Platelet inhibition by low-dose aspirin is not influenced by body mass or weight

Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of plat...

Full description

Saved in:
Bibliographic Details
Published inPlatelets (Edinburgh) Vol. 33; no. 8; pp. 1208 - 1213
Main Authors Heffron, Sean P., Windheim, Joseph, Barrett, Tessa J., Voora, Deepak, Berger, Jeffrey S.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 17.11.2022
Taylor & Francis Group
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0-57.5 kg/m 2 and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass - suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.
AbstractList Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0-57.5 kg/m 2 and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass - suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.
Aspirin’s clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin’s inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0–57.5 kg/m2 and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass – suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.
Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0-57.5 kg/m and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass - suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.
Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0-57.5 kg/m2 and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass - suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence for this in non-diabetic patients is sparse. We investigated the influence of body weight and mass on aspirin's inhibition of platelet aggregation in healthy adults without diabetes. Cohort one (NYU, n = 84) had light transmission aggregometry (LTA) of platelet-rich plasma to submaximal adenosine diphosphate (ADP) and arachidonic acid (AA) before and following 1 week of daily 81 mg non-enteric coated aspirin. Subjects in the validation cohort (Duke, n = 66) were randomized to 81 mg or 325 mg non-enteric coated aspirin for 4 weeks, immediately followed by 4 weeks of the other dose, with LTA to submaximal collagen, ADP, and AA before and after each dosage period. Body mass index (BMI) range was 18.0-57.5 kg/m2 and 25% were obese. Inhibition of platelet aggregation was similar irrespective of BMI, body weight and aspirin dose. There was no correlation between platelet aggregation before or after aspirin with BMI or body weight. Our data demonstrate that aspirin produces potent inhibition of direct and indirect COX1-mediated platelet aggregation in healthy adults without diabetes regardless of body weight or mass - suggesting that other mechanisms explain lower preventive efficacy of low-dose aspirin with increasing body weight/mass.
Author Barrett, Tessa J.
Heffron, Sean P.
Berger, Jeffrey S.
Windheim, Joseph
Voora, Deepak
Author_xml – sequence: 1
  givenname: Sean P.
  surname: Heffron
  fullname: Heffron, Sean P.
  organization: NYU Center for the Prevention of Cardiovascular Disease, NYU Langone Health
– sequence: 2
  givenname: Joseph
  surname: Windheim
  fullname: Windheim, Joseph
  organization: Leon H Charney Division of Cardiology, Department of Medicine, NYU Grossman School of Medicine
– sequence: 3
  givenname: Tessa J.
  surname: Barrett
  fullname: Barrett, Tessa J.
  organization: Leon H Charney Division of Cardiology, Department of Medicine, NYU Grossman School of Medicine
– sequence: 4
  givenname: Deepak
  surname: Voora
  fullname: Voora, Deepak
  organization: Duke Center for Applied Genomics & Precision Medicine
– sequence: 5
  givenname: Jeffrey S.
  surname: Berger
  fullname: Berger, Jeffrey S.
