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Patients with multiple rib fractures and con­cern for sternal fractures often will need contrast enhanced CT scan to make certain underlying pulmonary or vascular injuries are not present.
6,7
Patients with nondisplaced sternal fractures can be considered for trauma protocol placement, but in most instances, retrosternal hematoma and more significant sternal fractures are not amenable to discharge within 24 hours. Age, medical comor­bidities, functional status prior to injury, ability to ambulate, ability to tolerate oral pain medica­tions, and location and number of fractures are all important considerations for disposition deci­sions in this patient population.
Head Injury
Clinical observation of the head injured patien ts is one of the most frequently managed patients on a trauma protocol in the OU. This approach has been found to be safe and effective and can reduce inappropriate inpatient admission in this patient population.
9,10
Many such patients have concomi­tant intoxicants on board that render the obser­vation period invaluable in clinically observing patients to determine if their mental status is appropriate for discharge (determination often not feasible directly from the ED).
The challenge with this patient population is
defining (prior to OU placement) the patients true GCS and making certain more significantly head injured patients are not placed in this care setting. Patients with mild head injuries can also be observed with the benefit of not having to perform a head CT (important for radiation stewardship particularly in younger patients).
9
More advanced OUs with neurosurgical backup have experience managing patients with isolated, mild head trauma on coumadin and other blood thinners. Such patients represent a high-risk cohort of patients to discharge directly from the ED. As long as these patients do not have evidence of significant intra-cranial pathology on initial imaging, monitoring the clinical status in the OU is often appropriate.
Penetrating Trauma
Select patients with penetrating trauma can be successfully managed in the OU. Patient selection is very important with this patient population as certain conditions are inappropriate for the level of care offered in the ED OU and would be more
appropriately offered (due to the critical nature and rapid deterioration) in the ICU setting. Patients can have neurovascular checks and be watched for compartment syndrome. Patients with superficial wounds to the thorax and abdomen are appropriate for OU placement and have a low incidence of poor outcome even after brief obser­vation.
11,12
At nontrauma hospitals, most penetrat­ing injuries to the thorax and abdomen will require transfer for initial evaluation by a trauma team prior to OU placement. In general, patients with penetrating neck trauma should not be placed in the OU setting unless cleared by a trauma team at a trauma facility with expertise in managing this patient population in the OU setting.
Isolated extremity penetrating wounds are well managed in most cases in the OU as a high proportion of these patients can be safely moni­tored and then discharged. Extremity trauma with signs of vascular compromise, compartment syn­drome, or delayed presentations of injury with infection should be excluded and require more extensive resources in the inpatient setting.
Mechanical Falls
Patients with significant blunt trauma from mechanical falls can be managed successfully in the OU. Patients with extremity fractures can be included in this patient cohort, but operative frac­tures like hip fractures and femur fractures should not be placed in the OU. A mechanical fall proto­col or accepting fall patients on a general observa­tion protocol for trauma can be particularly beneficial with elderly patients. If such patients have gait instability and risk for further falls, then resources such as physical therapy need to be available for the clinician managing the patient in the OU. Often such patients require additional resources such as case management, social work, and even pharmacists to aid in management and safe disposition. Occult fractures and underlying medical comorbidities can prevent discharge in some cases as can the patients social situation, living environment, and support system (or lack thereof). (See also geriatric Chapter 55.)
Management/Intervention
Frequent vital signs are the mainstay of observation for the injured trauma patient. Frequent neurologic checks should take place for intoxicated or head injured patients. Specific therapeutic interventions
Trauma
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like pain and antiemetic medications, IV fluids, and other needs will be patient and protocol spe­cific. Frequency of vital signs should be consistent with nursing resources and patient acuity. Vascu­lar checks in higher risk patients looking for vas­cular compromise and compartment syndrome should be delineated. Patients should be transi­tioned from IV therapies to oral therapies as one data point to determine suitability for discharge and to see if continued outpatient management is appropriate. At trauma facilities it is important to delineate who will be doing repeat examinations, whether the OU providers or members of the trauma team. Cervical spine clearance, if not done initially prior to OU placement, should also be protocolized and consistent with national guidelines. Many trauma patients will need social services support to facilitate follow-up, medica­tion assistance, and even drug and alcohol coun­seling. As such, social worker coverage for the OU is essential when managing trauma patients. Resources such as physical therapy will depend on the type of patient managed, but can be invaluable in providing information about ongoing fall risk for elderly patients.
