Medication adherence and persistence in patients with rheumatoid arthritis, psoriasis, and psoriatic arthritis: a systematic literature review

Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biolo...

Full description

Saved in:
Bibliographic Details
Published inPatient preference and adherence Vol. 12; pp. 1483 - 1503
Main Authors Murage, Mwangi, Tongbram, Vanita, Feldman, Steven, Malatestinic, William, Larmore, Cynthia, Muram, Talia, Burge, Russel, Bay, Charles, Johnson, Nicole, Clifford, Sarah, Araujo, Andre
Format Journal Article
LanguageEnglish
Published New Zealand Dove Medical Press Limited 01.01.2018
Dove Medical Press
Subjects
Online AccessGet full text
ISSN1177-889X
1177-889X
DOI10.2147/PPA.S167508

Cover

Loading…
Abstract Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence. Using various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA. Using the medication possession ratio or the percentage of days covered >80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a ≥45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns. Biologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors - including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability - can inform targeted approaches to improve these rates.
AbstractList Purpose: Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence. Patients and methods: Using various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA. Results: Using the medication possession ratio or the percentage of days covered .80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a [greater than or equal to]45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns. Conclusion: Biologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors--including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability--can inform targeted approaches to improve these rates. Keywords: biologics, compliance, nonadherence, nonpersistence, factors, discontinuation
Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence.PURPOSEProper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence.Using various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA.PATIENTS AND METHODSUsing various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA.Using the medication possession ratio or the percentage of days covered >80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a ≥45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns.RESULTSUsing the medication possession ratio or the percentage of days covered >80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a ≥45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns.Biologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors - including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability - can inform targeted approaches to improve these rates.CONCLUSIONBiologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors - including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability - can inform targeted approaches to improve these rates.
Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence. Using various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA. Using the medication possession ratio or the percentage of days covered >80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a ≥45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns. Biologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors - including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability - can inform targeted approaches to improve these rates.
Mwangi J Murage,1 Vanita Tongbram,2 Steven R Feldman,3 William N Malatestinic,1 Cynthia J Larmore,1 Talia M Muram,1 Russel T Burge,1,4 Charles Bay,2 Nicole Johnson,2 Sarah Clifford,5 Andre B Araujo1 1Eli Lilly and Company, Indianapolis, IN, USA; 2ICON Plc, New York, NY, USA; 3Wake Forest University School of Medicine, Winston-Salem, NC, USA; 4University of Cincinnati, Division of Pharmaceutical Sciences, Winkle College of Pharmacy, Cincinnati, OH, USA; 5ICON Plc, San Francisco, CA, USA Purpose: Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and psoriatic arthritis (PsA). We systematically describe current adherence and persistence patterns for RA, PsO, and PsA, with a focus on biologics and identifying factors associated with adherence and persistence. Patients and methods: Using various databases, a systematic literature review of US-based studies published from 2000 to 2015 on medication adherence and persistence to biologics and associated factors was conducted among patients with RA, PsO, and PsA. Results: Using the medication possession ratio or