  email: jeffrey.berger@nyulangone.org, Deepak.voora@duke.edu
  organization: Division of Vascular Surgery, Department of Surgery, NYU Grossman School of Medicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/35768902$$D View this record in MEDLINE/PubMed
BookMark eNqFkc1u3CAUhVGUKplM-witWHbjFIwNWN20ivoTKVKzSNbo8pcQYTMFRqN5-9idSRZdtBuQ0HcOV_e7QKdTmhxC7ym5pESST2TomaCku2xJ286HFJLLE7SijA8N5aw_RauFaRboHF2U8kQIlYT3Z-ic9YLLgbQrdHsbobroKg7TY9ChhjRhvccx7RqbisNQNiGHCYeCp7RQPm7dZJxdKJ3sHo9QCk4Z71x4eKxv0RsPsbh3x3uN7r9_u7v62dz8-nF99fWmMZ0YatMKaYFT1xlmeqEJdJq0jA5Db8B7o6WXnpPO0MEwwan1GsACJcwI4k1r2BpdH3ptgie1yWGEvFcJgvrzkPKDglyDiU5JxkC6VnRGuK4bQFPb-04YTYa5Uuu56-Oha5PT760rVY2hGBcjTC5ti2q5nOdlfF7rGn04ols9Ovv68ctGZ6A_ACanUrLzrwglajGnXsypxZw6mptzn__KmVBh0VEzhPjf9JdDevaT8gi7lKNVFfYxZZ9hMqEo9u-KZx16sTU
CitedBy_id crossref_primary_10_1161_ATVBAHA_122_318020
Cites_doi 10.1111/j.1751-553X.2011.01360.x
10.1016/j.jacc.2016.11.049
10.1016/j.trsl.2012.12.015
10.2337/db07-0707
10.1111/jth.14445
10.1371/journal.pone.0126767
10.1016/j.atherosclerosis.2018.12.029
10.7326/M16-0577
10.1016/j.amjcard.2009.07.015
10.1161/01.STR.0000162719.11058.bd
10.2353/ajpath.2010.091082
10.1161/HYPERTENSIONAHA.111.181404
10.1161/01.STR.0000231683.43347.ec
10.1093/eurheartj/ehy066
10.1038/nature13479
10.1016/S0140-6736(18)31133-4
10.1161/JAHA.119.014726
10.1080/09537104.2018.1536261
10.1007/s40262-017-0611-8
10.1172/JCI110576
10.1111/bph.13707
10.1016/j.atherosclerosis.2015.04.015
10.1016/j.jacc.2005.06.058
10.1016/j.cjca.2014.10.025
10.1038/s41598-017-10441-8
10.1096/fj.201500155R
10.3109/09537104.2013.863857
10.1016/j.bcp.2017.06.128
10.3109/09537104.2013.793794
10.1111/j.1751-7141.2009.00058.x
10.1111/j.1538-7836.2010.03997.x
10.1016/j.vph.2020.106819
10.1016/j.amjcard.2007.02.081
10.1016/j.thromres.2011.05.008
10.1161/CIRCRESAHA.119.315897
ContentType Journal Article
Copyright 2022 Taylor & Francis Group, LLC 2022
Copyright_xml – notice: 2022 Taylor & Francis Group, LLC 2022
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOA
DOI 10.1080/09537104.2022.2087868
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList

MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1369-1635
EndPage 1213
ExternalDocumentID oai_doaj_org_article_833a8e274c7e449ab1d5f47cb09da1bb
35768902
10_1080_09537104_2022_2087868
2087868
Genre Research Article
Randomized Controlled Trial
Journal Article
GrantInformation_xml – fundername: NHLBI NIH HHS
  grantid: R01 HL139909
– fundername: NHLBI NIH HHS
  grantid: T32 HL098129
– fundername: NHLBI NIH HHS
  grantid: R01 HL118049
– fundername: NHLBI NIH HHS
  grantid: R01 HL157430
– fundername: NHLBI NIH HHS
  grantid: R35 HL144993
– fundername: NHLBI NIH HHS
  grantid: K23 HL135398
– fundername: NHLBI NIH HHS
  grantid: R01 HL114978
GroupedDBID ---
00X
03L
0BK
0YH
123
29O
36B
4.4
AALUX
AAMIU
AAPUL
AAQRR
ABBKH
ABDBF
ABEIZ
ABJNI
ABLIJ
ABLKL
ABUPF
ABXYU
ACENM
ACGEJ
ACGFS
ACUHS
ADCVX
ADRBQ
ADXPE
AECIN
AENEX
AEOZL
AFKVX
AGDLA
AGFJD
AGRBW
AGYJP
AIJEM
AJWEG
AKBVH
ALMA_UNASSIGNED_HOLDINGS
ALQZU
ALYBC
AMDAE
BABNJ
BLEHA
BOHLJ
CCCUG
CS3
DKSSO
DU5
EAP
EBC
EBD
EBS
EMB
EMK
EMOBN
EPL
ESX
F5P
H13
HZ~
KRBQP
KSSTO
KWAYT
KYCEM
LJTGL
M4Z
O9-
RNANH
RVRKI
SV3
TBQAZ
TDBHL
TERGH
TFDNU
TFL
TFW
TUROJ
TUS
UEQFS
V1S
~1N
AAGDL
AAYXX
ABWVI
ADYSH
AFRVT
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
GROUPED_DOAJ
ID FETCH-LOGICAL-c479t-278da61e4c3c57b0a4b0231995caffcb8f8f604c19c3761dfbaada103c70fc2c3
IEDL.DBID DOA
ISSN 0953-7104
1369-1635
IngestDate Wed Aug 27 01:32:25 EDT 2025
