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S/S and complications of Chlamydia
-S/S
Usually asymptomatic so routine screening is essential
Abdominal pain if PID occurs
-Complications
Acute salpingitis
Pelvic inflammatory disease (PID)
Most serious complication of chlamydial infections, and past chlamydial infections, is associated with an increased risk of acquiring HIV infection
S/S and complications of Gonorrhea
-S/S
Women often asymptomatic
Screening is crucial
When symptoms are present, they are often less specific than symptoms in men
Purulent endocervical discharge, but this is more often minimal or absent
Mucopurulent drainage: This is characterized by thick, purulent (pus-like), and something malodorous vaginal discharge
Menstrual irregularities or women may report pain. It may be chronic or acute severe pelvic or lower abdominal pain or longer, more painful menses
Following symptoms may occur infrequently: dysuria, vague abdominal pain, or low backache prompt a woman to seek care
Rectal gonorrhea may be completely asymptomatic or have severe symptoms with profuse purulent anal discharge, rectal pain, and blood in the stool
-Complications
Perinatal complications of gonococcal infection
Prelabor rupture of membranes, preterm birth, chorioamnionitis, neonatal sepsis, intrauterine growth restriction, and maternal postpartum sepsis
Gonococcal infections in pregnancy can affect the pregnant woman and the fetus
Ophthalmia neonatorum, a neonatal gonococcal infection, it is highly contagious, and if left untreated, it may lead to blindness of the newborn
S/S and complications of Pelvic Inflammatory Disease (PID)
-S/S
Mucopurulent drainage
Cramping or pain
-Complications
Tubal damage and infertility: Inflammation and infection cause scar tissue adhesions that can block or kink the fallopian tubes. While sperm may pass through, a larger fertilized egg cannot complete the journey to the uterus.
Ectopic pregnancy: Damaged tubes with adhesions prevent the fertilized egg from reaching the uterine cavity, resulting in tubal implantation. This can completely destroy the tube and is life-threatening if untreated.
Hydrosalpinx: Fluid buildup inside damaged fallopian tubes. This fluid is toxic to embryos and negatively impacts pregnancy rates in women undergoing infertility treatment.
Chronic pelvic pain: Ongoing inflammation and adhesions
Tubal factor infertility: Past chlamydial infections (the most common cause of PID) are strongly associated with increased risk of infertility
S/S and complications of Syphilis
-S/S
Primary Phase: This stage typically begins 5 to 90 days after the initial sexual encounter. The hallmark symptom is a chancre, which is a sore or lesion located in the reproductive area, such as the penis, labia, or vulva. This sore will eventually go away on its own.
Secondary Phase: This stage occurs 6 weeks to 6 months later. Key symptoms include:
Systemic rash: A classic indicator of syphilis is a rash that appears on the palms of the hands and soles of the feet.
Genital lesions: Infectious lesions may appear throughout the genital area.
Flu-like symptoms: Patients may experience mild fever or general malaise.
Like the primary stage, these symptoms are self-limiting and will eventually clear up, leading the patient to believe the infection is gone.
Tertiary Phase: This final stage can take years or even decades to manifest after the initial infection
-Complications
Neurological Complications: During the tertiary phase, the disease can cause significant damage to the nervous system.
Systemic Damage: If not treated with penicillin, the disease can lead to widespread systemic issues.
Death: Syphilis can be fatal if the infection is allowed to progress to its final stages without medical intervention.
Congenital Risks: While not detailed extensively in the syphilis section, the sources note that "torch infections" (which includes syphilis) acquired during pregnancy can have detrimental effects on a developing fetus
Neurologic, cardiovascular, musculoskeletal, or multiple organ–system complications can develop in the tertiary stage
S/S and complications of Human Papillomavirus (HPV)
-Signs and symptoms
Asymptomatic: Many individuals have no symptoms at all and may not realize they are infected.
Genital Warts: These are benign (non-cancerous) growths that can be unsightly, uncomfortable, and embarrassing. They may hurt or irritate the area and often interfere with sexuality.
