Updated: Oct 27, 2008
Epistaxis, or nosebleed, is a common pediatric complaint. Most incidents are rarely life threatening but cause significant parental concern.1 Most nosebleeds are benign, self-limiting, and spontaneous but may also be recurrent. Many uncommon causes are also noted.
Epistaxis can be divided into 2 categories, anterior bleeds and posterior bleeds, based on where the bleeding originates.
Bleeding typically occurs when the mucosa is eroded and vessels become exposed and subsequently break. More than 90% of bleeds occur anteriorly and arise from the Little area, where the Kiesselbach plexus forms on the septum.2 The Kiesselbach plexus is where vessels from both the internal carotid artery (anterior and posterior ethmoid arteries) and the external carotid (sphenopalatine and branches of the internal maxillary arteries) converge. These capillary or venous bleeds provide a constant ooze, rather than the profuse pumping of blood observed from an arterial origin.
Posterior bleeds arise further back in the nasal cavity, are usually more profuse, and are often of arterial origin. A posterior source presents a greater risk of airway compromise, aspiration of blood, and greater difficulty controlling bleeding.
Epistaxis usually occurs in children aged 2-10 years. Occurrence is unusual in infants in the absence of a coagulopathy or nasal pathology (eg, choanal atresia, neoplasm). Local trauma (eg, nose picking) does not occur until later in the toddler years. Older children and adolescents also have a less frequent incidence. Consider cocaine abuse in adolescent patients.
In all children in whom lesions are not observed in the Kiesselbach area, consider an otolaryngology consult for evaluation with a flexible or rigid rhinoscopy and nasopharyngoscopy to search for the source of bleeding and to rule out any lesions causing the bleeding. This is particularly important when epistaxis is combined with nasal airway obstruction, especially when unilateral obstruction is present. Most children older than 6 years can tolerate a well-coached flexible fiberoptic examination of the nasal cavity with a 3-mm scope without significant discomfort or mental trauma if the nose is anesthetized and decongested.
Other reasons for consultations are as follows:
While bleeding is occurring and the assessment is in process, the child should remain nothing by mouth (NPO). Once bleeding is controlled, a full diet can be started.
Patients with a simple controlled bleed may resume regular activity; however, instruct individuals not to forcefully blow or pick their noses. For a few days, avoiding contact sports or activities that may directly traumatize the nose is probably prudent.
Antibiotics with staphylococcal and streptococcal coverage are required if nasal packing is placed. The oral route is used most commonly because most patients are treated on an outpatient basis. If the patient requires admission, initially use intravenous medications. Continue all antibiotics until the packing is removed.
First-generation cephalosporin arrests bacterial growth by inhibiting bacterial cell wall synthesis.
250-500 mg PO qid
25-50 mg/kg/d PO divided qid
Coadministration with aminoglycosides increases nephrotoxic potential
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in renal impairment
First-generation semisynthetic cephalosporin that arrests bacterial cell wall synthesis, inhibiting bacterial growth. Parenteral antibiotic.
1 g IV q6h until packing removed or can tolerate PO
25-50 mg/kg/d IV divided q6-8h until packing removed or can tolerate PO
Probenecid prolongs effect of cefazolin; coadministration with aminoglycosides may increase renal toxicity; may yield false-positive urine-dipstick test results for glucose
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in renal impairment; superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy
Binds to one or more penicillin-binding proteins, which, in turn, inhibits synthesis of bacterial cell walls. For treatment of infections caused by penicillinase-producing staphylococci. Available as a susp of 62.5 mg/5 mL.
250-500 mg PO qid
12.5-25 mg/kg/d PO divided qid
Decreases efficacy of PO contraceptives; increases effects of anticoagulants; probenecid and disulfiram may increase penicillin levels
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Monitor PT in patients taking anticoagulant medications; toxicity may increase in patients with renal impairment
Parenteral penicillinase-resistant (antistaphylococcal) penicillin.
1-2 g IV q4h
50-200 mg/kg/d IV divided q4-6h
Associated with warfarin resistance when administered concurrently; effects may decrease with bacteriostatic action of tetracycline derivatives
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
To optimize therapy, determine causative organisms and susceptibility
Inhibits bacterial growth by inhibiting synthesis of dihydrofolic acid.
