MOBILE VIEW  | 

BODY STUFFERS

Classification   |    Detailed evidence-based information

Therapeutic Toxic Class

    A) BODY STUFFERS hastily ingest or insert into body orifices illegal drug packets to evade law enforcement officials. Unlike body packers, body stuffers are more likely to ingest or insert into body orifices drugs that are poorly wrapped, and the actual amount ingested or inserted is often difficult to determine.
    B) Please refer to individual managements (e.g., cocaine) for information on poisoning.
    C) Please refer to "COCAINE" management for further information on cocaine.
    D) Please refer to "OPIOIDS/OPIOID ANTAGONIST" management for further information on heroin.
    E) Please refer to "HALLUCINOGENIC AMPHETAMINES" management for further information on ecstasy.
    F) Please refer to "AMPHETAMINES AND RELATED DRUGS" management for further information on amphetamines.
    G) Please refer to "METHAMPHETAMINE" management for further information on methamphetamine.
    H) Please refer to "PLANTS-MARIJUANA" management for further information on marijuana.

Specific Substances

    1) Mini packers

Available Forms Sources

    A) FORMS
    1) Body stuffers may ingest drugs or insert them into body orifices (eg; rectum and/or vagina) unwrapped or wrapped in plastic bags, balloons, cellophane paper, aluminium foil, glass crack vials, or condoms (Kashani & Ruha, 2004; Fineschi et al, 2002; June et al, 2000; Sporer & Firestone, 1997).

Life Support

    A) This overview assumes that basic life support measures have been instituted.

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) This management will discuss the evaluation and decontamination of body stuffers. Please refer to the individual managements for detailed information regarding the clinical presentation, laboratory evaluation, and treatment of specific drug exposures (e.g. heroin, cocaine, etc.).
    B) BACKGROUND: Body stuffing occurs when dealers or users of illegal substances swallow drugs in an attempt to evade police detection. Drugs may be stuffed orally (most common), vaginally or rectally. Often, the drug is poorly packaged and dose ingested is higher than doses used recreationally. The most commonly stuffed drugs are cocaine and opioids. Other sympathomimetics and hallucinogens have also been reported.
    C) EPIDEMIOLOGY: Body stuffing is common, but the majority of these patients develop mild toxicity or are asymptomatic.
    D) WITH POISONING/EXPOSURE
    1) TOXICITY
    a) SYMPATHOMIMETICS (PRIMARILY COCAINE): Mild overdose patients often present with mild tachycardia and hypertension. Patients with moderate to severe toxicity will often present with severe tachycardia, hypertension, hyperthermia, and agitation, along with aggression, seizures and cardiac dysrhythmias.
    b) OPIOIDS (PRIMARILY HEROIN): Patients with mild toxicity may present with mild CNS/respiratory depression. In moderate to severe exposures, patients will present with respiratory/CNS depression, hypoxia, hypotension, hypothermia, and respiratory failure.
    c) HALLUCINOGENIC AMPHETAMINES: In general, most cases of MDMA and MDEA toxicity result in mild symptoms that can include fatigue, difficulty concentrating, agitation, hypertension, tachycardia, mydriasis, trismus, and diaphoresis. Occasionally, intense dysphoria (depression, anxiety), confusion, or delirium can occur. Severe overdoses appear to follow a clear pattern of toxicity characterized by hyperthermia, disseminated intravascular coagulation (DIC), rhabdomyolysis, acidosis, hyperkalemia, dysrhythmias, seizures, and acute renal failure. Severe toxicity can develop after typical recreational doses. Ecstasy-associated (MDMA) morbidity and mortality have been related to hyponatremia, dehydration, hyperthermia, hypertensive crisis, and cardiac dysrhythmias.
    d) Patients may also present with signs of an anticholinergic toxidrome (mydriasis, tachycardia, decreased bowel sounds, and dry/flushed skin) as these agents are often ingested to delay the passage of packets.

Laboratory Monitoring

    A) No specific studies are required for most asymptomatic patients. Urine drug screens may confirm exposure but cannot distinguish recreational use from drug absorption after stuffing.
    B) In symptomatic patients, institute continuous cardiac monitoring and obtain serial ECGs.
    C) In a patient with signs of toxicity after stuffing a sympathomimetic agent, monitor electrolytes, CBC, CPK, and urinalysis. Obtain a head CT to evaluate for hemorrhage in patients with abnormal mental status.
    D) When opioids are stuffed, monitor electrolytes, glucose, pulse oximetry/capnometry, and chest radiograph (if hypoxic).
    E) Abdominal x rays are rarely helpful in body stuffers.

