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Br J Clin Pharmacol. 1998 Jun;45(6):605-7.

Trying to improve compliance with prophylactic penicillin therapy in children with sickle cell disease.

Author information

1
Division of Pediatrics, Assaf Harofeh Medical Center, Sackler School of Medicine, Tel-Aviv University, Israel.

Abstract

AIMS:

To evaluate compliance with prophylactic penicillin therapy in sickle cell disease (SCD) in children.

METHODS:

Forty-five children aged 37 +/- 19 (9-84) months [mean +/- s.d; range] with homozygous SCD were recruited. After a baseline period of 2 months the patients were randomized to either the intervention or non-intervention group. The intervention consisted of a slide show explaining the pathogenesis of sickle cell disease and its complications; weekly phone calls by the clinic social worker; and a calendar. Compliance was again evaluated after the 2 month intervention period and after a further 2 month monitoring period without intervention. Compliance was monitored using the Medication Event Monitoring System. At the end of the 6 months, parents in both groups completed a questionnaire the aims of which were to determine knowledge and understanding of sickle cell disease and previous experience with infection. Patient admissions to the hospital during the study were recorded.

RESULTS:

Compliance during the 2 month baseline assessment was 66.0 +/- 32.5 (1.3-98.2)% and 69.3+25.4 (19.8-96.5)% in the intervention (n = 13) and non-intervention (n = 10) groups respectively (P = 0.79). During the next 2 months, compliance in the intervention group (n = 11) was 79.0 +/- 31.4 (11.0-100.0)% and in the non-intervention group (n = 9) was 66.0 +/- 20.2 (42.2-96.8)% (P = 0.297). In the final 2 month monitoring period compliance was 82.0 +/- 34.7 (3.8-100.0)% and 65.8 +/- 25.3 (25.0-98.2)% in the intervention (n = 7) and the non-intervention (n = 6) groups respectively (P = 0.366). No statistically significant differences were found when comparing compliance between the groups.

CONCLUSIONS:

Compliance with prophylactic antibiotic therapy in children with sickle cell disease is highly variable and its evaluation is problematic.

PMID:
9663818
PMCID:
PMC1873646
DOI:
10.1046/j.1365-2125.1998.00730.x
[Indexed for MEDLINE]
Free PMC Article

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