A 32-year-old multigravida at 36 weeks gestation presents wi… | 마이메르시 MyMerci
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Maternal Newborn Health
문제

A 32-year-old multigravida at 36 weeks gestation presents with complaints of severe headache, blurred vision, and right upper quadrant pain. Her blood pressure is 172/114 mmHg, and she has 4+ proteinuria. Which assessment finding would be most indicative of impending eclampsia?

해설
Hyperreflexia with clonus is the key neurological sign of impending eclampsia in severe preeclampsia, necessitating urgent intervention. Other options are less specific indicators of progression.
같은 주제 다음 문제A 28-year-old primigravida at 34 weeks gestation presents to the labor and delivery unit w…

심화 해설

Clinical Reasoning and Pathophysiology
The scenario describes a patient at 36 weeks gestation with severe hypertension (172/114 mmHg), 4+ proteinuria, severe headache, blurred vision, and right upper quadrant pain. This clinical picture is consistent with severe preeclampsia, a multisystem disorder characterized by new-onset hypertension and proteinuria (or other end-organ dysfunction) after 20 weeks of gestation [2][3]. The underlying pathophysiology involves a reduction in utero-placental perfusion leading to placental ischemia and an angiogenic imbalance, which triggers widespread maternal endothelial dysfunction [2][3]. This endothelial damage results in vasospasm, increased capillary permeability, and reduced perfusion to organs such as the brain, liver, and kidneys. The question asks for the finding most indicative of impending eclampsia, which is the onset of grand mal seizure activity in a patient with preeclampsia [1].

Analysis of Assessment Findings
The central nervous system manifestations of severe preeclampsia are the most reliable harbingers of seizure activity. Cerebral vasospasm and edema increase neuronal irritability, which manifests clinically as hyperreflexia. When this neuromuscular irritability becomes severe, it progresses to sustained, rhythmic muscle contractions upon sudden stretching of a tendon, known as clonus. The presence of hyperreflexia with clonus indicates a highly excitable central nervous system and is a direct precursor to generalized tonic-clonic seizures [1]. While the other options represent signs of severe disease and organ dysfunction, they are not as immediately predictive of a seizure as CNS hyperexcitability. Decreased urine output (400 mL in 24 hours) reflects renal involvement and oliguric injury. Facial edema and weight gain indicate fluid retention from capillary leak and hypoalbuminemia. A blood pressure of 160/100 mmHg on two occasions confirms the diagnosis of severe preeclampsia, but it is the neurological status that directly signals the imminent risk of eclampsia [2][3].
References (research sources)
  • [1]
    Diagnosis and Treatment of Eclampsia.Research articleKatsi V, Svigkou A, Dima I, Tsioufis K. (2024) · DOI: 10.3390/jcdd11090257
  • [2]
    Preeclampsia and Related Problems.Research articleNarkhede AM, Karnad DR. (2021) · DOI: 10.5005/jp-journals-10071-24032
  • [3]
    Preeclampsia: Narrative review for clinical use.Research articleVigil-De Gracia P, Vargas C, Sánchez J, Collantes-Cubas J. (2023) · DOI: 10.1016/j.heliyon.2023.e14187

임상 시나리오

Clinical Practice Guide: Monitoring for Impending Eclampsia

In a patient with severe preeclampsia, the neurological examination is paramount for detecting the transition to eclampsia. The presence of hyperreflexia with sustained clonus is a critical, direct indicator of central nervous system irritability and a reliable precursor to generalized tonic-clonic seizures. This finding should trigger immediate seizure prophylaxis, typically with intravenous magnesium sulfate, and preparation for urgent delivery. While oliguria, facial edema, and severe-range blood pressures confirm the severity of the disease and indicate end-organ damage, they do not carry the same immediate predictive value for an impending seizure as clonus. Continuous, focused assessment of deep tendon reflexes and clonus must be performed hourly in patients on magnesium sulfate to monitor for both therapeutic effect and toxicity.

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