Disposition after Observation
A significant majority of trauma patients can be discharged from the OU after an appropriate period of observation.
3,4
All such patients should have stable vital signs, have normal GCS, be clin­ically sober, be able to ambulate, and be able to tolerate oral intake. The ability to ambulate and tolerate symptoms with oral medications is crit­ical to ensure that such patients do not bounce back to the ED in short order. Imaging studies (which can be significant for this population) should be finalized by radiology and available to
the clinician prior to disposition so radiographic abnormalities can be addressed. The patient should have a documented disposition examination; such an examination should be comprehensive from head to toe and include observation of the patient ambulating. Follow-up should be time and action specific related to reevaluation needs and specific for the condition affecting the patient.
For more significantly injured patients, prompt reevaluation is important. This can be a challenge for patients without a primary care physician. Unfortunately in this trauma patient population (younger, more socioeconomically troubled), many will not have access to health care, will be uninsured or underinsured, and will be poorly resourced. As such, bringing the patient back to the ED for wound checks or injury checks in 48–72 hours is a consideration if outpatient follow-up can not be obtained in a timely fashion. Patients are generally discharged with symptom control medications for several days, particularly for blunt trauma patients for whom musculoskel­etal soft tissue injury can lead to prolonged pain and symptoms.
Summary
Trauma patients are clearly a very viable patient population to consider for the OU. As with all clinical conditions managed in the OU, careful patient selection is paramount to ensure success­ful discharge in the majority of managed patients. Clear exclusion criteria should be set to ensure that critically injured patients are not placed in the OU setting. More so than most clinical patient populations managed in the OU, local resources need to be carefully considered to ensure adequate backup is available, particularly at nontrauma hospitals.
References
1. Conrad L, Markovchick V, Mitchiner J, et al. The role of an emergency department observation unit in the management of trauma patients. J Emerg Med 1985; 2(5): 325–333.
2. Cowell VL, Ciraula D, Gabram S, et al. Trauma 24-hour observation critical path. J Trauma 1998; 45(1): 147–150.
3. Madsen TE, Bledsoe JR, Bossart PJ. Observation unit admission as an alternative to inpatient admission for trauma activation patients. Emerg Med J 2009; 26(6): 421–423.
4. Holly J, Bledsoe J, Black K, et al. Prospective evaluation of an ED observation unit protocol for trauma activation patients. Am J Emerg Med 2012; 30(8): 1402–1406.
5. Rivara FP, Jurkovich GJ, Gurney JG, et al. The magnitude of acute and chronic alcohol abuse in trauma patients. Arch Surg 1993. Aug; 128(8): 907–912.
6. Kendall JL, Kestler AM, Whitaker KT, et al. Blunt abdominal trauma patients are at very low risk for intra­abdominal injury after emergency department
Mark G. Moseley and Miles P. Hawley
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observation. West J Emerg Med
2011. Nov; 12 (4): 496–504.
7. Menditto VG, Gabrielli B, Marcosignori M, et al. A management of blunt thoracic trauma in an emergency department observation unit: pre-post observation study. J Trauma
2012. Jan; 72(1): 222–228.
8. Ammons MA, Moore EE, Rosen P. Role of the observation unit in the
management of thoracic trauma. J Emerg Med 1986; 4 (4): 279–282.
9. Holsti M, Kadish HA, Sill BL, et al. Pediatric closed head injuries treated in an observation unit. Pediatr Emerg Care 2005. Oct;21(10): 649–644.
10. MacLaren RE, Ghoorahoo HI, Kirby NG. Use of an accident and emergency department observation ward in management of head injury.
Br J Surg 1993. Feb; 80(2): 215–217.
11. Leppaniemi AK, Voutilainen PE, Haapiainen RK. Indications for early mandatory laparotomy in abdominal stab wounds. Br J Surg 1999. Jan; 86(1): 76–80.
12. Ordog GJ, Wasserberger J, Balasubramanium S, et al. Asymptomatic stab wounds of the chest. J Trauma 1994. 36 (5): 680–684.