the percentage of days covered>80%, RA and PsO adherence rates for etanercept, adalimumab, and infliximab ranged from 16% to 73%, 21% to 70%, and 38% to 81%, respectively. Using the criteria of a ≥45-day gap, RA persistence rates for etanercept, adalimumab, and infliximab ranged from 46% to 89%, 42% to 94%, and 41% to 76%, respectively. In PsO, persistence rates for etanercept and adalimumab ranged from 34% to 50% and 50% to 62%, respectively. Similar persistence rates were observed in PsA. Experienced biologics users showed better adherence and persistence. Younger age, female gender, higher out-of-pocket costs, greater disease severity, and more comorbidities were associated with lower adherence and persistence rates. Qualitative surveys revealed that nonpersistence was partly due to perceived ineffectiveness and safety/tolerability concerns. Conclusion: Biologic adherence and persistence rates in RA, PsO, and PsA in the United States were low, with significant opportunity for improvement. Various factors - including decrease in disease severity; reduction of comorbidities; lower out-of-pocket costs; refilling at specialty pharmacies; and awareness of drug effectiveness, safety, and tolerability - can inform targeted approaches to improve these rates. Keywords: biologics, compliance, nonadherence, nonpersistence, factors, discontinuation
Audience Academic
Author Murage, Mwangi
Burge, Russel
Clifford, Sarah
Larmore, Cynthia
Feldman, Steven
Malatestinic, William
Johnson, Nicole
Araujo, Andre
Muram, Talia
Tongbram, Vanita
Bay, Charles
AuthorAffiliation 1 Eli Lilly and Company, Indianapolis, IN, USA, murage_mwangi_james@lilly.com
3 Wake Forest University School of Medicine, Winston-Salem, NC, USA
4 University of Cincinnati, Division of Pharmaceutical Sciences, Winkle College of Pharmacy, Cincinnati, OH, USA
2 ICON Plc, New York, NY, USA
5 ICON Plc, San Francisco, CA, USA
AuthorAffiliation_xml – name: 2 ICON Plc, New York, NY, USA
– name: 1 Eli Lilly and Company, Indianapolis, IN, USA, murage_mwangi_james@lilly.com
– name: 3 Wake Forest University School of Medicine, Winston-Salem, NC, USA
– name: 5 ICON Plc, San Francisco, CA, USA
– name: 4 University of Cincinnati, Division of Pharmaceutical Sciences, Winkle College of Pharmacy, Cincinnati, OH, USA
Author_xml – sequence: 1
  givenname: Mwangi
  surname: Murage
  fullname: Murage, Mwangi
– sequence: 2
  givenname: Vanita
  orcidid: 0000-0002-5220-3569
  surname: Tongbram
  fullname: Tongbram, Vanita
– sequence: 3
  givenname: Steven
  orcidid: 0000-0002-0090-6289
  surname: Feldman
  fullname: Feldman, Steven
– sequence: 4
  givenname: William
  surname: Malatestinic
  fullname: Malatestinic, William
– sequence: 5
  givenname: Cynthia
  surname: Larmore
  fullname: Larmore, Cynthia
– sequence: 6
  givenname: Talia
  surname: Muram
  fullname: Muram, Talia
– sequence: 7
  givenname: Russel
  orcidid: 0000-0001-7907-6400
  surname: Burge
  fullname: Burge, Russel
– sequence: 8
  givenname: Charles
  orcidid: 0000-0003-1226-1147
  surname: Bay
  fullname: Bay, Charles
– sequence: 9
  givenname: Nicole
  surname: Johnson
  fullname: Johnson, Nicole
– sequence: 10
  givenname: Sarah
  surname: Clifford
  fullname: Clifford, Sarah
– sequence: 11
  givenname: Andre
  surname: Araujo
  fullname: Araujo, Andre
BackLink https://www.ncbi.nlm.nih.gov/pubmed/30174415$$D View this record in MEDLINE/PubMed
BookMark eNqNk1uL1DAUgIusuBd98l0Kggg6Y25NUx-EYfGysOKCCr6FND2dZmmbmqS77J_wN5t2xnVGlkX60OT0O1_SwznHyUFve0iSpxgtCWb5m4uL1fIr5nmGxIPkCOM8XwhR_DjYWR8mx95fIsQpJ_hRckgRzhnD2VHy6zNURqtgbJ-qqgEHvYZU9VU6gPPGh3lv-nSIDPTBp9cmNKlrYOxUsKZKlQuNM8H41-ngrTPKT8vZMG-D0X-Zt6lK_U20dnO8NQGcCqOD1MGVgevHycNatR6ebN8nyfcP77-dflqcf_l4dro6X2jOaFhgJpgquMC6ZlCUGcswLXlJKgyVooKTshZEkyLTimPFBaKqJnmOC13wkmlET5Kzjbey6lIOznTK3UirjJwD1q1lvLPRLUhKcs0wZFkea4ZYVdZZKYACwowjqGh0vdu4hrHsoNKxSk61e9L9L71p5NpeSY4xIvkkeLkVOPtzBB9kZ7yGtlU92NFLgooC0UJgFtHnG3St4tVMX9to1BMuV5wQzJFg-b1UJigVsS8mankHFZ8KOqNjj9Umxve0_5Wwe8KLnYQGVBsab9tx6ja_b74X3DU-2631bZH_NHQEXm0A7az3DupbBCM5jYuM4yK34xJp_A-tTZiHIf6Zae_M-Q1NexZA
CitedBy_id crossref_primary_10_1002_der2_90
crossref_primary_10_1002_jcph_2322
crossref_primary_10_2147_PPA_S289692
crossref_primary_10_1002_jac5_1417
crossref_primary_10_2147_RMHP_S265264
crossref_primary_10_18553_jmcp_2023_29_12_a_s2
crossref_primary_10_1007_s10067_024_06930_7
crossref_primary_10_18553_jmcp_2023_29_12_a_s1
crossref_primary_10_1097_ACI_0000000000000704
crossref_primary_10_1080_09546634_2020_1772454
crossref_primary_10_2196_34906
crossref_primary_10_51847_QVOwcxjCwX
crossref_primary_10_1007_s10067_020_05027_1
