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Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study
Background Demographic and biochemical variations in newborn children as compared to adults are attributable to variable prognosis to blood transfusions. Aims of this mixed cohort study of Platelets with/without Plasma (PLT/PZ); only Plasma (PZ) transfusions in ≤ 24 months children is as follows: An...
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Published in: | The Gazette of the Egyptian Paediatric Association 2024-12, Vol.72 (1), p.64-10, Article 64 |
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description | Background
Demographic and biochemical variations in newborn children as compared to adults are attributable to variable prognosis to blood transfusions. Aims of this mixed cohort study of Platelets with/without Plasma (PLT/PZ); only Plasma (PZ) transfusions in ≤ 24 months children is as follows: An Association of demography towards hospital mortality, and an association of laboratory investigations (LI) with hospital mortality.
Methods
PLT/PZ (
n
= 72) and PZ (
n
= 79) children ≤ 24 months were followed up for a total length of hospital stay (LOS(D)). We calculated the Odds Ratio (OR) of demographic, and laboratory parameters for mortality, survival studies of demographic, laboratory parameters , Kaplan Meier Survival curve, Log-Rank significance (KMLR) and Multivariable regression (
r
2
) with outcome as death.
Results
The present study is in 2019–2022. Higher OR for hospital-based mortality for PLT/PZ and PZ cohort were age ≤ 1 m, weight ≤ 1500 g, preterm, gestational age ≤ 34 weeks, hospital length of stay {LOS(D)} 0–7 days, APGAR score ≤ 5, and Hb ≤ 7 g/dl. High OR, mortality was observed with Female gender, Length of stay before first transfusion {LOS(F)}, 0-7d, WHO Grade of bleeding (GOB) 4,
PT
>50 sec,
INR
>1·7,
aPTT
>75sec, PLT counts (μl) ≤25000/μl (PLT/PZ) and GOB 3, 4 (PZ). Higher OR for mortality was also observed with a lower derangement of coagulative parameters
PT
≤50s,
INR
≤1·7,
aPTT
≤75s (PZ).
Higher survival was observed for (PLT/PZ) LOS(F) 0–7 days across age (m), weight (g) (
P
= 0·002; |
doi_str_mv | 10.1186/s43054-024-00302-1 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_0b71cb910a5b40fba72799953b24ec8d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A810468870</galeid><doaj_id>oai_doaj_org_article_0b71cb910a5b40fba72799953b24ec8d</doaj_id><sourcerecordid>A810468870</sourcerecordid><originalsourceid>FETCH-LOGICAL-c377t-e630f196474c7a3353e7e9e1336b751bb3409cfa437c097346cabb6f9c8bb31a3</originalsourceid><addsrcrecordid>eNp9Uk2P1SAUbYwmTsb5A65IXHeEQktZTiZ-TDKJLnRNLpT28dJCBV707fwHbvyF_hLvm5qnJsYQci-Xcw4XOFX1nNFrxvruZRactqKmDU7KaVOzR9VFQxWtlRLN4z_yp9VVzntKKZOKt31_UX177wYPJXlLBrfEKcG6wxxyjhbrPgby2Zcd2cW8-gIzWWLC4MuR-EDWGYqbXck1gTCclnmBuiQIeTxkN5BjPISJrOczVpR0oWTy4-t3AmTxXxBk4w5FSS6H4fisejLCnN3Vr3hZfXz96sPt2_r-3Zu725v72nIpS-06TkemOiGFlcB5y510yjHOOyNbZgwXVNkRBJeWKslFZ8GYblS2xz0G_LK623SHCHu9Jr9AOuoIXj8UYpo0pOLt7DQ1klmjGIXWCDoakI1USrXcNMLZfkCtF5vWmuKng8tF7-MhBWxfc6r6tpUC_-WMmgBFfRgjvpNdfLb6pmdUdH0vT6jrf6Bw4O94G4MbPdb_IjQbwaaYc3Lj-TKM6pM99GYPjfbQD_bQDEl8I2UEh8ml3x3_h_UTIxG-3Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3098557400</pqid></control><display><type>article</type><title>Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study</title><source>Publicly Available Content Database</source><source>Springer Nature - SpringerLink Journals - Fully Open Access </source><creator>Sharma, Sankalp ; Padhi, Phalguni</creator><creatorcontrib>Sharma, Sankalp ; Padhi, Phalguni</creatorcontrib><description>Background
Demographic and biochemical variations in newborn children as compared to adults are attributable to variable prognosis to blood transfusions. Aims of this mixed cohort study of Platelets with/without Plasma (PLT/PZ); only Plasma (PZ) transfusions in ≤ 24 months children is as follows: An Association of demography towards hospital mortality, and an association of laboratory investigations (LI) with hospital mortality.
