Clinical evaluation of type 2 disease status in a real‐world population of difficult to manage asthma using historic electronic healthcare records of blood eosinophil counts

Background Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti‐IL‐5/IL‐5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophili...

Full description

Saved in:
Bibliographic Details
Published inClinical and experimental allergy Vol. 51; no. 6; pp. 811 - 820
Main Authors Azim, Adnan, Newell, Colin, Barber, Clair, Harvey, Matthew, Knight, Deborah, Freeman, Anna, Fong, Wei Chern Gavin, Dennison, Paddy, Haitchi, Hans Michael, Djukanovic, Ratko, Kurukulaaratchy, Ramesh, Howarth, Peter
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.06.2021
Subjects
Online AccessGet full text
ISSN0954-7894
1365-2222
1365-2222
DOI10.1111/cea.13841

Cover

Loading…
Abstract Background Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti‐IL‐5/IL‐5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable. Methods We interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10‐year retrospective period from the index WATCH assessment were investigated (n = 11,176). Results In 235 biological therapy‐naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post‐bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation. Conclusions This highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.
AbstractList Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti-IL-5/IL-5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable.BACKGROUNDBlood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti-IL-5/IL-5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable.We interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10-year retrospective period from the index WATCH assessment were investigated (n = 11,176).METHODSWe interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10-year retrospective period from the index WATCH assessment were investigated (n = 11,176).In 235 biological therapy-naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post-bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation.RESULTSIn 235 biological therapy-naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post-bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation.This highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.CONCLUSIONSThis highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.
Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti-IL-5/IL-5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable. We interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10-year retrospective period from the index WATCH assessment were investigated (n = 11,176). In 235 biological therapy-naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post-bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation. This highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.
Background Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti‐IL‐5/IL‐5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable. Methods We interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10‐year retrospective period from the index WATCH assessment were investigated (n = 11,176). Results In 235 biological therapy‐naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post‐bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation. Conclusions This highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.
BackgroundBlood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for anti‐IL‐5/IL‐5Rα biological therapies. However, assessing such measures over limited time spans may not reveal the true underlying eosinophilic phenotype, as treatment, including daily oral corticosteroid therapy, suppresses eosinophilic inflammation and asthma is intrinsically variable.MethodsWe interrogated the electronic healthcare records of patients in the Wessex AsThma CoHort of difficult asthma (WATCH) study (UK). In 501 patients being evaluated in this tertiary care centre for difficult to control asthma, all requested full blood count test results in a 10‐year retrospective period from the index WATCH assessment were investigated (n = 11,176).ResultsIn 235 biological therapy‐naïve participants who had 10 or more measures in this time period, 40.3% were eosinophilic (blood eosinophils ≥300 cells/µl) at WATCH enrolment whilst an additional 43.1%, though not eosinophilic at enrolment, demonstrated eosinophilia at least once in the preceding decade. Persistent eosinophilia was associated with worse post‐bronchodilator airway obstruction and higher Fractional exhaled Nitric Oxide (FeNO). In contrast, the 16.6% of patients who never demonstrated eosinophilia at this blood eosinophil threshold showed preserved lung function and lower markers of Type 2 inflammation.ConclusionsThis highlights the central role that type 2 inflammation, as indicated by blood eosinophilia, has in difficult asthma and suggests that longitudinal electronic healthcare record analysis can be an important tool in clinical asthma phenotyping, providing insight that may help understand disease progression and better guide more specific treatment approaches.
Author Barber, Clair
Howarth, Peter