Pregnancy-Related Changes: Warts often become more obvious or appear during pregnancy due to the mother's slight immunosuppression.
Cervical Cell Changes: Internally, HPV can cause hyperplastic or neoplastic cell changes (abnormal cell growth) on the cervix, which are detected during a Pap smear
"Bumps" on vulva or labia (patient-reported)
Small lesions: 2-3 mm in diameter, 10-15 mm in height
Appearance: Soft, papillary swellings occurring singly or in clusters
Location in women: Posterior introitus (most common), buttocks, vulva, vagina, anus, and cervix
Long-duration infections: May appear as cauliflower-like mass
Moist areas: Multiple fine finger-like projections
Cervical lesions: Flat-topped papules (1-4 mm diameter), often only visible under magnification
Color: Flesh-colored or slightly darker based on skin tone
Usually painless but may be uncomfortable when very large, inflamed, or ulcerated
-Complications
Cervical Cancer: HPV is the predominant cause of cervical cancer. It causes slow-growing malignant changes in cervical cells.
Can be cancers of the cervix, vagina, vulva, anus, penis, and oropharynx
Persistent Infection: In some patients, particularly those with compromised immune systems, the infection can live in their cells for the rest of their lives, meaning they remain infectious.
Surgical Interventions: If abnormal cervical cells persist or worsen, complications may lead to the need for advanced diagnostic procedures like a colposcopy or major surgeries, such as a partial hysterectomy to remove the cervix or entire uterus
S/S and complications of Herpes Simplex Virus (HSV)
Herpes simplex virus 1 (HSV-1) → Transmitted non-sexually
Herpes simplex virus 2 (HSV-2) → Transmitted sexually
-Signs and symptoms
Initial Outbreak: The first infection, particularly with HSV-2, is often severe and can be devastating. Symptoms include:
Painful Lesions: These appear as vesicles or blisters filled with a high concentration of the virus.
Flu-like Symptoms: Patients often experience fever and chills.
Severe Dysuria: Urination can cause a severe burning sensation, leading some patients to avoid urinating because of the intense pain.
A history of having viral symptoms such as malaise, headache, fever, or myalgia is suggestive. Local symptoms such as vulvar pain, dysuria, itching, or burning at the site of infection and painful genital lesions that heal spontaneously are also highly suggestive of HSV infection.
Recurring Outbreaks: While medications like acyclovir can suppress outbreaks and shorten their duration, the virus remains in the body for life.
Painful recurrent genital ulcers
Generally less severe than primaru infection
-Complications
Neonatal Infection: If a mother has an active infection, the virus can be passed to the infant during passage through the vaginal canal. This can lead to a herpes viral infection of the eye in the newborn.
Detrimental Fetal Effects: HSV is classified as a "torch infection," meaning that if acquired during pregnancy, it can have serious, detrimental effects on the developing fetus.
Surgical Intervention (C-Section): If a woman in labor has visible, active lesions, a C-section is automatically advised to prevent the baby from coming into contact with the virus in the vaginal canal. If no lesions are present, a vaginal delivery may be allowed.