Methods
PLT/PZ (
n
= 72) and PZ (
n
= 79) children ≤ 24 months were followed up for a total length of hospital stay (LOS(D)). We calculated the Odds Ratio (OR) of demographic, and laboratory parameters for mortality, survival studies of demographic, laboratory parameters , Kaplan Meier Survival curve, Log-Rank significance (KMLR) and Multivariable regression (
r
2
) with outcome as death.
Results
The present study is in 2019–2022. Higher OR for hospital-based mortality for PLT/PZ and PZ cohort were age ≤ 1 m, weight ≤ 1500 g, preterm, gestational age ≤ 34 weeks, hospital length of stay {LOS(D)} 0–7 days, APGAR score ≤ 5, and Hb ≤ 7 g/dl. High OR, mortality was observed with Female gender, Length of stay before first transfusion {LOS(F)}, 0-7d, WHO Grade of bleeding (GOB) 4,
PT
>50 sec,
INR
>1·7,
aPTT
>75sec, PLT counts (μl) ≤25000/μl (PLT/PZ) and GOB 3, 4 (PZ). Higher OR for mortality was also observed with a lower derangement of coagulative parameters
PT
≤50s,
INR
≤1·7,
aPTT
≤75s (PZ).
Higher survival was observed for (PLT/PZ) LOS(F) 0–7 days across age (m), weight (g) (
P
= 0·002; < 0·01), and
INR
≤ 1·7;
aPTT
≤ 75 s across LOS(D) (
P
< 0·01,0·018); (PZ) LOS(D) ≤ 7 days across age (m) and weight (g) (
P
= 0·036, 0·001); and GOB across LOS(D) (PLT/PZ; PZ) (
P
= 0·052, 0·005). Demography (PLT/PZ)
r
2
= 50·36% (
P
= 0·021), laboratory investigations
r
2
= 10·44% (
P
= 0·47), LOS(F) (
P
= 0·010), LOS(D) (
P
= 0·003), and GOB (
P
= 0·03) were the predictors. Demography (PZ)
r
2
(
P
= 0·095), investigations
r
2
= 8·79% (
P
= 0·254), LOS(D) (
P
= 0·026), and GOB (
P
= 0·012) were the predictors.
