The vital signs provide clues to volume status, presence of shock, and the presence of increased intracranial pressure. The constellation of systemic hypertension, bradycardia, and respiratory depression (Cushing triad) is a late sign of increased intracranial pressure. Head circumference should be measured at the time of admission in children younger than 18 months of age.
“In prospective surveillance of nearly 400,000 neonates in the United States (2006-2009), 72 percent of those who had sepsis or meningitis within 72 hours of birth had infection caused by GBS and E. coli.”Stoll BJ, Hansen NI, Sánchez PJ, et al. Early onset neonatal sepsis: the burden of group B Streptococcal and E. coli disease continues. Pediatrics 2011; 127:817.
“Nevertheless, even after institution of universal immunization with PCV7, pneumococcus remains the most common etiologic agent of bacterial meningitis in children, accounting for one-third of cases. Importantly, half of the children with pneumococcal meningitis were infected with serotypes not included in the vaccine (so-called “nonvaccine-type” strains). In our study population, many cases of pneumococcal meningitis were due to serotypes that have emerged as important causes of invasive pneumococcal disease in the post–conjugate vaccine era (such as serotypes 19A, 15C, and 33F)”. Nigrovic LE, Kuppermann N, Malley R, Bacterial Meningitis Study Group of the Pediatric Emergency Medicine Collaborative Research Committee of the American Academy of Pediatrics. Children with bacterial meningitis presenting to the emergency department during the pneumococcal conjugate vaccine era. Acad Emerg Med 2008; 15:522.
“In the non-hospitalized neonate who is strongly suspected to have bacterial meningitis, but whose CSF parameters are not immediately available or not entirely consistent with bacterial meningitis (eg, negative Gram stain), ampicillin plus an aminoglycoside plus cefotaxime should be initiated. In one survey of febrile infants younger than 90 days who presented to an emergency center, nearly 80 percent of infants with meningitis had ampicillin-resistant pathogens”. Byington CL, Rittichier KK, Bassett KE, et al. Serious bacterial infections in febrile infants younger than 90 days of age: the importance of ampicillin-resistant pathogens. Pediatrics 2003; 111:964. “ The authors recommended that the initial regimen contain ampicillin and gentamicin plus a third-generation cephalosporin because of the risk of GBS and L. monocytogenes infection in this age group, as well as for treatment of cefotaxime susceptible organisms. When meningitis resulting from a gram-negative organism is strongly suspected, for example when the CSF Gram stain reveals gram-negative bacilli, the empirical regimen of ampicillin and an aminoglycoside should be expanded to include cefotaxime.” Clin Microbiol Rev. 2010 July; 23(3): 467–492. doi: Epidemiology, Diagnosis, and Antimicrobial Treatment of Acute Bacterial Meningitis Matthijs C. Brouwer,1 Allan R. Tunkel,2 and Diederik van de Beek. “Keep HSV in differential if rash, Increase liver transaminases, sepsis like syndrome: controversy over adding acyclovir: can be d/c’d once HSV PCR and cultures are negative or alternative dx is made; enteroviral PCR. Viral isolates usually grow in tissue by 4-8 days. HSV meningitis: neonatal 60mg/kg per day divided in 3 divided doses x 14-21 days.” “When meningitis resulting from a gram-negative organism is strongly suspected, for example when the CSF Gram stain reveals gram-negative bacilli, the empirical regimen of ampicillin and an aminoglycoside should be expanded to include cefotaxime.” “Late-onset sepsis without meningitis in neonates who remain hospitalized is treated with vancomycin and an aminoglycoside. When lumbar puncture suggests meningitis, cefotaxime should be added to provide an extended spectrum for gram-negative enterics and for optimal activity in the CSF against pneumococci. Ampicillin should be added to a vancomycin-aminoglycoside regimen if GBS or L. monocytogenes is suspected (eg, on the basis of the Gram stain), because vancomycin concentrations in the CSF are not bactericidal for these organisms”. Albanyan EA, Baker CJ. Is lumbar puncture necessary to exclude meningitis in neonates and young infants: lessons from the group B streptococcus cellulitis- adenitis syndrome. Pediatrics 1998; 102:985.