Trauma
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Subpart IVO
Chapter
59
Clinical – Toxicology
Toxicology
Steven J. Walsh, MD Marsha Ford, MD, FACEP
Toxicologic disorders account for over 4 million U.S. emergency department (ED) visits annually.
1
Many patients are discharged to home or to a psychiatric facility after ED evaluation. However, a significant number of poisoned individuals require admission for further observation and management. A large number of these patients do not require an extended hospital stay, making admission to the observation unit (OU) a reason­able disposition option.
The OU should be well-equipped to provide care for the poisoned patient. Continuous cardio­pulmonary monitoring, expeditious diagnostic testing (electrocardiography, radiography, labora­tory analysis, etc.), a variety of commonly used medications/antidotes (including but not limited to dextrose, antiemetics, analgesics, benzodiazep­ines, naloxone), a low nurse-to-patient ratio (most OUs have a 1:5 or 1:4 nurse patient ratio), and one­to-one sitters for patient safety/psychiatric obser­vation (if needed) should be available at all times. Any items that could be used for self-harm by suicidal individuals should be placed in a secure location, and all patients should be searched for such prior to admission to the OU. Providers caring for these patients should be familiar with common toxicities and toxidromes (such as opiate/ opioid, benzodiazepine, sympathomimetic, and anticholinergic), as well as the dosing, administra­tion, and adverse effects of the aforementioned commonly used medications. All staff should be aware of the Poison Help Hotline (800-222-1222 in the United States), which provides around-the­clock,free, confidential,and expert advice regarding poisoned patients.
A variety of poisonings are appropriate for OU care. In general, toxicologic admissions to the OU should include those patients whose anticipated stay is less than 24 hours and who have normal or near-normal vital signs. Somno­lent but arousable patients are appropriate for
observation care, as are those with mild central nervous system (CNS) hyperexcitation (hyperre­flexia/clonus, mild altered mental status/agitation controlled with benzodiazepines).
Not all poisoned patients are appropriate for observation-type admissions, however. Individ­uals who will likely require more than 23 hours of observation/management should be admitted to an inpati ent service. Those with significant tachycardia (heart rate [HR] > 110/minute) after appropriate toxicologic treatment, severe delirium, agitation and/or psychosis that cannot be con­trolled with benzodiazepines, significant laboratory and/or EKG derangements (e.g., QRS duration > 120 milliseconds [ms], QTc interval > 500 ms), a high likelihood of clinical deterioration, and patients requiring ICU care should not be admitted to the OU.
While impossible to discuss each and every poisoning that is/is not appropriate for observa­tion admission, some specific toxicities that lend themselves to observation-type care are listed as follows.
Substance: Acetaminophen (APAP)
Observation Admission Criteria:
– Single, acute APAP ingestion (defined as
ingestion of the entire amount of APAP
within 8 hours
2
) presenting within 24 hours requiring treatment based upon Rumack­Matthew nomogram
3
– Patients receiving the oral (PO)/intravenous
(IV) bolus dose of N-acetylcysteine (NAC) within 8 hours of acute ingestion
3,4
– Nausea/vomiting/abdominal pain controlled
with PO/IV antiemetics/non-APAP analgesics
– Lack of concomitant toxic ingestion that
would likely preclude disposition within 24 hours (i.e., sa licylate toxicity requiring
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21:22:48
bicarbonate infusion, long-acting opiate/ opioid toxicity requiring naloxone infusion)
Contraindications to Observation Admission:
– Ingestions other than single acute
ingestions
3,5
– Individuals receiving the bolus dose of NAC
greater than 8 hours after acute ingestion
3
– Patients with baseline hepatic dysfunction
(elevated aspartate aminotransferase [AST]/alanine amino transferase [ALT]/ international normalized ratio [INR] secondary to alcoholic liver disease, infectious hepatitis, or other underlying pathology)
– Elevated transaminases (AST and/or ALT