Psychological Impact: Because viral STIs like herpes are recurring and currently incurable, they can carry a significant amount of stigma and shame for the patient
Viremia in the Context of HSV and Pregnancy
In relation to HSV (herpes simplex virus) during pregnancy:
Primary HSV infection can cause viremia in the pregnant woman
During viremia, the virus circulates in the maternal bloodstream
This creates a risk for transplacental transmission to the fetus
However, congenital HSV infection through this route is rare
S/S and complications of Hepatitis A
-Transmission Routes
Fecal-oral route
Contaminated sources (like water or shellfish)
Risk factors are unhours populations
-S/S
Characterized by flulike symptoms with malaise, fatigue, anorexia, nausea, pruritus, fever, and right upper quadrant pain
-Complications
Dehydration:
Can result from severe nausea and vomiting
May require hospitalization for fluid replacement
Acute Liver Failure:
Rare but serious complication
Requires hospitalization
Women showing signs or symptoms need immediate medical attention
S/S and complications of Hepatitis B
-Identified as acute or chronic based on the presence of specific antibodies and antigens in blood tests
-S/S
Common Symptoms:
Arthralgias (joint pain) and arthritis
Lassitude (weakness/fatigue)
Anorexia (loss of appetite)
Nausea and vomiting
Headache
Fever
Mild abdominal pain
Later-Stage Symptoms:
Clay-colored stools
Dark urine
Increased abdominal pain
Jaundice
-Complications
Most threatening to the fetus and neonate
Disease of the liver and often a silent infection
Chronic HBV Infection:
Persistence of HBsAg in the blood indicates chronic infection
Can lead to chronic liver disease
Requires referral to specialized care provider for evaluation and management
FDA-approved therapeutic agents can result in sustained suppression of HBV replication and remission of liver disease
Perinatal Transmission (Most Significant Complication):
HBV is the virus most threatening to the fetus and neonate
Transmission most often occurs in infants of mothers with acute infection in late third trimester or during intrapartum/postpartum period
Exposure through HBsAg-positive vaginal secretions, blood, amniotic fluid, saliva, and breast milk
Neonatal Management:
Infants born to HBsAg-positive mothers should receive HBV vaccine and HBIG within 12 hours after birth
Must complete recommended vaccine series followed by postvaccination serologic testing
Universal HBV immunization recommended for all neonates before hospital discharge
-Note
Hepatitis B is often a "silent infection" - many people have no symptoms
The course can be sudden and severe in adults
Some individuals become asymptomatic chronic HBV carriers with persistence of HBsAg
All pregnant women should be screened for HBsAg at firts prenatal visit
S/S and complications of Hepatitis C
-S/S
Fatigue
Muscle weakness
Jaundice
Pruritus
-Complications
Liver fibrosis/cirrhosis
GI varices
Hepatocellular carcinoma
S/S and complications of Human immunodeficiency virus (HIV)
-S/S (Mnemonic= Feverish Hikers Need More Gear; Muscles Numb, Digestion Weak, Skin Reacts)
Fever
Headache
Night sweats
Malaise
Generalized lymphadenopathy
Myalgias
Nausea
Diarrhea
Weight loss
Sore throat
Rash
-Complications
Frequent opportunistic infections, etc.
AIDs
Endometriosis S/S
Pain Characteristics:
Pelvic pain - most common symptom (present in 33% of women with chronic pelvic pain)
Specifically, deep pelvic dyspareunia
Pain often begins a few days before menses
Can be present at ovulation and continue through the first days of menses
May start after menstrual flow has begun
Dull lower abdominal aching that radiates to the back or thighs
Acyclic pain (especially in adolescents)
Menstrual-Related Symptoms:
Dysmenorrhea (painful menstruation)
Abnormal vaginal bleeding
Other Common Symptoms:
Feelings of bloating or pelvic fullness
Gastrointestinal symptoms: diarrhea, constipation, and urgency (especially in adolescents)
Migraines (more common in adolescents with endometriosis)
Fertility Impact:
30% to 45% of infertile women have endometriosis
Risks for breast cancer
Nonmodifiable Risk Factors
Hormonal and Reproductive History:
Menarche before age 12 - longer exposure to hormones
Menopause after age 55 - longer exposure to hormones
Length of time on unopposed estrogen - significant risk factor
Never having children
First pregnancy after age 30
Not breastfeeding
Personal and Family History:
Personal history of breast cancer - constant risk for developing a second malignancy
Family history of breast or ovarian cancer in a first-degree relative or multiple relatives
BRCA1 or BRCA2 mutations:
55% to 72% lifetime risk with BRCA1 mutation
45% to 69% lifetime risk with BRCA2 mutation
General population: ~13% lifetime risk
Other Factors:
Female sex
Increasing age
Higher breast density - increases risk and makes mammography interpretation more difficult
Fibrocystic disease with proliferative diseases with atypia
Atypical hyperplasia (ADH or ALH) - 4 to 5 times greater risk
Diethylstilbestrol (DES) exposure - drug used decades ago to maintain pregnancy
Modifiable Risk Factors
Lifestyle Factors:
Overweight or obesity after menopause
Moderate to high alcohol consumption
Physical inactivity
Hormone Use:
Hormone replacement therapy during menopause for more than 5 years
Oral contraceptives
Side effects and drug interactions with IUDs
-Side effects
Heavier periods with Paragrad, periods, cramping
-Drug Interactions
??