Conclusions
PLT/PZ, demographic parameters, were significant cause of mortality with LOS(F), LOS(D), and GOB as predictors. PZ, demography attributed to mortality with LOS(D), and GOB as predictors. A higher OR of morality with lower derangement of laboratory profile is indicative of unnecessary transfusions in the age group. Laboratory investigations by themselves are not significant predictors of mortality.</description><identifier>ISSN: 2090-9942</identifier><identifier>ISSN: 1110-6638</identifier><identifier>EISSN: 2090-9942</identifier><identifier>DOI: 10.1186/s43054-024-00302-1</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Age groups ; Apgar score ; Blood platelets ; Blood transfusion ; Children ; Cohort analysis ; Comparative analysis ; Confidence intervals ; Demographic ; Fresh ; Frozen plasma ; Gestational age ; Health aspects ; Hospital patients ; Hospital stays ; Hospitalization ; Hypotheses ; Laboratories ; Length of stay ; Length of stay before first transfusion ; Medical prognosis ; Medical research ; Medicine ; Medicine & Public Health ; Medicine, Experimental ; Mortality ; Newborn babies ; Patient outcomes ; Patients ; Pediatrics ; Plasma ; Premature babies ; Premature birth ; Prognosis ; Thrombocytopenia ; Variables</subject><ispartof>The Gazette of the Egyptian Paediatric Association, 2024-12, Vol.72 (1), p.64-10, Article 64</ispartof><rights>The Author(s) 2024</rights><rights>COPYRIGHT 2024 Springer</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c377t-e630f196474c7a3353e7e9e1336b751bb3409cfa437c097346cabb6f9c8bb31a3</cites><orcidid>0009-0004-8494-8866 ; 0000-0003-0467-606X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3098557400/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3098557400?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Sharma, Sankalp</creatorcontrib><creatorcontrib>Padhi, Phalguni</creatorcontrib><title>Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study</title><title>The Gazette of the Egyptian Paediatric Association</title><addtitle>Egypt Pediatric Association Gaz</addtitle><description>Background
Demographic and biochemical variations in newborn children as compared to adults are attributable to variable prognosis to blood transfusions. Aims of this mixed cohort study of Platelets with/without Plasma (PLT/PZ); only Plasma (PZ) transfusions in ≤ 24 months children is as follows: An Association of demography towards hospital mortality, and an association of laboratory investigations (LI) with hospital mortality.
Methods
PLT/PZ (
n
= 72) and PZ (
n
= 79) children ≤ 24 months were followed up for a total length of hospital stay (LOS(D)). We calculated the Odds Ratio (OR) of demographic, and laboratory parameters for mortality, survival studies of demographic, laboratory parameters , Kaplan Meier Survival curve, Log-Rank significance (KMLR) and Multivariable regression (
r
2
) with outcome as death.
Results
The present study is in 2019–2022. Higher OR for hospital-based mortality for PLT/PZ and PZ cohort were age ≤ 1 m, weight ≤ 1500 g, preterm, gestational age ≤ 34 weeks, hospital length of stay {LOS(D)} 0–7 days, APGAR score ≤ 5, and Hb ≤ 7 g/dl. High OR, mortality was observed with Female gender, Length of stay before first transfusion {LOS(F)}, 0-7d, WHO Grade of bleeding (GOB) 4,
PT
>50 sec,
INR
>1·7,
aPTT
>75sec, PLT counts (μl) ≤25000/μl (PLT/PZ) and GOB 3, 4 (PZ). Higher OR for mortality was also observed with a lower derangement of coagulative parameters
PT
≤50s,
INR
≤1·7,
aPTT
≤75s (PZ).
Higher survival was observed for (PLT/PZ) LOS(F) 0–7 days across age (m), weight (g) (
P
= 0·002; < 0·01), and
INR
≤ 1·7;
aPTT
≤ 75 s across LOS(D) (
P
< 0·01,0·018); (PZ) LOS(D) ≤ 7 days across age (m) and weight (g) (
P
= 0·036, 0·001); and GOB across LOS(D) (PLT/PZ; PZ) (
P
= 0·052, 0·005). Demography (PLT/PZ)
r
2
= 50·36% (
P
= 0·021), laboratory investigations
r
2
= 10·44% (
P
= 0·47), LOS(F) (
P
= 0·010), LOS(D) (
P
= 0·003), and GOB (
P
= 0·03) were the predictors. Demography (PZ)
r
2
(
P
= 0·095), investigations
r
2
= 8·79% (
P
= 0·254), LOS(D) (
P
= 0·026), and GOB (
P
= 0·012) were the predictors.