greater than the upper limit of laboratory reference ranges)
– Coagulopathy (INR greater than the upper
limit of laboratory reference range)
– Renal insufficiency (creatinine greater than
the upper limit of laboratory reference range, oliguria/anuria)
Altered mental statusGravid patientPresence of concomitant toxicity that would
likely prevent disposition within 24 hours (i.e., long-acting opiate/opioid toxicity requiring naloxone infusion, salicylate toxicity requiring bicarbonate infusion)
– Provider judgment
Observation Management:
– IV or PO (NAC) per individual facilitys
protocol
3,4
Antiemetics as needed (PRN)Psychiatric consultation PRN
Discharge Criteria:
– Patient is cli nically w ell after NAC course
(resolution of abdominal pain, no nausea/ emesis, normal mentation)
3,4
– Undetectable [APAP] after NAC course
3,4
– Normal AST/ALT after NAC course
3,4
Comments:
– NAC protocols vary between facilities/
regions; consult your regional poison center
(800-222-1222 in the United States) for treatment recommendations
– Patients may require extension of NAC course
if evidence of liver injury develops (elevated AST/ALT, INR greater than 1.4, etc.; consult your regional poison center for treatment recommendations)
3
Substance: Benzodiazepines
Observation Admission Criteria:
– Confirmed/suspected symptomatic ingestion
(adult or child) after a 6-hour-or-less ED observation period
Somnolence/stupor
Slurred speech
Ataxia
Contraindications to Observation Admission:
– Hypoxia refractory to supplemental oxygen
delivered via nasal cannula
– Significant rhabdomyolysis (pressure ulcers/
blisters/bullae, creatine phosphokinase [CPK] greater than eight times upper limit of laboratory reference range, myoglobinuria) or compartment syndrome (elevated compartment pressures)
– Clinically significant aspiration pneumonitis
(fever, tachypnea, hypoxia, cough productive of sputum, infiltrate on chest radiograph)
– Presence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Observation Management:
Continuous cardiopulmonary monitoringPrevention of respiratory compromise/
aspiration (head-of-bed elevation, supplemental oxygen administration)
– Psychiatric consultation PRN
Discharge Criteria:
Normal mentationFluent (nonslurred) speechAmbulatory with a steady gaitNormal pulse oximetry/respiratory rate
Toxicology
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21:22:48
Comments:
– Use caution when considering pharmacologic
reversal with flumazenil (may precipitate acute withdrawal, including seizures, in patients with chronic use/abuse of gamma­aminobutyric acid [GABA] agonists [e.g., benzodiazepines])
6
– Many benzodiazepines are not detected by
rapid bedside drugs of abuse screens (high false negative rate)
7
– Consider aspiration pneumonitis and
rhabdomyolysis/compartment syndrome in patients found unresponsive or with altered mental status
Substance: Bupropion
Observation Admission Criteria:
– Any confirmed/suspected symptomatic
ingestion responsive to benzodiazepines
Mild CNS hyperexcitation (altered mental status, mild agitation, hyperreflexia, clonus)
Tachycardia/hypertension
– Confirmed/suspected asymptomatic
ingestion of:
10 mg/kg in children
900 mg in adults
Contraindications to Observation Admission:
– Mild CNS hyperexcitation unresponsive to
benzodiazepines
Seizure activityQRS interval > 120 msPresence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Observation Management:
18- to 24-hour period of observationContinuous cardiopulmonary monitoringPrevention of respiratory compromise/
aspiration
Benzodiazepines PRN agitationPsychiatric consultation PRN
Discharge Criteria:
Normal mentation/vital signsAbsence of seizure activity during observation
period
– QRS < 120 ms
Comments:
– Many ingestions seize late (hours 15–18)
8,9,10
; 18-hour period of observation is adequate if patient has remained asymptomatic to that point
– All patients who seize should be admitted to
the hospital (rather than the OU)
– Consider aspiration pneumonitis in patients
found with altered mental status and those who seize
Substance: Sulfonylureas
Observation Admission Criteria:
– Confirmed/suspected symptomatic ingestion
(adult or child)
11,12,13
Signs/symptoms of hypoglycemia
– Altered mental status/confusion/
somnolence, generalized weakness, tremor, diaphoresis, piloerection, nausea, etc.
