Over a period of four years, 114 children (> 28 days to ≤ 12 years) with seropositive brucellosis were admitted to Khamis Mushayt Civil Hospital, constituting 1% of all pediatric admissions. History of contact with domestic animals and ingestion of raw milk was positive, and over 84% of the patients were from the rural areas of Asir. The male:female ratio was 1.2:1, over 59% were of ≤ 5 years of age. Common clinical features observed were fever (80.7%), hepatosplemomegaly (38%), arthropathies (29%), and anemia (34%). Over 36% of the children were undernourished. Serological identification of etiological agents revealed Abortus and melitensis (53.5%), Abortus (32.5%) and melitensis (14%). All patients were treated with a combination of rifampicin and septrin. There were no deaths, drug-induced hepatitis was observed in two cases. It would appear that brucellosis is one of the major causes of morbidity in the pediatric population located in the Asir region and there is an urgent need for an effective control program. Brucellosis is one of the major health problems in both rural and urban Saudi Arabia [1]. While the epidemiology of the disease in the adult population is well documented [2,3], there is a paucity of data on its clinical pattern in Saudi children. This retrospective study was undertaken to evaluate the magnitude of the problem and to analyze the factors related to its clinical presentation in a selected population of pediatric patients requiring hospitalization in a district general hospital in the Asir Province of Saudi Arabia.
Material and MethodsCase records of all children (> 28 days to 12 years) with seropositive diagnosis of brucellosis admitted to Khamis Mushayt Civil Hospital over a period of four years (1406H to 1409H) were reviewed. Clinical laboratory, radiological and histological materials were reviewed and the diagnosis was verified or revised in each case. Of a total of 10,973 pediatric admissions, 114 children were identified to have a brucella agglutination titer 1:160. The serological diagnosis of brucellosis was made by collecting 5 cc of blood from each patient and the sera subjected to the slide agglutination test and tube agglutination test using gamma antigen preparation (Gamma Biologicals Inc., Houston, Texas, USA). A double dilution of serum from 1:10 to 1:2560 in tube method and 1:20 to 1:360 in slide method were used for the agglutination test. The tubes were incubated at 37°C for 48 hours. Positive and negative control sera were used for each batch of tests; against both strains of Brucella (B. abortus and B. melitensis) a significant titer of 1:160 was considered as positive for brucellosis.For bacteriological isolation of brucella organism, blood cultures using tryptic soy broth and CO 2 under vacuum (Difco Laboratories, Houston, Texas, USA) were used; standard methods [4] for incubation, subcultures, bacterial identification and antibiotic sensitivity testing procedures were employed.
Brucellosis in Pediatric Patients: A Review of 114 Cases from Asir Region
Annals of Sau...