“Repeat lumbar puncture — Lumbar puncture should be repeated routinely at 24 to 48 hours after initiation of antimicrobial therapy to document CSF sterilization. Gram-positive bacteria usually clear rapidly (within 24 to 48 hours) from the CSF after initiation of appropriate antimicrobial therapy, whereas gram-negative may persist for several days in severe cases.” “Reevaluation of the CSF 24 to 48 hours after initiation of antimicrobial therapy is important for several reasons: •Delayed sterilization of the CSF is associated with an increased risk of developing neurologic sequelae. •The persistent identification of organisms on a Gram-stained smear may be an early indication of inadequacy of antimicrobial therapy (eg, the organism is not susceptible to the concentration of antibiotic that is attained in the CSF. Persistence of viable organisms more than 48 hours after initiation of antimicrobial therapy is an indication for diagnostic neuroimaging because it can indicate a purulent focus (eg, obstructive ventriculitis, multiple small vessel thrombi) that can require additional intervention or increased duration of antimicrobial therapy. •Sterilization of the CSF is a criterion for discontinuing combination therapy for some pathogens (eg, GBS, Listeria). In uncomplicated neonatal meningitis, the CSF culture obtained 24 to 48 hours after initiation of therapy is sterile. If there is just a colony or two, it is appropriate to obtain a third CSF culture when it is known that the second is positive (ie, after an additional 24 to 48 hours). However, as indicated above, a positive culture obtained 24 to 48 hours after initiation of therapy with more than one or two colonies raises a concern for ventriculitis. The additional evaluation and management of infants with possible ventriculitis is individualized and should be undertaken in consultation with specialists in pediatric infectious diseases and pediatric neurosurgery. Treatment and outcome of bacterial meningitis in the neonate Authors Morven S Edwards, MD Carol J Baker, MD June 1, 2011. Treatment and outcome of bacterial meningitis in the neonate” Positive CSF culture — The duration of antimicrobial therapy depends upon the causative organism and the clinical course: •A 14-day course is sufficient for neonates with uncomplicated GBS meningitis and for meningitis caused by other gram-positive organisms, such as L. monocytogenes or Enterococcus. •A longer course of therapy is required for neonates with GBS meningitis who have a complicated course. •A 21-day course is the minimum for neonates with meningitis resulting from E. coli or other gram-negative pathogens. •Prolonged treatment, sometimes for as long as eight weeks, may be required for neonates with ventriculitis, abscesses, or multiple areas of infarction. “ Negative CSF culture — The duration of antibiotic therapy for neonates with negative cultures must be determined on an individual clinical basis. •For neonates with suspected but unproven bacterial meningitis, we usually suggest discontinuation of antimicrobials after 48 to 72 hours of negative CSF culture. •For neonates with CSF pleocytosis and bacteremia, but a negative CSF culture, we usually continue meningeal doses of antimicrobial therapy for 10 days for gram-positive bacteremia (ie, GBS) and 14 days for gram-negative bacteremia. “ E. Coli Ampicillin Resistant: 3rd Generation Cephalosporin plus Aminoglycoside Minimum 7 - 14 days combination plus total 21 days of 3rd generation cephalosporin or 14 days after CSF Sterility whichever is longer ( A III ) “Duration of therapy depends on individual patient response, though generalized guidelines according to the responsible pathogen are as follows: Neisseria meningitidis or H. influenzae, seven days; S. pneumoniae, 10 to 14 days; Streptococcus agalactiae, 14 to 21 days; aerobic gram-negative bacilli, 21 days (two weeks beyond the first sterile CSF culture in neonates); Listeria monocytogenes, 21 days or longer. Intravenous therapy is recommended throughout to maintain sufficient CSF concentrations. In neonates with meningitis caused by gram-negative bacilli, the duration of therapy should be determined in part by repeated lumbar punctures documenting CSF sterilization (A-III). Patients who have not responded clinically after 48 hours of appropriate therapy also should be monitored with repeated CSF analysis (A-III), particularly those with meningitis caused by resistant strains and those who have received adjunctive dexamethasone.” After Discharge: check audiology screen (also prior to d/c), consider earlier cochlear implant. Hearing test after 4-6 weeks. Check the following: hearing loss, orthopedic complication, skin complication, psychosocial problems, neurological and developmental problems, renal failure. Do Immune testing if more than 1 episode of meningococcal dz, if serotypes other than ACY W135, plus menigococcal dz plus other bacterial meningitis. Coagulase-negative staphylococci — Vancomycin is the antimicrobial of choice for proven meningitis caused by coagulase-negative staphylococci. These organisms rarely invade the meninges except as a complication of bacteremia accompanying intraventricular hemorrhage in very LBW infants (birth weight <1500 g) or as a result of surgical manipulations or placement of a ventriculoperitoneal shunt. Such infections invariably are of late onset.