Conclusions
PLT/PZ, demographic parameters, were significant cause of mortality with LOS(F), LOS(D), and GOB as predictors. PZ, demography attributed to mortality with LOS(D), and GOB as predictors. A higher OR of morality with lower derangement of laboratory profile is indicative of unnecessary transfusions in the age group. Laboratory investigations by themselves are not significant predictors of mortality.</description><subject>Age groups</subject><subject>Apgar score</subject><subject>Blood platelets</subject><subject>Blood transfusion</subject><subject>Children</subject><subject>Cohort analysis</subject><subject>Comparative analysis</subject><subject>Confidence intervals</subject><subject>Demographic</subject><subject>Fresh</subject><subject>Frozen plasma</subject><subject>Gestational age</subject><subject>Health aspects</subject><subject>Hospital patients</subject><subject>Hospital stays</subject><subject>Hospitalization</subject><subject>Hypotheses</subject><subject>Laboratories</subject><subject>Length of stay</subject><subject>Length of stay before first transfusion</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Medicine, Experimental</subject><subject>Mortality</subject><subject>Newborn babies</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Plasma</subject><subject>Premature babies</subject><subject>Premature birth</subject><subject>Prognosis</subject><subject>Thrombocytopenia</subject><subject>Variables</subject><issn>2090-9942</issn><issn>1110-6638</issn><issn>2090-9942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9Uk2P1SAUbYwmTsb5A65IXHeEQktZTiZ-TDKJLnRNLpT28dJCBV707fwHbvyF_hLvm5qnJsYQci-Xcw4XOFX1nNFrxvruZRactqKmDU7KaVOzR9VFQxWtlRLN4z_yp9VVzntKKZOKt31_UX177wYPJXlLBrfEKcG6wxxyjhbrPgby2Zcd2cW8-gIzWWLC4MuR-EDWGYqbXck1gTCclnmBuiQIeTxkN5BjPISJrOczVpR0oWTy4-t3AmTxXxBk4w5FSS6H4fisejLCnN3Vr3hZfXz96sPt2_r-3Zu725v72nIpS-06TkemOiGFlcB5y510yjHOOyNbZgwXVNkRBJeWKslFZ8GYblS2xz0G_LK623SHCHu9Jr9AOuoIXj8UYpo0pOLt7DQ1klmjGIXWCDoakI1USrXcNMLZfkCtF5vWmuKng8tF7-MhBWxfc6r6tpUC_-WMmgBFfRgjvpNdfLb6pmdUdH0vT6jrf6Bw4O94G4MbPdb_IjQbwaaYc3Lj-TKM6pM99GYPjfbQD_bQDEl8I2UEh8ml3x3_h_UTIxG-3Q</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Sharma, Sankalp</creator><creator>Padhi, Phalguni</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><general>SpringerOpen</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0004-8494-8866</orcidid><orcidid>https://orcid.org/0000-0003-0467-606X</orcidid></search><sort><creationdate>20241201</creationdate><title>Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study</title><author>Sharma, Sankalp ; Padhi, Phalguni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-e630f196474c7a3353e7e9e1336b751bb3409cfa437c097346cabb6f9c8bb31a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Age groups</topic><topic>Apgar score</topic><topic>Blood platelets</topic><topic>Blood transfusion</topic><topic>Children</topic><topic>Cohort analysis</topic><topic>Comparative analysis</topic><topic>Confidence intervals</topic><topic>Demographic</topic><topic>Fresh</topic><topic>Frozen plasma</topic><topic>Gestational age</topic><topic>Health aspects</topic><topic>Hospital patients</topic><topic>Hospital stays</topic><topic>Hospitalization</topic><topic>Hypotheses</topic><topic>Laboratories</topic><topic>Length of stay</topic><topic>Length of stay before first transfusion</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Medicine, Experimental</topic><topic>Mortality</topic><topic>Newborn babies</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Plasma</topic><topic>Premature babies</topic><topic>Premature birth</topic><topic>Prognosis</topic><topic>Thrombocytopenia</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sharma, Sankalp</creatorcontrib><creatorcontrib>Padhi, Phalguni</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</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 China</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>The Gazette of the Egyptian Paediatric Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sharma, Sankalp</au><au>Padhi, Phalguni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study</atitle><jtitle>The Gazette of the Egyptian Paediatric Association</jtitle><stitle>Egypt Pediatric Association Gaz</stitle><date>2024-12-01</date><risdate>2024</risdate><volume>72</volume><issue>1</issue><spage>64</spage><epage>10</epage><pages>64-10</pages><artnum>64</artnum><issn>2090-9942</issn><issn>1110-6638</issn><eissn>2090-9942</eissn><abstract>Background
Demographic and biochemical variations in newborn children as compared to adults are attributable to variable prognosis to blood transfusions. Aims of this mixed cohort study of Platelets with/without Plasma (PLT/PZ); only Plasma (PZ) transfusions in ≤ 24 months children is as follows: An Association of demography towards hospital mortality, and an association of laboratory investigations (LI) with hospital mortality.
