Investigation on the effects of long-term antibiotic therapy in sickle cell disease associated with molar-incisor hypomineralisation-a pilot study
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Kumar, Harleen
[1
,2
]
Mccafferty, Kathleen
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Boston Childrens Hosp, Dept Dent, Boston, MA 02115 USA
Harvard Sch Dent Med, Boston, MA 02115 USAUniv Sydney, Fac Med & Hlth, Sch Dent, Sydney, NSW 2000, Australia
Mccafferty, Kathleen
[3
,4
]
Neboda, Chaturi
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Univ Sydney, Fac Med & Hlth, Sch Dent, Sydney, NSW 2000, Australia
Sydney Dent Hosp & Oral Hlth Serv, Sydney Local Hlth Dist, Surry Hills, NSW 2010, AustraliaUniv Sydney, Fac Med & Hlth, Sch Dent, Sydney, NSW 2000, Australia
Neboda, Chaturi
[1
,2
]
Chase, Isabelle
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Boston Childrens Hosp, Dept Dent, Boston, MA 02115 USA
Harvard Sch Dent Med, Boston, MA 02115 USAUniv Sydney, Fac Med & Hlth, Sch Dent, Sydney, NSW 2000, Australia
Chase, Isabelle
[3
,4
]
机构:
[1] Univ Sydney, Fac Med & Hlth, Sch Dent, Sydney, NSW 2000, Australia
[2] Sydney Dent Hosp & Oral Hlth Serv, Sydney Local Hlth Dist, Surry Hills, NSW 2010, Australia
[3] Boston Childrens Hosp, Dept Dent, Boston, MA 02115 USA
The term Molar-Incisor Hypomineralisation (MIH) is used to describe hypomineralised defects of systemic origin that affect at least one of the first permanent molars and often involves the permanent incisors. Antibiotic therapy during amelogenesis may be associated with enamel hypomineralisation. By examining children with Sickle Cell Disease (SCD), who take prophylactic antibiotics daily from birth until age five, it may be possible to determine if there is an increased prevalence of MIH in this population. The aim of this study was to determine the effect of long-term antibiotic use on the prevalence and severity of MIH in children with SCD. In a prospective cohort pilot study over a period of seven months, children aged 7-17 years, with SCD at Boston Children's Hospital (n = 18) were examined for MIH. Information regarding peri-natal concerns, incidence of illness and antibiotic use were also collected. The results were compared to a group of control patients (n = 63) for prevalence and severity of MIH using Fisher's exact test. The patients with SCD, 4/18 (22%) taking daily antibiotics did not show a statistically significant greater prevalence of MIH compared to the control group, 24/63 (38%). There was no correlation between MIH and pneumonia, asthma, fever, flu, otitis media, breastfeeding, gender and birth weight. However, an association was noted between premature birth and MIH (p <= 0.05). No correlation was found between long -term antibiotic use and higher prevalence of MIH in the SCD group compared to the control group. However, MIH may be more severe in those with a history of long-term antibiotics.
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Childrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Res Ctr Oakland, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Hoppe, Carolyn
Kuypers, Frans
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Childrens Hosp, Oakland Res Inst, Red Cell Lab, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Kuypers, Frans
Larkin, Sandra
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Childrens Hosp, Oakland Res Inst, Red Cell Lab, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Larkin, Sandra
Hagar, Ward
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Childrens Hosp, Oakland Res Inst, Adult Sickle Cell Ctr, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Hagar, Ward
Vichinsky, Elliott
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Childrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Res Ctr Oakland, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Vichinsky, Elliott
Styles, Lori
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Childrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
Res Ctr Oakland, Oakland, CA 94609 USAChildrens Hosp, Dept Haematol Oncol, Oakland, CA 94609 USA
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Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Tolu, Seda S.
Wang, Kai
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Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Wang, Kai
Yan, Zi
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Albert Einstein Coll Med, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Yan, Zi
Crouch, Andrew
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Montefiore Med Ctr, Albert Einstein Coll Med, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Crouch, Andrew
Sebastian, Gracy
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Montefiore Med Ctr, Sickle Cell Ctr, 111 E 210th St, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Sebastian, Gracy
Chaitowitz, Mark
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Montefiore Med Ctr, New York, NY USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Chaitowitz, Mark
Fornari, Eric
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Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Fornari, Eric
Schwechter, Evan
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Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Schwechter, Evan
Uehlinger, Joan
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Montefiore Med Ctr, 111 E 210th St, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Uehlinger, Joan
Manwani, Deepa
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Childrens Hosp Montefiore, Bronx, NY USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Manwani, Deepa
Minniti, Caterina P.
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Montefiore Med Ctr, Albert Einstein Coll Med, Div Hematol, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
Minniti, Caterina P.
Bouhassira, Eric E.
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Albert Einstein Coll Med, Div Hematol & Cell Biol, Bronx, NY 10467 USAMontefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA