Dental Care for a Child with Congenital Hydrocephalus: A Case Report with 12-Month Follow-Up

Yasser Alsayed Tolibah, Chaza Kouchaji, Thuraya Lazkani, Mohammad Tamer Abbara, Saffana Jbara, Ziad D Baghdadi, Yasser Alsayed Tolibah, Chaza Kouchaji, Thuraya Lazkani, Mohammad Tamer Abbara, Saffana Jbara, Ziad D Baghdadi

Abstract

Hydrocephalus affects the central nervous system as a result of progressive ventricular dilatation from the accumulation of cerebrospinal fluid in the brain's lateral ventricles. This paper reports on the oral characteristics of a child with congenital hydrocephalus, discusses her complex dental care needs, and presents dental management of this case. Despite the complex and challenging dental needs, this child received dental treatment in a chairside approach without general anesthesia. A thorough knowledge of the patient's medical condition, together with expert clinical skills, was indispensable for managing the child and improving the quality and length of her life.

Keywords: child; dental care for the chronically ill; dental care for the disabled; facial asymmetry; hydrocephalus; oral health; tooth diseases.

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(A) Frontal view of the child. (B) Lateral view of the child. Note the enlargement in the head’s posterior region due to hydrocephalus. (C) The ventriculoperitoneal (VP) shunt in the neck’s left side.
Figure 2
Figure 2
(A) The upper arch. (B) Frontal view of both arches in occlusion. (C) The lower arch.
Figure 3
Figure 3
A panoramic radiograph showing teeth #46 and #36 with extremely large carious lesions and periapical radiolucencies, tooth #16 with an extensive carious lesion, and large carious lesions in the upper primary molars.
Figure 4
Figure 4
(A) Apical lesions with extensive decay in tooth #36. (B) Verifying the placement of the MTA plug. (C) Completed root canal treatment and placement of a metallic crown.
Figure 5
Figure 5
(A) Apical lesions with extensive decay in tooth #46. (B) Biodentine placement, completed root canal treatment, and placement of a metallic crown.
Figure 6
Figure 6
(A) A pinpoint pulp exposure in tooth #16. (B) MTA placed.
Figure 7
Figure 7
(A) Cavitated carious lesion and hypomineralized spots on the buccal surface of tooth #21. (B) Resin-bonded restoration after finishing and polishing.
Figure 8
Figure 8
1 month after treatment. (A) The upper arch. (B) Anterior view in occlusion. (C) The lower arch.
Figure 9
Figure 9
(A) The upper arch with a palatal crib. (B) The palatal crib in occlusion. (C) The lower arch with the lingual holding arch.
Figure 10
Figure 10
(A) A panoramic radiograph one year after treatment. (B) The lower-right permanent molar immediately after the treatment. (C) The lower-right permanent molar one year after the treatment. Note apical healing. (D) The lower-left permanent molar immediately after the treatment. (E) The lower-left permanent molar one year after the treatment. Note apical healing. (F) The upper arch one year after the treatment. (G) Both arches in occlusion. Note the reduction in an open bite. (H) The lower arch one year after the treatment.
Figure 10
Figure 10
(A) A panoramic radiograph one year after treatment. (B) The lower-right permanent molar immediately after the treatment. (C) The lower-right permanent molar one year after the treatment. Note apical healing. (D) The lower-left permanent molar immediately after the treatment. (E) The lower-left permanent molar one year after the treatment. Note apical healing. (F) The upper arch one year after the treatment. (G) Both arches in occlusion. Note the reduction in an open bite. (H) The lower arch one year after the treatment.