Fri Jul 11 09:21:41 EDT 2025
Wed Feb 19 02:08:56 EST 2025
Tue Jul 01 04:01:54 EDT 2025
Thu Apr 24 23:04:28 EDT 2025
Wed Dec 25 09:06:53 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 8
Keywords body weight
Aspirin
cyclooxygenase 1
obesity
platelet aggregation
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c479t-278da61e4c3c57b0a4b0231995caffcb8f8f604c19c3761dfbaada103c70fc2c3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
OpenAccessLink https://doaj.org/article/833a8e274c7e449ab1d5f47cb09da1bb
PMID 35768902
PQID 2682783616
PQPubID 23479
PageCount 6
ParticipantIDs informaworld_taylorfrancis_310_1080_09537104_2022_2087868
pubmed_primary_35768902
crossref_primary_10_1080_09537104_2022_2087868
doaj_primary_oai_doaj_org_article_833a8e274c7e449ab1d5f47cb09da1bb
proquest_miscellaneous_2682783616
crossref_citationtrail_10_1080_09537104_2022_2087868
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-11-17
PublicationDateYYYYMMDD 2022-11-17
PublicationDate_xml – month: 11
  year: 2022
  text: 2022-11-17
  day: 17
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle Platelets (Edinburgh)
PublicationTitleAlternate Platelets
PublicationYear 2022
Publisher Taylor & Francis
Taylor & Francis Group
Publisher_xml – name: Taylor & Francis
– name: Taylor & Francis Group
References cit0011
cit0033
cit0012
cit0034
cit0031
cit0010
cit0032
cit0030
cit0019
cit0017
cit0018
cit0015
cit0016
cit0013
cit0035
cit0014
cit0022
cit0001
cit0023
cit0020
cit0021
cit0008
cit0009
cit0006
cit0028
cit0007
cit0029
cit0004
cit0026
cit0005
cit0027
cit0002
cit0024
cit0003
cit0025
References_xml – ident: cit0017
  doi: 10.1111/j.1751-553X.2011.01360.x
– ident: cit0027
  doi: 10.1016/j.jacc.2016.11.049
– ident: cit0030
  doi: 10.1016/j.trsl.2012.12.015
– ident: cit0013
  doi: 10.2337/db07-0707
– ident: cit0019
  doi: 10.1111/jth.14445
– ident: cit0009
  doi: 10.1371/journal.pone.0126767
– ident: cit0014
  doi: 10.1016/j.atherosclerosis.2018.12.029
– ident: cit0018
  doi: 10.7326/M16-0577
– ident: cit0031
  doi: 10.1016/j.amjcard.2009.07.015
– ident: cit0035
  doi: 10.1161/01.STR.0000162719.11058.bd
– ident: cit0026
  doi: 10.2353/ajpath.2010.091082
– ident: cit0008
  doi: 10.1161/HYPERTENSIONAHA.111.181404
– ident: cit0006
  doi: 10.1161/01.STR.0000231683.43347.ec
– ident: cit0028
  doi: 10.1093/eurheartj/ehy066
– ident: cit0022
  doi: 10.1038/nature13479
– ident: cit0003
  doi: 10.1016/S0140-6736(18)31133-4
– ident: cit0015
  doi: 10.1161/JAHA.119.014726
– ident: cit0021
  doi: 10.1080/09537104.2018.1536261
– ident: cit0011
  doi: 10.1007/s40262-017-0611-8
– ident: cit0004
  doi: 10.1172/JCI110576
– ident: cit0024
  doi: 10.1111/bph.13707
– ident: cit0033
  doi: 10.1016/j.atherosclerosis.2015.04.015
– ident: cit0007
  doi: 10.1016/j.jacc.2005.06.058
– ident: cit0002
  doi: 10.1016/j.cjca.2014.10.025
– ident: cit0023
  doi: 10.1038/s41598-017-10441-8
– ident: cit0025
  doi: 10.1096/fj.201500155R
– ident: cit0029
  doi: 10.3109/09537104.2013.863857
– ident: cit0012
  doi: 10.1016/j.bcp.2017.06.128
– ident: cit0016
  doi: 10.3109/09537104.2013.793794
– ident: cit0010
  doi: 10.1111/j.1751-7141.2009.00058.x
– ident: cit0005
  doi: 10.1111/j.1538-7836.2010.03997.x
– ident: cit0020
  doi: 10.1016/j.vph.2020.106819
– ident: cit0032
  doi: 10.1016/j.amjcard.2007.02.081
– ident: cit0034
  doi: 10.1016/j.thromres.2011.05.008
– ident: cit0001
  doi: 10.1161/CIRCRESAHA.119.315897
SSID ssj0018065
Score 2.3255754
Snippet Aspirin's clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence...
