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060 A randomised study of autologous bone marrow-derived stem cells in pediatric cardiomyopathy

IntroductionBone marrow mononuclear cell fraction has been used as therapy for dilated cardiomyopathy in adults. Although case series are reported, there are no randomised controlled studies in children.MethodsWe designed a randomised, crossover, controlled pilot study to determine safety and feasib...

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Published in:Archives of disease in childhood 2018-12, Vol.103 (Suppl 2), p.A25-A25
Main Authors: Pincott, ES, Ridout, D, Brocklesby, M, McEwan, A, Muthurangu, V, Burch, M
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container_title Archives of disease in childhood
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creator Pincott, ES
Ridout, D
Brocklesby, M
McEwan, A
Muthurangu, V
Burch, M
description IntroductionBone marrow mononuclear cell fraction has been used as therapy for dilated cardiomyopathy in adults. Although case series are reported, there are no randomised controlled studies in children.MethodsWe designed a randomised, crossover, controlled pilot study to determine safety and feasibility of intracoronary stem cell therapy in children. The primary safety end-point was freedom from death and transplantation or any complication that could be considered related to bone marrow injection or anaesthesia (e.g., infection, malignancy, anaphylaxis, renal deterioration). Other end-points were magnetic resonance imaging measurements and N-terminal prohormone brain natriuretic peptide. Participants with cardiomyopathy (New York Heart Association/Ross Classification II-IV) were identified, the study included 10 children (6 M; 4 F), with a mean age of 7.2 years (range, 2.2–14.1 years). Patients were crossed over at 6 months.ResultsThe original protocol was completed by 9 patients. The safety end-point was achieved in all. Ratio of the geometric means for treatment effect, adjusting for baseline, was assessed for end-diastolic and end-systolic volumes (EDV, ESV). The ratio for EDV was 0.93 (95% confidence interval 0.88–0.99, p=0.01), this indicated that EDV was on average 7% lower in patients after stem cell treatment compared with placebo. The ratio for ESV was 0.90 (95% confidence interval 0.82–1.00, p=0.05), this indicated that ESV was on average 10% lower after stem cell treatment compared with placebo. The primary efficacy end-point ejection fraction was not met.DiscussionBone marrow mononuclear cell therapy for cardiomyopathy is feasible and safe in children. Left ventricular volumes were significantly reduced 6 months after stem cell injection compared with placebo, which may reflect reverse remodelling.
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Although case series are reported, there are no randomised controlled studies in children.MethodsWe designed a randomised, crossover, controlled pilot study to determine safety and feasibility of intracoronary stem cell therapy in children. The primary safety end-point was freedom from death and transplantation or any complication that could be considered related to bone marrow injection or anaesthesia (e.g., infection, malignancy, anaphylaxis, renal deterioration). Other end-points were magnetic resonance imaging measurements and N-terminal prohormone brain natriuretic peptide. Participants with cardiomyopathy (New York Heart Association/Ross Classification II-IV) were identified, the study included 10 children (6 M; 4 F), with a mean age of 7.2 years (range, 2.2–14.1 years). Patients were crossed over at 6 months.ResultsThe original protocol was completed by 9 patients. The safety end-point was achieved in all. Ratio of the geometric means for treatment effect, adjusting for baseline, was assessed for end-diastolic and end-systolic volumes (EDV, ESV). The ratio for EDV was 0.93 (95% confidence interval 0.88–0.99, p=0.01), this indicated that EDV was on average 7% lower in patients after stem cell treatment compared with placebo. The ratio for ESV was 0.90 (95% confidence interval 0.82–1.00, p=0.05), this indicated that ESV was on average 10% lower after stem cell treatment compared with placebo. The primary efficacy end-point ejection fraction was not met.DiscussionBone marrow mononuclear cell therapy for cardiomyopathy is feasible and safe in children. Left ventricular volumes were significantly reduced 6 months after stem cell injection compared with placebo, which may reflect reverse remodelling.</description><identifier>ISSN: 0003-9888</identifier><identifier>EISSN: 1468-2044</identifier><identifier>DOI: 10.1136/goshabs.60</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Anaphylaxis ; Anesthesia ; Bone imaging ; Bone marrow ; Bone marrow transplantation ; Bone remodeling ; Brain natriuretic peptide ; Cardiomyopathy ; Cell death ; Cell therapy ; Children ; Dilated cardiomyopathy ; Feasibility studies ; Heart ; Injection ; Magnetic resonance imaging ; Malignancy ; Neuroimaging ; Patients ; Pediatrics ; Placebos ; Safety ; Stem cells</subject><ispartof>Archives of disease in childhood, 2018-12, Vol.103 (Suppl 2), p.A25-A25</ispartof><rights>2018 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3079945767/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3079945767?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,21378,21394,27924,27925,33611,33877,43733,43880,74221,74397</link.rule.ids></links><search><creatorcontrib>Pincott, ES</creatorcontrib><creatorcontrib>Ridout, D</creatorcontrib><creatorcontrib>Brocklesby, M</creatorcontrib><creatorcontrib>McEwan, A</creatorcontrib><creatorcontrib>Muthurangu, V</creatorcontrib><creatorcontrib>Burch, M</creatorcontrib><title>060 A randomised study of autologous bone marrow-derived stem cells in pediatric cardiomyopathy</title><title>Archives of disease in childhood</title><description>IntroductionBone marrow mononuclear cell fraction has been used as therapy for dilated cardiomyopathy in adults. Although case series are reported, there are no randomised controlled studies in children.MethodsWe designed a randomised, crossover, controlled pilot study to determine safety and feasibility of intracoronary stem cell therapy in children. The primary safety end-point was freedom from death and transplantation or any complication that could be considered related to bone marrow injection or anaesthesia (e.g., infection, malignancy, anaphylaxis, renal deterioration). Other end-points were magnetic resonance imaging measurements and N-terminal prohormone brain natriuretic peptide. Participants with cardiomyopathy (New York Heart Association/Ross Classification II-IV) were identified, the study included 10 children (6 M; 4 F), with a mean age of 7.2 years (range, 2.2–14.1 years). Patients were crossed over at 6 months.ResultsThe original protocol was completed by 9 patients. The safety end-point was achieved in all. Ratio of the geometric means for treatment effect, adjusting for baseline, was assessed for end-diastolic and end-systolic volumes (EDV, ESV). The ratio for EDV was 0.93 (95% confidence interval 0.88–0.99, p=0.01), this indicated that EDV was on average 7% lower in patients after stem cell treatment compared with placebo. The ratio for ESV was 0.90 (95% confidence interval 0.82–1.00, p=0.05), this indicated that ESV was on average 10% lower after stem cell treatment compared with placebo. The primary efficacy end-point ejection fraction was not met.DiscussionBone marrow mononuclear cell therapy for cardiomyopathy is feasible and safe in children. 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Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Education Database (ProQuest)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Archives of disease in childhood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pincott, ES</au><au>Ridout, D</au><au>Brocklesby, M</au><au>McEwan, A</au><au>Muthurangu, V</au><au>Burch, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>060 A randomised study of autologous bone marrow-derived stem cells in pediatric cardiomyopathy</atitle><jtitle>Archives of disease in childhood</jtitle><date>2018-12-01</date><risdate>2018</risdate><volume>103</volume><issue>Suppl 2</issue><spage>A25</spage><epage>A25</epage><pages>A25-A25</pages><issn>0003-9888</issn><eissn>1468-2044</eissn><abstract>IntroductionBone marrow mononuclear cell fraction has been used as therapy for dilated cardiomyopathy in adults. Although case series are reported, there are no randomised controlled studies in children.MethodsWe designed a randomised, crossover, controlled pilot study to determine safety and feasibility of intracoronary stem cell therapy in children. The primary safety end-point was freedom from death and transplantation or any complication that could be considered related to bone marrow injection or anaesthesia (e.g., infection, malignancy, anaphylaxis, renal deterioration). Other end-points were magnetic resonance imaging measurements and N-terminal prohormone brain natriuretic peptide. Participants with cardiomyopathy (New York Heart Association/Ross Classification II-IV) were identified, the study included 10 children (6 M; 4 F), with a mean age of 7.2 years (range, 2.2–14.1 years). Patients were crossed over at 6 months.ResultsThe original protocol was completed by 9 patients. The safety end-point was achieved in all. Ratio of the geometric means for treatment effect, adjusting for baseline, was assessed for end-diastolic and end-systolic volumes (EDV, ESV). The ratio for EDV was 0.93 (95% confidence interval 0.88–0.99, p=0.01), this indicated that EDV was on average 7% lower in patients after stem cell treatment compared with placebo. The ratio for ESV was 0.90 (95% confidence interval 0.82–1.00, p=0.05), this indicated that ESV was on average 10% lower after stem cell treatment compared with placebo. The primary efficacy end-point ejection fraction was not met.DiscussionBone marrow mononuclear cell therapy for cardiomyopathy is feasible and safe in children. Left ventricular volumes were significantly reduced 6 months after stem cell injection compared with placebo, which may reflect reverse remodelling.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/goshabs.60</doi></addata></record>
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subjects Anaphylaxis
Anesthesia
Bone imaging
Bone marrow
Bone marrow transplantation
Bone remodeling
Brain natriuretic peptide
Cardiomyopathy
Cell death
Cell therapy
Children
Dilated cardiomyopathy
Feasibility studies
Heart
Injection
Magnetic resonance imaging
Malignancy
Neuroimaging
Patients
Pediatrics
Placebos
Safety
Stem cells
title 060 A randomised study of autologous bone marrow-derived stem cells in pediatric cardiomyopathy
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