Side effects and drug interactions with Nexplanon (LARCs or long active reversible contraceptives)
-Side effects
Irregular bleeding
-Drug interactions
?
Side effects and drug interactions with Progestin-only contraception (Short acting/hormonal)
-Side effects
Irregular bleeding/spotting
Breast tenderness
Acne
Lower libido
Headaches
Nausea
Ovarian cysts
Depression
-Drug interactions
?
Side effects and drug interactions with Oral contraceptives
-Side effects
Sore breasts
Nausea
Spotting
Decreased sex drive
-Drug interactions
?
Drug interactions with COCs
-Anticonvulsants (Dilantin) → reduces effects of COCs
-Fosamprenavir, rifampin, or rifabutin (HIV/TB medications)
Contraindications to COCs
-History of thrombosis
-Stroke
-Heart disease/hypertension
-Breast cancer
-Positive antiphospholipid antibodies
-Migraines with aura
-Prolonged immobility (Surgery, MS, etc.)
-Diabetes with vascular complications
-Gallbladder
-Disease
-Hepatic disease or disorder
-Pregnancy
-Use of fosamprenavier, rifampin, or rifabutin (HIV/TB meds)
-Use of some anticonvulsants (Dilantin)
-Less than 6-week PP (postpartum)
-Smoker over 35 (vasoconstriction and compromised vascular system)
Signs of pregnancy
-Presumptive
Those changes felt by the woman
Nausea
Vomiting
Breast tenderness
Fatigue
-Probable
Those changes observed by an examiner, can still be attributed to other causes!
Chadwick’s: Blue/violet color of vaginal mucosa/cervic
Hegar’s: Softening of the lower uterine segment
Goodell’s sign: Softening of the tip of cervix
Pregnancy test (urine or serum)
-Positive
Those signs attributed only to presence of a fetus
Fetal movement on ultrasound, fetal heartbeat
Anemia in pregnancy
-Dilutional anemia, especially common in 2nd trimester
Hgb = RBC/plasma volume
Plasma volume increases more than RBC mass
Should not decrease less than 11 g/dL (normal is 12 g/dL)
If lower, investigate pathological anemia instead of physiologic anemia
Iron and folate supplementation can be recommended
Physiologic anemia of pregnancy is a normal occurrence where hemoglobin and hematocrit decrease due to greater plasma volume expansion compared to red blood cell production. This is most noticeable in the second trimester.
Complications:
Associated with preterm birth and low-birth-weight infants
Fetus usually receives adequate iron stores even from anemic mother, further depleting maternal iron levels
What can be normal findings for a patient in 1st trimester (1-13 weeks)?
Uterine Changes:
Uterus remains a pelvic organ until 12 weeks
Size progression: large hen's egg (7 weeks) → orange (10 weeks) → grapefruit (12 weeks)
Changes from pear shape to spherical/globular shape
Can be palpated above symphysis pubis between 12-14 weeks
Cardiovascular:
Heart rate begins increasing at ~5 weeks
Increase of 15-20 beats/min above baseline by 32 weeks (persists to term)
Increased frequency of isolated premature atrial and ventricular contractions
Respiratory:
Maternal oxygen consumption begins increasing
Early structural adaptations begin
Common Symptoms:
Nausea and vomiting
Fatigue
Breast tenderness
Urinary frequency
-Fetus’s organs are starting to form
What can be normal findings for a patient in 2nd trimester (14-27 weeks)?