References

    1. Acs G., Cozzi E. Antibiotic prophylaxis for patients with hydrocephalus shunts: A survey of pediatric dentistry and neurosurgery program directors. Pediatr. Dent. 1992;14:246–250.
    1. Akhter R., Hassan N.M.M., Martin E.F., Muhit M., Smithers-Sheedy H., Badawi N., Khandaker G. Caries experience and oral health-related quality of life (OHRQoL) of children and adolescents with cerebral palsy in a low-resource setting. BMC Oral Health. 2019;19:15. doi: 10.1186/s12903-018-0704-2.
    1. Akinwonmi B.A., Kolawole K.A., Folayan M.O., Adesunloye A.M. Orthodontic treatment need of children and adolescents with special healthcare needs resident in Ile-Ife, Nigeria. Eur. Arch. Paediatr. Dent. 2020;21:355–362. doi: 10.1007/s40368-019-00492-y.
    1. Aptekar A., Sandor G.K. Point of care. What precautions and measures do I have to consider when treating a patient with ventriculoperitoneal vs ventriculoatrial shunt? J. Can. Dent. Assoc. 2006;72:627–628.
    1. Ausili E., Tabacco F., Focarelli B., Nucera E., Patriarca G., Rendeli C. Prevalence of latex allergy in spina bifida: Genetic and environmental risk factors. Eur. Rev. Med. Pharmacol. Sci. 2007;11:149–153.
    1. Becker A., Shapira J., Chaushu S. Orthodontic treatment for disabled children--a survey of patient and appliance management. J. Orthod. 2001;28:39–44. doi: 10.1093/ortho/28.1.39.
    1. Becker A., Shapira J., Chaushu S. Orthodontic treatment for the special needs child. Semin. Orthod. 2004;10:281–292. doi: 10.1053/j.sodo.2004.09.009.
    1. Bignardi L., Prates T., De Rossi A., Nelson-Filho P., de Carvalho F.K., de Siqueira Mellara T., de Queiroz A.M. Strategies and dental care in the treatment of patients with myelomeningocele. Spec. Care Dent. 2018;38:89–94. doi: 10.1111/scd.12276.
    1. De Castilho L.S., Abreu M.H.N.G., Pires ESouza L.G.A., Romualdo L.T.A., Souza ESilva M.E., Resende V.L.S. Factors associated with anterior open bite in children with developmental disabilities. Spec. Care Dent. 2018;38:46–50. doi: 10.1111/scd.12262.
    1. De Morais Gallarreta F.W., Bernardotti F.P., de Freitas A.C., de Queiroz A.M., Faria G. Characteristics of individuals with hydrocephalus and their dental care needs. Spec. Care Dent. 2010;30:72–76. doi: 10.1111/j.1754-4505.2009.00122.x.
    1. Den Hollander N.S., Vinkesteijn A., Schmitz-van Splunder P., Catsman-Berrevoets C.E., Wladimiroff J.W. Prenatally diagnosed fetal ventriculomegaly; prognosis and outcome. Prenat. Diagn. 1998;18:557–566. doi: 10.1002/(SICI)1097-0223(199806)18:6<557::AID-PD303>;2-3.
    1. Deshpande A.N., Pradhan N.R., Patel K.S., Mulchandani V.R. Consequences of Severe Epileptic Attack in a 3-year-old Girl with Congenital Hydrocephalus. Contemp. Clin. Dent. 2018;9:498–501. doi: 10.4103/ccd.ccd_140_18.
    1. Garg A., Revankar A.V. Spina bifida and dental care: Key clinical issues. J. Calif. Dent. Assoc. 2012;40:868–869.
    1. Huggare J.A., Kantomaa T.J., Rönning O.V., Serlo W.S. Craniofacial morphology in shunt-treated hydrocephalic children. Cleft Palate J. 1986;23:261–269.
    1. Kahle K.T., Kulkarni A.V., Limbrick D.D., Jr., Warf B.C. Hydrocephalus in children. Lancet. 2016;387:788–799. doi: 10.1016/S0140-6736(15)60694-8.
    1. Kalyvas A.V., Kalamatianos T., Pantazi M., Lianos G.D., Stranjalis G., Alexiou G.A. Maternal environmental risk factors for congenital hydrocephalus: A systematic review. Neurosurg. Focus. 2016;41:E3. doi: 10.3171/2016.8.FOCUS16280.
    1. Kestle J.R., Walker M.L., Strata Investigators A multicenter prospective cohort study of the Strata valve for the management of hydrocephalus in pediatric patients. J. Neurosurg. 2005;102(Suppl. 2):141–145;. doi: 10.3171/jns.2005.102.2.0141.
    1. Kinsman S.L., Johnston M.V. Nelson Textbook of Pediatrics E-Book. 21st ed. Elsevier; Amsterdam, The Netherlands: 2020. Hydrocephalus.
