uterus. The right ovarian vein complex, which is remarkably dilated during pregnancy, lies obliquely over the right ureter and may contribute significantly to right ureteral dilatation. High levels of progesterone likely have some effect but estrogen has no effect on the smooth muscle of the ureter
Thyroid in pregnancy
Thyroid binding globulin (TBG) is increased due to increased circulating estrogens with a concomitant increase in the total thyroxine. Free thyroxine (T4) remains relatively constant. Total triiodothyroxine (T3) levels also increase in pregnancy while free T3 levels do not change. In a pregnant patient without iodine deficiency, the thyroid gland may increase in size up to 10%.
ultrasound reveals heterogeneous cystic tissue in the uterus (snowstorm pattern)
This patient’s presentation is classic for a molar pregnancy (A molar pregnancy starts when an egg is fertilized, but instead of a normal, viable pregnancy resulting, the placenta develops into an abnormal mass of cysts). Beta-hCG levels in normal pregnancy do not reach one million. A chest x-ray would be the most appropriate step, as the lungs are the most common site of metastatic disease in patients with gestational trophoblastic disease. Though a repeat quantitative Beta-hCG will be required on a weekly basis, an immediate post-operative value will be of little clinical utility.
Recommendations concerning weight gain in pregnancy
The recommendations are: underweight (BMI 30 kg/m2) total weight gain 11 - 20 pounds.
When does fetal organ formation occur?
3-10 week estimated gestational age
Mom brother has sickle cell disease. odds that this couple will have a child with sickle cell anemia, if the carrier rate for sickle cell disease in the African American population is 1/10?
Sickle cell anemia is an autosomal recessive condition that occurs in 1/500 births in the African-American population. The carrier state, or sickle-cell trait, is found in approximately 1/10 African-Americans. Since the patient’s brother is affected, both of their parents have to be carriers. Each time two carrier parents for an autosomal recessive condition conceive there is a 1/4 chance of having either an affected or an unaffected child and a 1/2 chance of having a child who is a carrier. Since the patient is unaffected, she has a 1/3 chance of not being a carrier and a 2/3 chance of being a carrier. The patient’s husband has a 1/10 chance of being a carrier (the general population risk for African-Americans). Thus, the chance that this couple will have a child with sickle cell anemia is: 2/3 X 1/10 X 1/4 = 1/60.
African American couple preconception counsel
Screening for carriers of both alpha and beta thalassemia is possible by evaluation of red cell indices. Although solubility tests for hemoglobin S or sickle cell preparations can be used for screening, hemoglobin electrophoresis is definitive and preferable because other hemoglobinopathies can also be detected including hemoglobin C trait and thalassemia minor. Although sickle cells can be identified on a blood smear in individuals with sickle cell disease, the cells may be absent in individuals with milder types of sickle cell disease and even in some individuals with severe sickle cell disease. Evaluation of a peripheral smear is not useful in detecting carriers for sickle cell disease.
Jewish decent genetic disorders (4)
Fanconi anemia (rare inherited bone marrow failure), Tay-Sachs disease (rare inherited disorder that progressively destroys nerve cells (neurons) in the brain and spinal cord), Cystic Fibrosis, and Niemann-Pick disease (lipid storage disorder that results from the deficiency of a lysosomal enzyme, acid sphingomyelinase) are all autosomal recessive conditions that occur at an increased incidence in Jews of Ashkenazi descent. The Beta thalassemia is seen mainly in Mediterranean populations.
Valproic acid effects on fetus
Valproic acid is associated with an increased risk for neural tube defects (specifically lumbar meningomyelocele), hydrocephalus (fluid build up in brain) and craniofacial malformations.
Fetal ultrasound examination at approximately 16 to 18 weeks gestation is recommended to detect neural tube defects.
diabetes immediately prior to conception and during organogenesis effect
Women with poorly controlled diabetes immediately prior to conception and during organogenesis have a four- to eight-fold risk of having a fetus with a structural anomaly. The majority of lesions involve the central nervous system (neural tube defects) and the cardiovascular system. Genitourinary and limb defects have also been reported. Although caudal regression malformation occurs at an increased incidence in individuals with diabetes, this condition is very rare.