crossref_primary_10_1080_03007995_2019_1668204
crossref_primary_10_1093_rap_rkaa015
crossref_primary_10_1016_j_xjidi_2023_100210
crossref_primary_10_1136_rmdopen_2022_002616
crossref_primary_10_1136_annrheumdis_2021_221640
crossref_primary_10_1590_1413_81232023285_13482022en
crossref_primary_10_1007_s40744_024_00647_4
crossref_primary_10_1002_acr2_11347
crossref_primary_10_1111_bjd_18851
crossref_primary_10_2196_48079
crossref_primary_10_1007_s12325_023_02600_3
crossref_primary_10_1016_j_msard_2022_103860
crossref_primary_10_1080_09546634_2019_1638880
crossref_primary_10_1080_09546634_2021_1898526
crossref_primary_10_14412_1996_7012_2019_4_18_25
crossref_primary_10_1080_09546634_2019_1690622
crossref_primary_10_1111_dth_14808
crossref_primary_10_36469_jheor_2022_31895
crossref_primary_10_1007_s12325_023_02671_2
crossref_primary_10_1001_jamadermatol_2024_6567
crossref_primary_10_1590_1413_81232023285_13482022
crossref_primary_10_1007_s13555_023_01075_y
crossref_primary_10_3899_jrheum_201568
crossref_primary_10_1016_j_therap_2020_08_003
crossref_primary_10_1007_s10067_019_04837_2
crossref_primary_10_1007_s00228_024_03676_8
crossref_primary_10_1111_dth_15227
crossref_primary_10_1177_09612033221115974
crossref_primary_10_18553_jmcp_2021_20560
crossref_primary_10_1097_RHU_0000000000002159
crossref_primary_10_7717_peerj_16418
crossref_primary_10_1136_bmjopen_2022_069681
crossref_primary_10_1007_s12325_023_02619_6
crossref_primary_10_1111_jocd_14610
crossref_primary_10_1007_s40801_024_00428_z
crossref_primary_10_1080_14737167_2020_1800456
crossref_primary_10_2147_TCRM_S248390
crossref_primary_10_3899_jrheum_2022_1277
crossref_primary_10_1016_j_jaad_2019_05_081
crossref_primary_10_1111_ddg_15448_g
crossref_primary_10_1111_jdv_15872
crossref_primary_10_1007_s12325_022_02084_7
crossref_primary_10_1177_0894318420921155
crossref_primary_10_1007_s12325_020_01501_z
crossref_primary_10_1186_s13561_024_00507_5
crossref_primary_10_1080_14737167_2021_1880322
crossref_primary_10_3390_jcm11061506
crossref_primary_10_33393_grhta_2024_3204
crossref_primary_10_1371_journal_pone_0215415
crossref_primary_10_1016_j_pec_2021_11_026
crossref_primary_10_1136_bmjopen_2018_027456
crossref_primary_10_1016_j_jaad_2021_05_049
crossref_primary_10_2147_BTT_S385422
crossref_primary_10_1186_s12875_022_01744_5
crossref_primary_10_3389_fmed_2021_718922
crossref_primary_10_1016_j_clinthera_2021_07_005
crossref_primary_10_1093_rheumatology_keab130
crossref_primary_10_1080_03009742_2020_1855365
crossref_primary_10_1111_bjd_19509
crossref_primary_10_1016_j_jaad_2019_11_015
crossref_primary_10_1002_acr_25442
crossref_primary_10_1183_20734735_0037_2021
crossref_primary_10_3389_fphar_2022_878972
crossref_primary_10_1007_s12325_022_02413_w
crossref_primary_10_1007_s13555_022_00686_1
crossref_primary_10_1177_08971900221131933
crossref_primary_10_1016_j_hlpt_2022_100697
crossref_primary_10_1590_s0004_2803_24612023_149
crossref_primary_10_1093_rap_rkaa070
crossref_primary_10_1007_s40744_020_00201_y
crossref_primary_10_18553_jmcp_2021_27_7_882
crossref_primary_10_1038_s41584_022_00810_7
crossref_primary_10_1016_j_jbspin_2021_105175
crossref_primary_10_1111_ijd_17163
crossref_primary_10_1007_s40744_021_00286_z
crossref_primary_10_1007_s40801_020_00217_4
crossref_primary_10_1136_ard_2022_222879
crossref_primary_10_1186_s13075_022_02884_w
crossref_primary_10_3390_biomedicines9080958
crossref_primary_10_1186_s12955_023_02134_w
crossref_primary_10_1136_annrheumdis_2021_220973
crossref_primary_10_1007_s40744_021_00285_0
crossref_primary_10_1016_j_anai_2020_07_026
crossref_primary_10_2147_BTT_S474733
crossref_primary_10_1007_s00296_023_05280_y
crossref_primary_10_2196_34017
crossref_primary_10_1016_j_chest_2020_10_050
crossref_primary_10_31718_2077_1096_22_3_4_65
crossref_primary_10_3390_healthcare10112152
crossref_primary_10_1186_s12913_021_07459_0
crossref_primary_10_14412_1996_7012_2022_4_40_45
crossref_primary_10_2147_PPA_S316263
crossref_primary_10_1111_ddg_15448
crossref_primary_10_12688_hrbopenres_13274_2
ContentType Journal Article
Copyright COPYRIGHT 2018 Dove Medical Press Limited
COPYRIGHT 2020 Dove Medical Press Limited
2018 Murage et al. This work is published and licensed by Dove Medical Press Limited 2018
Copyright_xml – notice: COPYRIGHT 2018 Dove Medical Press Limited
– notice: COPYRIGHT 2020 Dove Medical Press Limited
– notice: 2018 Murage et al. This work is published and licensed by Dove Medical Press Limited 2018
DBID AAYXX
CITATION
NPM
7X8
5PM
DOA
DOI 10.2147/PPA.S167508
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList



