Ciguatera Toxicity

Etiology

Consuming ciguatoxin-contaminated seafood is mainly responsible for the manifestations of ciguatera poisoning. Warmer months, eg, May through August in the northern hemisphere, are associated with an increased risk of poisoning, as phytoplanktons proliferate the fastest during these months.[8][9] However, warmer ocean temperatures from climate change and increased water carbon dioxide content favor phytoplankton and algal bloom occurrences throughout the year. Thus, ciguatera poisoning outbreaks can occur even in relatively cooler seasons. Additionally, rising ocean temperatures have expanded ciguatera-affected regions by enabling the growth of ciguatoxin-carrying marine species in previously nonendemic sites.[10] 

Due to bioaccumulation, tropical predator species are most likely to cause ciguatera toxicity. Barracudas, groupers, moray eels, snapper, and amberjacks are commonly implicated. However, ciguatera contamination has also been reported in over 400 reef fish species. Any part of the fish can contain the toxin, and concentrations of 0.1 parts per billion in the fish's flesh is enough to cause illness.[11] Ciguatoxin is tasteless, odorless, lipid-soluble, and heat-resistant. Therefore, the poison can evade the senses and cannot be easily destroyed by cooking contaminated food. People who consume seafood may not know if they have ingested the toxin unless they can connect the incident to publicly reported toxic algal blooms.[12]

Epidemiology

Ciguatera toxicity is the most common worldwide nonbacterial fish poisoning, with up to 50,000 to 500,000 cases occurring globally annually. This number is likely underreported, as most physicians are probably unaware that ciguatera poisoning is reportable. People's exposure risk may increase when highly contaminated fish visceral tissues are consumed.[13] Fortunately, the mortality rate of this condition is low at less than 1%.[14] However, symptoms typically last for weeks to months and sometimes years.[15]

Ciguatera poisoning is endemic to the South Pacific and Caribbean, though ciguatoxin contamination of marine species has also been detected in the Indian Ocean. Ciguatoxin has numerous types, but the most common are Pacific and Caribbean ciguatoxin-1. Pacific ciguatoxin-1 is 10 times more toxic than Caribbean ciguatoxin-1.

Pathophysiology

Ciguatoxin is a potent sodium channel poison in mammals. The toxin causes sustained sodium channel activation and blocks potassium channels. These actions combined lead to membrane depolarization and spontaneous, repetitive action potential firing (see Image. Sites and Modes of Action of Ciguatoxins).

Increased sodium influx damages excitable cells, particularly the neurons and cardiac myocytes. Swelling of the axons, nerve terminals, and perisynaptic Schwann cells occurs in the neurons. Meanwhile, in the cardiac myocytes, animal studies demonstrate that sodium channel-mediated ciguatoxin action influences cardiac contractility. Moderate ciguatoxin concentrations have indirect and direct positive inotropic actions, while high toxin levels produce negative inotropic effects.[16]

Ciguatoxin’s activation of calcium as a secondary messenger contributes to the cardiovascular, musculoskeletal, and gastrointestinal manifestations of the illness. Intracellular calcium increases due to inositol triphosphate-mediated stored calcium release, terminal calcium channel activation, and sodium-calcium exchanger stimulation. Consequently, spontaneous and tetanic contractions occur in the heart, skeletal, and smooth muscles. Intestinal smooth muscle contraction disturbances lead to intestinal fluid stimulation and diarrhea without mucosal injury. Synaptic vesicle recycling is also impaired, exhausting neurotransmitter reserves.

The toxin causes pruritus owing to deranged low-frequency discharge in C-polymodal nociceptive fibers (cutaneous afferent unmyelinated fibers), which are not normally active in undamaged skin at normal temperatures.[17] Cold allodynia or cold temperature inversion is due to increased nerve depolarization of type Aδ and C fibers.