Treatment Overview

    0.4.2) ORAL/PARENTERAL EXPOSURE
    A) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Asymptomatic patients should be observed in an emergency setting for at least 6 hours. A cardiac monitor should be placed. Activated charcoal can be offered to any patient who presents with normal mental status. Patients with mild tachycardia and hypertension can be treated with benzodiazepines. Treat mild to moderate sympathomimetic exposures with IV fluids and benzodiazepines. For mild to moderate opioid exposures, monitor for respiratory or CNS depression, and administer naloxone if clinically indicated.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Initiate resuscitation for unstable patients. For severe sympathomimetic exposures, patients should be aggressively sedated (large doses of benzodiazepines may be necessary), and if this is not effective, patients should be paralyzed and intubated. If the patient develops signs of sodium channel blockade (eg; QRS widening), administer hypertonic sodium bicarbonate. Severe toxicity from opioid overdose can be effectively reversed with naloxone boluses. Initiate a naloxone infusion if repeated doses are needed, and titrate to reverse respiratory depression but avoid acute withdrawal. If a patient arrives intubated, do not administer naloxone as this may precipitate withdrawal and a difficult airway. Allow the patient to metabolize the opioid while providing excellent symptomatic and supportive care.
    C) DECONTAMINATION
    1) PREHOSPITAL: Activated charcoal adsorbs sympathomimetics and opioids effectively. Activated charcoal can be utilized in any patient who presents early with normal mental status or if the airway is protected.
    2) HOSPITAL: Activated charcoal can be utilized in any patient who presents early with normal mental status or if the airway is protected. Gastric lavage is generally not indicated. Whole bowel irrigation can be utilized, but is usually not necessary for most body stuffers.
    D) AIRWAY MANAGEMENT
    1) Intubate patients not responsive to naloxone or who are seizing, hemodynamically unstable, agitated, or obtunded.
    E) ANTIDOTE
    1) Patients who present with QRS widening or wide complex tachycardia after stuffing cocaine or cocaine containing products, may be treated with sodium bicarbonate (1 to 2 mEq/kg bolus; repeat as needed to maintain arterial pH between 7.45 and 7.55). Monitor acid-base status and serum sodium, as aggressive sodium bicarbonate therapy may cause alkalemia and hypernatremia. Treat seizures with benzodiazepines.
    2) Patients who stuff opioids can be treated with the opioid antagonist naloxone (0.4 mg IV and titrate to effect). A naloxone infusion can be started at 0.4 to 0.8 mg/hour in normal saline or 5% dextrose titrated to clinical effects, or infuse 2/3 the initial dose needed to awaken the patient each hour.
    F) ENHANCED ELIMINATION
    1) The most commonly stuffed drugs are not effectively removed by hemodialysis or hemoperfusion.
    G) PATIENT DISPOSITION
    1) OBSERVATION CRITERIA: Anyone who develops signs of toxicity should be admitted. Imaging is rarely helpful. Although the optimal duration of observation for asymptomatic patients is controversial, the best available data suggest that patients who are asymptomatic, have received activated charcoal and have normal vital signs after 6 hours, are unlikely to deteriorate.
    2) ADMISSION CRITERIA: Any patient who develops clinical symptoms from ingested drug should be admitted to a monitored setting in a hospital. Patients who develop signs of severe toxicity should be admitted to the ICU. Patients can be discharged from the medical facility with complete resolution of symptoms.
    3) CONSULT CRITERIA: Consult a poison center or medical toxicologist for any questions, concerns or cases of moderate to severe toxicity.
    H) PITFALLS
    1) Errors are made when patients with a history of stuffing are not appropriately referred to a healthcare facility for evaluation, or if they are discharged with clinical signs of toxicity or an inadequate duration of observation.
    I) TOXICOKINETICS
    1) Packaging will alter the onset and duration of action of these medications. Patients may have delayed presentation compared to the ingestion of an unpackaged drug.

Range Of Toxicity

    A) TOXICITY: Toxicity is dependent on the agent(s) ingested.
    B) Although the estimated minimum lethal dose of cocaine is 1.2 g, fatalities have been reported after 30 mg of cocaine applied to mucous membranes. Fatalities have been reported after the ingestion of 1 to 3 grams of cocaine in powder form.
    C) Ingestion of a single capsule of MDMA could be lethal.
    D) The lethal dose of opioids varies and depends on purity of the drug and the habituation of the involved individual.