160 mg (trimethoprim)/800 mg (sulfamethoxazole) PO q12h (ie, 1 double-strength [DS] tab q12h)
5-10 mg/kg/d (based on trimethoprim component) PO divided bid
May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly patients; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine
Documented hypersensitivity; megaloblastic anemia due to folate deficiency
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Do not use near term in pregnancy because of risk of kernicterus in the newborn; discontinue at first appearance of rash or sign of adverse reaction; obtain CBCs frequently; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; caution in folate deficiency (eg, chronic alcoholics, elderly patients, those receiving anticonvulsant therapy, or those with malabsorption syndrome); hemolysis may occur in individuals with G-6-PD deficiency; patients with AIDS may not tolerate or respond; caution in renal or hepatic impairment (perform urinalyses and renal function tests during therapy); give fluids to prevent crystalluria and stone formation
Semisynthetic derivative of lincomycin that inhibits protein synthesis by binding to 50s ribosomal subunit. Available as 75-mg/5 mL oral suspension.
300 mg PO qid
600 mg IV q8h
8-25 mg/kg/d PO divided tid/qid
20-40 mg/kg/d IV divided q6-8h
Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects of clindamycin; antidiarrheals may delay absorption of clindamycin
Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Benzyl alcohol is used as a preservative and has demonstrated toxicity in neonates; adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile
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epistaxis, nosebleed, nose bleed, nasal hemorrhage, anterior bleed, posterior bleed, airway compromise, cocaine abuse, nasal stenosis, leukemia, von Willebrand disease, hematemesis, melena, rhinitis, allergic rhinitis, Osler-Weber Rendu syndrome, nasal tumors, hemophilia, pertussis, cystic fibrosis, intranasal rhabdomyosarcoma, nasal angiofibroma
William Gluckman, DO, MBA, FACEP, Assistant Professor, Department of Surgery, Section of Emergency Medicine, University of Medicine and Dentistry of New Jersey, University Hospital; Attending Emergency Physician, St Joseph's Regional Medical Center; President and CEO, FastER Urgent Care
William Gluckman, DO, MBA, FACEP is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Robert Barricella, DO, FAAP, FACEP, Director of Pediatric Emergency Department and Emergency Fellowship, Assistant Professor, Department of Pediatrics, University of Medicine and Dentistry of New Jersey
Robert Barricella, DO, FAAP, FACEP is a member of the following medical societies: American Academy of Pediatrics, American College of Emergency Physicians, and American Medical Association
Disclosure: Nothing to disclose.
Huma Quraishi, MD, Division Director, Assistant Professor, Department of Pediatrics, Division of Otolaryngology, University of Medicine and Dentistry of New Jersey
Huma Quraishi, MD is a member of the following medical societies: American Academy of Otolaryngic Allergy and American Academy of Otolaryngology-Head and Neck Surgery
Disclosure: Nothing to disclose.
Sangeeta Lamba, MD, Resident Physician, Section of Emergency Medicine, University Hospital, University of Medicine and Dentistry of New Jersey
Sangeeta Lamba, MD is a member of the following medical societies: American College of Emergency Physicians, American College of Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Orval Brown, MD, Director of Otolaryngology Clinic, Professor, Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center at Dallas
Orval Brown, MD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Medical Association, American Society of Pediatric Otolaryngology, Society for Ear, Nose and Throat Advances in Children, and Society of University Otolaryngologists-Head and Neck Surgeons
Disclosure: Nothing to disclose.
Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from broker recommendation; Avanir Pharma Stock Investment from broker recommendation
John E McClay, MD, Assistant Professor, Department of Otolaryngology, Division of Pediatric Otolaryngology, Children's Medical Center, University of Texas Southwestern Medical School
John E McClay, MD is a member of the following medical societies: American Academy of Otolaryngic Allergy, American Academy of Otolaryngology-Head and Neck Surgery, American College of Surgeons, and American Medical Association
Disclosure: Nothing to disclose.
Paul D Petry, DO, FACOP, FAAP, Consulting Staff, Freeman Pediatric Care, Freeman Health System
Paul D Petry, DO, FACOP, FAAP is a member of the following medical societies: American Academy of Osteopathy, American Academy of Pediatrics, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.
Glenn C Isaacson, MD, FACS, FAAP, Professor of Otolaryngology-Head and Neck Surgery and Pediatrics, Temple University School of Medicine
Glenn C Isaacson, MD, FACS, FAAP is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Laryngological Rhinological and Otological Society, American Society of Pediatric Otolaryngology, and Society of University Otolaryngologists-Head and Neck Surgeons
Disclosure: Covidien Honoraria Consulting
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