    1. Kuru E., Eden E. Success of Two Caries Risk Assessment Tools in Children: A Pilot Study With a 3-Year Follow-Up. Int. Q. Community Health Educ. 2020;40:317–320. doi: 10.1177/0272684X19892356.
    1. Limbrick D.D., Jr., Baksh B., Morgan C.D., Habiyaremye G., McAllister J.P., 2nd, Inder T.E., Mercer D., Holtzman D.M., Strahle J., Wallendorf M.J., et al. Cerebrospinal fluid biomarkers of infantile congenital hydrocephalus. PLoS ONE. 2017;12:e0172353. doi: 10.1371/journal.pone.0172353.
    1. Löppönen T., Saukkonen A.L., Serlo W., Tapanainen P., Ruokonen A., Knip M. Accelerated pubertal development in patients with shunted hydrocephalus. Arch. Dis. Child. 1996;74:490–496. doi: 10.1136/adc.74.6.490.
    1. Moazzam A.A., Nehrer E., Da Silva S.L., Polido J.C., Arakelyan A., Habibian M., Krieger M.D. The association between dental health and procedures and developing shunt infections in pediatric patients. J. Neurosurg. Pediatr. 2014;14:508–513. doi: 10.3171/2014.8.PEDS1444.
    1. Pirttiniemi P., Lahtela P., Huggare J., Serlo W. Head posture and dentofacial asymmetries in surgically treated muscular torticollis patients. Acta Odontol. Scand. 1989;47:193–197. doi: 10.3109/00016358909007700.
    1. Pirttiniemi P., Poikela A., Huggare J., Löppönen T. Dental maturation in children with shunt-treated hydrocephalus. Cleft Palate Craniofac. J. 2004;41:651–654. doi: 10.1597/03-018.1.
    1. Poonia A., Chengappa M.D., Mitra R., Jain P., Ghavri T. Full-mouth Rehabilitation of a Ventriculoperitoneal Shunt-treated Hydrocephalic Pediatric Patient: A Case Report. Int. J. Clin. Pediatr. Dent. 2020;13:103–106. doi: 10.5005/jp-journals-10005-1744.
    1. Rajasekharan S., Martens L.C., Cauwels R.G.E.C., Anthonappa R.P. Biodentine™ material characteristics and clinical applications: A 3 year literature review and update. Eur. Arch. Paediatr. Dent. 2018;19:1–22. doi: 10.1007/s40368-018-0328-x.
    1. Ramasamy C. Relationship between Dental Procedures and Shunt Infections in Hydrocephalic Patients: A Narrative Review. J. Clin. Pediatr. Dent. 2018;42:67–71. doi: 10.17796/1053-4628-42.1.12.
    1. Sacar S., Turgut H., Toprak S., Cirak B., Coskun E., Yilmaz O., Tekin K. A retrospective study of central nervous system shunt infections diagnosed in a university hospital during a 4-year period. BMC Infect Dis. 2006;6:43. doi: 10.1186/1471-2334-6-43.
    1. Seda G., Tsai S., Lee-Chiong T. Medication effects on sleep and breathing. Clin. Chest Med. 2014;35:557–569. doi: 10.1016/j.ccm.2014.06.011.
    1. Schubert-Bast S., Berghaus L., Filmann N., Freiman T., Strzelczyk A., Kieslich M. Risk and risk factors for epilepsy in shunt-treated children with hydrocephalus. Eur. J. Paediatr. Neurol. 2019;23:819–826. doi: 10.1016/j.ejpn.2019.09.004.
    1. Shaheen R., Sebai M.A., Patel N., Ewida N., Kurdi W., Altweijri I., Sogaty S., Almardawi E., Seidahmed M.Z., Alnemri A., et al. The genetic landscape of familial congenital hydrocephalus. Ann. Neurol. 2017;81:890–897. doi: 10.1002/ana.24964.
    1. Stojicic S., Shen Y., Qian W., Johnson B., Haapasalo M. Antibacterial and smear layer removal ability of a novel irrigant, QMiX. Int. Endod. J. 2012;45:363–371. doi: 10.1111/j.1365-2591.2011.01985.x.
    1. Stone S.S., Warf B.C. Combined endoscopic third ventriculostomy and choroid plexus cauterization as primary treatment for infant hydrocephalus: A prospective North American series. J. Neurosurg. Pediatr. 2014;14:439–446. doi: 10.3171/2014.7.PEDS14152.
    1. Tully H.M., Dobyns W.B. Infantile hydrocephalus: A review of epidemiology, classification and causes. Eur. J. Med. Genet. 2014;57:359–368. doi: 10.1016/j.ejmg.2014.06.002.
    1. Watanabe J., Okamoto K., Ohashi T., Natsumeda M., Hasegawa H., Oishi M., Miyatake S., Matsumoto N., Fujii Y. Malignant Hyperthermia and Cerebral Venous Sinus Thrombosis After Ventriculoperitoneal Shunt in Infant with Schizencephaly and COL4A1 Mutation. World Neurosurg. 2019;127:446–450. doi: 10.1016/j.wneu.2019.04.156.

Source: PubMed

3
Abonnieren