Harvey, Matthew
Azim, Adnan
Knight, Deborah
Newell, Colin
Djukanovic, Ratko
Fong, Wei Chern Gavin
Haitchi, Hans Michael
Kurukulaaratchy, Ramesh
Freeman, Anna
Dennison, Paddy
Author_xml – sequence: 1
  givenname: Adnan
  orcidid: 0000-0001-5960-1159
  surname: Azim
  fullname: Azim, Adnan
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 2
  givenname: Colin
  surname: Newell
  fullname: Newell, Colin
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 3
  givenname: Clair
  surname: Barber
  fullname: Barber, Clair
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 4
  givenname: Matthew
  surname: Harvey
  fullname: Harvey, Matthew
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 5
  givenname: Deborah
  surname: Knight
  fullname: Knight, Deborah
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 6
  givenname: Anna
  surname: Freeman
  fullname: Freeman, Anna
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 7
  givenname: Wei Chern Gavin
  orcidid: 0000-0003-2546-156X
  surname: Fong
  fullname: Fong, Wei Chern Gavin
  organization: St Mary’s Hospital
– sequence: 8
  givenname: Paddy
  surname: Dennison
  fullname: Dennison, Paddy
  organization: University Hospital Southampton NHS Foundation Trust
– sequence: 9
  givenname: Hans Michael
  orcidid: 0000-0001-8603-302X
  surname: Haitchi
  fullname: Haitchi, Hans Michael
  organization: University of Southampton
– sequence: 10
  givenname: Ratko
  surname: Djukanovic
  fullname: Djukanovic, Ratko
  organization: University of Southampton
– sequence: 11
  givenname: Ramesh
  surname: Kurukulaaratchy
  fullname: Kurukulaaratchy, Ramesh
  email: R.J.Kurukulaaratchy@soton.ac.uk
  organization: St Mary’s Hospital
– sequence: 12
  givenname: Peter
  surname: Howarth
  fullname: Howarth, Peter
  organization: University of Southampton
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33528864$$D View this record in MEDLINE/PubMed
BookMark eNp9kc1u1TAQRi1URG8LC14AWWIDi7R2HCfOsroqP1IlNrCOJvakceXEwXao7q6PwJvwTjwJvr2li0owG2_Od2bk74QczX5GQl5zdsbznGuEMy5UxZ-RDRe1LMo8R2TDWlkVjWqrY3IS4w1jTMhWvSDHQshSqbrakF9bZ2erwVH8AW6FZP1M_UDTbkFaUmMjQkQaE6Q1UjtToAHB_b77eeuDM3Txy-oeU8YOg9WrSzR5OsEM10ghpnECukY7X9PRxuSD1RQd6hR8Xk3H7EujhoBZrX0wca_qnfeGos8xv4zWUe3XOcWX5PkALuKrh_eUfPtw-XX7qbj68vHz9uKq0EIpXnDTV6YB0yphWgRpKl4ilmVbS142mpWsUn3-i6qRtRKsGdqWKQYNDL2pZS_FKXl38C7Bf18xpm6yUaNzMKNfY1dWSkquWlln9O0T9MavYc7XdaUUXDLB1V745oFa-wlNtwQ7Qdh1f6vIwPsDoIOPMeDwiHDW7Wvucs3dfc2ZPX_CapvuW0gBrPtf4tY63P1b3W0vLw6JPxwzu3g
CitedBy_id crossref_primary_10_1016_j_jaip_2021_08_038
crossref_primary_10_1016_j_jaci_2023_06_005
crossref_primary_10_1111_all_15375
crossref_primary_10_1016_j_jaip_2023_05_028
crossref_primary_10_3389_fmed_2022_992565
crossref_primary_10_1080_17476348_2024_2404673
crossref_primary_10_2147_JIR_S295038
crossref_primary_10_1111_cea_14109
crossref_primary_10_1080_02770903_2024_2449229
crossref_primary_10_2147_JAA_S378505
crossref_primary_10_1111_cea_13893
crossref_primary_10_1016_j_jaip_2021_07_056
crossref_primary_10_3390_jpm12010070
crossref_primary_10_1016_j_waojou_2021_100547
crossref_primary_10_2147_JAA_S474338
crossref_primary_10_1016_j_anai_2022_02_021
crossref_primary_10_3389_fphar_2023_1315540
crossref_primary_10_1016_j_jaip_2023_02_020
crossref_primary_10_1080_02770903_2023_2241905
crossref_primary_10_3238_PersPneumo_2021_12_17_05
crossref_primary_10_2147_JAA_S430183
crossref_primary_10_33590_emj_HTIQ1028
crossref_primary_10_1016_j_rmed_2022_106915
crossref_primary_10_1016_j_chest_2021_05_030
crossref_primary_10_1055_a_1709_7899
crossref_primary_10_1186_s13223_024_00917_4
crossref_primary_10_3390_jcm13164801
crossref_primary_10_1016_j_jacig_2024_100343
crossref_primary_10_1080_07853890_2024_2417184
crossref_primary_10_3390_jpm12091435
crossref_primary_10_1186_s13223_023_00863_7
crossref_primary_10_1016_j_chest_2021_04_013
crossref_primary_10_1016_j_jaip_2023_05_011
Cites_doi 10.1111/j.1440-1843.2006.00784.x
10.1016/S0140-6736(02)11679-5
10.1183/09031936.00165106
10.1016/j.jaci.2015.11.020
10.1016/j.anai.2016.08.010
10.1016/j.jaip.2017.12.019
10.1016/j.jaip.2020.05.053
10.1111/cea.13310
10.1136/thoraxjnl-2014-205634
10.1080/02770903.2018.1502301
10.1016/j.anai.2014.04.011
10.1183/13993003.02536-2017
10.1136/pgmj.2006.049551
10.1016/j.it.2004.07.006
10.1016/j.jaci.2010.01.003
10.1002/alr.21793
10.1016/S0140-6736(16)31322-8
10.1016/j.rmed.2019.04.020
10.1136/bmj.k1479
10.1056/NEJMoa1403290
10.1186/s12890-018-0689-2
10.1164/rccm.200711-1754OC
10.1164/rccm.201109-1640OC
10.1016/j.rmed.2010.03.030
10.1016/S0140-6736(16)31324-1
10.1164/rccm.200402-230OC
10.1136/thoraxjnl-2016-209919
10.1373/clinchem.2016.267450
10.1177/2040622315609251
10.1111/cea.12345
10.1016/j.jaci.2011.03.010
10.1164/rccm.201304-0775OC
10.1016/S2213-2600(17)30125-X
10.1183/13993003.00938-2018
10.1097/MCP.0b013e32835b118e
10.1016/j.jaci.2014.04.005
10.1016/j.rmed.2018.06.025
10.1016/j.jaci.2010.02.008
10.1126/scitranslmed.3001456
10.1016/S2213-2600(15)00367-7
10.2174/1389450119666180212120012
10.1111/j.1751-553X.2011.01365.x
10.1186/s12890-019-0862-2
10.1371/journal.pone.0100645
ContentType Journal Article
Copyright 2021 The Authors. published by John Wiley & Sons Ltd.