Summary Of Exposure

    A) This management will discuss the evaluation and decontamination of body stuffers. Please refer to the individual managements for detailed information regarding the clinical presentation, laboratory evaluation, and treatment of specific drug exposures (e.g. heroin, cocaine, etc.).
    B) BACKGROUND: Body stuffing occurs when dealers or users of illegal substances swallow drugs in an attempt to evade police detection. Drugs may be stuffed orally (most common), vaginally or rectally. Often, the drug is poorly packaged and dose ingested is higher than doses used recreationally. The most commonly stuffed drugs are cocaine and opioids. Other sympathomimetics and hallucinogens have also been reported.
    C) EPIDEMIOLOGY: Body stuffing is common, but the majority of these patients develop mild toxicity or are asymptomatic.
    D) WITH POISONING/EXPOSURE
    1) TOXICITY
    a) SYMPATHOMIMETICS (PRIMARILY COCAINE): Mild overdose patients often present with mild tachycardia and hypertension. Patients with moderate to severe toxicity will often present with severe tachycardia, hypertension, hyperthermia, and agitation, along with aggression, seizures and cardiac dysrhythmias.
    b) OPIOIDS (PRIMARILY HEROIN): Patients with mild toxicity may present with mild CNS/respiratory depression. In moderate to severe exposures, patients will present with respiratory/CNS depression, hypoxia, hypotension, hypothermia, and respiratory failure.
    c) HALLUCINOGENIC AMPHETAMINES: In general, most cases of MDMA and MDEA toxicity result in mild symptoms that can include fatigue, difficulty concentrating, agitation, hypertension, tachycardia, mydriasis, trismus, and diaphoresis. Occasionally, intense dysphoria (depression, anxiety), confusion, or delirium can occur. Severe overdoses appear to follow a clear pattern of toxicity characterized by hyperthermia, disseminated intravascular coagulation (DIC), rhabdomyolysis, acidosis, hyperkalemia, dysrhythmias, seizures, and acute renal failure. Severe toxicity can develop after typical recreational doses. Ecstasy-associated (MDMA) morbidity and mortality have been related to hyponatremia, dehydration, hyperthermia, hypertensive crisis, and cardiac dysrhythmias.
    d) Patients may also present with signs of an anticholinergic toxidrome (mydriasis, tachycardia, decreased bowel sounds, and dry/flushed skin) as these agents are often ingested to delay the passage of packets.

Cardiovascular

    3.5.2) CLINICAL EFFECTS
    A) CARDIOVASCULAR FINDING
    1) WITH POISONING/EXPOSURE
    a) In one retrospective study of 98 cases of crack cocaine body stuffers, tachycardia, hypertension, and chest pain were observed in 55%, 24%, and 14% of patients, respectively (Sporer & Firestone, 1997).
    b) Ventricular fibrillation has been reported in cocaine body stuffers, with onset before or immediately after presentation to the emergency department. Generalized seizures have usually developed in these patients shortly before the onset of ventricular fibrillation (June et al, 2000).
    c) CASE REPORT - To hide methamphetamine packets from law enforcement officials, a 20-year-old woman concealed drugs enclosed in plastic bags in her vagina. While in police custody, she experienced a self-limited grand mal seizure and later developed multiple seizures, altered mental status, tachycardia (HR 141 beats per minute) and hypertension (144/31 mmHg). ECG revealed sinus tachycardia with a ventricular rate of 151 beats per minute. Although the patient was clinically well on the fourth day, except for persistent sinus tachycardia at rest in the 120's, she signed out of the hospital (Kashani & Ruha, 2004).

Neurologic

    3.7.2) CLINICAL EFFECTS
    A) PSYCHOMOTOR AGITATION
    1) WITH POISONING/EXPOSURE
    a) In one retrospective study of 98 cases of crack cocaine body stuffers, agitation was observed in 22% of patients (Sporer & Firestone, 1997).
    b) DELAYED ONSET/CASE REPORT - A 25-year-old man ingested methamphetamine wrapped in a sealable plastic bag, in an attempt to provide sustained drug release. He developed abdominal pain and presented to the ED 12 hours after ingestion with no clinical evidence of methamphetamine effects and a negative toxicology screen; he remained asymptomatic and was discharged 24 hours after ingestion. He returned 18 hours later with acute delirium, hypertension, tachycardia (210 beats/minute) and fever (38.3 C). He was treated supportively (sedation, intubation, whole bowel irrigation) and recovered (Hendrickson et al, 2006).
    B) SEIZURE
    1) WITH POISONING/EXPOSURE
    a) Seizures were reported in a patient who ingested 20 "small rocks" of crack cocaine. The first seizure developed about 10 hours after ingestion, a second occurred 23 hours after ingestion and a third 24 hours after ingestion and shortly after presentation to the emergency department (Pollack et al, 1992).
    b) In one retrospective study of 98 cases of crack cocaine body stuffers, seizures were observed in 4% of patients; all occurring within 2 hours of the reported crack cocaine ingestion (Sporer & Firestone, 1997).
    c) CASE REPORT - To hide methamphetamine packets from law enforcement officials, a 20-year-old woman concealed drugs enclosed in plastic bags in her vagina. While in police custody, she experienced a self-limited grand mal seizure and later developed multiple seizures, altered mental status, tachycardia and hypertension. Neurological examination revealed significant agitation, intermittent myoclonic jerking of all four extremities, clonus and hyperreflexia. Although the patient was clinically well on the fourth day, except for persistent sinus tachycardia at rest in the 120's, she signed out of the hospital (Kashani & Ruha, 2004).