Van de Beek D et al. Clinical features and prognostic features in adults with bacterial meningitis. NEJM. 28 October 2004. “Sixty-three percent of patients with meningococcal meningitis present with a rash that is usually petechial. Petechial rash may also be caused by Haemophilus influenzae or Streptococcus pneumoniae infection. Pneumococcal meningitis is more likely than meningococcal meningitis to be associated with seizures, focal neurologic findings, and altered consciousness. Clinical or laboratory feature Sensitivity (%) Two of the following features: fever, neck stiffness, altered mental status, and headache 95 Cerebrospinal fluid white blood cell count ≥ 100 per μL (0.10 × 109 per L) 93 Headache 87 Neck stiffness 83 Fever ≥ 100.4°F (38°C)77 Nausea74 Altered mental status (Glasgow Coma Scale score < 14)69 Growth of organism in blood culture 66 Triad of fever, neck stiffness, and altered mental status 44 Focal neurologic signs33 Seizure 5 Papilledema 3”
“5% sensitivity and 95% specificity for kernigs and brudzinski’s signs; 30% sensitivity for Nuchal rigidity-late presentation in children. Meningeal signs — Although meningeal signs are present at the time of admission in the majority of patients, they are not invariably present. In one review of 1064 cases of acute bacterial meningitis in children older than one month, 16 (1.5 percent) had no meningeal signs during their entire period of hospitalization. Nuchal rigidity may not be elicited in comatose patients or those with focal or diffuse neurologic deficits. In addition, nuchal rigidity may occur late in the course, particularly in young children. When meningitis was defined as ≥6 white cells/microL of CSF, the sensitivity was extremely low (5 percent for each sign and 30 percent for nuchal rigidity); the specificity was 95 percent for each sign and 68 percent for nuchal rigidity. Neither Kernig's nor Brudzinski's sign performed much better among the 29 patients with moderate or the four patients with severe meningeal inflammation, defined as ≥100 and ≥1000 white cells/microL, respectively. Nuchal rigidity was present in all four patients with severe meningeal irritation but had a specificity of only 70 percent”: Clinical Features of Bacterial Meningitis UpToDate.