Uterine Changes:
Pregnancy may "show" after week 14 (varies by body type and parity)
Uterus rises to umbilicus level by 20-22 weeks
Uterus rotates to the right as it enlarges
Enlargement primarily from mechanical pressure of growing fetus
Cardiovascular:
Audible splitting of S1 and S2 by end of first trimester/early second
Third heart sound (S3) after midpregnancy
Systolic ejection murmurs in ~96% of women (most audible over left sternal border)
Heart elevated upward and rotated forward to left
PMI shifted upward and laterally 1-1.5 cm
Respiratory:
Physiologic dyspnea common (begins first or second trimester)
Diaphragm rises up to 4 cm
Costal angle increases; lower rib cage flares out
Transverse thoracic diameter increases ~2 cm
Chest breathing replaces abdominal breathing
-Fetus’s organ system are maturing
What can be normal findings for a patient in 3rd trimester (More than 28 weeks)?
Uterine Changes:
Fundus nearly reaches xiphoid process at term
Lightening occurs weeks 38-40 (fundal height decreases as fetus descends)
Nulliparas: ~2 weeks before labor
Multiparas: at labor onset
Cardiovascular:
Heart rate remains 15-20 beats/min above baseline
All cardiovascular changes persist until term
Respiratory:
Oxygen consumption reaches 40% above nonpregnant levels by term
Mechanical pressure increases dyspnea in late pregnancy
-Getting ready/into position, etc. for delivery
How do you determine gestational age/due date with Naegele's rule?
Naegele's Rule Calculation
The Formula:
Identify the first day of the last menstrual period (LMP)
Subtract 3 months from that date
Add 7 days to the result
Add 1 year (if needed)
Example:
LMP: January 10, 2024
Subtract 3 months: October 10, 2023
Add 7 days: October 17, 2023
Add 1 year: October 17, 2024 (EDB)
Important Assumptions
Naegele's rule assumes:
28-day menstrual cycle
Ovulation/fertilization occurred on day 14 of the cycle
Accurate recall of LMP date
Key Points About Accuracy
Limitations:
Only about 5% of women give birth spontaneously on the EDB calculated by Naegele's rule
Most births occur within 7 days before to 7 days after the EDB
Most Accurate Method:
First trimester ultrasound measurement of the embryo or fetus provides the most accurate EDB assessment
The EDB is determined based on both the LMP date AND first accurate ultrasound examination
How do you determine gestational age/due date?
Methods for Determining Gestational Age and Due Date
Most Accurate Method: First Trimester Ultrasound
Crown-rump length or maximum embryo length measured during first trimester
Commonly accepted as the most accurate method for determining gestational age
The estimated date of birth (EDB) is determined based on both the LMP date AND first accurate ultrasound examination
After First Trimester Ultrasound:
Measurements used: biparietal diameter (BPD), head circumference, abdominal circumference, and femur length
Combination of these measurements is the most accepted method after the first trimester
What is Gravidity, Gravida, Parity, Primipara, Multipara, and Nullipara
-Gravidity: Pregnancy
-Gravida: Whoman who is pregnant
-Parity: Number of pregnancies in which fetus or fetuses have reached viability, not number of fetuses (e.g., twins) born
Whether fetus is born alive or is still born (fetus who shows no signs of life at birth) after viability is reached does not affect parity
Gestational definition of viability is reaching 20 weeks gestation
Vs. ability to survive extrauterine life is approximately 22-23 weeks
-Primara: Woman who has completed one pregnancy with fetus or fetuses who have reached stage of fetal viability
-Multipara: Woman who has completed two or more pregnancies to stage of fetal viability
-Nullipara: Woman who have not completed a pregnancy with fetus or fetuses who have reached stage of fetal viability
What does GTPAL stand for?
-Gravidity/Gravida (number of pregnancies, including this one)
-Term (pregnancies, 37 weeks 0 days and beyond)
-Preterm (pregnancies, between 20 weeks 0 days and 36 weeks 6 days gestation)
-Abortion (Number of pregnancies that ended in miscarriage or elective termination before 20 weeks or weighted less than 500 g at birth)
-Living (Number of children currently living)
Where is the fundus at 20 weeks?
