MEDICATION
- Ampicillin/sulbactam: 3 g (peds: 100–200 mg ampicillin/kg/24 h) IV q6h
- Cefoxitin: 2 g (peds: 80–100 mg/kg/24 h) IV q6h
- Ceftriaxone: 1 g (peds: 50–100 mg/kg) IV q24h
- Ciprofloxacin: 400 mg (peds: 20–40 mg/kg) IV q12h
- Ertapenem: 1 g IM/IV q24h
- Metronidazole: 500 mg (peds: 30–50 mg/kg/24 h) IV q8–12h
- Morphine sulfate: 3–5 mg (peds: 0.1–0.2 mg/kg per dose q2–q4h) IV, every 15 min titrated to effect
- Piperacillin/tazobactam: 3.375 g (peds: 150–300 mg/kg/d if <6 mo; 240–400 mg/kg/d if >6 mo) IV q6h
FOLLOW-UP
DISPOSITION
Admission Criteria
- Surgical intervention of acute appendicitis
- Observation or further diagnostic workup if diagnosis is uncertain
Discharge Criteria
Patients with abdominal pain thought not to be appendicitis may be discharged if they meet the following criteria:
- Resolved or resolving symptoms
- Minimal or no abdominal tenderness
- No lab/radiologic abnormalities
- Able to tolerate PO intake
- Adequate social support and able to return if symptoms worsen
FOLLOW-UP RECOMMENDATIONS
24–48 hr recheck for patients discharged from the ED with abdominal pain of unclear etiology
PEARLS AND PITFALLS
- Pediatric and geriatric patients present atypically and have increased perforation rates
- Imaging is not required in a classic presentation of acute appendicitis
- Appendicitis cannot be ruled out on any imaging modality if the appendix is not visualized
ADDITIONAL READING
- Basaran A, Basaran M. Diagnosis of acute appendicitis during pregnancy: A systematic review.
Obstet Gynecol Surv
. 2009;64(7):481–488.
- Hennelly KE, Bachur R. Appendicitis update.
Curr Opin Pediatr
. 2011;23:281–285.
- Long SS, Long C, Lai H, et al. Imaging strategies for the right lower quadrant pain in pregnancy.
AJR Am J Roentgenol
. 2011;196:4–12.
- Singh A, Danrad R, Hahn PF, et al. MR imaging of the acute abdomen and pelvis: Acute appendicitis and beyond.
Radiographics
. 2007;27:1419–1431.
See Also (Topic, Algorithm, Electronic Media Element)
- Abdominal Pain
- Vomiting, Adult; Vomiting, Pediatric
CODES
ICD9
- 540.1 Acute appendicitis with peritoneal abscess
- 540.9 Acute appendicitis without mention of peritonitis
- 541 Appendicitis, unqualified
ICD10
- K35.3 Acute appendicitis with localized peritonitis
- K35.80 Unspecified acute appendicitis
- K37 Unspecified appendicitis
ARSENIC POISONING
Vinodinee L. Dissanayake
BASICS
DESCRIPTION
- Acute toxicity:
- Caused by intentional ingestion, malicious poisoning, or medication error
- Minimal lethal ingested dose ∼2 mg/kg
- Chronic toxicity:
- Resulting from occupational exposures, water or food contamination, or use of folk remedies containing arsenic
- Ingestion is the primary route of exposure
- Inhalational toxicity is possible from arsine gas exposure
ETIOLOGY
- Most cases seen in the ED result from intentional ingestion or malicious poisoning
- Sodium arsenate, found in ant killer, is the most common acute exposure in the US
- Contaminated food and water supplies are the most common cause worldwide
- Inorganic arsenic trioxide has been recently approved as a chemotherapeutic agent for acute myelogenous leukemia (AML)
- Melarsoprol, an organic arsenical, has been used to treat trypanosomiasis since 1949
- Found in pesticides, certain folk remedies (herbal balls), industrial wood preservatives
- May be released as arsine gas from combustion of zinc- and arsenic-containing compounds
Mechanism
- Arsenic exists in several forms—gas (arsine, or lewisite), organic, elemental, and inorganic