Gastrointestinal

    3.8.2) CLINICAL EFFECTS
    A) ABDOMINAL PAIN
    1) WITH POISONING/EXPOSURE
    a) In one retrospective study of 98 cases of crack cocaine body stuffers, abdominal pain was observed in 20% of patients (Sporer & Firestone, 1997).

Dermatologic

    3.14.2) CLINICAL EFFECTS
    A) EXCESSIVE SWEATING
    1) WITH POISONING/EXPOSURE
    a) In one retrospective study of 98 cases of crack cocaine body stuffers, diaphoresis was observed in 13% of patients (Sporer & Firestone, 1997).

Monitoring Parameters Levels

    4.1.1) SUMMARY
    A) No specific studies are required for most asymptomatic patients. Urine drug screens may confirm exposure but cannot distinguish recreational use from drug absorption after stuffing.
    B) In symptomatic patients, institute continuous cardiac monitoring and obtain serial ECGs.
    C) In a patient with signs of toxicity after stuffing a sympathomimetic agent, monitor electrolytes, CBC, CPK, and urinalysis. Obtain a head CT to evaluate for hemorrhage in patients with abnormal mental status.
    D) When opioids are stuffed, monitor electrolytes, glucose, pulse oximetry/capnometry, and chest radiograph (if hypoxic).
    E) Abdominal x rays are rarely helpful in body stuffers.
    4.1.2) SERUM/BLOOD
    A) BLOOD/SERUM CHEMISTRY
    1) In a patient with signs of toxicity after stuffing a sympathomimetic agent, monitor electrolytes, CBC, CPK, and urinalysis. Obtain a head CT to evaluate for hemorrhage in patients with abnormal mental status.
    2) When opioids are stuffed, monitor electrolytes, glucose, pulse oximetry/capnometry, and chest radiograph (if hypoxic).
    3) In symptomatic patients, institute continuous cardiac monitoring and obtain serial ECGs.
    4.1.3) URINE
    A) URINARY LEVELS
    1) Rapid urine testing for drugs may assist in determining the packet content (Nelson, 2002). However, as many of these patients use recreational drugs, positive urine tests may reflect drug use that occurred any time within the past several days.
    2) In one retrospective study of 98 cases of crack cocaine body stuffers, urine toxicologic screening was performed in 11% of patients; results were positive for cocaine metabolite in slightly more than half (Sporer & Firestone, 1997).
    3) Severe methamphetamine toxicity has been reported following intravaginal body stuffing. Urine test was positive for methamphetamine and the amphetamine metabolite (Kashani & Ruha, 2004).

Radiographic Studies

    A) It is important to recognize the limitation of radiographic studies; packets have been missed on every radiographic modality.
    B) ABDOMINAL RADIOGRAPHY
    1) Abdominal radiography may be of value in locating cocaine packets in cocaine smuggler "body-packers" (Souka, 1999; Beerman et al, 1986). However, radiographic detection of the containers is more difficult in the stuffer than in the packer (Pollack et al, 1992). In several case series of body stuffers, results were rarely positive (Sporer & Firestone, 1997).
    a) In one retrospective study of 98 cases of crack cocaine body stuffers, abdominal radiographs were obtained in 17% of patients; the findings were negative in all cases (Sporer & Firestone, 1997). In another study, abdominal radiographs were not of value for stuffers ingesting cellophane-wrapped packets (June et al, 2000).
    b) Although drugs in a glass or hard plastic crack vials may be visualized on a plain film, soft plastic bags may not be observed. Some studies have reported some degree of radiopacity of crack cocaine "rocks," detected on plain radiography and CT (Schwartz, 2002).
    2) KUB
    a) The Kidney Ureter Bladder Radiograph (KUB) is often negative in body stuffers (Eng et al, 1999; Sporer & Firestone, 1997). Routine use of KUB in these patients is not warranted.
    b) In one body stuffer, the KUB film revealed a faint radiopaque density in the right lower quadrant that was suspicious for a foreign body (Pollack et al, 1992).
    3) ABDOMINAL CT
    a) Upper abdominal CT scan and abdominal radiography with Gastrografin(R) have been reported to result in better visualization (June et al, 2000; Sporer & Firestone, 1997; Marc et al, 1990; Diamant-Berger et al, 1988; Hartoko et al, 1988). In a few cases, plastic "baggies" have been visualized by abdominal CT (Schwartz, 2002).
    b) A case of a false-negative abdominal CT scan without contrast in a cocaine body stuffer has been reported (Eng et al, 1999).
    4) MRI
    a) Magnetic resonance does not visualize packets because of the lack of protons (Kersschot et al, 1985).

