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Author: Aaron Laskey, MD, Staff Physician, Department of Emergency Medicine, New York University

Aaron Laskey is a member of the following medical societies: American Academy of Emergency Medicine

Coauthor(s): Ugo Anthony Ezenkwele, MD, MPH, Assistant Professor, Assistant Professor of Emergency Medicine, Department of Emergency Medicine, New York University School of Medicine/Bellevue Hospital Center; Eric L Weiss, MD, DTM&H, Director of Stanford Travel Medicine, Medical Director of Stanford Lifeflight, Assistant Professor, Departments of Emergency Medicine and Infectious Diseases, Stanford University School of Medicine

Editors: Mark Louden, MD, FACEP, Assistant Medical Director, Emergency Department, Duke Raleigh Hospital; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Jon Mark Hirshon, MD, MPH, Associate Professor, Department of Emergency Medicine, University of Maryland School of Medicine; John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center; Jonathan Adler, MD, Attending Physician, Department of Emergency Medicine, Massachusetts General Hospital; Division of Emergency Medicine, Harvard Medical School

Author and Editor Disclosure

Synonyms and related keywords: Ascaris lumbricoides, A lumbricoides, roundworm, intestinal roundworm, human parasite, nematode infection, ascariasis, malnutrition, iron-deficiency anemia, bowel obstruction, Ascaris suum, eosinophilic pneumonia, Löffler syndrome

Background

Intestinal nematode infections affect one fourth to one third of the world's population. Of these, the intestinal roundworm Ascaris lumbricoides is the most common. While the vast majority of these cases are asymptomatic, infected persons may present with pulmonary or gastrointestinal complaints. Ascariasis predominates in areas of poor sanitation and is associated with malnutrition, iron-deficiency anemia, and impairments of growth and cognition.

Pathophysiology

A lumbricoides is the largest of the intestinal nematodes affecting humans, measuring 15-35 cm in length. Infection begins with the ingestion of embryonated (infective) eggs in feces-contaminated soil. Once ingested, eggs hatch, releasing small larvae that penetrate the intestinal wall. Larvae migrate to the pulmonary bed via the portal veins, during which time they may cause pulmonary symptoms (eg, cough, wheezing). After migrating up the respiratory tract and being swallowed, they mature, copulate, and lay eggs in the intestines. Adult worms may live in the gut for 6-24 months, where they can cause partial or complete bowel obstruction in large numbers, or they can migrate into the appendix, hepatobiliary system, or pancreatic ducts. From egg ingestion to new egg passage takes approximately 9 weeks, with an additional 3 weeks needed for egg molting before they are capable of infecting a new host.

Frequency

United States

In the United States, approximately 4 million people are believed to be infected. High-risk groups include international travelers, recent immigrants (especially from Latin America and Asia), refugees, and international adoptees. Ascariasis is indigenous to the rural southeast, where cross-infection by pigs with the nematode Ascaris suum is thought to occur.

International

Worldwide, 1.4 billion people are infected with A lumbricoides, with prevalence among developing countries as low as 4% in Mafia Island, Zanzibar, to as high as 90% in some areas of Indonesia. Local practices (eg, termite mound–eating in Kenya) may predispose to ascariasis in some populations.

Mortality/Morbidity

The rate of complications secondary to ascariasis ranges from 11-67%, with intestinal and biliary tract obstruction representing the most common serious sequelae. Although infection with A lumbricoides is rarely fatal, it is responsible for an estimated 8,000-100,000 deaths annually, mainly in children.

Race

No racial predilection is known. A genetic predisposition has been described in a study of families from Nepal.

Sex

Male children are thought to be infected more frequently, owing to a greater propensity to eat soil.

Age

Children, because of their habits (eg, directly or indirectly consuming soil), are more commonly and more heavily infected than adults. Neonates may be infected by transplacental infection.



History

Most patients are asymptomatic. When symptoms occur, they are divided in 2 categories: early (larval migration) and late (mechanical effects).