– Documented hypoglycemia (blood
glucose less than lower limit of laboratory reference range)
– Confirmed/suspected asymptomatic ingestion
(adult or child)
11,12,13
Contraindications to Observation Admission:
– Multiple hypoglycemic episodes prehospital
and/or in ED
Signs/symptoms of severe hypoglycemia
Hypothermia, focal neurologic deficit,
seizure, coma
– Hypoglycemia refractory to dextrose 5% in
water (D5W) administration
– Presence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Steven J. Walsh and Marsha Ford
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21:22:48
Observation Management:
Correct hypoglycemia with IV dextrose PRN
Empiric dextrose is not indicated in the absence of suspected/documented hypoglycemia (wait until patient becomes symptomatic/hypoglycemic)
– Check blood glucose every 2 hours while
awake and every hour while asleep
Meals/activity as toleratedPsychiatric consultation PRN
Discharge Criteria:
Normal vital signs/blood glucoseNo clinical evidence of hypoglycemia
Normal mentation, steady gait, lack of piloerection/diaphoresis, etc.
– No hypoglycemic episodes during a 24-hour
observation period
Each time the patient requires dextrose, the clock is reset and an additional 24­hour observation period is required from time of dextrose administration
Comments:
– After second episode of hypoglycemia
requiring dextrose administration, admit for further evaluation/treatment with dextrose/ octreotide
11–15
Substance: Carbon Monoxide (CO)
Observation Admission Criteria:
– Non-gravid patients exposed to CO who may
benefit from hyperbaric oxygen (HBO) therapy
Syncope/loss of consciousness
Altered mental status/confusion
Abnormal neurologic (particularly cerebellar) examination
Initial carboxyhemoglobin > 25%
No evidence of significant end-organ damage
Normal EKGNormal troponinNo renal insufficiency
Contraindications to Observation Admission:
Evidence of end-organ damage
Persistently abnormal neurologic (particularly cerebellar) examination
CT evidence of cerebral ischemia/ hemorrhage
Abnormal EKG
Elevated troponin
Renal insufficiency
– Significant rhabdomyolysis and/or
compartment syndrome
– Clinically significant aspiration
pneumonitis
Gravid patientPresence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Observation Management:
Continuous cardiopulmonary monitoring100% oxygen administrationHyperbaric oxygen (HBO) as indicatedSymptomatic care (nasal decongestants, etc.)
between HBO treatments
– Psychiatric consultation PRN
Discharge Criteria:
Completion of facilitys HBO regimenNormal neurologic/cerebellar examination
Comments:
– Consider aspiration pneumonitis and/or
rhabdomyolysis/compartment syndrome in patients found unresponsive or with altered mental status
– Indications for HBO are somewhat
controversial
16–18
; consult your regional poison center (800-222-1222 in the United States) for recommendations
– Hyperoxygenation therapy is not without risk
(fire in the HBO chamber, seizure, hollow organ rupture, pulmonary/middle ear barotrauma, etc.)
Substance: Opiates/opioids
Observation Admission Criteria:
– Confirmed/suspected symptomatic ingestion
(adult or child) after 6-hour-or-less ED observation period
Somnolence/stupor
Slurred speech Ataxia
Toxicology
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21:22:48
Contraindications to Observation Admission:
– Hypoxia refractory to supplemental oxygen
delivered via nasal cannula
– Significant rhabdomyolysis and/or
compartment syndrome
– Clinically significant aspiration
pneumonitis
– Signs/symptoms requiring continuous
naloxone infusion
– Patients with QTc interval > 500 ms
19
– Presence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Observation Management:
Continuous cardiopulmonary monitoringPrevention of respiratory compromise/
aspiration
– Psychiatric consultation PRN
Discharge Criteria:
Normal mentationFluent speechAmbulatory with a steady gaitNormal pulse oximetry/respiratory rate
Comments:
– Consider aspiration pneumonitis and
rhabdomyolysis/compartment syndrome in patients found unresponsive or with altered mental status
– Use naloxone for bradypnea/hypopnea/
hypoxia, not for somnolence
Use naloxone with caution in patients with suspected or confirmed tramadol and/or propoxyphene toxicity (may precipitate seizure)
– If patient requires more than two doses of
naloxone, begin continuous infusion/admit for further evaluation/management
Substance: Neuroleptics
Observation Admission Criteria:
– Confirmed/suspected symptomatic ingestion
(adult or child) after 6-hour-or-less ED observation period
Altered mental status (somnolence/stupor, agitation/confusion)
Slurred speech
Ataxia
Hyperreflexia/clonus
Contraindications to Observation Admission:
