Yw. Miller et al., SEQUENTIAL ANTIBIOTIC-THERAPY FOR ACNE PROMOTES THE CARRIAGE OF RESISTANT STAPHYLOCOCCI ON THE SKIN OF CONTACTS, Journal of antimicrobial chemotherapy, 38(5), 1996, pp. 829-837
The selection of a predominantly resistant staphylococcal skin flora i
n acne patients during antibiotic treatment has been extensively docum
ented. This study sought to determine whether antibiotic therapy for a
cne had any effect on skin carriage of resistant coagulase-negative st
aphylococci (CNS) by close contacts of treated patients. Bacterial sam
ples were obtained using a scrub wash technique from facial skin of 41
contacts (parents, siblings or partners) of patients who had been tre
ated with at least three different antibiotics over a minimum period o
f 2 years. Samples were also obtained from 41 control subjects who had
no known contact with any antibiotic treated acne patient. None of th
e contacts or controls had received any antibiotic therapy in the prec
eding two years. The number, percentage and prevalence of CNS resistan
t to each of seven antibiotics was estimated by plating serial ten-fol
d dilutions of wash fluid directly onto antibiotic-containing and anti
biotic-free medium. Significantly more contacts than controls carried
strains resistant to erythromycin, clindamycin, fusidic acid, trimetho
prim and chloramphenicol as well as more multiply resistant strains (P
< 0.05, chi(2)) The number and percentage of staphylococci resistant
to tetracycline, erythromycin, clindamycin, fusidic acid and chloramph
enicol were also significantly raised (P < 0.05, Mann-Whitney U-test)
in contacts. Only aminoglycoside resistance was not increased by any o
f the above criteria. These observations provide evidence that sequent
ial antibiotic therapy for acne exerts selective pressure for increase
d skin carriage of resistant CNS not only in patients but also in thei
r close contacts.