  • In the early phase (4-16 d after egg ingestion), respiratory symptoms result from the migration of larvae through the lungs. Classically, these symptoms occur in the setting of eosinophilic pneumonia (Löffler syndrome).
    • Fever
    • Nonproductive cough
    • Dyspnea
    • Wheezing
  • In the late phase (6-8 wk after egg ingestion), gastrointestinal symptoms occur.
    • Passage of worms (from mouth, nares, anus)
    • Diffuse or epigastric abdominal pain
    • Nausea, vomiting

Physical

  • General
    • Fever
    • Jaundice (in biliary obstruction)
    • Cachexia (due to malnutrition)
    • Mental retardation
  • Pulmonary
    • Wheezing
    • Rales
    • Diminished breath sounds
  • Abdominal
    • Abdominal tenderness, which may be diffuse (in obstructive infections), or localized to the right lower (appendicitis) or right upper quadrant (hepatobiliary infections)
    • Peritoneal signs in cases of bowel perforation
  • Migrating larvae may transmit other organisms, causing bacterial pneumonia. Rare cases of airway obstruction have also been reported. Other much less common presentations include lacrimal drainage obstruction, acute interstitial nephritis, and encephalopathy.

Causes

Symptoms are typically associated with early larval migration, heavy intestinal burdens of adult worms, or aberrant worm migration. Worm migration may be stimulated by anesthetic agents or subtherapeutic anthelmintic treatment or by use of certain anthelmintics (eg, pyrantel pamoate).



Appendicitis, Acute
Asthma
Cholangitis
Cholecystitis and Biliary Colic
Hookworm
Obstruction, Large Bowel
Obstruction, Small Bowel
Pancreatitis
Strongyloides Stercoralis

Other Problems to be Considered

Hepatic abscess
Tropical pulmonary eosinophilia
Visceral larva migrans



Lab Studies

  • Early infection (larval migration)
    • Complete blood count (CBC) may show eosinophilia.
    • Sputum analysis may reveal larvae or Charcot-Leyden crystals.
    • Stool examination findings are typically normal in absence of previous infection.
  • Established infection (adult phase): Stool examination findings include characteristic eggs. Adult females lay about 200,000 eggs per day, aiding microscopic identification of characteristic eggs.

Imaging Studies

  • Early infection (larval migration): Chest radiography may reveal patchy infiltrates of eosinophilic pneumonia.
  • Established infection (adult phase)
    • Abdominal radiography may reveal adult worms (especially with contrast).
    • Obstructing Ascaris lesions cause cylindrical filling defects on contrast computed tomography (CT) scans.
    • Cholangiopancreatography by endoscopy (ERCP) or magnetic resonance imaging (MRCP, or magnetic resonance cholangiopancreatography) may detect adult worms in bile or pancreatic ducts.
    • Ultrasonography may detect worms in gallbladder.



Emergency Department Care

  • Early infection (larval migration)
    • Inhaled beta-agonists may be indicated.
    • Steroids for pulmonary symptoms are controversial.
    • Whether anthelmintic therapy is effective against larval stages is unclear.
  • Established infection (adult phase)
    • Benzimidazoles are the mainstay of treatment of symptomatic and asymptomatic infections. They are poorly systemically absorbed and exert their action directly on worms.
    • Treatment of bowel obstruction includes intravenous hydration, nasogastric suctioning, electrolyte monitoring, and laparotomy if conservative measures fail.
    • Piperazine citrate, a helminth paralytic, has been suggested in cases of obstruction; however, it is no longer commercially available in the United States.
    • Hepatobiliary ascariasis typically responds to similarly conservative therapy, but it may require invasive intervention (eg, ERCP).

Consultations

Bowel or hepatobiliary obstruction may require surgical or gastroenterologic consultation.



Benzimidazoles are effective for the treatment of intestinal ascariasis, although some authors recommend against their use in the first year of life due to their teratogenic effects in animal studies. The most commonly recommended agents are albendazole and mebendazole. Ivermectin and pyrantel pamoate are alternatives, the latter having been suggested for pregnant patients in whom benzimidazoles are contraindicated. A new anthelmintic agent from China, tribendimidine, has recently been show to be as efficacious as albendazole.

Drug Category: Anthelmintics

Parasite biochemical pathways are sufficiently different from the human host to allow selective interference by chemotherapeutic agents in relatively small doses.

