LE 1 Pregnancu Flashcards
A 29-year-old G2P1 (1001) pregnant woman at 33 weeks AOG by LMP came into the ER in preterm labor. She is hypertensive and diabetic with uncontrolled glucose levels. She is non-compliant with her medications. The attending OB-GYN decided to give her medication for fetal lung maturation. Which of the following is an adverse effect of a corticosteroid?
A. Increases risk for intrauterine growth restriction of the fetus
B. Decreases incidence of neonatal sepsis
C. Triggers increase in maternal glucose level
D. Induces fetal lung maturation
C. Triggers increase in maternal glucose level
Rationale: Corticosteroids, such as betamethasone and dexamethasone, are commonly given to pregnant women at risk of preterm labor to accelerate fetal lung maturation. One of the known adverse effects of corticosteroids is the elevation of maternal glucose levels, which is particularly significant in this case as the patient is diabetic with uncontrolled glucose levels.
Which of the following clinical uses of uterine relaxants is NOT TRUE?
A. To prevent or arrest preterm labor
B. To treat severe dysmenorrhea during menses
C. To reverse inadvertent overstimulation
D. To facilitate intrauterine manipulations
B. To treat severe dysmenorrhea during menses
Rationale: Uterine relaxants, also known as tocolytics, are primarily used to prevent or arrest preterm labor, reverse uterine overstimulation, and facilitate intrauterine manipulations. They are not typically used to treat severe dysmenorrhea during menses, which is managed with other types of medication such as NSAIDs.
A 25-year-old G2P1 (1001) at 33 weeks AOG came into the ER with regular uterine contractions. On PE: Uterine contractions were at 5-minute intervals, moderate; IE: 1 cm, beginning effacement, intact BOW, cephalic, St -2. After 2 hours, the patient’s uterine contractions decreased in interval and intensity. What is the first-line oral tocolytic agent that can be given to the patient?
A. Nifedipine
B. Diphenhydramine
C. Atosiban
D. Celecoxib
A. Nifedipine
Rationale: Nifedipine, a calcium channel blocker, is commonly used as a first-line oral tocolytic agent to manage preterm labor. It works by inhibiting calcium influx into smooth muscle cells, thereby reducing uterine contractions.
Expressed in volume per unit of time:
A. Half-life
B. Clearance
B. Clearance
Rationale: Clearance is a pharmacokinetic parameter that describes the volume of plasma from which a drug is completely removed per unit time. It is often expressed in units such as mL/min or L/hr.
Effects of aging on absorption, except:
A. Lower peak concentration
B. Delayed time to peak concentration
C. Overall bioavailability is decreased
D. Overall bioavailability is unchanged
C. Overall bioavailability is decreased
Rationale: Aging generally affects drug absorption by decreasing the rate of absorption, leading to a lower peak concentration and delayed time to peak concentration. However, the overall bioavailability of most drugs remains unchanged unless there are significant changes in first-pass metabolism or other age-related physiological changes.
What factor affects drug transfer and drug effect on the fetus?
A. Rate of drug that crosses the placenta
B. Maternal bioavailability of the drug
C. Physical property of the drug
D. Volume of distribution
A. Rate of drug that crosses the placenta
Rationale: The rate at which a drug crosses the placenta is a critical factor affecting drug transfer and its effects on the fetus. Other factors such as maternal bioavailability, physical properties of the drug, and volume of distribution are also important but secondary to the rate of placental transfer.
A patient is admitted with exacerbation of congestive heart failure. What would you expect to find during your admission assessment?
A. Flat neck and hand veins
B. Furrowed dry tongue
C. Increased blood pressure and crackles throughout the lungs
D. Bradycardia
E. Pitting edema in lower extremities
C. Increased blood pressure and crackles throughout the lungs
Rationale: Exacerbation of congestive heart failure typically presents with increased blood pressure due to fluid overload and crackles throughout the lungs from pulmonary congestion. Other findings may include pitting edema, but increased blood pressure and pulmonary crackles are more direct indicators of heart failure exacerbation.
When a patient’s sodium serum level is 120 mEq/L, as the medical clerk on duty, your priority is to monitor the status of which body system?
A. Neurological
B. Gastrointestinal
C. Pulmonary
D. Hepatic
E. Endocrine
A. Neurological
Rationale: A sodium serum level of 120 mEq/L indicates significant hyponatremia, which can lead to neurological symptoms such as confusion, seizures, and even coma. Monitoring the neurological status is therefore a priority in managing severe hyponatremia.
The time course and intensity of the pharmacologic effect of a drug:
A. Pharmacodynamics
B. Pharmacokinetics
A. Pharmacodynamics
Rationale: Pharmacodynamics refers to the study of the biochemical and physiological effects of drugs and their mechanisms of action, including the time course and intensity of drug effects.
