We appreciate the work by Garro et al (1) prospectively validating
the clinical prediction model for Lyme meningitis we developed from a
retrospective cohort (2). In fact, our model was also recently validated
in a retrospective cohort of children from Belgium (3). Garro and
colleagues (1) should be commended for their work as prediction models are
rarely validated. Despite the relatively small number of enrolled
subjects, this prospective validation provides further support for
performing a multicenter study to determine whether a prediction model can
address two key issues in caring for pediatric patients presenting with
aseptic meningitis. Firstly, can the model decrease antibiotic use in
children who are at “low risk” for Lyme meningitis? Secondly, for those
children at “high risk” for LM, can early treatment with parental
antibiotics while awaiting confirmatory serology testing reduce the number
of days an indwelling catheter is needed, thus reducing the risk of a
catheter-related complications?
While the “Rule of 7’s” suggested by Garro et al (1) is an easy
concept to remember, it should noted that facial nerve palsy is not the
only cranial neuropathy seen in Lyme meningitis (4). It is unclear
whether Garro et al (1) or Tuerlinckx et al (3) considered the presence of
papilledema, as we did in our model, to be classified as cranial neuritis.
In our own clinical experience, abducens nerve palsy and papilledema are
excellent clues, in the correct context, to raise your suspicion for Lyme
meningitis versus aseptic meningitis. Papilledema has been reported to be
the only neurologic finding in patients with Lyme meningitis prior to
their progression to meningitis (5). As papilledema caused by Lyme
meningitis can lead to vision loss (6), a fundus examination and
measurement of cerebrospinal fluid opening pressure in all children with
suspected meningitis are important elements in the evaluation of children
with Lyme meningitis.
Robert A. Avery, D.O.
Children’s Hospital of Philadelphia
Philadelphia, PA
Stephen C. Eppes, M.D.
A.I. duPont Hospital for Children
Wilmington, DE
Samir S. Shah, M.D., M.S.C.E.
Children’s Hospital of Philadelphia
Philadelphia, PA
References
1. Garro AC, Rutman M, Simonsen K, Jaeger KL, Chapin K, Lockhart G.
Prospective validation of a clinical prediction model for Lyme meningitis
in children. Pediatrics. 2009; 123:e829-834.
2. Avery RA, Frank G, Glutting JJ, Eppes SC. Prediction of Lyme
meningitis in children from a Lyme disease-endemic region: A logistic-
regression model using history, physical, and laboratory findings.
Pediatrics. 2006; 117:e1-7
3. Tuerlinckx D, Bodart E, Jamart J, Glupczynski Y. Prediction of
Lyme meningitis based on a logistic regression model using clinical and
cerebrospinal fluid analysis: A European model. Pediatr Infect Dis J.
2009; 28:394-397.
4. Shah SS, Zaoutis TE, Turnquist J, Hodinka RL, Coffin SE. Early
differentiation of Lyme from Enteroviral meningitis. Pediatr Infect Dis
J. 2005;24:542-545.
5. Steenhoff AP, Smith MJ, Shah SS, Coffin SE. Neuroborreliosis with
progression from pseudotumor cerebri to aseptic meningitis. Pediatr
Infect Dis J. 2006; 25:91-92.
6. Raucher HS, Kaufman DM, Goldfarb J, Jacobson RI, Roseman B. Wolff
RR. Pseudotumor cerebri and Lyme disease: a new association. J Pediatr.
1985; 107:931-933.
Conflict of Interest:
None declared