Toxicokinetics

Ciguatoxin toxicokinetics have not been extensively studied. However, Pacific ciguatoxin-1 was investigated in a rat model. The peak serum concentration after oral ingestion was achieved after 2 hours. The half-life after oral ingestion was calculated to be 82 hours. Ciguatoxin activity remained in the liver, muscle, and brain 96 hours after intraperitoneal and oral dosing. Elimination was primarily fecal, with a small fraction cleared by the renal route.[18]

History and Physical

Ciguetera poisoning is a clinical diagnosis. A thorough history and physical examination are crucial to diagnostic accuracy and timeliness. No laboratory or radiologic studies are available to aid in diagnosis. The clinical symptoms of this condition include gastrointestinal and neurological effects that may start within 1 hour or upwards of 1 to 2 days after consuming contaminated fish.

Diarrhea is the most commonly reported symptom. However, patients may also present with other signs of gastrointestinal involvement, like abdominal pain, nausea, vomiting, gastric upset, and belching. Symptom onset is highly variable and may occur in as short as 30 minutes to 1 hour after ingestion or be delayed until 48 hours. About 90% of cases occur within 12 hours. Diarrhea lasts about 5 days on average.

Mouth, hand, and foot paresthesias are the predominant neurological manifestations of ciguatera poisoning. Other neurological symptoms include headache, ataxia, dizziness or vertigo, seizures, perioral paresthesia, numbness, metallic taste in the mouth, blurred vision, ataxia, pruritus, meningismus, tremors, and hallucinations. Severe ciguatera toxicity may present with cold allodynia or a burning sensation on contact with a cold object. Cold allodynia has other possible causes but is essentially pathognomonic of substance poisoning in the right setting.[19]

Dermatologic effects that have been reported are pruritus, urticaria, and bullous or desquamating skin effects.[20][21][22] Pruritus is present in 50-65% of cases and may be severe.[23] Pruritus may also be aggravated by ethanol use.[24]

Cardiovascular effects are rare but may include bradycardia, hypotension, and ectopic beats.[25][26][27] Patients must be asked about palpitations, positional dizziness, dyspnea, and lightheadedness, as the toxin can cause bradycardia and ventricular arrhythmia. However, cardiac symptoms are typically only present in the early stages of the toxicity and improve with time.[28]

Sexual and obstetrical complications include reports of dyspareunia in a female patient following sexual intercourse with a person known to have ciguatera toxicity. This occurrence suggests that the toxin may be transmitted through semen.[29] Ciguatoxin is not known to be teratogenic. However, the poison has been shown to cross the placental barrier and cause abnormal fetal movements.[30] Ciguatoxin thus increases the risk of preterm labor and spontaneous abortions.[27] Lastly, affected mothers have reported diarrhea and facial rashes in their breastfeeding infants.[31]

Musculoskeletal manifestations of ciguatera poisoning include myalgias and arthralgias. Dysuria, hypersalivation, and sleep disturbances may also be reported.

Most patients with ciguatera symptoms recover after a few days to weeks. However, some individuals may remain symptomatic for years. Alcohol consumption during toxin ingestion has been found to increase the risk of developing bradycardia, hypotension, and altered skin sensation. Relapses may be triggered by consuming alcohol, nuts, seeds, fish, chicken, and eggs.[32]

The patient's travel and social history and dietary patterns must be elicited during history taking. A detailed physical examination must be performed for every patient. Particular attention should be given to the exam's gastrointestinal, cardiac, neuromuscular, and dermatologic segments. Pelvic examination may be performed in individuals reporting urogenital symptoms.

Evaluation

Multiple tests can detect ciguatoxin, such as liquid chromatography-mass spectrometry, cytotoxicity assays, and receptor-binding immunoassays.[33][34] However, these tests are used more in an academic or research setting and are typically not clinically available. Additionally, these tests take days to yield results and are thus inappropriate for emergency department visits.

Routine diagnostic tests are often nonspecific. However, some tests are useful for monitoring ciguatoxin effects in the body. For example, metabolic panels may help determine fluid and electrolyte imbalances due to abdominal symptoms. Fecalysis may not show pathologic organisms. An electrocardiogram can help look for arrhythmia in patients with cardiovascular symptoms. Imaging tests can help rule out neurologic lesions if lateralizing neurologic signs are present on physical examination. The clinical presentation must guide the choice of diagnostic exams.