Methods

    A) Severe methamphetamine toxicity has been reported following intravaginal body stuffing. Gas chromatography and mass spectrometry were used to detect methamphetamine and the amphetamine metabolite in the patient's urine (Kashani & Ruha, 2004).

Life Support

    A) Support respiratory and cardiovascular function.

Patient Disposition

    6.3.1) DISPOSITION/ORAL EXPOSURE
    6.3.1.1) ADMISSION CRITERIA/ORAL
    A) Any patient who develops clinical symptoms from ingested drug should be admitted to a monitored setting in a hospital. Patients who develop signs of severe toxicity should be admitted to the ICU. Patients can be discharged from the medical facility with complete resolution of symptoms.
    B) In one retrospective study of 98 cases of crack cocaine body stuffers, the length of observation was 5 hours or less in 51%, and 6 to 10 hours in another 23%. The authors recommended 6 hours of observation in the asymptomatic body stuffer (Sporer & Firestone, 1997).
    6.3.1.3) CONSULT CRITERIA/ORAL
    A) Consult a poison center or medical toxicologist for any questions, concerns or cases of moderate to severe toxicity.
    6.3.1.5) OBSERVATION CRITERIA/ORAL
    A) Anyone who develops signs of toxicity should be admitted. Imaging is rarely helpful. Although the optimal duration of observation for asymptomatic patients is controversial, the best available data suggest that patients who are asymptomatic, have received activated charcoal and have normal vital signs after 6 hours, are unlikely to deteriorate.

Monitoring

    A) No specific studies are required for most asymptomatic patients. Urine drug screens may confirm exposure but cannot distinguish recreational use from drug absorption after stuffing.
    B) In symptomatic patients, institute continuous cardiac monitoring and obtain serial ECGs.
    C) In a patient with signs of toxicity after stuffing a sympathomimetic agent, monitor electrolytes, CBC, CPK, and urinalysis. Obtain a head CT to evaluate for hemorrhage in patients with abnormal mental status.
    D) When opioids are stuffed, monitor electrolytes, glucose, pulse oximetry/capnometry, and chest radiograph (if hypoxic).
    E) Abdominal x rays are rarely helpful in body stuffers.