2021 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd.
2021. This article 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.
Copyright_xml – notice: 2021 The Authors. published by John Wiley & Sons Ltd.
– notice: 2021 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd.
– notice: 2021. This article 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.
DBID 24P
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7T5
H94
K9.
7X8
DOI 10.1111/cea.13841
DatabaseName Wiley Online Library Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Immunology Abstracts
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Immunology Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE

AIDS and Cancer Research Abstracts
Database_xml – sequence: 1
  dbid: 24P
  name: Wiley Online Library Open Access
  url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html
  sourceTypes: Publisher
– 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 Medicine
Biology
EISSN 1365-2222
EndPage 820
ExternalDocumentID 33528864
10_1111_cea_13841
CEA13841
Genre article
Research Support, Non-U.S. Gov't
Journal Article
Observational Study
GrantInformation_xml – fundername: Novartis
– fundername: AAIR Charity
– fundername: National Institute for Health Research Southampton Biomedical Research Centre
– fundername: Medical Research Council
  grantid: G0802804
– fundername: MRF_
  grantid: MRF-009-0003-RG-HAITC
GroupedDBID ---
.3N
.55
.GA
.Y3
05W
0R~
10A
1OB
1OC
24P
29B
31~
33P
36B
3O-
3SF
4.4
4P2
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5RE
5VS
66C
6J9
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
A8Z
AAESR
AAEVG
AAHHS
AAHQN
AAIPD
AAKAS
AAMNL
AANHP
AANLZ
AAONW
AASGY
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABDBF
ABEML
ABJNI
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACRPL
ACSCC
ACUHS
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZCM
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFEBI
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHEFC
AHMBA
AIACR
AITYG
AIURR
AIWBW
AJBDE
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
AOETA
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CAG
COF
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
DU5
EAD
EAP
EAS
EBB
EBC
EBD
EBS
EBX
EDH
EJD
EMB
EMK
EMOBN
ESX
EX3
F00
F01
F04
F5P
FEDTE
FUBAC
FZ0
G-S
G.N
GODZA
H.X
HF~
HGLYW
HVGLF
HZI
HZ~
IHE
IX1
J0M
K48
KBYEO
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
Q~Q
R.K
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
SV3
TEORI
TUS
UB1
V8K
V9Y
W8V
W99
WBKPD
WHWMO
WIH
WIJ
WIK
WOHZO
WOW
WQJ
WRC
WUP
WVDHM
WXI
WXSBR
X7M
XG1
YFH
YUY
ZGI
ZXP
ZZTAW
~IA
~WT
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
CGR
CUY
CVF
ECM
EIF
NPM
7T5
H94
K9.
7X8
ID FETCH-LOGICAL-c3881-1db4d7ad983d9ea5d412ee22965127c02048b59847568307f99080a7afbd65b53
IEDL.DBID 24P
ISSN 0954-7894
1365-2222
IngestDate Fri Jul 11 01:38:14 EDT 2025
Sat Jul 26 02:22:43 EDT 2025
Mon Jul 21 05:35:33 EDT 2025
Thu Apr 24 22:59:01 EDT 2025
Tue Jul 01 02:53:30 EDT 2025
Wed Jan 22 16:28:42 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 6
Keywords epidemiology
eosinophils
asthma
Language English
License Attribution
2021 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3881-1db4d7ad983d9ea5d412ee22965127c02048b59847568307f99080a7afbd65b53
Notes Funding information
Kurukulaaratchy and Howarth contributed equally.