Methods
PLT/PZ (
n
= 72) and PZ (
n
= 79) children ≤ 24 months were followed up for a total length of hospital stay (LOS(D)). We calculated the Odds Ratio (OR) of demographic, and laboratory parameters for mortality, survival studies of demographic, laboratory parameters , Kaplan Meier Survival curve, Log-Rank significance (KMLR) and Multivariable regression (
r
2
) with outcome as death.
Results
The present study is in 2019–2022. Higher OR for hospital-based mortality for PLT/PZ and PZ cohort were age ≤ 1 m, weight ≤ 1500 g, preterm, gestational age ≤ 34 weeks, hospital length of stay {LOS(D)} 0–7 days, APGAR score ≤ 5, and Hb ≤ 7 g/dl. High OR, mortality was observed with Female gender, Length of stay before first transfusion {LOS(F)}, 0-7d, WHO Grade of bleeding (GOB) 4,
PT
>50 sec,
INR
>1·7,
aPTT
>75sec, PLT counts (μl) ≤25000/μl (PLT/PZ) and GOB 3, 4 (PZ). Higher OR for mortality was also observed with a lower derangement of coagulative parameters
PT
≤50s,
INR
≤1·7,
aPTT
≤75s (PZ).
Higher survival was observed for (PLT/PZ) LOS(F) 0–7 days across age (m), weight (g) (
P
= 0·002; < 0·01), and
INR
≤ 1·7;
aPTT
≤ 75 s across LOS(D) (
P
< 0·01,0·018); (PZ) LOS(D) ≤ 7 days across age (m) and weight (g) (
P
= 0·036, 0·001); and GOB across LOS(D) (PLT/PZ; PZ) (
P
= 0·052, 0·005). Demography (PLT/PZ)
r
2
= 50·36% (
P
= 0·021), laboratory investigations
r
2
= 10·44% (
P
= 0·47), LOS(F) (
P
= 0·010), LOS(D) (
P
= 0·003), and GOB (
P
= 0·03) were the predictors. Demography (PZ)
r
2
(
P
= 0·095), investigations
r
2
= 8·79% (
P
= 0·254), LOS(D) (
P
= 0·026), and GOB (
P
= 0·012) were the predictors.
Conclusions
PLT/PZ, demographic parameters, were significant cause of mortality with LOS(F), LOS(D), and GOB as predictors. PZ, demography attributed to mortality with LOS(D), and GOB as predictors. A higher OR of morality with lower derangement of laboratory profile is indicative of unnecessary transfusions in the age group. Laboratory investigations by themselves are not significant predictors of mortality.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1186/s43054-024-00302-1</doi><tpages>10</tpages><orcidid>https://orcid.org/0009-0004-8494-8866</orcidid><orcidid>https://orcid.org/0000-0003-0467-606X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
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ispartof | The Gazette of the Egyptian Paediatric Association, 2024-12, Vol.72 (1), p.64-10, Article 64 |
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language | eng |
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source | Publicly Available Content Database; Springer Nature - SpringerLink Journals - Fully Open Access |
subjects | Age groups Apgar score Blood platelets Blood transfusion Children Cohort analysis Comparative analysis Confidence intervals Demographic Fresh Frozen plasma Gestational age Health aspects Hospital patients Hospital stays Hospitalization Hypotheses Laboratories Length of stay Length of stay before first transfusion Medical prognosis Medical research Medicine Medicine & Public Health Medicine, Experimental Mortality Newborn babies Patient outcomes Patients Pediatrics Plasma Premature babies Premature birth Prognosis Thrombocytopenia Variables |
title | Pediatric demographic association with hospital mortality in platelets- and plasma-transfused young pediatric patients — a mixed cohort study |
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