Oral Exposure

    6.5.1) PREVENTION OF ABSORPTION/PREHOSPITAL
    A) ACTIVATED CHARCOAL
    1) Activated charcoal adsorbs sympathomimetics and opioids effectively.
    2) PREHOSPITAL ACTIVATED CHARCOAL ADMINISTRATION
    a) Consider prehospital administration of activated charcoal as an aqueous slurry in patients with a potentially toxic ingestion who are awake and able to protect their airway. Activated charcoal is most effective when administered within one hour of ingestion. Administration in the prehospital setting has the potential to significantly decrease the time from toxin ingestion to activated charcoal administration, although it has not been shown to affect outcome (Alaspaa et al, 2005; Thakore & Murphy, 2002; Spiller & Rogers, 2002).
    1) In patients who are at risk for the abrupt onset of seizures or mental status depression, activated charcoal should not be administered in the prehospital setting, due to the risk of aspiration in the event of spontaneous emesis.
    2) The addition of flavoring agents (cola drinks, chocolate milk, cherry syrup) to activated charcoal improves the palatability for children and may facilitate successful administration (Guenther Skokan et al, 2001; Dagnone et al, 2002).
    3) CHARCOAL DOSE
    a) Use a minimum of 240 milliliters of water per 30 grams charcoal (FDA, 1985). Optimum dose not established; usual dose is 25 to 100 grams in adults and adolescents; 25 to 50 grams in children aged 1 to 12 years (or 0.5 to 1 gram/kilogram body weight) ; and 0.5 to 1 gram/kilogram in infants up to 1 year old (Chyka et al, 2005).
    1) Routine use of a cathartic with activated charcoal is NOT recommended as there is no evidence that cathartics reduce drug absorption and cathartics are known to cause adverse effects such as nausea, vomiting, abdominal cramps, electrolyte imbalances and occasionally hypotension (None Listed, 2004).
    b) ADVERSE EFFECTS/CONTRAINDICATIONS
    1) Complications: emesis, aspiration (Chyka et al, 2005). Aspiration may be complicated by acute respiratory failure, ARDS, bronchiolitis obliterans or chronic lung disease (Golej et al, 2001; Graff et al, 2002; Pollack et al, 1981; Harris & Filandrinos, 1993; Elliot et al, 1989; Rau et al, 1988; Golej et al, 2001; Graff et al, 2002). Refer to the ACTIVATED CHARCOAL/TREATMENT management for further information.
    2) Contraindications: unprotected airway (increases risk/severity of aspiration) , nonfunctioning gastrointestinal tract, uncontrolled vomiting, and ingestion of most hydrocarbons (Chyka et al, 2005).
    6.5.2) PREVENTION OF ABSORPTION
    A) RADIOGRAPHY
    1) Radiographic detection of the containers may be more difficult in the body stuffer than in the packer (Pollack et al, 1992).
    2) Abdominal CT may be required in the patients with protracted symptoms.
    B) ACTIVATED CHARCOAL
    1) Activated charcoal may adsorb cocaine or other drugs leaking or leaching from packets, as well as serve as a marker for GI transit. It has been suggested that some packets are semipermeable and do not need to rupture to cause death from toxicity (Queen & Glauser, 2002; Wetli & Mittleman, 1981).
    2) Although activated charcoal has been used in body packers, its spillage into the peritoneum secondary to perforation of the bowel wall or during surgery is of concern (Olmedo et al, 2001).
    3) CHARCOAL ADMINISTRATION
    a) Consider administration of activated charcoal after a potentially toxic ingestion (Chyka et al, 2005). Administer charcoal as an aqueous slurry; most effective when administered within one hour of ingestion.
    4) CHARCOAL DOSE
    a) Use a minimum of 240 milliliters of water per 30 grams charcoal (FDA, 1985). Optimum dose not established; usual dose is 25 to 100 grams in adults and adolescents; 25 to 50 grams in children aged 1 to 12 years (or 0.5 to 1 gram/kilogram body weight) ; and 0.5 to 1 gram/kilogram in infants up to 1 year old (Chyka et al, 2005).
    1) Routine use of a cathartic with activated charcoal is NOT recommended as there is no evidence that cathartics reduce drug absorption and cathartics are known to cause adverse effects such as nausea, vomiting, abdominal cramps, electrolyte imbalances and occasionally hypotension (None Listed, 2004).
    b) ADVERSE EFFECTS/CONTRAINDICATIONS
    1) Complications: emesis, aspiration (Chyka et al, 2005). Aspiration may be complicated by acute respiratory failure, ARDS, bronchiolitis obliterans or chronic lung disease (Golej et al, 2001; Graff et al, 2002; Pollack et al, 1981; Harris & Filandrinos, 1993; Elliot et al, 1989; Rau et al, 1988; Golej et al, 2001; Graff et al, 2002). Refer to the ACTIVATED CHARCOAL/TREATMENT management for further information.
    2) Contraindications: unprotected airway (increases risk/severity of aspiration) , nonfunctioning gastrointestinal tract, uncontrolled vomiting, and ingestion of most hydrocarbons (Chyka et al, 2005).
    C) WHOLE BOWEL IRRIGATION
    1) WHOLE BOWEL IRRIGATION may be a relatively safe and effective means of rapid decontamination for the body stuffer, and may be considered in some patients (primarily those who are suspected to have ingested multiple packets) (Olmedo et al, 2001; Betzelos & Mueller, 1991; Hoffman et al, 1990). Activated charcoal should be administered prior to beginning whole bowel irrigation as polyethylene glycol (PEG) solution decreases the ability of charcoal to adsorb charcoal in vitro (Makosiej et al, 1993).
    a) WHOLE BOWEL IRRIGATION/INDICATIONS: Whole bowel irrigation with a polyethylene glycol balanced electrolyte solution appears to be a safe means of gastrointestinal decontamination. It is particularly useful when sustained release or enteric coated formulations, substances not adsorbed by activated charcoal, or substances known to form concretions or bezoars are involved in the overdose.
    1) Volunteer studies have shown significant decreases in the bioavailability of ingested drugs after whole bowel irrigation (Tenenbein et al, 1987; Kirshenbaum et al, 1989; Smith et al, 1991). There are no controlled clinical trials evaluating the efficacy of whole bowel irrigation in overdose.
    b) CONTRAINDICATIONS: This procedure should not be used in patients who are currently or are at risk for rapidly becoming obtunded, comatose, or seizing until the airway is secured by endotracheal intubation. Whole bowel irrigation should not be used in patients with bowel obstruction, bowel perforation, megacolon, ileus, uncontrolled vomiting, significant gastrointestinal bleeding, hemodynamic instability or inability to protect the airway (Tenenbein et al, 1987).