The WATCH study makes use of the NIHR SBRC and Clinical Research Facility at UHS‐NHS‐FT that are funded by the NIHR. The WATCH study itself is not externally funded. Funding assistance for database support for the WATCH study was initially obtained from a non‐promotional grant from Novartis (£35,000). Funding assistance for relevant patient costs (eg parking) was initially provided by a charitable grant (£3500) from the Asthma, Allergy & Inflammation Research (AAIR) Charity.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ObjectType-Undefined-3
ORCID 0000-0001-8603-302X
0000-0003-2546-156X
0000-0001-5960-1159
OpenAccessLink https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcea.13841
PMID 33528864
PQID 2531503185
PQPubID 36521
PageCount 10
ParticipantIDs proquest_miscellaneous_2485518956
proquest_journals_2531503185
pubmed_primary_33528864
crossref_primary_10_1111_cea_13841
crossref_citationtrail_10_1111_cea_13841
wiley_primary_10_1111_cea_13841_CEA13841
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate June 2021
2021-06-00
20210601
PublicationDateYYYYMMDD 2021-06-01
PublicationDate_xml – month: 06
  year: 2021
  text: June 2021
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: Oxford
PublicationTitle Clinical and experimental allergy
PublicationTitleAlternate Clin Exp Allergy
PublicationYear 2021
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2017; 5
2018; 141
2018; 361
2012; 185
2017; 63
2005; 171
2015; 3
2019; 53
2015; 70
2006; 11
2010; 125
2004; 25
2010; 104
2019; 56
2016; 388
2013; 188
2019; 19
2014; 371
2007; 30
2012; 34
2014; 44
2014; 134
2014; 113
2013; 19
2020; 8
2018; 19
2006; 82
2018; 6
2016; 6
2018; 18
2016; 7
2011; 128
2002; 360
2017; 11
2019; 49
2016; 117
2018; 51
2018; 73
2016; 138
2008; 178
2014; 9
2019; 152
2010; 2
e_1_2_10_23_1
e_1_2_10_46_1
e_1_2_10_24_1
e_1_2_10_45_1
e_1_2_10_21_1
e_1_2_10_44_1
e_1_2_10_22_1
e_1_2_10_43_1
Sreeparvathi A (e_1_2_10_41_1) 2017; 11
e_1_2_10_42_1
e_1_2_10_20_1
e_1_2_10_40_1
e_1_2_10_2_1
e_1_2_10_4_1
e_1_2_10_18_1
e_1_2_10_3_1
e_1_2_10_19_1
e_1_2_10_6_1
e_1_2_10_16_1
e_1_2_10_39_1
e_1_2_10_5_1
e_1_2_10_17_1
e_1_2_10_38_1
e_1_2_10_8_1
e_1_2_10_14_1
e_1_2_10_37_1
e_1_2_10_7_1
e_1_2_10_15_1
e_1_2_10_36_1
e_1_2_10_12_1
e_1_2_10_35_1
e_1_2_10_9_1
e_1_2_10_13_1
e_1_2_10_34_1
e_1_2_10_10_1
e_1_2_10_33_1
e_1_2_10_11_1
e_1_2_10_32_1
e_1_2_10_31_1
e_1_2_10_30_1
e_1_2_10_29_1
e_1_2_10_27_1
e_1_2_10_28_1
e_1_2_10_25_1
e_1_2_10_26_1
e_1_2_10_47_1
References_xml – volume: 11
  start-page: 54
  issue: 1
  year: 2006
  end-page: 61
  article-title: Inflammatory subtypes in asthma: assessment and identification using induced sputum
  publication-title: Respirology
– volume: 185
  start-page: 612
  issue: 6
  year: 2012
  end-page: 619
  article-title: A large subgroup of mild‐to‐moderate asthma is persistently noneosinophilic
  publication-title: Am J Respir Crit Care Med
– volume: 73
  start-page: 107
  issue: 2
  year: 2018
  end-page: 115
  article-title: Functional phenotypes determined by fluctuation‐based clustering of lung function measurements in healthy and asthmatic cohort participants
  publication-title: Thorax
– volume: 49
  start-page: 163
  issue: 2
  year: 2019
  end-page: 170
  article-title: Variability of blood eosinophils in patients in a clinic for severe asthma
  publication-title: Clin Exp Allergy
– volume: 70
  start-page: 115
  issue: 2
  year: 2015
  end-page: 120
  article-title: External validation of blood eosinophils, FE(NO) and serum periostin as surrogates for sputum eosinophils in asthma
  publication-title: Thorax
– volume: 11
  start-page: MC08
  issue: 2
  year: 2017
  end-page: MC11
  article-title: Significance of blood eosinophil count in patients with chronic rhinosinusitis with nasal polyposis
  publication-title: J Clin Diagn Res
– volume: 360
  start-page: 1715
  issue: 9347
  year: 2002
  end-page: 1721
  article-title: Asthma exacerbations and sputum eosinophil counts: a randomised controlled trial