Chorionic villi sampling
CVS is generally performed at 10-12 weeks gestation. The procedure involves sampling of the chorionic frondosum, which contains the most mitotically active villi in the placenta. CVS can be performed using a transabdominal or transcervical approach. The sampled placental tissue may be analyzed for fetal chromosomal abnormalities, biochemical, or DNA-based studies including testing for the mutations associated with cystic fibrosis
Highest detection rate for trisomy 21
All of the tests screen for trisomy 21 and trisomy 18. Cell-free DNA screening has a trisomy 21 detection rate of over 99% at a 0.2% false-positive rate. The other options may also be used to screen for trisomy 21. Detection rates provided at a 5% false positive screen rate.
- First trimester combined test: first trimester nuchal translucency, PAPP-A (pregnancy associated plasma protein A) and Beta-hCG – 85% Detection Rate
- Triple screen: second trimester AFP (alpha fetoprotein), Beta-hCG, uE3 (unconjugated estriol) – 69% Detection Rate
- Quad screen: (second trimester Triple screen + inhibin A) – 81% Detection Rate
- Sequential screen: (first trimester NT and PAPP-A + second trimester quad screen) – 93% Detection Rate
- Serum integrated screen, when unable to obtain nuchal translucency: (first trimester PAPP-A + second trimester quad screen) – 85-88% Detection Rate
risk of fetal loss associated with CVS
The risk of fetal loss associated with CVS is approximately 1% and is not related to her prior miscarriage Hx
Most common syndrome of inherited mental retardation?
Fragile X syndrome is the most common form of inherited mental retardation. The syndrome occurs in approximately 1 in 3,600 males and 1 in 4,000 to 6,000 females. Down syndrome is genetic but the majority of cases are not inherited.
This patient has three values on the three-hour glucose tolerance test that were abnormal.
Begin a diabetic diet and blood glucose monitoring
Initial management should include teaching the patient how to monitor her blood glucose levels at home on a schedule that would include a fasting blood sugar and one- or two-hour post-prandial values after all three meals, daily. Goals for blood sugar management would be to maintain blood sugars when fasting below 90 and one- and two-hour post-meal values below 120. A repeat glucose tolerance test would not add any value, as an abnormal test has already been documented. Oral hypoglycemic agents and insulin are not indicated at this time, as the patient may achieve adequate glucose levels with diet modification alone. Gestational diabetes varies in prevalence. The prevalence rate in the United States has varied from 1.4 to 14% in various studies. Risk factors for gestational diabetes include: a previous large baby (greater than 9 lb), a history of abnormal glucose tolerance, pre-pregnancy weight of 110% or more of ideal body weight, and member of an ethnic group with a higher than normal rate of type 2 diabetes, such as American Indian or Hispanic descent.
Gestational diabetes
Intrauterine growth restriction is typically seen in women with pre-existing diabetes and not with gestational diabetes. Shoulder dystocia, metabolic disturbances, preeclampsia, polyhydramnios and fetal macrosomia are all associated risks of gestational diabetes.
Folic acid intake
In 1991, the Centers for Disease Control and Prevention recommended that all women with a previous pregnancy complicated by a fetal neural tube defect ingest 4 mg of folic acid daily before conception and through the first trimester. In one analysis, this dose of folic acid in women at high risk reduced the incidence of neural tube defects by 85%. According to ACOG, tThe recommended dose for non-high risk patients is at least 0.4-.8 mg/day.
Maternal serum alpha fetoprotein
Ninety to ninety-five percent of cases of elevated MSAFP are caused by conditions other than neural tube defects including under-estimation of gestational age, fetal demise, multiple gestation, ventral wall defects and a tumor or liver disease in the patient. Incorrect dating, specifically under-estimation of gestational age, is the most common explanation for an elevated MSAFP. The next appropriate step in the management of this patient is to obtain an ultrasound to assess the gestational age, viability, rule out multiple gestation as well as a fetal structural abnormality.