What is the initial workup and management for a patient presenting with nausea and vomiting?

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Initial Workup and Management of Nausea and Vomiting

Immediate Assessment and Risk Stratification

Begin by determining if this is acute (≤7 days) or chronic (≥4 weeks) presentation, as this fundamentally changes your diagnostic and therapeutic approach. 1, 2

Key Historical Elements to Obtain

  • Timing and duration: Acute onset suggests gastroenteritis, food poisoning, medication effect, or acute migraine; chronic suggests gastroparesis, functional disorders, or malignancy 3, 2
  • Medication review: Recent initiation of opioids, chemotherapy, antibiotics, or antifungals is a common culprit 4, 3
  • Associated symptoms requiring urgent evaluation: Severe headache (CNS pathology), acute abdominal pain (surgical abdomen), fever with altered mental status (infection/sepsis), or signs of dehydration 3, 2
  • Metabolic red flags: Check for constipation, hypercalcemia, uremia, diabetic ketoacidosis, or electrolyte disturbances 4, 3
  • Pregnancy status in women of childbearing age 3, 2

Physical Examination Priorities

  • Hydration status: Assess mucous membranes, skin turgor, orthostatic vital signs, and mental status to determine need for IV fluids 5
  • Abdominal examination: Look for peritoneal signs, distension, or masses suggesting obstruction or surgical pathology 3
  • Neurologic examination: If headache or altered mental status present, evaluate for increased intracranial pressure or meningismus 3

Initial Laboratory and Imaging Workup

For Acute Nausea/Vomiting Without Alarm Features

  • Minimal testing needed: Urine pregnancy test in women of childbearing age 3
  • Consider basic metabolic panel only if: Severe or prolonged symptoms, concern for dehydration, or suspicion of metabolic cause 3

For Acute Nausea/Vomiting With Alarm Features or Moderate-Severe Symptoms

  • Complete metabolic panel: To assess electrolytes, renal function, glucose, and calcium 3
  • Complete blood count: To evaluate for infection or anemia 3
  • Urinalysis: To assess for urinary tract infection or ketones 3
  • Lipase/amylase: If epigastric pain suggests pancreatitis 3
  • Thyroid-stimulating hormone: If chronic symptoms or other signs of thyroid disease 3
  • Abdominal imaging: Plain radiographs for suspected obstruction; CT abdomen if acute abdomen or unclear diagnosis 3
  • Head CT: If severe headache, altered mental status, or focal neurologic signs suggest intracranial pathology 3

For Chronic Nausea/Vomiting (≥4 weeks)

  • Esophagogastroduodenoscopy (EGD): First-line test if alarm symptoms (weight loss, dysphagia, age >50 with new onset) or risk factors for gastric malignancy 3
  • Gastric emptying study: If gastroparesis suspected (early satiety, postprandial fullness, diabetes) 3
  • Consider: Small bowel imaging, metabolic workup, and psychiatric evaluation if initial testing unrevealing 3, 6

Pharmacologic Management

For Acute Vomiting (First-Line)

Ondansetron (5-HT3 antagonist) is the preferred initial agent, with sublingual formulation (4-8 mg every 8-12 hours) potentially improving absorption in actively vomiting patients. 5, 7

For Acute Vomiting (Alternative or Adjunctive Agents)

If ondansetron fails or is contraindicated, use dopamine antagonists on a fixed schedule rather than as-needed 8:

  • Metoclopramide 10-20 mg PO/IV every 6 hours 8, 9
  • Prochlorperazine 5-10 mg PO/IV every 6 hours or 25 mg rectal suppository 5, 8, 9
  • Promethazine 12.5-25 mg PO/IV/rectal every 4-6 hours 5, 10

For Refractory or Intractable Vomiting

Immediately start a dopamine receptor antagonist on a fixed schedule (not as-needed) to maintain constant therapeutic levels, prioritizing metoclopramide 10-20 mg every 6 hours or haloperidol 0.5-2 mg every 4-6 hours. 8