  publication-title: Lancet
– volume: 3
  start-page: 849
  issue: 11
  year: 2015
  end-page: 858
  article-title: Blood eosinophil count and prospective annual asthma disease burden: a UK cohort study
  publication-title: Lancet Respir Med
– volume: 51
  start-page: 1702536
  issue: 4
  year: 2018
  article-title: Associations between blood eosinophils and decline in lung function among adults with and without asthma
  publication-title: Eur Respir J
– volume: 8
  start-page: 3396
  issue: 10
  year: 2020
  end-page: 3406
  article-title: New perspectives on difficult asthma; sex and age of asthma‐onset based phenotypes
  publication-title: J Allergy Clin Immunol Pract
– volume: 5
  start-page: 390
  issue: 5
  year: 2017
  end-page: 400
  article-title: Efficacy of mepolizumab add‐on therapy on health‐related quality of life and markers of asthma control in severe eosinophilic asthma (MUSCA): a randomised, double‐blind, placebo‐controlled, parallel‐group, multicentre, phase 3b trial
  publication-title: Lancet Respir Med
– volume: 6
  start-page: 980
  issue: 3
  year: 2018
  end-page: 986
  article-title: Asthma exacerbations associated with lung function decline in patients with severe eosinophilic asthma
  publication-title: J Allergy Clin Immunol Pract
– volume: 152
  start-page: 60
  year: 2019
  end-page: 66
  article-title: Increase in blood eosinophils during follow‐up is associated with lung function decline in adult asthma
  publication-title: Respir Med
– volume: 104
  start-page: 1254
  issue: 9
  year: 2010
  end-page: 1262
  article-title: Airway eosinophilia in remission and progression of asthma: accumulation with a fast decline of FEV(1)
  publication-title: Respir Med
– volume: 188
  start-page: 1193
  issue: 10
  year: 2013
  end-page: 1201
  article-title: The effects of airway microbiome on corticosteroid responsiveness in asthma
  publication-title: Am J Respir Crit Care Med
– volume: 371
  start-page: 1198
  issue: 13
  year: 2014
  end-page: 1207
  article-title: Mepolizumab treatment in patients with severe eosinophilic asthma
  publication-title: N Engl J Med
– volume: 18
  start-page: 119
  issue: 1
  year: 2018
  article-title: Anti‐IL‐5 therapy in patients with severe eosinophilic asthma ‐ clinical efficacy and possible criteria for treatment response
  publication-title: BMC Pulm Med
– volume: 178
  start-page: 218
  issue: 3
  year: 2008
  end-page: 224
  article-title: Cluster analysis and clinical asthma phenotypes
  publication-title: Am J Respir Crit Care Med
– volume: 82
  start-page: 823
  issue: 974
  year: 2006
  end-page: 829
  article-title: Factors contributing to inappropriate ordering of tests in an academic medical department and the effect of an educational feedback strategy
  publication-title: Postgrad Med J
– volume: 125
  start-page: 1028
  issue: 5
  year: 2010
  end-page: 1036
  article-title: Analyses of asthma severity phenotypes and inflammatory proteins in subjects stratified by sputum granulocytes
  publication-title: J Allergy Clin Immunol
– volume: 44
  start-page: 1137
  issue: 9
  year: 2014
  end-page: 1145
  article-title: Full blood count parameters for the detection of asthma inflammatory phenotypes
  publication-title: Clin Exp Allergy
– volume: 388
  start-page: 2115
  issue: 10056
  year: 2016
  end-page: 2127
  article-title: Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high‐dosage inhaled corticosteroids and long‐acting beta2‐agonists (SIROCCO): a randomised, multicentre, placebo‐controlled phase 3 trial
  publication-title: Lancet
– volume: 128
  start-page: 293
  issue: 2
  year: 2011
  end-page: 300
  article-title: Fluctuation phenotyping based on daily fraction of exhaled nitric oxide values in asthmatic children
  publication-title: J Allergy Clin Immunol
– volume: 63
  start-page: 823
  issue: 4
  year: 2017
  end-page: 832
  article-title: Association of blood eosinophil and blood neutrophil counts with asthma exacerbations in the copenhagen general population study
