2001
DOI: 10.1097/00006250-200105000-00001
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Vaginal Clindamycin in Preventing Preterm Birth and Peripartal Infections in Asymptomatic Women With Bacterial Vaginosis

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Cited by 8 publications
(26 citation statements)
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“…Randomized clinical trials (RCTs) of antibiotic administration to reduce the rate of pre-term birth have yielded conflicting results (Morales et al 1994, Hauth et al 1995, McDonald et al 1997, Carey et al 2000, Paavonen et al 2000, Rosenstein et al 2000, Kekki et al 2001, Lamont 2003, Ugwumadu et al 2003) and there is no uniform proof that antibiotic use reduces risk of pre-term birth. The reader is referred to the original trials and systematic reviews for details (Brocklehurst et al 2000, Guise et al 2001, Klebanoff et al 2003, Leitich et al 2003b.…”
Section: Infection and Adverse Pregnancy Outcomementioning
confidence: 99%
“…Randomized clinical trials (RCTs) of antibiotic administration to reduce the rate of pre-term birth have yielded conflicting results (Morales et al 1994, Hauth et al 1995, McDonald et al 1997, Carey et al 2000, Paavonen et al 2000, Rosenstein et al 2000, Kekki et al 2001, Lamont 2003, Ugwumadu et al 2003) and there is no uniform proof that antibiotic use reduces risk of pre-term birth. The reader is referred to the original trials and systematic reviews for details (Brocklehurst et al 2000, Guise et al 2001, Klebanoff et al 2003, Leitich et al 2003b.…”
Section: Infection and Adverse Pregnancy Outcomementioning
confidence: 99%
“…Antibacterial vaginosis treatment in asymptomatic women proved ineffective for the reduction in the rate of peripartum infection. On the other hand, recurrent bacterial vaginosis increased the risk for this complication as shown by a randomised, controlled trial that used vaginal clindamycin in bacterial vaginosis [48].…”
Section: Prophylaxismentioning
confidence: 99%
“…1,[3][4][5]15,17,18 Although many studies have suggested a link between periodontal disease and preterm delivery and bacterial vaginosis and preterm delivery, treatment studies of low-risk patients have not demonstrated any risk reduction in preterm birth with treatment of either. 14,17,19 These findings, in combination with our finding that the presence of both periodontal disease and BV is not synergistic, suggest that perhaps BV and periodontal disease are clinical markers for a genetic susceptibility or other environmental factors rather than causative agents. It is possible that the polymorphisms in the inflammatory pathway that make subjects more likely to have BV or periodontal disease also place them at higher risk for preterm delivery.…”
Section: Discussionmentioning
confidence: 79%