Drug NameAlbendazole (Albenza)
DescriptionDecreases ATP production in worm, causing energy depletion, immobilization, and finally death.
Adult Dose400 mg/d PO single dose; repeat in 3 wk if not cured
Pediatric Dose<2 years: 200 mg/d PO single dose; repeat in 3 wk if not cured
>2 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsCoadministration with carbamazepine may decrease efficacy; dexamethasone and praziquantel may increase toxicity
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsDiscontinue use if LFT values increase significantly (resume when levels decrease to pretest values); GI symptoms (nausea, vomiting, diarrhea) or CNS symptoms (dizziness, headache, meningeal signs) may occur; granulocytopenia, thrombocytopenia, and pancytopenia have been reported

Drug NameMebendazole (Vermox)
DescriptionCauses worm death by selectively and irreversibly blocking uptake of glucose and other nutrients in susceptible adult intestine where helminths dwell.
Adult Dose100 mg PO bid on 3 consecutive days
Administer second course if not cured within 3-4 wk
Pediatric Dose<2 years: Not established
>2 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsCarbamazepine and phenytoin may decrease effects
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsAdjust dose in hepatic impairment; GI symptoms (nausea, vomiting, abdominal pain, diarrhea) and CNS symptoms (headache, dizziness) are common; alopecia may be associated with high doses; rare reactions include angioedema, seizures, and agranulocytosis

Drug NamePiperazine citrate
DescriptionRecommend for GI or biliary obstruction secondary to ascariasis; causes flaccid paralysis of the helminth by blocking response to worm muscle to acetylcholine.
Adult Dose3.5 g PO qd for 2 d
Pediatric Dose75 mg/kg PO qd for 2 d; not to exceed 3.5 g/dose
ContraindicationsDocumented hypersensitivity
InteractionsCoadministration with chlorpromazine may increase toxicity
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsMost commonly reported reactions include GI and CNS effects; discontinue therapy if effects become significant; prolonged, repeated, or excessive therapy should be avoided because of potential neurotoxicity

Drug NamePyrantel pamoate (Antiminth)
DescriptionDepolarizing neuromuscular blocking agent; inhibits cholinesterases, resulting in spastic paralysis of worm.
Adult Dose11 mg/kg/dose PO as single dose; not to exceed 1 g
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity; hepatic disease
InteractionsPyrantel and piperazine are mutually antagonistic and should not be used concomitantly
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsCaution in liver impairment, anemia, and malnutrition; GI effects, headache, insomnia, rash, tenesmus, and elevated LFT values may occur

Drug NameIvermectin (Stromectol)
DescriptionBinds selectively with glutamate-gated chloride ion channels in invertebrate nerve and muscle cells, causing cell death.
Adult Dose150-200 mcg/kg PO once
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsNone reported
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsSerious reactions include Stevens-Johnson syndrome, asthma exacerbation, and vision loss (rare); common reactions include pruritus, rash, headache, myalgias, and elevated LFT values

Drug NameLevamisole (Ergamisol)
DescriptionMay inhibit worm copulation via agonism of L-subtype nicotinic acetylcholine receptors in male nematode muscles.
Adult Dose2.5 mg/kg PO once
Pediatric DoseAdminister as in adults
ContraindicationsDocumented hypersensitivity
InteractionsIncreases toxicity and serum levels of phenytoin; causes disulfiram reactions when taken with alcohol
PregnancyC - Safety for use during pregnancy has not been established.
PrecautionsAgranulocytosis can occur asymptomatically



Further Inpatient Care

  • Further inpatient care is warranted for patients with complications due to worm migration.

Further Outpatient Care

  • Primary care follow up is suggested to confirm cure.
  • Presumptive administration of albendazole to all immigrants at risk for parasitosis has been suggested and shown to save lives and money. However, current recommendations do not include its implementation.

Deterrence/Prevention

  • Screening programs for the carrier state may assist in eradication in endemic areas.
  • Given the association with poverty and malnutrition, long-term control will require sustained economic growth in developing countries.

Complications

  • Complications are typically due to worm migration.

Prognosis

  • The prognosis is excellent.

Patient Education

  • Recommend good personal hygiene and food handling techniques: discriminate defecation, hand-washing, cleaning fruits and vegetables, and avoiding soil consumption.



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Ascaris Lumbricoides excerpt

Article Last Updated: Feb 14, 2007