– Tachycardia (HR > 110/min) and/or agitation
unresponsive to benzodiazepine administration
– Hypoxia refractory to supplemental oxygen
delivered via nasal cannula
Seizure activitySignificant rhabdomyolysis and/or
compartment syndrome
– Clinically significant aspiration
pneumonitis
– Evidence of serotonin syndrome (SS)
20
Fever (core temperature > 38° C)
Autonomic instability (tachycardia/ bradycardia, hypertension/hypotension)
Altered mental status (typically confusion or somnolence/stupor)
Tremor/hyperreflexia/clonus and/or hypertonicity (often greater in the lower extremities)
– Evidence of neuroleptic malignant syndrome
(NMS)
21,22
Fever
Autonomic instability
Altered mental status (typically somnolence, confusion, or agitation/ hyperactivity)
Lead-pipehypertonicity/rigidity
QRS duration > 120 msQTc interval > 500 msPresence of concomitant toxic ingestion that
would likely prevent disposition within 24 hours
– Provider judgment
Observation Management:
Continuous cardiopulmonary monitoringPrevention of respiratory compromise/
aspiration
IV crystalloid hydrationBenzodiazepines PRN agitationPsychiatric consultation PRN
Steven J. Walsh and Marsha Ford
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21:22:48
Discharge Criteria:
Normal mental statusFluent speechAmbulatory with a steady gaitQRS duration < 120 msQTc interval < 500 msNo signs/symptoms consistent with SS/NMS
Comments:
– Consider aspiration pneumonitis and
rhabdomyolysis/compartment syndrome in patients found unresponsive or with altered mental status
– Neuroleptics are a heterogenous group of
medications, each with specific toxicities. Contact your regional poison center (800-222­1222 in the United States) for specific recommendations.
Substance: Latrodectus Mactans (Black Widow Spider) Envenomation
Observation Admission Criteria:
– Confirmed/suspected symptomatic grade I/II
envenomation (defined below) after 6-hour­or-less ED observation/treatment period controlled with PO/IV analgesics and/or benzodiazepines
23
Normal VS
Pain at the bite site that may be migratory to the trunk
Contraindications to Observation Admission:
– Grade I/II envenomation requiring
continuous infusion of opiates/opioids and/or benzodiazepines
– Grade III envenomation
23,24,25
Autonomic instability, respiratory distress, cardiac ischemia, severe muscle spasm/ rigidity, generalized myalgias/diaphoresis, nausea/emesis, headache
Evidence of superinfectionGravid patient
Observation Management:
– PO/IV analgesics/benzodiazepines PRN
tachycardia/pain/muscle spasm
– Tetanus prophylaxis
Discharge Criteria:
– Pain/muscle spasm well-controlled with PO
analgesics
– No evidence of superinfection
Comments:
– Avoid administration of calcium, dantrolene,
and centrally acting muscle relaxants (methocarbamol, cyclobenzaprine, metaxalone, etc.)
24,25
– Consult your regional poison center before
administering Latrodectus antivenom, which may cause anaphylaxis/anaphylactoid reaction and serum sickness
Substance: Crotalid (Pit Viper) Envenomation
Observation Admission Criteria:
– Progression of swelling halted with elevation
in conjunction with antivenom administration (see Commentsregarding antivenom) and elevation of affected extremity
Intact neurovascular statusNo evidence of coagulopathy (normal platelet
count/PT/INR/fibrinogen)
– Pain controlled with IV/PO analgesics
Observation Admission Contraindications:
Anaphylaxis to venom/antivenomCompartment syndrome (very rare)Clinically significant hemorrhage (very rare)Pain requiring continuous opiate/opioid
infusion
Observation Management:
Local wound careSplinting/elevation/serial circumferential
measurements of affected extremity
Debridement of hemorrhagic blebs PRNTetanus prophylaxisIV/PO analgesics PRNAntivenom PRN
Discharge Criteria:
– Stable laboratory studies (no worsening
thrombocytopenia/hypofibrinogenemia/INR elevation)
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21:22:48
Intact neurovascular statusPain controlled with PO analgesics
Comments:
– Consult with your regional poison center
prior to antivenom administration; some envenomations may not require antivenom
administration; additionally, antivenom can cause anaphylactoid/anaphylactic reactions as well as serum sickness
– Incision and suction of venom and/or ice
application to the bite site/affected extremity is not recommended
26–28
(See also Snakebites Chapters 84 and 85 under Specialized Clinical Protocols)
References
1. Substance Abuse and Mental Health Services Administration, Center for Behavioral Health Statistics and Quality. (July 2,
2012). The DAWN Report:
Highlights of the 2010 Drug Abuse Warning Network (DAWN) Findings on Drug­Related Emergency Department Visits. Rockville, MD.