  publication-title: Clin Chem
– volume: 361
  start-page: k1479
  year: 2018
  article-title: Biases in electronic health record data due to processes within the healthcare system: retrospective observational study
  publication-title: BMJ
– volume: 141
  start-page: 81
  year: 2018
  end-page: 86
  article-title: Diagnosing persistent blood eosinophilia in asthma with single blood eosinophil or exhaled nitric oxide level
  publication-title: Respir Med
– volume: 19
  start-page: 99
  issue: 1
  year: 2019
  article-title: Protocol for the Wessex AsThma CoHort of difficult asthma (WATCH): a pragmatic real‐life longitudinal study of difficult asthma in the clinic
  publication-title: BMC Pulm Med
– volume: 138
  start-page: 61
  issue: 1
  year: 2016
  end-page: 75
  article-title: Multidimensional endotyping in patients with severe asthma reveals inflammatory heterogeneity in matrix metalloproteinases and chitinase 3‐like protein 1
  publication-title: J Allergy Clin Immunol
– volume: 19
  start-page: 1882
  issue: 16
  year: 2018
  end-page: 1896
  article-title: Blood eosinophils as biomarkers to drive treatment choices in asthma and COPD
  publication-title: Curr Drug Targets
– volume: 7
  start-page: 34
  issue: 1
  year: 2016
  end-page: 51
  article-title: Eosinophilic airway inflammation: role in asthma and chronic obstructive pulmonary disease
  publication-title: Ther Adv Chronic Dis
– volume: 34
  start-page: 91
  issue: 1
  year: 2012
  end-page: 97
  article-title: The use of the white cell count and haemoglobin in combination as an effective screen to predict the normality of the full blood count
  publication-title: Int J Lab Hematol
– volume: 6
  start-page: 926
  issue: 9
  year: 2016
  end-page: 934
  article-title: Peripheral blood eosinophilia correlates with hyperplastic nasal polyp growth
  publication-title: Int Forum Allergy Rhinol
– volume: 117
  start-page: 551
  issue: 5
  year: 2016
  end-page: 553
  article-title: Variability of blood eosinophil count as an asthma biomarker
  publication-title: Ann Allergy Asthma Immunol
– volume: 19
  start-page: 60
  issue: 1
  year: 2013
  end-page: 65
  article-title: Induced sputum in asthma: diagnostic and therapeutic implications
  publication-title: Curr Opin Pulm Med
– volume: 388
  start-page: 2128
  issue: 10056
  year: 2016
  end-page: 2141
  article-title: Benralizumab, an anti‐interleukin‐5 receptor alpha monoclonal antibody, as add‐on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double‐blind, placebo‐controlled phase 3 trial
  publication-title: Lancet
– volume: 53
  start-page: 1800938
  issue: 1
  year: 2019
  article-title: "T2‐high" in severe asthma related to blood eosinophil, exhaled nitric oxide and serum periostin
  publication-title: Eur Respir J
– volume: 134
  start-page: 287
  issue: 2
  year: 2014
  end-page: 294
  article-title: Lung function decline and variable airway inflammatory pattern: longitudinal analysis of severe asthma
  publication-title: J Allergy Clin Immunol
– volume: 2
  issue: 57
  year: 2010
  article-title: Achieving a nationwide learning health system
  publication-title: Sci Transl Med
– volume: 171
  start-page: 109
  issue: 2
  year: 2005
  end-page: 114
  article-title: Decline in lung function in the Busselton Health Study: the effects of asthma and cigarette smoking
  publication-title: Am J Respir Crit Care Med
– volume: 9
  issue: 6
  year: 2014
  article-title: Potentially pathogenic airway bacteria and neutrophilic inflammation in treatment resistant severe asthma
  publication-title: PLoS One
– volume: 25
  start-page: 477
  issue: 9
  year: 2004
  end-page: 482
  article-title: A role for eosinophils in airway remodelling in asthma
  publication-title: Trends Immunol
– volume: 56
  start-page: 808
  issue: 8
  year: 2019
  end-page: 815
  article-title: Effects of systemic corticosteroids on blood eosinophil counts in asthma: real‐world data