    c) ADMINISTRATION: Polyethylene glycol balanced electrolyte solution (e.g. Colyte(R), Golytely(R)) is taken orally or by nasogastric tube. The patient should be seated and/or the head of the bed elevated to at least a 45 degree angle (Tenenbein et al, 1987). Optimum dose not established. ADULT: 2 liters initially followed by 1.5 to 2 liters per hour. CHILDREN 6 to 12 years: 1000 milliliters/hour. CHILDREN 9 months to 6 years: 500 milliliters/hour. Continue until rectal effluent is clear and there is no radiographic evidence of toxin in the gastrointestinal tract.
    d) ADVERSE EFFECTS: Include nausea, vomiting, abdominal cramping, and bloating. Fluid and electrolyte status should be monitored, although severe fluid and electrolyte abnormalities have not been reported, minor electrolyte abnormalities may develop. Prolonged periods of irrigation may produce a mild metabolic acidosis. Patients with compromised airway protection are at risk for aspiration.
    D) SURGICAL THERAPY
    1) Rarely, intra-abdominal surgery is indicated if bowel obstruction is present, if the patient has severe symptoms of toxicity (primarily from cocaine) or if abdominal radiography shows residual packets remaining in the gastrointestinal tract not removed by WBI (Peake et al, 2009; Queen & Glauser, 2002; Olmedo et al, 2001; Hollander & Hoffman, 2002; Olmedo et al, 1999; Souka, 1999).
    2) Follow-up plain radiography and a barium swallow with small bowel follow-through should be considered in patients who have ingested large numbers of packets (Peake et al, 2009; Olmedo et al, 2001; Hollander & Hoffman, 2002; Olmedo et al, 2001).
    3) Heroin body stuffers may be managed nonsurgically using WBI and naloxone. Surgery should be performed if the body stuffer has a bowel obstruction (Jordan et al, 2009; Nelson, 2002; Olmedo et al, 2001).
    E) ENDOSCOPY
    1) Attempts at endoscopic removal (mainly in body packers) have resulted in spontaneous rupture of packets and this procedure is NOT RECOMMENDED (Peake et al, 2009; Queen & Glauser, 2002; McCleave, 1993; Suarez et al, 1977), although in certain circumstances it may be "cautiously attempted" (Hoffman et al, 1990; Sherman & Zingler, 1990), particularly if the packet will not pass through the pylorus (Peake et al, 2009). Tap water enemas have also resulted in package rupture (Queen & Glauser, 2002; Jonsson et al, 1983); enemas should be avoided (Souka, 1999; McCleave, 1993).
    F) CATHARTICS
    1) To avoid possible package rupture or deterioration, gentle laxatives which do not directly stimulate the bowel should be considered (McCleave, 1993). Psyllium, sodium sulfate, and bisacodyl suppositories have been used (Queen & Glauser, 2002).
    2) Bisacodyl (Dulcolax) or other rectal suppository may be administered to enhance fecal excretion of the packages. Care must be taken not to perforate drug packets which might be in the rectum.
    3) CASE SERIES: Utecht et al (1993) present a series of 14 patients, nine of whom swallowed heroin-containing packets and five of whom inserted them rectally. Thirteen had evidence of packets on KUB. Bisacodyl suppositories were used to evacuate packets from the rectum. No patient received gastric lavage (Utecht et al, 1993).
    4) Psyllium hydrophilic mucilloid or other bulk laxative may be given to facilitate passage and removal of packages (Dose: 3.5 grams 2 to 3 times daily).
    5) Liquid paraffin or mineral oil may dissolve latex packets and should be avoided (Visser et al, 1998; McCleave, 1993).
    6) In a retrospective cohort study of 98 cocaine body stuffers, 7% of patients were treated with magnesium citrate (Sporer & Firestone, 1997).
    G) CRACK VIALS
    1) Crack vials ingested to avoid arrest have also caused symptomatic intoxication. In a study of 23 patients with a history of having ingested crack vials, four patients developed mild to severe symptomatology (Hoffman et al, 1990).
    2) Vials were retrieved in 2 of 3 patients given ipecac, and in 2 of 5 patients treated with whole bowel irrigation (Hoffman et al, 1990).
    3) Although vials were ultimately recovered from eleven patients, abdominal radiographies were positive in only two. Thus, radiography may not reveal the presence of crack vials in the gastrointestinal tract (Hoffman et al, 1990).
    6.5.3) TREATMENT
    A) MONITORING OF PATIENT
    1) No specific studies are required for most asymptomatic patients. Urine drug screens may confirm exposure but cannot distinguish recreational use from drug absorption after stuffing.
    2) In symptomatic patients, institute continuous cardiac monitoring and obtain serial ECGs.
    3) In a patient with signs of toxicity after stuffing a sympathomimetic agent, monitor electrolytes, CBC, CPK, and urinalysis. Obtain a head CT to evaluate for hemorrhage in patients with abnormal mental status.
    4) When opioids are stuffed, monitor electrolytes, glucose, pulse oximetry/capnometry, and chest radiograph (if hypoxic).
    5) Abdominal x rays are rarely helpful in body stuffers.
    B) PSYCHOMOTOR AGITATION
    1) INDICATION
    a) If patient is severely agitated, sedate with IV benzodiazepines.
    2) DIAZEPAM DOSE
    a) ADULT: 5 to 10 mg IV initially, repeat every 5 to 20 minutes as needed (Brophy et al, 2012; Prod Info diazepam IM, IV injection, 2008; Manno, 2003).
    b) CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed (Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    3) LORAZEPAM DOSE
    a) ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed (Manno, 2003).
    b) CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed (Brophy et al, 2012; Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    4) Extremely large doses of benzodiazepines may be required in patients with severe intoxication in order to obtain adequate sedation. Titrate dose to clinical response and monitor for hypotension, CNS and respiratory depression, and the need for endotracheal intubation.
    5) In a retrospective cohort study of 98 cocaine body stuffers, 15% of patients were treated with benzodiazepines for agitation (Sporer & Firestone, 1997).
    C) PROCHLORPERAZINE
    1) In a retrospective cohort study of 98 cocaine body stuffers, 4% of patients were treated with prochlorperazine (Sporer & Firestone, 1997).