Sadoun, Tania and Amandeep Singh. Adult Bacterial Meningitis in the United States: 2009 Update. Emergency Medicine Practice. September 2009.Volume 11, Number 9. OBTAIN an extensive travel and exposure history. --exposure to rodents (LCM), ticks (lyme), TB --Sexual activity (HSV-2, HIV, Syphillis) --Contacts with patients with viral exanthems (enterovirus) --Use of meds Physical exam: Rash: maculopauluar exanthem; enterovirus, HIV, syphillis, meningococcal, RMSF --parotitis ---severe vesicular/ulcerative genital lesions HSV-2 ---oropharyngeal thrush and cervical lymphadenopathy—HIV ---asymmetric flaccid paralysis: WNV. Meningitis: uncomfortable, lethargic, ha, cerebral function mostly normal can have seizure Encephalitis: AMS, as above, motor or sensory deficits, altered behavior, personality changes, speech or movement d/o. May present with meningoencephalitis a combo of both. Meds as cuase: A delayed hypersensitivity type reaction or 2 direct meningeal irritation. CSF with CSF RBC >2000 in nontraumatic tab: HSV Encephalatis: 0-27,000 RBCs also ct with frontal and temporal edema. RESOLVES WITHOUT SPECIFIC THERAPY. PCR for CSF Enterovirus: confirms diagnosis, decreases cost of unnecessary antibiotics, shorten stays in hospital. LCM: lymphocytic Choriomeningitis Virus. Human Zoonosis—Rodent borne areanovirus. Common in winter: excreted in feces of mice, rats,. HSV-2: Sexualy Activity: think of HSV- 2, HIV, Syphillis. IF GENITAL LESION present current OR week prior to meningeal symtpoms: Strong suggestion of HSV -2: 85% genital lesion present or preceded by about 1 week. USE ACYCLOVIR 10mg/kg q 8 hour oral agent at D/C x 10-14 days. PCR for HSVDNA in the CSF. IF recurrent HSV2 meningitis: a form of recurrent benign lymphocytic meningitis (RBLSM) : >3 episodes of fever and mengismus lasting 2-5 days caused by HSV2: Recurrent Mollaret’s Meningitis. “Successful management of intracranial abscess involves the administration of parenteral antibiotics and neurosurgical consultation. The combination of a third-generation cephalosporin (cefotaxime 50 mg/kg IV every 4 hours, with a maximum dose of 2 gm; or ceftriaxone 50 mg/kg IV every 12 hours, with a maximum dose of 2 gm), metronidazole (15 mg/kg IV every 12 hours), and vancomycin (15 mg/kg IV every 6 hours with a maximum dose of 500 mg) can be used in most patients who are presumed to have a contiguous source of infection (eg, an ear, sinus, or dental infection). Although some experimental evidence suggests that corticosteroids (dexamethasone 10 mg IV followed by 4 mg every 6 hours) reduce edema surrounding brain abscesses,36,37 no quality trials in humans have demonstrated clinical benefits from corticosteroid therapy. Emergent neurosurgical drainage should be considered in patients with signs of increased ICP; otherwise, patients may be observed for clinical response to parenteral antibiotics.”
“Prior administration of antimicrobial agents, particularly oral antibiotics, tends to have minimal effects on CSF cytology . However, CSF chemistry results in pretreated patients must be interpreted with caution. In a retrospective review of 231 children with bacterial meningitis in the post-Hib and pneumococcal conjugate vaccine era, 85 children received antibiotics before LP . Receipt of antibiotics for ≥12 hours before LP was associated with increased median CSF glucose concentration (48 versus 29 mg/dL [2.66 versus 1.6 mmol/L]) and decreased median CSF protein concentration (121 versus 178 mg/dL [1.21 versus 1.78 g/L]). Although the use of antimicrobial therapy before LP affects the CSF culture and perhaps the Gram stain, conventional teaching has been that a pathogen still can be identified in the CSF in the majority of patients up to several hours after the administration of antibiotics . However, a review of 128 children with bacterial meningitis specifically addressed this question and found that the time interval between antibiotic administration and negative CSF cultures may be shorter than appreciated for children who receive parenteral antibiotics : Among children with meningococcal meningitis who were treated with a parenteral dose of an extended-spectrum cephalosporin, three of nine LPs were sterile within one hour (occurring as early as 15 minutes), and all were sterile by two hours. Sterilization of the CSF was slower with pneumococcal meningitis. The first negative culture was obtained four hours after administration of antibiotics, and five of seven were negative by 10 hours. Rarely, patients with bacterial meningitis may present with normal or near-normal white blood cell counts, glucose levels, and protein levels. This has been observed in young children with neutropenia and other immunocompromised states, and very early in the course of meningococcal meningitis. Blood cultures should be obtained before antibiotic therapy is initiated in patients with suspected meningitis. Positive blood cultures are obtained in approximately two-thirds of patients with bacterial meningitis”: Van de Beek D, de Gans J, Spanjaard L, Weisfelt M, Reitsma JB, Vermeulen M. Clinical features and prognostic factors in adults with bacterial meningitis. N Engl J Med. 2004;351(18):1849-1859. (Prospective; 696 cases). “CSF culture remains the gold standard for the diagnosis of bacterial meningitis; aerobic culturing techniques are obligatory for community-acquired bacterial meningitis. Anaerobic culture may be important for postneurosurgical meningitis or for the investigation of CSF shunt meningitis. “ Clin Microbiol Rev. 2010 July; 23(3): 467–492. doi: Epidemiology, Diagnosis, and Antimicrobial Treatment of Acute Bacterial MeningitisMatthijs C. Brouwer,1 Allan R. Tunkel,2 and Diederik van de Beek also with these same authors: Blood Culture Blood cultures are valuable to detect the causative organism and establish susceptibility patterns if CSF cultures are negative or unavailable. Blood culture positivity differs for each causative organism: 50 to 90% of H. influenzae meningitis patients, 75% of pneumococcal meningitis patients, and 40% of children and 60% of adult patients with meningococcal meningitis. The yield of blood cultures was decreased by 20% for pretreated patients in two studies.