Which of the following is considered a mild adverse effect of OCPs?
A. Weight gain
B. Hirsutism
C. Withdrawal bleeding
D. Breakthrough bleeding
D. Breakthrough bleeding
Rationale: Breakthrough bleeding is a common and mild adverse effect of oral contraceptive pills (OCPs). Other effects such as weight gain, hirsutism, and withdrawal bleeding can occur but are less common or not considered mild adverse effects.
What is the teratogenic effect of barbiturates when taken during the critical period in a developing embryo or fetus?
A. Neural tube defect
B. Neonatal lethargy
C. Neonatal dependence
D. Neonatal toxicity
A. Neural tube defect
Rationale: Barbiturates have been associated with an increased risk of congenital malformations, including neural tube defects, when taken during the critical period of embryonic development. Other effects such as neonatal lethargy, dependence, and toxicity are possible but are not classified as teratogenic effects.
A 25-year-old G2P1 (1001) at 33 weeks AOG came into the ER with regular uterine contractions. On PE: Uterine contractions were at 5-minute intervals, moderate; IE: 1 cm, beginning effacement, intact BOW, cephalic, St -2. After 24 hours, the patient again had regular uterine contractions with increasing intensity and frequency. You decided to use Magnesium sulfate for neuroprotection in case labor ensues. What is the mode of action of MgSO4?
A. MgSO4 limits Ca++ influx by blocking L-type Ca channels in smooth muscle.
B. MgSO4 inhibits prostaglandin synthesis by inhibiting cyclooxygenase.
C. MgSO4 inhibits oxytocin receptors during active labor.
D. MgSO4 acts as a divalent cation and competes with Ca++ in myometrial cells.
D. MgSO4 acts as divalent cation and competes with Ca++ in myometrial cells.
Rationale: Magnesium sulfate’s mechanism of action in the context of preterm labor is related to its role as a divalent cation that competes with calcium ions (Ca++) in myometrial cells. This competition reduces calcium availability for muscle contraction, thereby relaxing the uterine muscles and potentially delaying labor.
This is an anti-progestin that can be used as a post-coital contraceptive:
A. Misoprostol
B. Mifepristone
C. Both A & B
D. Neither A & B
B. Mifepristone
Rationale: Mifepristone is an anti-progestin that can be used as a post-coital contraceptive. It works by blocking the action of progesterone, which is necessary for maintaining pregnancy. Misoprostol, on the other hand, is a prostaglandin used to induce uterine contractions and is not used as a post-coital contraceptive on its own.
What FDA category of drugs can be given to pregnant patients?
A. Category A
B. Category B
C. Category C
D. Category A & B
E. Category A, B, C
D. Category A & B
Rationale: FDA categories A and B drugs are considered safe for use in pregnant patients. Category A drugs have been shown to pose no risk to the fetus in controlled human studies, while Category B drugs have shown no evidence of harm in animal studies and no adequate studies in humans, or have shown adverse effects in animals but not in controlled human studies. Category C drugs should be used with caution as they have shown adverse effects in animal studies and lack adequate human studies.
Phase I metabolic pathway:
A. Converts to inactive metabolites
B. Converts to metabolites of greater activity
C. Converts to metabolites of equal activity
D. Converts to metabolites of lesser activity
B. Converts to metabolites of greater activity
Rationale: Phase I metabolic pathways often introduce or unmask a functional group (such as hydroxyl, amine, or carboxyl) on the drug molecule through oxidation, reduction, or hydrolysis reactions. These modifications can lead to the formation of metabolites that are more active, less active, or equally active compared to the parent drug. However, it is commonly associated with increasing activity or preparing for further metabolism in Phase II.
Potential serious adverse reactions to contraceptives include:
A. Myocardial infarction
B. Pulmonary embolism
C. Thrombophlebitis
D. All of the above
D. All of the above
Rationale: Serious adverse reactions to contraceptives can include myocardial infarction, pulmonary embolism, and thrombophlebitis, particularly in women who smoke or have other risk factors for cardiovascular disease.
Progesterone is synthesized in the following, EXCEPT:
A. Ovary
B. Placenta
C. Testes
D. Adrenals
C. Testes
Rationale: Progesterone is primarily synthesized in the ovaries, placenta, and adrenal glands. The testes primarily produce androgens such as testosterone, not progesterone.
Renal tubule reabsorption is affected by hormones:
A. Aldosterone
B. Renin/angiotensin
C. Atrial Natriuretic Peptide (ANP)
D. All of the above
E. A and B only
D. All of the above
Rationale: Renal tubule reabsorption is influenced by several hormones including aldosterone, the renin-angiotensin system, and atrial natriuretic peptide (ANP), which all play roles in regulating fluid and electrolyte balance.
