94 Preterm premature rupture of membranes
Pathophysiology
When membranes rupture before the onset of labor it is called premature rupture of membranes (PROM). Preterm premature rupture of membranes (PPROM) is the leakage of amniotic fluid before term (38-41 wk gestation). From early in pregnancy, the slightly alkaline (pH 7.0-7.5) amniotic fluid is produced within the amniotic sac. As pregnancy advances, fetal urine significantly contributes to the volume. Fetal breathing and swallowing reabsorb the amniotic fluid, which is formed, absorbed, and replaced within a 4-hr period. Amniotic fluid volume at term is approximately 500-1500 mL. It provides an environment that protects the fetus from trauma and injury, provides even distribution of temperature, contains an antibacterial substance, and enables the fetus to move and develop without pressure. It also plays a major role in fetal development of the lungs and kidneys. Although the cause of PPROM is unknown, it is considered the cause of one-third of the preterm births before 36 wk gestation (Jorgensen, 2008; Weitz, 2001). Risk for a preterm birth is high. The majority of patients with PPROM deliver from within 24 hr to 2 wk of onset.
Assessment
Complications—fetal:
Diagnostic tests
Blood Rh factor and antibody screen:
Nursing diagnosis:
Risk for infection
related to bacterial spread (often from upward movement of vaginal bacteria)
ASSESSMENT/INTERVENTIONS | RATIONALES |
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Assist health care provider with sterile speculum examination, collection of amniotic fluid, Nitrazine paper test, and observation of ferning by microscope. | These assessments are able to confirm the diagnosis of PPROM. |
Assist with collecting specimens from amniocentesis or vaginal secretions for laboratory culture. | Group B streptococcus, Chlamydia trachomatis, gonorrhea, bacterial vaginosis, or trichomoniasis organisms are common causes of maternal vaginal tract infections and chorioamnionitis. |
After PPROM has been confirmed, begin maternal assessments: monitor maternal vital signs q2-4h; palpate uterus for tenderness; and observe vaginal secretions for color, amount, and odor q8h. | Fever, uterine tenderness, and changes in vaginal discharge are signs of infection. Prompt notification of signs to the health care provider may decrease the risk of further compromise to the fetus or mother. |
Apply external fetal heart rate (FHR) monitor and assess with nonstress test (NST) q8h. | Fetal tachycardia is a sign of infection. A nonreactive NST result is associated with infection. Late decelerations in labor are a sign of a compromised fetus struggling with oxygenation demands during labor. |
Arrange for other tests of fetal well-being (e.g., BPP, amniocentesis for lecithin to sphingomyelin [L/S] ratio, and phosphatidyl glycerol [PG], and ultrasound for AFI). | BPP assesses deviations in growth and development and assesses for subclinical infection. |
Collect serial maternal specimens of blood for complete blood count (CBC) and urine for urinalysis as prescribed by the health care provider (e.g., daily). | White blood cell differential rises with infection. Bacteria is present in the urine if a urinary tract infection (UTI) develops. |
Administer antibiotics as prescribed by the health care provider. | Prophylactic antibiotics prevent or reduce effects of maternal-fetal infections and may reduce morbidity and prolong the pregnancy. |
Instruct and assist patient with good hygiene: frequent hand hygiene, wiping perineum from front to back, and changing the peripad q2h (if a pad is worn). | These practices prevent spread of microorganisms from the environment to the genital area. A moist, warm peripad fosters bacterial growth. |