Kaplan, Sheldon et al. Neurologic complications of bacterial meningitis in children. UpToDate. 24 Jan 2011. “In one review of 235 children with bacterial meningitis, approximately 78 percent were irritable or lethargic, 7 percent were somnolent, and 15 percent semicomatose or comatose at the time of admission . Among patients with pneumococcal meningitis, 29 percent were semicomatose or comatose at the time of admission. All of the children with hearing loss had one or more of the following risk factors at presentation: Symptoms for ≥2 days before admission Absence of petechiae CSF glucose concentration ≤10.8 mg/dL (0.6 mmol/L) S. pneumoniae infection Ataxia Hearing loss is two to three times more common in children with pneumococcal meningitis than with other forms of bacterial meningitis . Ataxia is commonly associated with hearing loss in children, since both are related to bacterial labyrinthitis.” Cranial nerve palsy The abducens (VI) nerve is the cranial nerve most commonly affected in meningitis, probably because its long intracranial segment adjacent to the brainstem is highly vulnerable to elevated intracranial pressure and the inflammatory reaction that can occur with meningitis.
Tunkel, Allan R. et al. Practice guidelines for the management of bacterial meningitis. Clin Infect Dis. 1 November 2004 Empiric regimen — The empiric regimen should include coverage for penicillin-resistant S. pneumoniae and N. meningitidis, the two most common causes of bacterial meningitis in infants and children. An appropriate empiric regimen (ie, one that covers antibiotic-resistant S. pneumoniae, N. meningitidis, and Hib) includes high doses of a third-generation cephalosporin (eg, cefotaxime, ceftriaxone) and vancomycin : Cefotaxime (300 mg/kg per day intravenously [IV], maximum dose 12 g/day, in 3 or 4 divided doses), or ceftriaxone (100 mg/kg per day IV, maximum dose 4 g/day, in 1 or 2 divided doses), plus: Vancomycin (60 mg/kg per day IV, maximum dose 4 g/day, in 4 divided doses) If ceftriaxone is used, twice daily dosing to avoid the possibility of inadequate treatment in the event of dosing errors, delayed doses, or missed doses . Some experts suggest the addition of rifampin to the empiric regimen if dexamethasone is administered. Consultation with an expert in pediatric infectious diseases is recommended for children in whom cephalosporins or vancomycin are contraindicated.
Prehospital: GET GCS or AVPU, Finger stick, O2, 2 largebore IV’s; universal precautions; chemoprophylaxis to those who intubate and have contact with mucous membranes as well as confirmed menigococcal meningitis.