  publication-title: J Asthma
– volume: 30
  start-page: 452
  issue: 3
  year: 2007
  end-page: 456
  article-title: Severe exacerbations predict excess lung function decline in asthma
  publication-title: Eur Respir J
– volume: 113
  start-page: 19
  issue: 1
  year: 2014
  end-page: 24
  article-title: High blood eosinophil count is associated with more frequent asthma attacks in asthma patients
  publication-title: Ann Allergy Asthma Immunol
– volume: 125
  start-page: 830
  issue: 4
  year: 2010
  end-page: 837
  article-title: Fixed airflow obstruction due to asthma or chronic obstructive pulmonary disease: 5‐year follow‐up
  publication-title: J Allergy Clin Immunol
– ident: e_1_2_10_28_1
  doi: 10.1111/j.1440-1843.2006.00784.x
– ident: e_1_2_10_3_1
  doi: 10.1016/S0140-6736(02)11679-5
– ident: e_1_2_10_33_1
  doi: 10.1183/09031936.00165106
– ident: e_1_2_10_39_1
  doi: 10.1016/j.jaci.2015.11.020
– ident: e_1_2_10_20_1
  doi: 10.1016/j.anai.2016.08.010
– ident: e_1_2_10_37_1
  doi: 10.1016/j.jaip.2017.12.019
– ident: e_1_2_10_25_1
  doi: 10.1016/j.jaip.2020.05.053
– ident: e_1_2_10_18_1
  doi: 10.1111/cea.13310
– ident: e_1_2_10_5_1
  doi: 10.1136/thoraxjnl-2014-205634
– ident: e_1_2_10_44_1
  doi: 10.1080/02770903.2018.1502301
– ident: e_1_2_10_9_1
  doi: 10.1016/j.anai.2014.04.011
– ident: e_1_2_10_8_1
  doi: 10.1183/13993003.02536-2017
– ident: e_1_2_10_22_1
  doi: 10.1136/pgmj.2006.049551
– ident: e_1_2_10_32_1
  doi: 10.1016/j.it.2004.07.006
– ident: e_1_2_10_35_1
  doi: 10.1016/j.jaci.2010.01.003
– ident: e_1_2_10_40_1
  doi: 10.1002/alr.21793
– ident: e_1_2_10_13_1
  doi: 10.1016/S0140-6736(16)31322-8
– ident: e_1_2_10_15_1
  doi: 10.1016/j.rmed.2019.04.020
– ident: e_1_2_10_47_1
  doi: 10.1136/bmj.k1479
– ident: e_1_2_10_11_1
  doi: 10.1056/NEJMoa1403290
– ident: e_1_2_10_46_1
  doi: 10.1186/s12890-018-0689-2
– ident: e_1_2_10_38_1
  doi: 10.1164/rccm.200711-1754OC
– ident: e_1_2_10_16_1
  doi: 10.1164/rccm.201109-1640OC
– ident: e_1_2_10_36_1
  doi: 10.1016/j.rmed.2010.03.030
– ident: e_1_2_10_14_1
  doi: 10.1016/S0140-6736(16)31324-1
– ident: e_1_2_10_34_1
  doi: 10.1164/rccm.200402-230OC
– ident: e_1_2_10_30_1
  doi: 10.1136/thoraxjnl-2016-209919
– ident: e_1_2_10_31_1
– ident: e_1_2_10_10_1
  doi: 10.1373/clinchem.2016.267450
– ident: e_1_2_10_2_1
  doi: 10.1177/2040622315609251
– ident: e_1_2_10_6_1
  doi: 10.1111/cea.12345
– ident: e_1_2_10_29_1
  doi: 10.1016/j.jaci.2011.03.010
– ident: e_1_2_10_43_1
  doi: 10.1164/rccm.201304-0775OC
– ident: e_1_2_10_12_1
  doi: 10.1016/S2213-2600(17)30125-X
– ident: e_1_2_10_45_1
  doi: 10.1183/13993003.00938-2018
– ident: e_1_2_10_4_1
  doi: 10.1097/MCP.0b013e32835b118e
– ident: e_1_2_10_17_1
  doi: 10.1016/j.jaci.2014.04.005
– ident: e_1_2_10_19_1
  doi: 10.1016/j.rmed.2018.06.025
– ident: e_1_2_10_27_1
  doi: 10.1016/j.jaci.2010.02.008
– ident: e_1_2_10_24_1
  doi: 10.1126/scitranslmed.3001456
– volume: 11
  start-page: MC08
  issue: 2
  year: 2017
  ident: e_1_2_10_41_1
  article-title: Significance of blood eosinophil count in patients with chronic rhinosinusitis with nasal polyposis
  publication-title: J Clin Diagn Res
– ident: e_1_2_10_7_1
  doi: 10.1016/S2213-2600(15)00367-7
– ident: e_1_2_10_21_1
  doi: 10.2174/1389450119666180212120012
– ident: e_1_2_10_23_1
  doi: 10.1111/j.1751-553X.2011.01365.x
– ident: e_1_2_10_26_1
  doi: 10.1186/s12890-019-0862-2
– ident: e_1_2_10_42_1
  doi: 10.1371/journal.pone.0100645
SSID ssj0003598
Score 2.4821925
Snippet Background Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for...
Blood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for...
BackgroundBlood eosinophil measurement is essential for the phenotypic characterization of patients with difficult asthma and in determining eligibility for...
SourceID proquest
pubmed
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 811
SubjectTerms Adult
Airway management
Anti-Asthmatic Agents - therapeutic use
