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   The Impact of Short-Term,Intensive Antifolate Treatment (with Pyrimethamine and Sulfadoxine) and Antibiotics Followed by Long-Term,Secondary Antifolate Prophylaxis on the Rate of Toxoplasmic Retinochoroiditis Recurrence  
   
نویسنده borkowski p.k. ,brydak-godowska j. ,basiak w. ,świtaj k. ,żarnowska-prymek h. ,olszyńska-krowicka m. ,kajfasz p. ,rabczenko d.
منبع plos neglected tropical diseases - 2016 - دوره : 10 - شماره : 8
چکیده    Purpose: to assess the impact of intensive antifolate treatment,followed by secondary antifolate prophylaxis (a-sp) on the recurrence rate of toxoplasmic retinochoroiditis (trc). to investigate whether there are any other factors potentially predisposing for recurrence. material and methods: a total of 637 medical records of trc patients,who had been treated in the years 1994–2013 were reviewed. all patients were treated with pyrimethamine /sulfadoxine one 25mg/500mg tablet daily (p/s 25/500mg) for 21 days with a double loading dose for the first two days. from day 2 the patients also received prednisone at a starting dose of 40mg and spiramycine 3 million iu three times daily,given for 10 days followed by azithromycin 500mg once daily for another 6 days. the analysis of the recurrence rate involved 352 patients who had completed 6-month secondary prophylaxis (p/s one 25 mg/500mg tablet twice a week). results: when secondary antifolate prophylaxis (a-sp) was instituted immediately after the treatment for trc,the probability of 3-year recurrence–free survival after the first course of a-sp was 90.9%. a recurrence was most likely approximately 3.5 years after the first treatment. a univariate cox regression model demonstrated that a risk for recurrence was 2.82 times higher (p = 0.02) in patients with retinal scars. in the multivariate analysis,the risk for recurrence was 2.41 higher (p = 0.06). in patients with haemorrhagic lesions the risk for recurrence was lower,arr = 0.17 (approaching borderline statistical significance p = 0.08). conclusions: with the institution of a-sp of immediately after the intensive treatment for trc,i.e. when a reactivation was most likely,there was no recurrence during a-sp. following a-sp the recurrence rates were low and recurrence-free periods tended to be longer. the treatment regimen employed had a beneficial effect on the recurrence interval as it reduced and delayed the highest probability of recurrence. © 2016 borkowski et al.
آدرس former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, department of ophthalmology,medical university of warsaw, Poland, former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, former department of zoonoses and tropical diseases,medical university of warsaw,present department of infectious,tropical diseases and hepatology,medical university of warsaw, Poland, department-centre for monitoring and analyses of population health status,national institute of public health—national institute of hygiene,warsaw, Poland
 
     
   
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