Dubos, Francois et al. Clinical decision rules for evaluating meningitis in children. Current Opinion in Neurology 2009, 22:288–293: “Refined Bacterial Meningitis Score: Introduced clinical variables and deleted less useful variables such as White count (peripheral ANC) and CSF neutrophil counts. So added purpura and added serum procalcitonin. The modified rule recommends antibiotic treatment and hospitalization for children with meningitis and presenting at least one of the following criteria: seizure, ‘toxic’ appearance (i.e.irritability, lethargy, or low capillary refill), purpura, positive CSF Gram staining, PCT of at least 0.5 ng/ml, or CSF protein at least 50 mg/dl. This modified rule, called the Meningitest, had a sensitivity of 100% in the derivation and internal validation sets (95% CI 78–100 and 65–100, respectively) and a specificity of 62 and 51%, respectively. The external validation of this Meningitest used the same European population (six hospitalbased cohort studies from five European countries) mentioned above. The sensitivity remained 100% (95%CI 96–100) but the specificity was lower [37% (95% CI 28–47)]. This would still make it possible to safely eliminate antibiotic treatments and hospital stays for 37% of the children with acute meningitis. insufficient validation for the Meningitest. Both can be used, though cautiously, bearing in mind the limitations of each rule: some rare false negative patients with the BMS and insufficient validation for the Meningitest.Large prospective multicenter studies are now needed to provide confirmation of their validity before the extensive generalization of their use. Exclusion Criteria: Neurosurgical history Immunosuppression CSF red blood cell count ≥ 0.01 × 106 per μL Antibiotic use in the previous 48 hours. 100% Sensitivity; 37-51% Specific n=365. Toxic appearance: irritability, lethargy, or low capillary refill. c The sensitivities of the rules are determined by presence of at least one criterion, and specificities by the absence of any criteria.”
Transcript of "Pediatric neurologic emergencies"
Seizures-neonatal, infants, febrile
STROKES in Pediatrics
brief and subtle
“bicycling” motion to limbs
typically sz’s can’t be provoked/consoled
EEG alone less predictable-unless together
with mri.(murray,boylan,r yan-pediatrics-2009 )
Presents within first day (0-24hrs)
congenital CNS anomalies
electrolyte abnormalities – hypoglycemia and hypocalcemia
CNS trauma – maternal drug toxicity
4 EPILEPTIC SYNDROMES:
1)Benign familial conv.2)fifth day fits
syn) 5) DE VIVO SYNDROME
HISTORY- PHYSICAL EXAM
RADIOLOGIC – EEG
2)CT-LOTS OF RADIATION
3)MRI- MORE DEF OF INFARTS
AND MORE ACCURATE FOR PROGNOSIS
Phenobarbital-20mg/kg slowly(can go up to
40mg/kg total in intractable seizures)
Phenitoin-20mg/kg iv slowly over 30-45 mts
Lorazepan-.1mg/kg q 6-8hrs
Piridoxin-50-100 mg iv after previous 3 meds
Neonatal seizure – in first 28 days of life
(typically first few days)
seizure lasting >30 mins
NB rose 5-10 mins
sequential seizures without regain LOC >30min
Febrile seizure – NIH defn. - event of
infancy/childhood, typically between age
3mo and 5yrs, with no evidence intracranial
infection or defined cause
Epilepsy - two or more seizures not provoked
by a specific event such as fever, trauma,
infection, or chemical change
partial – focal onset
tonic, clonic, tonic-clonic, myoclonic, atonic, absence
simple partial – no LOC
complex partial – LOC
partial secondarily generalized
age 3mo – 5yrs
peak age 9-20 mo
2-5% children will have before age 5
25-40% will have family history
80 – 97% simple
3 - 20% complex
< 15 mins
no focal features
no greater than 1 episode in 24h
neurologically and developmentally normal
febrile epilepticus >30min or recurrent without
regaining consciousness > 30min
recurrence within 24h
risk recurrence 25-50%
risk recurrence after 2nd – 50%
most recurrences within 6-12 mo
(20% within same febrile illness)
Risk of epilepsy
2-3% (baseline 1%)
family history of epilepsy
abnormal developmental status
complex febrile seizure
seizure lasting >30 mins
NB Rosen 5-10 mins
sequential seizures without regain LOC >30min
mortality in pediatric status epilepticus 4%
morbidity may be as high as 30%
brief directed Hx and Px
if meningitis/encephalitis considered
anything at all?
what about first time seizures? recurrent?
septic work-up (CBC, BC, urine C+S, CXR, LP)
< 12 - 18 mo
therapeutic drug levels
TORCH, ammonia, amino acids in neonate
CPK, lactate, prolactin – ?confirm seizure?
patients at greatest risk for meningitis
under 18 months of age
seizure in the ED
focal or prolonged seizure
seen a physician within the past 48 hours
concern about follow-up
prior treatment with antibiotics
The American Academy of Pediatrics
“strongly consider” in infants under 12 months of age with a first
WHO? which patients?
WHAT? CT vs. MRI
ultrasound in neonates
WHEN? emergent vs. elective
predictors of abnormal findings of computed tomography of the head
in pediatric patients presenting with seizures
Warden CR - Ann Emerg Med - 01-Apr-1997; 29(4): 518-23
retrospective case series
predicts CT scan results normal if
no underlying high-risk condition
malignancy, NCT, recent CHI, or recent CSF shunt revision
older than 6 months
sustained a seizure of 15 minutes or less
no new-onset focal neurologic deficit
not prospectively validated
correct underlying pathology, if any
antipyretics ineffective in febrile seizure
anti-epileptic choice often trial and error
no anti-epileptic 100% effective
febrile seizure – diazepam, phenobarbital, valproic acid
Currently AAP does not recommend
neonatal - phenobarbital
generalized TC – phenytoin, phenobarbital, carbamazepine, valproic
absence – ethosuximide, valproic acid
new anti-epileptics – felbamate, gabapentin, lamotrigine,
topiramate, tiagabine, vigabatrine
in consultation with neurologist
Fever or hypothermia
Irritability or lethargy
Tachypnea or apnea
Bulging fontanelle (late)
Vomiting or diarrhea
Altered Sleep Pattern
***INCREASE INTRACRANIAL PRES.3 DE CUSHING
Norris, Cecilia M.R. et al. Aseptic Meningitis in the Newborn and Young Infant. AAFP.
15 May 1999; 59.
Affects all age groups
Male = Female
Newborns ( 0 - 4 weeks )
Group b strep ( 50 % )
E. coli ( 25 % )
Other gram - negative rods ( 8 % )
Listeria monocytogenes ( 6 % )
S. pneumoniae ( 5 % )
Stoll BJ, Hansen NI, Sanchez PJ, et al. Early onset neonatal sepsis: the burden of group B
Streptococcal and E. Coli disease continues. Pediatrics 2011; 127: 817.
Infants ( > 1 month - < 3 months )
Group b streptococcus ( 39 % )
Gram-negative bacilli ( 32 % )
S. pneumoniae ( 14 % )
N. meningitidis ( 12 % )
Nigrovic LE, Kuppermann N, Malley R, Bacterial Meningitis Study Group of the Emergency Medicine
Collaborative Research Committee of the American Academy of Pediatrics. Children with bacterial
meningitis presenting to the emergency department during the pneumococcal conjugate vaccine era. Acad
Emerg Med 2008; 15: 522.
< 1 month old
Amp + Aminoglycoside
Amp + 3rd Gen Ceph
Amp + aminoglycoside + 3rd Gen Ceph
No Ceftriaxone in above = Kernicterus
1 – 23 months old
Vancomycin + 3rd Gen Ceph
Tunkel, Allan R. Practice guidelines for the management of bacterial meningitis.
Clinical Infectious Disease. 1 November 2004.
GBS + : Pen G or Amp for 14 - 21 days
E. Coli Amp Resistant: 3rd Gen Ceph plus
Must repeat LP with all Gram Neg Bacilli
Min 7 - 14 days combination + total 21 days of 3rd gen
ceph or 14 days after CSF Sterility whichever is longer ( A
L. Monocytogenes: Amp x 14 – 21 days
Tunkel, Allan R. Practice guidelines for the management of bacterial meningitis. Clinical Infectious
Disease. 1 November 2004.
