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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 |
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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. Left ventricular volumes were significantly reduced 6 months after stem cell injection compared with placebo, which may reflect reverse remodelling.</description><subject>Anaphylaxis</subject><subject>Anesthesia</subject><subject>Bone imaging</subject><subject>Bone marrow</subject><subject>Bone marrow transplantation</subject><subject>Bone remodeling</subject><subject>Brain natriuretic peptide</subject><subject>Cardiomyopathy</subject><subject>Cell death</subject><subject>Cell therapy</subject><subject>Children</subject><subject>Dilated cardiomyopathy</subject><subject>Feasibility studies</subject><subject>Heart</subject><subject>Injection</subject><subject>Magnetic resonance imaging</subject><subject>Malignancy</subject><subject>Neuroimaging</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Placebos</subject><subject>Safety</subject><subject>Stem cells</subject><issn>0003-9888</issn><issn>1468-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>CJNVE</sourceid><sourceid>M0P</sourceid><recordid>eNqNyjFOwzAUgGGrAolQunCCJzGnfa5TxxkRAnGA7pUbu62rJC_1s0HZWLgoJwEhDsD0D_8nxL3EpZRKr47EJ7vnpcaZKGSlTbnGqroSBSKqsjHG3Ihb5jOiXBujCmFR49fH5yNEOzjqA3sHnLKbgA5gc6KOjpQZ9jR46G2M9F46H8Pbr_M9tL7rGMIAo3fBphhaaG10gfqJRptO0524PtiO_eKvc_Hw8rx9ei3HSJfsOe3OlOPws3YK66apNrWu1f_UN6xMTOo</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Pincott, ES</creator><creator>Ridout, D</creator><creator>Brocklesby, M</creator><creator>McEwan, A</creator><creator>Muthurangu, V</creator><creator>Burch, M</creator><general>BMJ Publishing Group LTD</general><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8A4</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20181201</creationdate><title>060 A randomised study of autologous bone marrow-derived stem cells in pediatric cardiomyopathy</title><author>Pincott, ES ; Ridout, D ; Brocklesby, M ; McEwan, A ; Muthurangu, V ; Burch, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_30799457673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anaphylaxis</topic><topic>Anesthesia</topic><topic>Bone imaging</topic><topic>Bone marrow</topic><topic>Bone marrow transplantation</topic><topic>Bone remodeling</topic><topic>Brain natriuretic peptide</topic><topic>Cardiomyopathy</topic><topic>Cell death</topic><topic>Cell therapy</topic><topic>Children</topic><topic>Dilated cardiomyopathy</topic><topic>Feasibility studies</topic><topic>Heart</topic><topic>Injection</topic><topic>Magnetic resonance imaging</topic><topic>Malignancy</topic><topic>Neuroimaging</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Placebos</topic><topic>Safety</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pincott, ES</creatorcontrib><creatorcontrib>Ridout, D</creatorcontrib><creatorcontrib>Brocklesby, M</creatorcontrib><creatorcontrib>McEwan, A</creatorcontrib><creatorcontrib>Muthurangu, V</creatorcontrib><creatorcontrib>Burch, M</creatorcontrib><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>Proquest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Education Database (ProQuest)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & 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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