Enhanced Elimination

    A) HEMODIALYSIS OR HEMOPERFUSION
    1) The most commonly stuffed drugs are not effectively removed by hemodialysis or hemoperfusion.

Summary

    A) TOXICITY: Toxicity is dependent on the agent(s) ingested.
    B) Although the estimated minimum lethal dose of cocaine is 1.2 g, fatalities have been reported after 30 mg of cocaine applied to mucous membranes. Fatalities have been reported after the ingestion of 1 to 3 grams of cocaine in powder form.
    C) Ingestion of a single capsule of MDMA could be lethal.
    D) The lethal dose of opioids varies and depends on purity of the drug and the habituation of the involved individual.

Minimum Lethal Exposure

    A) GENERAL
    1) COCAINE
    a) Although the estimated minimum lethal dose of cocaine is 1.2 g, fatalities have been reported after 30 mg of cocaine applied to mucous membranes (Fineschi et al, 2002).
    b) Fatalities have been reported after the ingestion of 1 to 3 grams of cocaine in powder form (McCarron & Wood, 1983).
    2) MDMA/MDEA
    a) A 29-year-old male with no history of heart disease, hypertension or other cardiovascular risk factors died of a Type 1 aortic dissection approximately 48 hours after ingesting 1 ecstasy tablet and a large quantity of alcohol (Duflou & Mark, 2000). Initial symptoms did not begin until approximately 36 hours after exposure.
    b) An 18-year-old woman who ingested an estimated 150 milligrams of MDMA in combination with alcohol developed ventricular fibrillation and died; postmortem MDMA levels were 1 milligram/liter (Dowling et al, 1987).
    c) A 16-year-old girl died of hyperthermia, coagulopathy, and rhabdomyolysis after ingestion of one tablet of "Ecstasy" (strength unknown) (Chadwick et al, 1991).
    d) An 18-year-old male died following ingestion of 3 tablets of "ecstasy". Serum MDMA concentration was 1.26 milligrams/liter on admission (Campkin & Davies, 1992).
    e) In a series of 7 fatalities related to MDMA use, the doses ingested ranged from 1 to 5 tablets (unknown dose in 2 patients) (Henry et al, 1992). MDMA plasma concentration ranged from 0.11 milligrams/liter to 1.26 milligrams/liter.

Serum Plasma Blood Concentrations

    7.5.2) TOXIC CONCENTRATIONS
    A) TOXIC CONCENTRATION LEVELS
    1) SERUM: In a case of methamphetamine toxicity following intravaginal body stuffing, quantitative serum levels of methamphetamine and amphetamine were 3100 ng/mL and 110 ng/mL, respectively. The patient experienced multiple seizures, altered mental status, tachycardia and hypertension (Kashani & Ruha, 2004).
    2) CASE REPORT: A 23-year-old woman was found unconscious and unresponsive in a county jail. She died after several unsuccessful cardiopulmonary resuscitation attempts. Autopsy revealed multiple small loosely wrapped plastic packages containing methamphetamine in the patient's vagina. Postmortem methamphetamine concentrations in her subclavian blood, vitreous fluid, and urine were 42.6 mg/L, 20.1 mg/L, and 771 mg/L, respectively. Concentrations of amphetamine (the active metabolite of methamphetamine) in subclavian blood, vitreous fluid, and urine were 1.3 mg/L, 0.5 mg/L, and 20.4 mg/L, respectively (Jones et al, 2014).

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