-Around the umbilicus
Important nutrition advice in pregnancy
Key Nutrition Recommendations
Preconception & Early Pregnancy:
Folic acid: 0.4 mg (400 mcg) daily for all women of childbearing age
During pregnancy: Increase to 0.6 mg (600 mcg) daily, especially in first trimester
History of NTD: 4 mg daily starting 1 month before conception through first trimester
Critical for preventing neural tube defects (spina bifida, anencephaly)
Iron Supplementation:
Recommended daily allowance: 27 mg during pregnancy
Supports maternal RBC expansion and fetal iron transfer
May be better tolerated if started after first trimester due to nausea
Include dietary iron sources even when taking supplements
Protein Intake:
71 g/day during pregnancy (increased from 46 g/day for nonpregnant adults)
Essential for fetal growth, placental development, and maternal tissue expansion
Sources: milk, meat, eggs, cheese, legumes, whole grains, nuts
General Dietary Guidance
Prenatal Vitamins:
Multiple micronutrient (MMN) supplement recommended before and throughout pregnancy
Especially important in first trimester when adequate folate and iron intake is less likely
Important: Supplements don't replace the need for a nutritious, well-balanced diet
Dietary Approach:
Consume a varied diet rich in vitamins and minerals
Counseling should begin in early prenatal care and continue throughout pregnancy
Most nutrient needs (except folate and iron) can be met through dietary sources alone
Foods to Promote Iron Absorption:
Certain foods can enhance or inhibit iron absorption from supplements
Discuss optimal timing and food combinations with healthcare provider
Special Considerations
Supplements are especially important for women with:
Known nutritional risk factors
Poor dietary intake
History of anemia
Multiple gestations
Appendicitis in pregnancy
Appendicitis in Pregnancy
Incidence & Diagnosis Challenges:
Most common nonobstetric surgical emergency during pregnancy
Occurs in approximately 1 in 1,000 pregnancies
Diagnosis often delayed because symptoms mimic normal pregnancy changes (nausea, vomiting, elevated WBC)
Rupture occurs in up to 40% of pregnant women with appendicitis due to delayed diagnosis
Clinical Presentation
Most Reliable Symptom:
Right lower quadrant abdominal pain (regardless of gestational age)
Less Reliable Indicators in Pregnancy:
Nausea and vomiting (common in normal pregnancy)
Loss of appetite (not reliable)
Fever, tachycardia, dry tongue, localized tenderness (less likely than in nonpregnant individuals)
WBC count (not helpful due to physiologic increase in pregnancy)
Anatomic Changes:
Appendix is displaced upward and laterally as pregnancy progresses
Pushed high and to the right, away from McBurney point
Makes diagnosis more difficult
Diagnostic Workup
Initial Tests:
Urinalysis (rule out UTI)
Chest x-ray (rule out right lower lobe pneumonia)
Both conditions can cause lower abdominal pain
Imaging:
Ultrasonography preferred during pregnancy (avoids fetal radiation exposure)
MRI is appropriate next step if ultrasound doesn't confirm diagnosis
CT scan avoided due to radiation exposure (though it's the test of choice in nonpregnant patients)
Treatment
Surgical Management:
Prompt surgical intervention is standard treatment
Appendectomy recommended even if appendicitis not evident at surgery
Performed via laparoscopy or laparotomy (surgeon's discretion)
Antibiotic Therapy:
Often administered for uncomplicated appendicitis
Definitely necessary if rupture, abscess, or peritonitis present
Safe options during pregnancy: penicillins, cephalosporins, metronidazole