If symptoms persist after 24-48 hours, escalate therapy by:

  • Adding a 5-HT3 antagonist: Ondansetron 4-8 mg every 8-12 hours or granisetron 1-2 mg daily 8
  • Adding corticosteroids: Dexamethasone 4-8 mg daily to potentiate antiemetic effect 4, 8
  • Adding benzodiazepine for anxiety component: Lorazepam 0.5-1 mg IV/PO every 4-6 hours 5, 8

For truly refractory cases:

  • Olanzapine 2.5-5 mg PO daily for persistent vomiting, especially effective in bowel obstruction 4, 8
  • Cannabinoids: Dronabinol 2.5-7.5 mg every 4 hours as last resort 4, 8
  • Haloperidol 0.5-2 mg IV with monitoring for QT prolongation 5

Important Medication Caveats

  • Start with reduced doses in elderly or debilitated patients (e.g., olanzapine 2.5 mg, not 5 mg) 8
  • Monitor for extrapyramidal symptoms with metoclopramide and prochlorperazine; have diphenhydramine 50 mg available for dystonic reactions 8
  • Avoid metoclopramide in suspected bowel obstruction 4
  • Use fixed scheduling for persistent symptoms, not as-needed dosing 8

Fluid and Electrolyte Management

For Mild Dehydration or Tolerating Oral Intake

Oral rehydration with small, frequent sips of electrolyte-rich fluids (sports drinks) is preferred. 5

For Moderate-Severe Dehydration or Unable to Tolerate Oral Intake

Initiate IV fluid therapy with balanced crystalloid solutions (lactated Ringer's preferred over normal saline to avoid hyperchloremic acidosis), starting with 500-1000 mL bolus followed by maintenance rate. 5

  • Add dextrose-containing fluids if prolonged fasting, concern for hypoglycemia, or cyclic vomiting syndrome 5

Special Clinical Scenarios

Opioid-Induced Nausea/Vomiting

  • Prophylactic antiemetics highly recommended if prior history of opioid-induced nausea 4
  • First assess and treat constipation, as this is often the underlying cause 4
  • Use phenothiazines (prochlorperazine) or dopamine antagonists (metoclopramide, haloperidol) as first-line 4
  • Add 5-HT3 antagonists (ondansetron, granisetron) if nausea persists, as they have lower CNS side effects 4
  • Consider opioid rotation if nausea persists beyond one week despite treatment 4

Chemotherapy-Induced Nausea/Vomiting

  • Combine 5-HT3 antagonist + corticosteroid for moderate-high emetogenic chemotherapy 4
  • Add aprepitant (neurokinin-1 antagonist) 125 mg day 1, then 80 mg days 2-3 for highly emetogenic regimens 4
  • For delayed emesis: Continue corticosteroids twice daily for several days after chemotherapy 4

Cyclic Vomiting Syndrome

Use an abortive cocktail of sumatriptan (nasal spray or subcutaneous) + ondansetron + benzodiazepine, with sedation using promethazine or lorazepam in a quiet, dark environment. 5

  • IV dextrose-containing fluids are essential in this population 5

Anticipatory Nausea/Vomiting

Lorazepam or similar benzodiazepines combined with behavioral techniques are most effective. 4

Reassessment and Follow-Up

  • Reevaluate within 24-48 hours after initiating treatment to assess symptom control 8
  • If nausea persists beyond one week, reassess for underlying causes including CNS pathology, hypercalcemia, bowel obstruction, or medication effects 4
  • Before next chemotherapy cycle (if applicable), modify antiemetic regimen that failed to provide adequate protection 8

References

Research

A Practical 5-Step Approach to Nausea and Vomiting.

Mayo Clinic proceedings, 2022

Research

Evaluation of nausea and vomiting: a case-based approach.

American family physician, 2013

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Acute Vomiting

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Nausea and vomiting in adults--a diagnostic approach.

Australian family physician, 2007

Guideline

Management of Intractable Vomiting

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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