Treatment / Management

The treatment of ciguatera poisoning is primarily supportive, as the toxin does not have a specific antidote. Nausea and vomiting should be treated with ondansetron or another antiemetic. Antidiarrheals may also be considered to treat diarrhea. Dehydration can occur due to vomiting and diarrhea. Thus, patients should be treated with oral fluids or, if unable to take fluids by mouth, intravenous fluids.

Antihistamines and amitriptyline may be considered for pruritus. Cold showers may also temporarily relieve skin burning and pruritus. Non-steroidal anti-inflammatory medications can relieve musculoskeletal pain. Evidence suggests that gabapentin and amitriptyline may also help treat neuropathies associated with ciguatera poisoning.[35][36] Seizures should be treated with benzodiazepines. For refractory seizures, barbiturates or propofol may be considered.(B3)

Neuropathic symptoms may be exacerbated by alcohol or vigorous exercise. Therefore, patients should be advised to avoid alcohol and vigorous physical activities for at least several months.[30] Others that patients must avoid include fresh or preserved fish, fish sauces, shellfish and shellfish products, nuts, and nut oils. Symptomatic bradycardia is treated with intravenous atropine.[37] Direct α-adrenergic agonists like phenylephrine may be given for orthostasis. (B3)

If the patient presents before the onset of nausea and vomiting, activated charcoal may be used in the first few hours of ingestion to prevent further intestinal ciguatoxin absorption.[38] However, aspiration and pneumonitis are possible risks if vomiting starts after activated charcoal administration. (B3)

Intravenous mannitol is a controversial treatment. Mannitol is an osmotic diuretic that can, in theory, reduce neuronal edema and abnormal action potentials. Anecdotal evidence suggests that this agent can decrease neuropathic symptoms or prevent the onset of neurologic symptoms. However, a double-blinded trial demonstrated that intravenous mannitol offers no added benefit to patients with ciguatera toxicity compared to normal saline.[39] Meanwhile, some physicians advocate for the treatment, suggesting that mannitol's benefits outweigh the potential for harm and thus must be considered in acute ciguatera poisoning management.[40] (B3)

Differential Diagnosis

Diagnosing ciguatera poisoning is often difficult due to the symptoms' nonspecificity, relative rarity in non-coastal locations, clinicians' lack of familiarity with the illness, and absence of ciguatera-specific diagnostic tests. However, some of the conditions that resemble ciguatera poisoning include the following:

• Shellfish poisoning, which has the amnesic (domoic acid), diarrheic (okadaic acid), neurotoxic (brevetoxin), and paralytic (saxitoxin) forms and is also related to algal blooms
• Scombroid poisoning
• Common enteroviruses
• Organophosphate toxicity
• Botulism
• Multiple sclerosis
• Guillain-Barre syndrome
• Acute gastroenteritis from other sources like Salmonella, Escherichia coli, Entamoeba histolytica

A careful collection of history and physical examination findings are key to diagnosis. Laboratory exams may help rule out other causes.

Prognosis

Ciguatera toxicity is generally self-limiting, with symptoms typically lasting for a few days. However, a prolonged symptomatology duration is possible, with some patients experiencing symptoms for months to years. Predisposing factors to a lengthy illness course are currently unknown. However, patients should be counseled to avoid fish, caffeine, alcohol, and nuts within 6 months of poisoning, as these foods and beverages can trigger symptom recurrences. Mortality has only been reported in 1% of patients who have ciguatera toxicity.

Complications

Besides the previously described organ-specific manifestations, untreated ciguatera poisoning may cause dehydration, weakness, palpitations, temperature sensitivity, and psychological disturbances. Some individuals may experience symptom recurrence months or even years after the initial toxin exposure. Fatalities are very rare but have been reported. The prognosis of this condition is overall very good.