Symptoms lasting < 24 hours ( 48 % )
Focal Neurologic Deficit ( 33 % )
Rash ( 26 % )
Coma ( 14 % )
Seizure ( 5 % )
Van de Beek D et al. Clinical features and prognostic features in adults with
bacterial meningitis. NEJM. 28 October 2004.
Exam for signs of infection
Glasgow Coma Scale
HSV – 1 Most common cause
Viral: Enterovirus, HIV, WNV, Mumps, LCM, HSV - 2
Fungal: Coccidioidomycosis, Cryptococcus
Parasites ( Angiostrongyliasis )
Ehrlichosis, RMSF, Lyme, Syphillis
Neoplasm of the leptomeninges
Drug - Induced: NSAIDs, Septra, Pyridium, Allopurinol
Sadoun, Tania and Amandeep Singh. Adult Bacterial Meningitis in the United States: 2009 Update.
Emergency Medicine Practice. September 2009.Volume 11, Number 9.
Leukocytosis or leukopenia
Normal renal function
+ Blood cultures ( 40 – 75 % )
WBC’s ( Neutrophils, Lymphocytes )
CULTURE – GOLD STANDARD
Banmberger, David, Diagnosis, Initial Management, and Prevention of Meningitis Am Fam Physician. 2010 Dec 15;82(12):
Impaired mental status ( most irritable / lethargic
15 % comatose at admission )
Cerebral edema and increased intracranial pressure
Seizures ( 20 – 30 % )-lorazepan + dilantin
Hearing loss ( 11 % )
CN VI - most commonly affected
Neuropsychological impairment ( 4 % )
Subdural effusion ( 10 – 33 % )
Kaplan, Sheldon et al. Neurologic complications of bacterial meningitis in children. UpToDate.
24 Jan 2011.
2 - 50 years of age - Empiric
Vancomycin + 3rd gen ceph
For Gram Stain +
N. meningitidis / H. influenzae: 3rd gen ceph
S. pneumoniae: Vancomycin + 3rd gen ceph
Tunkel, Allan R. et al. Practice guidelines for the management of bacterial meningitis. Clin Infect
Dis. 1 November 2004.
Inpatient ( often ICU )
Appropriate Antibiotic Therapy
Supportive Care(hemo-dinamic ,respiratory,
renal & electrolytes, myocardial support)
Treat coexisting conditions(seizures ,brain
Prevent hypothermia and dehydration
Tunkel, Allan R. et al. Practice guidelines for the management of bacterial meningitis.
Clin Infect Dis. 1 November 2004.
CSF positive Gram staining
Presence of purpura
CSF protein > 50 mg / dl
Serum Procalcitonin > 0.5 ng / ml
Dubos, Francois et al. Clinical decision rules for evaluating meningitis in children. Current Opinion in
Neurology 2009, 22:288–293.
Etiology: more with pneumococcal
Seizure after 72 hours
CSF sugar < 20 mg per dl at admission
Delayed sterilization of CSF : > 24 hours
Estado patologico caracterizado por
1)inconciencia profunda-perdida de via
area , broncoaspiracion.
3)resistencia a estimulos externos
4)DISFUNCION de ARAS
5)Bien en tronco o hemisferios cer.
6)requiere minimo una hora para
distingirlo de contusion,sincope u otras entidades
de aparicion transitoria.
Management of ABC ,S comes first
Airway clearing comes first
If hx. Of trauma or not CSPINE stabilization
Respiratory effort evaluation + 02 supp or
May need assist control respiration plus
Evaluation of “DERM”
D- depth of coma or response to stimuli
E- pupils equal ,reactive ,dilated ,constricted
R- respiration altered?taquipnea,distress ?
M- paralysis? Motor response? How is the
response ? Decorticate? Decerabrate?
CUSHING TRIAD(icp high)
Injuries causing coma?-injuries caused by fall?
What do witness referred?
Causes: not enough 02? Low sugar?
Decreased brain perfusion with decrease 02
Structural causes: trauma plus consequences
Metabolic, toxins, infection, fever?
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