Antibodies, Monoclonal, Humanized - therapeutic use
Asthma
Asthma - blood
Asthma - classification
Asthma - drug therapy
Asthma - physiopathology
Blood
Bronchodilators
Cohort Studies
Corticosteroids
Electronic Health Records
Eosinophilia
Eosinophilia - blood
Eosinophils
epidemiology
Female
Forced Expiratory Volume
Fractional Exhaled Nitric Oxide Testing
Glucocorticoids - therapeutic use
Humans
Immunoglobulin E - blood
Immunotherapy
Inflammation
Leukocyte Count
Leukocytes (eosinophilic)
Male
Middle Aged
Nitric oxide
Omalizumab - therapeutic use
Patient Selection
Patients
Phenotypes
Phenotyping
Respiratory function
Sputum - cytology
Vital Capacity
Title Clinical evaluation of type 2 disease status in a real‐world population of difficult to manage asthma using historic electronic healthcare records of blood eosinophil counts
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcea.13841
https://www.ncbi.nlm.nih.gov/pubmed/33528864
https://www.proquest.com/docview/2531503185
https://www.proquest.com/docview/2485518956
Volume 51
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3NatwwEB5CQksvIU3_tknLtPTQi4sty7ZMTiE_hEJKKQ3kZiRL7ga29hLvHnrrI_RN8k55kszIWiehKfRiDJZk49GMRqOZ7wP4UMemsXVhorLUWSQt7VlLlbqoSZWOdUxLbMm1w6df8pMz-fk8O1-DvVUtzIAPMQbcWDO8vWYF16a_o-S105-SVHHR-gaX1jJ9gZBfRzPM0HQD0J6MClXKACvEaTxj1_uL0V8e5n2H1a84x1uwGVxF3B9k-xTWXLsNjwbyyF_b8Pg0HIs_g6uA7jnDW_Bu7Brk-CoKDIcwyMVDyx4vWtRIvuLs-vcfD5iK85HFi3sxZ4pH5MBFh0N2K-p-Mf2pkbPkf-A0QIvgLYcOTsc8MhziPj0P5dPi0XXUrZtPL2boqSn653B2fPT94CQKTAxRnSqVRIk10hbakhht6XRmZSKcE6LMyV8oai6wVYb-tyyyXJHVaGiNU7EudGNsnpksfQHrbde6V4BlYWtGsTdxamXslDYuZd5ILRoaVYkJfFyJpKoDTDmzZcyq1XaFpFd56U3g_dh0PmBzPNRodyXXKqhnXwmyPBmbs2wC78bHpFh8WqJb1y2pDcPmJIr2jxN4OcyH8S1cqKZULulj_QT59-urg6N9f_P6_5vuwBPBmTM-1rML64vLpXtDrs_CvPVTnK6H38QNSD0Bhw
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3NbtQwEB5VRUAvCMrfQoEBceASlDhO4khcqqrVAt2KQyv1Ftmxw1ZaklWze-DGI_AmvBNPwozjTakAiVuk-CfK_Ho88w3A6zo2ja0LE5WlziJp6cxaqtRFTap0rGMysSXXDs9O8umZ_HCenW_Bu00tzIAPMQbcWDK8vmYB54D0b1JeO_02SRVXrd-Q5JczTwv5adTDjE03IO3JqFClDLhCnMczTr1ujf5wMa97rN7kHN2FO8FXxP2BuPdgy7W7cHPoHvl1F27Nwr34ffgR4D0XeIXejV2DHGBFgeEWBrl6aN3jRYsayVlc_Pz23SOm4nJs48WzuGmKh-TAVYdDeivqfjX_opHT5D_jPGCL4FUTHZyPiWQ4BH56XsrnxaPraFq3nF8s0Pem6B_A2dHh6cE0Cq0YojpVKokSa6QttCU62tLpzMpEOCdEmZPDUNRcYasM_W9ZZLkitdGQkVOxLnRjbJ6ZLH0I223XuseAZWFrhrE3cWpl7JQ2LuXGkVo0tKoSE3izIUlVB5xybpexqDbnFaJe5ak3gVfj0OUAzvG3QXsbulZBPvtKkOrJWJ9lE3g5vibJ4usS3bpuTWMYNydRdICcwKOBH8ZduFJNqVzSx3oG-ff21cHhvn948v9DX8Dt6ensuDp-f_LxKewITqPxgZ892F5drt0z8oNW5rln918x9wQT
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwEB5Vrai4oFJeCwUGxIFLUOI4iSNOVemqPFr1QKXeIjt22EpLsiK7B278BP5J_1N_CTOON6UCJG6R4keU8Tw8j28AXtWxaWxdmKgsdRZJS3fWUqUualKlYx2Tii25dvj4JD86kx_Os_MNeLuuhRnwIUaHG3OGl9fM4Avb_MbktdNvklRx0foWB_s4n0_I01EMMzTdALQno0KVMsAKcRrPOPWmMvrDwrxpsHqNM92BO8FUxP2Btndhw7W7cGtoHvl9F7aPQ1j8HlwGdM85XoN3Y9cg-1dRYAjCIBcPrXq8aFEj2Yrzqx8_PWAqLsYuXjyLe6Z4RA5cdjhkt6Lul7OvGjlL_gvOArQIXvfQwdmYR4aD36fnpXxaPLqOpnWL2cUcfWuK_j6cTQ8_HxxFoRNDVKdKJVFijbSFtkRGWzqdWZkI54Qoc7IXipoLbJWh_y2LLFckNRrScSrWhW6MzTOTpQ9gs-1a9wiwLGzNKPYmTq2MndLGpdw3UouGVlViAq_XJKnqAFPO3TLm1fq6QtSrPPUm8HIcuhiwOf42aG9N1yqwZ18JkjwZi7NsAi_G18RYHC3RretWNIZhcxJF98cJPBzOw7gLF6oplUv6WH9A_r19dXC47x8e___Q57B9-m5afXp_8vEJ3BacROPdPnuwufy2ck_JClqaZ_60_wKTKgM8
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=Clinical+evaluation+of+type+2+disease+status+in+a+real-world+population+of+difficult+to+manage+asthma+using+historic+electronic+healthcare+records+of+blood+eosinophil+counts&rft.jtitle=Clinical+and+experimental+allergy&rft.au=Azim%2C+Adnan&rft.au=Newell%2C+Colin&rft.au=Barber%2C+Clair&rft.au=Harvey%2C+Matthew&rft.date=2021-06-01&rft.eissn=1365-2222&rft.volume=51&rft.issue=6&rft.spage=811&rft_id=info:doi/10.1111%2Fcea.13841&rft_id=info%3Apmid%2F33528864&rft.externalDocID=33528864
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0954-7894&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0954-7894&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0954-7894&client=summon