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he had a recurrence of peritonitis caused by the same microorganism&#44; and then he was treated with oral ciprofloxacin adjusted to antibiogram results without achieving a negative peritoneal fluid culture&#46; Given the suspicion of recurring peritonitis due to a biofilm&#44; intravenous &#40;IV&#41; daptomycin was started at a dose of 500<span class="elsevierStyleHsp" style=""></span>mg&#47;48<span class="elsevierStyleHsp" style=""></span>h &#40;residual diuresis 400<span class="elsevierStyleHsp" style=""></span>ml&#47;24<span class="elsevierStyleHsp" style=""></span>h&#41;&#46; After 10 days of treatment&#44; the fluid remained slightly cloudy &#40;220<span class="elsevierStyleHsp" style=""></span>cells&#47;&#956;l&#44; 55&#37; polymorphonuclear cells&#44; 45&#37; monomorphonuclear cells&#41;&#44; with a positive culture for <span class="elsevierStyleItalic">S&#46; epidermidis</span>&#46; Therefore&#44; treatment was started with IP daptomycin &#40;200<span class="elsevierStyleHsp" style=""></span>mg loading dose followed by 40<span class="elsevierStyleHsp" style=""></span>mg in each exchange&#41; and maintained for 14 days&#46; Throughout this time&#44; the patient received associated antifungal prophylaxis&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">The peritoneal fluid culture during and after treatment was negative&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">After completing intraperitoneal antibiotic treatment&#44; the patient resumed his usual therapy &#40;automatic PD with a daytime exchange&#41;&#46; He was scheduled for daptomycin lseal therapy&#44; administered once per week for 4 weeks&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The sealing therapy protocol was performed using 35<span class="elsevierStyleHsp" style=""></span>mg of daptomycin in 7<span class="elsevierStyleHsp" style=""></span>ml of lactated Ringer&#39;s solution&#44; with the abdomen empty for a minimum of 12<span class="elsevierStyleHsp" style=""></span>h&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Currently&#44; the patient remains asymptomatic&#44; and has had no more episodes of peritonitis&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Daptomycin is a lipopeptide antibiotic indicated in the treatment of bacteraemia&#44; right-sided endocarditis and complicated skin infections&#44; with anti-biofilm activity&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Several cases of treatment of peritonitis in PD with both IV and IP daptomycin have been reported&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Goedecke et al&#46; showed that intravenous administration of daptomycin achieved plasma and peritoneal fluid levels greater than the minimum inhibitory concentration for microorganisms sensitive to this antibiotic&#46; However&#44; the study was conducted in a single patient&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Subsequently&#44; several cases were reported of peritonitis in PD that were successfully treated with IV daptomycin&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">A study of the pharmacokinetics of daptomycin in PD&#44; with the dual aim of evaluating the drug&#39;s penetration of the peritoneal cavity and obtaining a dose regimen to be administered in this type of patients that offered safety and prevented toxicity&#44; concluded that administration at doses of 4&#8211;6<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#47;48<span class="elsevierStyleHsp" style=""></span>h is an appropriate regimen for treating non-peritoneal systemic infections in patients who receive continuous ambulatory PD but&#44; owing to its limited penetration of the abdominal cavity&#44; its administration by the IV route is not safe for the treatment of peritonitis&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">In the case presented&#44; daptomycin administered by the intravenous route did not achieve a negative peritoneal fluid culture&#46; At the time of administration&#44; peritoneal inflammation was not substantial&#44; and the percentage of polymorphonuclear cells was only 55&#37;&#44; given that the patient was undergoing antibiotic treatment with ciprofloxacin&#44; and the even lower penetration in the abdominal cavity could be attributed to this&#46; Although there have been no studies on how peritoneal inflammation influences the concentration of daptomycin in the peritoneum&#44; a study by Cardone et al&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> suggested that the peritoneal inflammation that occurs in the patients studied should to a certain extent promote the drug&#39;s penetration of the peritoneal cavity&#44; without being able to ensure whether suitable levels would be achieved as the inflammatory process decreases&#46;</p></span>"
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Letter to the Editor
Daptomycin in peritoneal dialysis, intraperitoneal or intravenous
Daptomicina en diálisis peritoneal, intraperitoneal o intravenosa
Cristina Pérez Melón
Corresponding author
cristicpm@hotmail.com

Corresponding author.
, Maria Borrajo Prol, Elena Iglesias, Beatriz Ferreiro, Maria Camba Caride
Servicio de Nefrología, Complejo Hospitalario Universitario de Orense, Orense, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Recurrent peritonitis due to a suspected biofilm causes substantial morbidity in patients with peritoneal dialysis &#40;PD&#41; and sometimes leads to permanent abandonment of the technique&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 55-year-old man with a prior history of meningitis due to listeria&#44; resolved with antibiotic treatment&#44; chronic kidney disease &#40;CKD&#41; secondary to membranous glomerulonephritis in PD and an adrenal incidentaloma&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">He visited our department owing to signs and symptoms of peritonitis due to clinically asymptomatic <span class="elsevierStyleItalic">Staphylococcus epidermidis</span>&#44; which resolved with intraperitoneal &#40;IP&#41; vancomycin administered for 14 days&#46; The post-treatment monitoring culture was negative&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Fifteen days after completion of antibiotic therapy&#44; he had a recurrence of peritonitis caused by the same microorganism&#44; and then he was treated with oral ciprofloxacin adjusted to antibiogram results without achieving a negative peritoneal fluid culture&#46; Given the suspicion of recurring peritonitis due to a biofilm&#44; intravenous &#40;IV&#41; daptomycin was started at a dose of 500<span class="elsevierStyleHsp" style=""></span>mg&#47;48<span class="elsevierStyleHsp" style=""></span>h &#40;residual diuresis 400<span class="elsevierStyleHsp" style=""></span>ml&#47;24<span class="elsevierStyleHsp" style=""></span>h&#41;&#46; After 10 days of treatment&#44; the fluid remained slightly cloudy &#40;220<span class="elsevierStyleHsp" style=""></span>cells&#47;&#956;l&#44; 55&#37; polymorphonuclear cells&#44; 45&#37; monomorphonuclear cells&#41;&#44; with a positive culture for <span class="elsevierStyleItalic">S&#46; epidermidis</span>&#46; Therefore&#44; treatment was started with IP daptomycin &#40;200<span class="elsevierStyleHsp" style=""></span>mg loading dose followed by 40<span class="elsevierStyleHsp" style=""></span>mg in each exchange&#41; and maintained for 14 days&#46; Throughout this time&#44; the patient received associated antifungal prophylaxis&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">The peritoneal fluid culture during and after treatment was negative&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">After completing intraperitoneal antibiotic treatment&#44; the patient resumed his usual therapy &#40;automatic PD with a daytime exchange&#41;&#46; He was scheduled for daptomycin lseal therapy&#44; administered once per week for 4 weeks&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The sealing therapy protocol was performed using 35<span class="elsevierStyleHsp" style=""></span>mg of daptomycin in 7<span class="elsevierStyleHsp" style=""></span>ml of lactated Ringer&#39;s solution&#44; with the abdomen empty for a minimum of 12<span class="elsevierStyleHsp" style=""></span>h&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Currently&#44; the patient remains asymptomatic&#44; and has had no more episodes of peritonitis&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Daptomycin is a lipopeptide antibiotic indicated in the treatment of bacteraemia&#44; right-sided endocarditis and complicated skin infections&#44; with anti-biofilm activity&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Several cases of treatment of peritonitis in PD with both IV and IP daptomycin have been reported&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Goedecke et al&#46; showed that intravenous administration of daptomycin achieved plasma and peritoneal fluid levels greater than the minimum inhibitory concentration for microorganisms sensitive to this antibiotic&#46; However&#44; the study was conducted in a single patient&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Subsequently&#44; several cases were reported of peritonitis in PD that were successfully treated with IV daptomycin&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">A study of the pharmacokinetics of daptomycin in PD&#44; with the dual aim of evaluating the drug&#39;s penetration of the peritoneal cavity and obtaining a dose regimen to be administered in this type of patients that offered safety and prevented toxicity&#44; concluded that administration at doses of 4&#8211;6<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#47;48<span class="elsevierStyleHsp" style=""></span>h is an appropriate regimen for treating non-peritoneal systemic infections in patients who receive continuous ambulatory PD but&#44; owing to its limited penetration of the abdominal cavity&#44; its administration by the IV route is not safe for the treatment of peritonitis&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">In the case presented&#44; daptomycin administered by the intravenous route did not achieve a negative peritoneal fluid culture&#46; At the time of administration&#44; peritoneal inflammation was not substantial&#44; and the percentage of polymorphonuclear cells was only 55&#37;&#44; given that the patient was undergoing antibiotic treatment with ciprofloxacin&#44; and the even lower penetration in the abdominal cavity could be attributed to this&#46; Although there have been no studies on how peritoneal inflammation influences the concentration of daptomycin in the peritoneum&#44; a study by Cardone et al&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> suggested that the peritoneal inflammation that occurs in the patients studied should to a certain extent promote the drug&#39;s penetration of the peritoneal cavity&#44; without being able to ensure whether suitable levels would be achieved as the inflammatory process decreases&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; P&#233;rez Mel&#243;n C&#44; Borrajo Prol M&#44; Iglesias E&#44; Ferreiro B&#44; Camba Caride M&#46; Daptomicina en di&#225;lisis peritoneal&#44; intraperitoneal o intravenosa&#46; Nefrolog&#237;a&#46; 2016&#59;36&#58;461&#8211;462&#46;</p>"
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ISSN: 20132514
Original language: English
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