Key Nursing Considerations
Maintain high index of suspicion for appendicitis in pregnant women with abdominal pain
Understand that typical signs may be absent or altered
Recognize urgency due to high rupture risk
Support timely diagnostic workup and surgical intervention
Cholecystitis in pregnancy
Cholecystitis in Pregnancy
Incidence & Pathophysiology:
Cholelithiasis (gallstones) occurs in 1-3% of pregnant women
Pregnancy increases risk due to elevated estrogen and progesterone levels, which encourage stone formation and slow gallbladder emptying
Cholecystitis (gallbladder inflammation) usually occurs when a gallstone obstructs the cystic duct
Third most common indication for nonobstetric surgery in pregnancy (~4 cases per 10,000 pregnancies)
Clinical Presentation
Cholelithiasis (Gallstones):
Most are asymptomatic during pregnancy
First symptom: biliary colic with epigastric or right upper quadrant pain
Pain may radiate to back or shoulders
Often triggered after high-fat meals or occurs spontaneously
Cholecystitis (Inflammation):
Epigastric or right upper quadrant pain (more severe and prolonged than biliary colic)
Nausea and vomiting
Fever
Management
Conservative Management:
Most women can be managed conservatively for remainder of pregnancy
Nutritional counseling emphasized (see dietary modifications below)
Surgery often postponed until postpartum period
Surgical Intervention:
Immediate cholecystectomy required for:
Recurrent biliary colic
Acute cholecystitis
Laparoscopic cholecystectomy is the preferred procedure
Can be safely performed in all trimesters (second trimester traditionally considered safest, but improved techniques allow surgery at any time)
Both laparoscopic and open cholecystectomy are safe options
Diagnostic Challenges
Pregnancy makes diagnosis more difficult due to:
Enlarged uterus
Displaced internal organs
Altered usual signs and symptoms
More difficult abdominal palpation
Key Nursing Considerations
Provide nutritional counseling for conservative management
Educate about avoiding high-fat meals
Monitor for worsening symptoms requiring surgical intervention
Support patient through surgical decision-making if needed
Ectopic pregnancy
Definition & Location:
Fertilized ovum implants outside the uterine cavity
70% occur in the ampulla (largest portion of fallopian tube)
Less common sites: abdominal cavity, ovary, cervix, cesarean scar
Accounts for 3% of all pregnancy-related maternal deaths in the U.S.
Risk Factors
Previous ectopic pregnancy
Fallopian tube abnormalities
Previous genital infections
Infertility
Smoking
Assisted reproductive technology (IVF)
Previous tubal ligation or IUD use
Classic Clinical Manifestations (Before Rupture)
Three Classic Symptoms:
Abdominal pain (occurs in almost every case)
Begins as dull, lower quadrant pain on one side
Progresses from dull → colicky → sharp, stabbing → diffuse, severe pain
Delayed menses (1-2 weeks late or lighter than usual)
Abnormal vaginal bleeding (mild-to-moderate dark red or brown spotting)
After Rupture
Additional Signs:
Referred shoulder pain (from diaphragmatic irritation due to blood in peritoneal cavity)
Generalized, one-sided, or deep lower quadrant acute abdominal pain
Signs of shock: faintness, dizziness (related to intraabdominal bleeding, not necessarily vaginal bleeding)
Cullen sign: ecchymotic blueness around umbilicus (indicates hemoperitoneum)
Diagnosis
Screening Criteria: Every woman with abdominal pain, vaginal spotting/bleeding, AND positive pregnancy test should be screened.
