Authority: IC 16-19-3-4; IC 16-41-2-1
Affected: IC 16-41-2; IC 16-41-9
Sec. 122.
The specific control measures for pertussis (infectious agent: Bordetella pertussis) are as follows:
A search for unrecognized or unreported, early, and atypical cases is indicated where a nonimmune infant or child is, or might be, at risk.
Table 1 | ||||
Agents for Treatment and Postexposure Prophylaxis of Pertussis | Alternate agent* | |||
Age group | Azithromycin | Erythromycin | Clarithromycin | TMP-SMZ |
<1 month | 10 mg/kg per day as a single dose for 5 days1 | 40 mg/kg per day in 4 divided doses for 14 days | Not recommended | Contraindicated at < 2 months |
1-5 months | See above | See above | 15 mg/kg per day in 2 divided doses for 7 days | >=2 months of age: TMP, 8 mg/kg per day; SMX, 40 mg/kg per day in 2 doses for 14 days |
>=6 months and children | 10 mg/kg as a single dose on day 1 (maximum 500 mg), then 5 mg/kg per day as a single dose on days 2-5 (maximum 250 mg) | See above (maximum 2 g/day) | See above (maximum 1 g/day) | See above |
Adolescents and adults | 500 mg in a single dose on day 1, then 250 as a single dose on days 2-5 | 2 g per day in 4 divided doses for 14 days | 1 g per day in 2 divided doses for 7 days | TMP, 320 mg per day; SMX, 1,600 mg/day in 2 divided doses for 14 days |
*TMP indicates trimethoprim; SMX, sulfamethoxazole. This drug can be an alternate in patients $2 months who are allergic to macrolides, who cannot tolerate macrolides, or who are infected with a rare macrolide resistant strain to Bordetella pertussis. | ||||
1 Preferred macrolide for this age because of risk of idiopathic hypertrophic pyloric stenosis associated with erythromycin. |
Infected persons shall be excluded from:
410 IAC 1-2.5-122