Aspirin’s clinical efficacy may be influenced by body weight and mass. Although inadequate platelet inhibition by aspirin is suggested as responsible, evidence...
SourceID doaj
proquest
pubmed
crossref
informaworld
SourceType Open Website
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1208
SubjectTerms Adenosine Diphosphate - pharmacology
Adult
Arachidonic Acid - pharmacology
Aspirin
Aspirin - pharmacology
Aspirin - therapeutic use
Blood Platelets
Body Weight
Collagen - pharmacology
cyclooxygenase 1
Humans
obesity
Platelet Aggregation
Platelet Aggregation Inhibitors - pharmacology
Platelet Aggregation Inhibitors - therapeutic use
Platelet Function Tests
Title Platelet inhibition by low-dose aspirin is not influenced by body mass or weight
URI https://www.tandfonline.com/doi/abs/10.1080/09537104.2022.2087868
https://www.ncbi.nlm.nih.gov/pubmed/35768902
https://www.proquest.com/docview/2682783616
https://doaj.org/article/833a8e274c7e449ab1d5f47cb09da1bb
Volume 33
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1LaxsxEBYlveQSkiZpnBcqlNw2Xa20ehzttiYUWnJoIDehJzE4uyF2CP730Wh3jQkUX3oVEgyj0Tw0M98g9DXSynsTRVEqawsWDS0Uj76IgdfG-WSxFDQn__7Db-7Yr_v6fmPUF9SEdfDAHeO-SUqNDCl2ciIwpowlvo5MOFsqb4i1oH2TzRuCqT5_AOnCDmWPQrUhG3p3AFU7rcFSig0r6MSSQgLO6oZVyuD976BL_-2AZkM03Ud7vQeJxx3lB-hDaD6hw3GToufHFb7CuaYzf5YfotvbefIl09XgWfMws7k8C9sVnrevhW8XARtItM8aPFvgpoVd_cgSD7ts61f4MXnXuH3Gr_kP9QjdTX_-_X5T9DMUCseEWhaVkN5wEpijrha2NMwC4ptStTMxOiujjLxkjiiXVA3x0RqT-FpSJ8roKkeP0U7TNuEEYVPJqEztIIfMkiOpODFlqIOrk1agVowQG3ioXQ8wDnMu5poMOKQ96zWwXvesH6Hr9bGnDmFj24EJXNB6MwBk54UkNroXG71NbEZIbV6vXub_kdgNM9F0CwFfBlnQ6TFChsU0oX1Z6IpLmFzCCR-hz52QrMmkENmpsjr9H-SfoV2gCJoiiThHO8vnl3CRvKOlvUQfx5Mfk-llfhBv5_AHzg
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Platelet+inhibition+by+low-dose+aspirin+is+not+influenced+by+body+mass+or+weight&rft.jtitle=Platelets+%28Edinburgh%29&rft.au=Heffron%2C+Sean+P&rft.au=Windheim%2C+Joseph&rft.au=Barrett%2C+Tessa+J&rft.au=Voora%2C+Deepak&rft.date=2022-11-17&rft.eissn=1369-1635&rft.volume=33&rft.issue=8&rft.spage=1208&rft_id=info:doi/10.1080%2F09537104.2022.2087868&rft_id=info%3Apmid%2F35768902&rft.externalDocID=35768902
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0953-7104&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0953-7104&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0953-7104&client=summon