Key Diagnostic Tools:
Quantitative β-hCG levels
Transvaginal ultrasound
Discriminatory Zone Concept:
When β-hCG >1500-2000 mIU/mL, normal intrauterine pregnancy should be visible on transvaginal ultrasound
If β-hCG >1500 mIU/mL but no intrauterine pregnancy visible → ectopic pregnancy very likely
β-hCG may be redrawn every 48 hours to assess viability
Differential Diagnosis: Miscarriage, ruptured corpus luteum cyst, appendicitis, salpingitis, ovarian cysts, ovarian torsion, UTI
STIs in pregnancy
STIs in Pregnancy: Key Considerations
Maternal & Fetal Impact:
STIs cause significant morbidity and mortality during pregnancy
Maternal consequences: infertility, sterility (lifelong effects)
Fetal consequences: affect child's length and quality of life
Outcomes depend on: coinfection with other STIs, timing of infection, and when treatment was initiated
TORCH infections → group of infections that are capable of crossing the placenta and adversely affecting the fetus
T - Toxoplasmosis
O - Other infections (hepatitis, HIV)
R - Rubella virus
C - Cytomegalovirus
H - Herpes simplex virus (HSV)
Screening Recommendations
HIV:
Universal screening at initial prenatal visit (opt-out approach)
Retest in third trimester for high-risk women
Rapid HIV testing in labor for women with unknown status
With antiretroviral therapy (ART), mother-to-child transmission reduced to <2%
ART given orally throughout pregnancy but may increase risk of preterm birth, low birth weight, and stillbirth
Syphilis:
Screen all pregnant women at first prenatal visit
Retest early third trimester and at delivery if high risk
Test all women who deliver stillborn infants
Partners must be evaluated, tested, and treated
Up to one-third with early primary syphilis may have nonreactive serologic tests initially
Chlamydia:
Yearly screening for all sexually active women <25 years
Screen women ≥25 years if high risk (new/multiple partners)
All pregnant women <25 years: screen at first prenatal visit
Pregnant women ≥25 years: screen if at increased risk
Retest during third trimester if <25 or at risk
Test of cure 4 weeks after treatment for pregnant women
Retest within 3 months after treatment
Public Health Concern
26 million new STI cases in 2018 (nearly half in ages 15-24)
61% of chlamydial infections in young women (2019)
10-15% of untreated STIs (chlamydia/gonorrhea) lead to pelvic inflammatory disease (PID)
PID can cause infertility and chronic pelvic pain
Maternal Harms
Immediate Complications:
Salpingitis (fallopian tube infection) - particularly with gonorrhea in first trimester
Pelvic inflammatory disease (PID) - 10-15% of untreated chlamydia/gonorrhea cases
Chorioamnionitis (infection of fetal membranes)
Postpartum sepsis
Prelabor rupture of membranes
Preterm birth
Long-Term Consequences:
Infertility and sterility (lifelong effects)
Increased risk of ectopic pregnancy (from past chlamydial infections)
Chronic pelvic/abdominal pain
Increased HIV transmission risk - cervical inflammation from chlamydia causes microscopic ulcerations, making HIV acquisition easier
Fetal & Neonatal Harms
In Utero Effects:
Intrauterine growth restriction (IUGR)
Congenital infection (rare with some STIs like HSV, but possible during maternal viremia)
Outcomes vary based on timing of infection and treatment
Neonatal Complications:
Gonorrhea:
Ophthalmia neonatorum (most common manifestation)
Highly contagious eye infection that can lead to blindness if untreated
Neonatal sepsis
Preventive erythromycin eye ointment applied to all newborns at birth
Chlamydia:
Most common infectious cause of ophthalmia neonatorum
>50% of exposed infants develop conjunctivitis or pneumonia
Standard neonatal eye prophylaxis does NOT prevent perinatal chlamydial transmission
Herpes Simplex Virus (HSV):
Neonatal herpes: 1,200-1,500 cases/year in U.S.
~20% mortality rate despite treatment advances
~20% of survivors have long-term neurologic sequelae
Highest risk: primary maternal infection near term
80% of infected infants born to mothers with no known HSV history
Why Timing Matters
The impact depends on:
When infection was acquired (early vs. late pregnancy)
Presence of coinfections with other STIs
When treatment was initiated
How does Chlamydia affect both mother and baby?
-Maternal
Prelabor rupture of membranes
Preterm labor
Postpartum endometritis
-Fetal effects
Low birth weight
How does Gonorrhea affect both mother and baby?
-Maternal
Prelabor rupture of membranes
Miscarriage
Preterm labor
Chorioammionitis
Postpartum endometritis
Postpartum sepsis
-Fetal effects
Preterm birth
Intrauterine growth restriction (IUGR)
How does Herpes simplex virus (HIV) affect both mother and baby?
-Maternal
Intrauterine infection (rare)
-Fetal effects
Congenital infection (rare)
How does Human papillomavirus (HPV) affect both mother and baby?
-Maternal
Dystocia from large lesions
Excessive bleeding from lesions after birth trauma
-Fetal effects
None known
How does Syphilis affect both mother and baby?
-Maternal
Miscarriage
Preterm labor
-Fetal effects
IUGR
Preterm birth
Stillbirth
Congenital infection