2. Dart RC, Erdman AR, Olson KR, et al. Acetaminophen poisoning: an evidence-based consensus guideline for out-of­hospital management. Clin Toxicol. 2006;44:1–18.
3. Rumack BH. Acetaminophen hepatotoxicity: the first 35 years. J Toxicol Clin Toxicol. 2002;40:3–20.
4. Buckley NA, Whyte IM, OConnell DL, et al. Oral or intravenous N-acetylcysteine: which is the treatment of choice for acetaminophen (paracetamol) poisoning.
J Toxicol Clin Toxicol.
1999;37:759–767.
5. Daly FF, OMalley GF, Heard K, et al. Prospective evaluation of repeated supratherapeutic acetaminophen (paracetamol) ingestion. Ann Emerg Med. 2004 Oct;44(4):393–398.
6. Amrein R, Leishman B, Bentzinger C, et al. Flumazenil in benzodiazepine antagonism: actions and clinical use in intoxications and anaesthesiology. Med Toxicol. 1987;2:411–429.
7. Dunn W. Various laboratory methods screen and confirm benzodiazepines. Emerg Med News. 2000;21–24.
8. Beuhler MC, Spiller HA, Sasser HC. The outcome of unintentional pediatric bupropion ingestions: a NPDS database review. J Med Toxicol. 2010 Mar;6(1):4–8.
9. Spiller HA, Bosse GM, Beuhler M, et al. Unintentional ingestion of bupropion in children. J Emerg Med 2010; 38:332–336.
10. Harmon T, Jurta D, Krenzelok E. Delayed seizures from sustained-release bupropion overdose. J Toxicol Clin Toxicol, 1998;36:522.
11. Quadrani DA, Spiller HA, Widder P. Five-year retrospective evaluation of sulfonylurea ingestion in children. J Toxicol Clin Toxicol. 1996;34:267–270.
12. Spiller HA, Villalobos D, Krenzelok EP, et al. Prospective multicenter study of sulfonylurea ingestion in children. J Pediatr. 1997;131:141–146.
13. Burkhart KK. When does hypoglycemia develop after sulfonylurea ingestion? Ann Emerg Med. 1998;31:771–772.
14. Boyle PJ, Justice K, Krentz AJ, et al. Octreotide reverses hyperinsulinemia and prevents hypoglycemia induced by sulfonylurea overdoses. J Clin
Endocrinol Metab.
1993;76:752–756.
15. Fasano CJ, OMalley G, Dominici P, et al. Comparison of octreotide and standard therapy versus standard therapy alone for the treatment of sulfonylurea-induced hypoglycemia. Ann Emerg Med 2008 Apr;51(4):400–406.
16. Weaver LK, Gesell LB. Carbon Monoxide Poisoning. In: Gesell LB, ed. Hyperbaric Oxygen
2009: Indications and Results The Hyperbaric Oxygen Therapy Committee Report.Durham:
Underwater and Hyperbaric Medical Society; 2008:19–28.
17. Myers RAM, Snyder SK, Emhoff TA. Subacute sequelae of carbon monoxide poisoning. Ann Emerg Med. 1985;14:1167.
18. Gorman DF, Clayton D, Gilligan JE, et al. A longitudinal study of 100 consecutive admissions for carbon monoxide poisoning to The Royal Adelaide Hospital.
Undersea Hyperb Med.
1992;20:311–316.
19. Martell BA, Arnsten JH, Krantz MJ, et al. Impact of methadone treatment on cardiac repolarization and conduction in opioid users. Am J Cardiol. 2005;95:915–918.
20. Mills KC: Serotonin syndrome. A clinical update. Crit Care Clin. 1997;13:763–783.
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