- Inorganic forms (pentavalent and trivalent arsenic) are most frequently involved in toxic exposures:
- Pentavalent arsenic uncouples oxidative phosphorylation
- Most pentavalent arsenic is converted to the more toxic trivalent arsenic in the body
- Trivalent arsenic binds sulfhydryl groups and interferes in hemoglobin production
- Some trivalent arsenic may be methylated into species of varying toxicity
- The more reactive species are DNA damaging and genotoxic
DIAGNOSIS
SIGNS AND SYMPTOMS
- CNS:
- Altered mental status/encephalopathy
- Neurodevelopmental deficits in children
- Peripheral neuropathy
- Acute: Sensory neuropathy
- Subacute: Sensorimotor neuropathy
- Peripheral dysesthesias
- Headache
- Seizures
- Cardiovascular:
- Prolonged QTc interval
- Hypotension (acute) or hypertension (chronic)
- Dysrhythmias, primarily ventricular
- Nonspecific ST segment changes
- Noncardiogenic pulmonary edema
- Pulmonary:
- Inhalational exposure increases lung cancer risk and respiratory mortality
- Large acute ingestion (8 mg/kg) may lead to severe respiratory distress
- Pulmonary edema, hemorrhagic bronchitis, and bronchopneumonia
- GI:
- Nausea, vomiting after ingestion and possibly inhalation
- Protracted and may be refractory to antiemetics at usual doses
- Can have hemorrhagic gastroenteritis; corrosive to GI tract
- Rice water diarrhea
- Abdominal pain
- Garlic odor to breath, vomit, stools
- Causes acute hepatitis; chronically, can cause portal HTN
- A possible association with diabetes mellitus in chronic exposure
- Miscellaneous (usually associated with chronic exposure)
- Acute rhabdomyolysis
- Blackfoot disease in Taiwan: Gangrene from loss of circulation to extremities
- Dermatitis, such as toxic erythroderma and hyperkeratotic, hyperpigmented lesions
- Hemolytic anemia (more pronounced with arsine gas exposure)
- Hypothyroidism (antagonizes thyroid hormone)
- Increased risk of carcinoma (liver/basal cell/squamous cell of skin/bronchogenic)
- Leukopenia (after several days)
- Mees lines (white bands across the nails owing to growth arrest caused by arsenic)
- Patchy alopecia
- Raynaud phenomenon and vasospasticity
ESSENTIAL WORKUP
- Spot urine arsenic level
- CBC
DIAGNOSIS TESTS & NTERPRETATION
Lab
- Spot urine arsenic level >1,000 μg/L may confirm diagnostic suspicion:
- Peaks 10–50 hr postingestion
- Definitive test is 24 hr urine collection with speciation into organic and inorganic types of arsenic.
- Blood levels not routinely helpful owing to short half-life in serum (∼2 hr)
- CBC to evaluate for anemia, leukopenia, basophilic stippling
- Electrolytes, BUN/creatinine, and glucose
- Urinalysis to look for evidence of hemolysis/rhabdomyolysis
- Liver function tests
- Total creatine phosphokinase (CPK) for rhabdomyolysis
- Hair and nail arsenic levels:
- Do not help in acute setting
- May help determine chronicity of exposure in select populations
Imaging
- Plain abdominal radiographs to look for radiopaque foreign body
- Cranial CT/other studies as indicated by patient’s condition
DIFFERENTIAL DIAGNOSIS
- Acute toxicity:
- Acute appendicitis/colitis/gastroenteritis
- Celiac disease
- Cholera
- Distributive shock
- Encephalopathy
- Toxic ingestions
- Amanita
mushroom poisoning
- Cyclic antidepressants or other seizure-inducing toxins
- Organophosphates
- Chronic toxicity:
- Addison disease
- Guillain–Barré syndrome or other neuropathy
- Raynaud phenomenon
- Thromboangiitis obliterans, or other vasculitides
- Vitamin deficiency (B
3
, B
6
, or B
12
)
- Wernicke–Korsakoff syndrome