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. 1997 Nov;8(6):323-8.
doi: 10.1155/1997/742365.

Varicella zoster virus infections in Canadian children in the prevaccine era: A hospital-based study

Affiliations

Varicella zoster virus infections in Canadian children in the prevaccine era: A hospital-based study

S Kuhn et al. Can J Infect Dis. 1997 Nov.

Abstract

Objective: To describe the clinical course of children admitted for varicella zoster virus (VZV) infections to a pediatric hospital before the release of VZV vaccine in Canada.

Design: Retrospective case series.

Setting: Tertiary pediatric hospital. Population studied was children aged 18 years or younger admitted to hospital between 1983 and 1992 who were discharged with a diagnosis of varicella or zoster. Of the 201 children who were identified, 36 were excluded, leaving 165 for analysis.

Results: There was a male:female ratio of 1.5:1 and a median age of 5.3 years (range two weeks to 18 years). The group included those who were previously healthy (70, 42.4%), immunocompromised (60, 36.4%), and those with nonimmunocompromising conditions (35, 21.2%). Comparison of immunocompetent and immunocompromised children revealed that complication of VZV infection was a more common reason for admission among the former (86 of 105, 81.9%, P<0.001), whereas treatment with acyclovir to limit dissemination was the most common reason in the latter (53 of 60, 88.3%, P<0.001). Skin and soft tissue infections were the most common complications in immunocompetent children (36 of 98) and those younger than five years (26 of 53), whereas pulmonary complications predominated among immunocompromised patients (eight of 98) and neurological complications in five- to 10-year-olds (16 of 36). Only one death (0.6%) occurred in an immunocompetent patient. Group A beta-hemolytic streptococci and Staphylococcus aureus caused equal numbers of secondary infections (92% of all isolates).

Conclusions: Complications of VZV infections and secondary prophylactic antiviral treatment of immunocompromised children explain the majority of hospitalizations in this institution, and can be monitored after VZV vaccine introduction. Complications vary significantly with underlying healthy status and age.

OBJECTIFS :: Décrire l’évolution clinique des enfants admis pour des infections au virus varicella-zona dans un hôpital pédiatrique avant la mise en marché d’un vaccin anti-VZV au Canada.

MODÈLE :: Série de cas rétrospectifs.

CONTEXTE :: Hôpital pédiatrique de soins tertiaires. La population étudiée regroupait des enfants de 18 ans ou moins admis à l’hôpital entre 1983 et 1992 et qui ont obtenu leur congé avec un diagnostic de varicelle ou de zona. Parmi les 201 enfants qui ont été identifiés, 36 ont été exclus, ce qui en laissait 165 pour l’analyse.

RÉSULTATS :: Le ratio hommes-femmes était de 1,5 2.1 et l’âge moyen était de 5,3 ans (variant de deux semaines à 18 ans). Le groupe comprenait les sujets auparavant en bonne santé (70, 42,4 %), des sujets immunodéprimés (60, 36,4 %) et des sujets présentant des maladies sans immunodépression (35, 21,2 %). La comparaison entre les enfants immunocompétents et immunodéprimés a révélé que la complication de l’infection au VZV était une raison plus fréquente d’admission chez le premier groupe (86 sur 105, 81,9 %, P < 0,001) alors que le traitement à l’acyclovir pour limiter la dissémination de l’infection a été la raison la plus fréquente dans le dernier groupe (53 sur 60, 88,3 %, P < 0,001). Les infections de la peau et des tissus mous ont été les complications les plus courantes chez les enfants immunocompétents (36 sur 98) et chez les sujets de moins de cinq ans (26 sur 53), alors que les complications pulmonaires ont prédominé chez les patients immunodéprimés (8 sur 98) et les complications neurologiques chez les 5 à 10 ans (16 sur 36). Un seul décès (0,6 %) est survenu chez un patient immunocompétent. Les streptocoques bêta-hémolytiques du groupe A et Staphylococcus aureus ont provoqué un nombre égal d’infections secondaires (92 % de tous les isolats).

CONCLUSIONS :: Les complications des infections à VZV et le traitement antiviral prophylactique secondaire des enfants immunodéprimés expliquent la majorité des hospitalisations dans cet établissement et peuvent être surveillées après l’introduction du vaccin anti-VZV. Les complications varient considérablement selon l’état de santé sous-jacent et l’âge.

Keywords: Childhood; Complications; Varicella zoster infections.

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Figures

Figure 1
Figure 1
Reason for admission to hospital with varicella zoster infections by patient health status. Nonimmunocompromising conditions include eight endocrinopathies (two panhypopituitarism, two congential adrenal hyperplasia, four insulin-dependent diabetes melllitus), six skin disorders (four eczema, one burn, one lamellar icthyosis), four seizure disorders, four congential heart disorders, three asthmatics, three infants born prematurely, portal hypertension, polycystic kidneys, recurrent severe emesis of unknown etiology, chronic idiopathic thrombocytopenic purpura, chromosomal anomaly, cystic fibrosis and mononucleosis. Immunocompromising conditions include acute lymphocytic leukemia (22), acute myeloblastic leukemia (one), lymphoma (three), solid tumour (12), immunosuppressive doses of steriods for nonmalignant conditions (16), bone marrow transplant (two), liver transplant (one), hypogammaglobulinemia/neutropenia (one), ataxia-telangiectasis (one) and neonate (one). *Comparisons made between immunocompetent (healthy and nonimmunocompromised conditions) and immunocompromised patients. Chronic skin disease (one of each eczema, lamellar icthyosis), V-1 zoster with underlying portal hypertenion (one), endocrinopathies for which replacement doses of corticosteriods were given (four), and congential heart disease (two)
Figure 2
Figure 2
Sites of varicella zoster virus complications leading to admission, by patient health status group. *Comparisons made between immunocompetent (healthy and nonimmunocompromising conditions) and immunocompromised patients. CNS Neurological complications; SST Skin and soft tissue infection
Figure 3
Figure 3
Anatomical sites among patients with complications by patient age group. *Comparisons were made between children younger than five years of age and children aged five to 10 years, given the small number of children older than 10 years of age. CNS Neurological complications; SST Skin and soft tissue infection

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