Phase 1 Metabolic Pathway includes:
A. Oxidation
B. Glucuronidation
C. Conjugation
D. Acetylation
A. Oxidation
Rationale: Phase I metabolic reactions involve the introduction or unmasking of a functional group on the drug molecule, commonly through oxidation. Glucuronidation, conjugation, and acetylation are typically Phase II reactions that involve the conjugation of the drug with another substance to increase its water solubility for excretion.
This FDA teratogenic risk category is described as either studies in animals have revealed adverse effects on the fetus and there are no controlled studies in women OR studies in women and animals are not available. Drugs should be given only if the potential benefit justifies the potential risk to the fetus.
A. Category A
B. Category B
C. Category C
D. Category D
E. Category X
C. Category C
What is the teratogenic effect of valproic acid when taken during the critical period in a developing embryo or fetus?
A. Neural tube defect
B. Fetal anemia
C. Hypothyroidism
D. Hypoplastic nasal bridge
A. Neural tube defect
Rationale: Valproic acid is well-documented to increase the risk of neural tube defects when taken during the critical period of embryonic development. This is why it is often contraindicated or used with extreme caution in pregnant women.
Estrogen is secreted in the following:
A. Corpus luteum
B. Placenta
C. Testes
D. All of the above
D. All of the above
Rationale: Estrogen is secreted by the corpus luteum, placenta, and testes. It plays significant roles in various reproductive and physiological processes in both males and females.
This anti-estrogen drug acts as a competitive inhibitor, which prevents bone loss and has a stimulatory effect on the uterus:
A. Raloxifene
B. Toremifene
C. Tamoxifen
D. Any of the above
B. Toremifene
Rationale: Toremifene is an anti-estrogen drug that acts as a competitive inhibitor. It is known to prevent bone loss and has a stimulatory effect on the uterus, which distinguishes it from other selective estrogen receptor modulators (SERMs) like raloxifene, which does not stimulate the uterus but still prevents bone loss and decreases atherosclerosis.
This anti-estrogen drug stimulates ovulation by preventing feedback inhibition:
A. Cyproterone acetate
B. Clomiphene citrate
C. Toremifene
D. Tamoxifen
B. Clomiphene citrate
Rationale: Clomiphene citrate is an anti-estrogen that stimulates ovulation by blocking estrogen receptors in the hypothalamus, preventing feedback inhibition and thereby increasing the release of gonadotropins (LH and FSH).
This drug is better absorbed when given with food:
A. Ciprofloxacin
B. Cefuroxime
C. Both
D. Neither
B. Cefuroxime
Rationale: Cefuroxime is better absorbed when taken with food, which enhances its bioavailability. Ciprofloxacin’s absorption can be impaired by the presence of certain food components, especially dairy products.
Edema is the accumulation of fluid within the interstitial spaces, which may be caused by the following EXCEPT:
A. Increased plasma osmotic pressure
B. Increased hydrostatic pressure
C. Increased capillary membrane permeability
D. Lymphatic channel obstruction
E. C and D only
A. Increased plasma osmotic pressure
Rationale: Edema is typically caused by factors that lead to fluid leakage into the interstitial spaces, such as increased hydrostatic pressure, increased capillary membrane permeability, and lymphatic channel obstruction. Increased plasma osmotic pressure, however, tends to pull fluid back into the vascular compartment, reducing the likelihood of edema.
The hormones aldosterone and ADH both have an important function in:
A. Fluid balance in the body
B. The regulation of acid concentration in the body
C. Stimulation of a conscious desire for water
D. The activity of buffer systems
A. Fluid balance in the body
Rationale: Both aldosterone and antidiuretic hormone (ADH) play crucial roles in maintaining fluid balance in the body. Aldosterone promotes sodium and water reabsorption in the kidneys, while ADH increases water reabsorption in the renal collecting ducts.
Which of the following is a contraindication to giving estrogen?
A. Pregnant women
B. Undiagnosed genital bleeding
C. History of DVT
D. All of the above
D. All of the above
Rationale: Estrogen is contraindicated in pregnant women, in cases of undiagnosed genital bleeding, and in individuals with a history of deep vein thrombosis (DVT) due to the increased risk of adverse effects and complications in these conditions.
What drug causes discoloration and defects on teeth?
A. Cytarabine
B. Amphetamines
C. Carbamazepine
D. Tetracycline
D. Tetracycline
Rationale: Tetracycline antibiotics are known to cause discoloration and defects in teeth, especially when administered to children whose teeth are still developing.
A high sodium diet:
A. Decreases lithium excretion
B. Increases lithium excretion
C. Has no effect on lithium excretion
D. Increases lithium blood level
B. Increases lithium excretion
Rationale: A high sodium diet increases the excretion of lithium because the kidneys process sodium and lithium similarly. Increased sodium intake leads to increased lithium excretion, potentially lowering lithium blood levels and reducing its therapeutic efficacy.