MEDLINE - Academic
PubMed

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
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1177-889X
EndPage 1503
ExternalDocumentID oai_doaj_org_article_327c41e55717404dbf5b8e3e01460ed3
PMC6110273
A622160847
A583381777
30174415
10_2147_PPA_S167508
Genre Journal Article
Review
GeographicLocations United States
GeographicLocations_xml – name: United States
GroupedDBID ---
0YH
123
29O
2WC
53G
5VS
7RV
8C1
8FI
8FJ
8G5
AAYXX
ABDBF
ABUWG
ACGFO
ACUHS
ADBBV
ADRAZ
AENEX
AFKRA
AIAGR
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BCNDV
BENPR
BKEYQ
BPHCQ
BVXVI
CCPQU
CITATION
DIK
DWQXO
E3Z
EBD
ESX
F5P
FYUFA
GNUQQ
GROUPED_DOAJ
GUQSH
GX1
HYE
IAO
IHR
IHW
IPNFZ
ITC
KQ8
M2O
M48
MK0
M~E
NAPCQ
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RIG
RNS
RPM
TDBHL
TR2
TUS
UKHRP
VDV
NPM
PJZUB
PPXIY
PMFND
7X8
5PM
ID FETCH-LOGICAL-c643t-1484a9681cf4e9b54513b6b2d1eda3862bf82c295ca61a6803af27719c96b4c03
IEDL.DBID M48
ISSN 1177-889X
IngestDate Wed Aug 27 01:27:26 EDT 2025
Thu Aug 21 14:02:30 EDT 2025
Fri Jul 11 02:51:26 EDT 2025
Tue Jun 17 21:10:21 EDT 2025
Wed Mar 19 01:47:07 EDT 2025
Tue Jun 10 20:42:38 EDT 2025
Sat Mar 08 18:47:36 EST 2025
Thu May 22 21:21:44 EDT 2025
Thu May 22 21:22:25 EDT 2025
Mon Jul 21 05:57:06 EDT 2025
Thu Apr 24 23:04:51 EDT 2025
Tue Jul 01 00:42:20 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords nonadherence
biologics
nonpersistence
compliance
discontinuation
factors
Language English
License http://creativecommons.org/licenses/by-nc/3.0
The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c643t-1484a9681cf4e9b54513b6b2d1eda3862bf82c295ca61a6803af27719c96b4c03
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
ObjectType-Review-3
content type line 23
ORCID 0000-0002-5220-3569
0000-0003-1226-1147
0000-0001-7907-6400
0000-0002-0090-6289
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.2147/PPA.S167508
PMID 30174415
PQID 2099039814
PQPubID 23479
PageCount 21
ParticipantIDs doaj_primary_oai_doaj_org_article_327c41e55717404dbf5b8e3e01460ed3
pubmedcentral_primary_oai_pubmedcentral_nih_gov_6110273
proquest_miscellaneous_2099039814
gale_infotracmisc_A622160847
gale_infotracmisc_A583381777
gale_infotracacademiconefile_A622160847
gale_infotracacademiconefile_A583381777
gale_healthsolutions_A622160847
gale_healthsolutions_A583381777
pubmed_primary_30174415
crossref_primary_10_2147_PPA_S167508
crossref_citationtrail_10_2147_PPA_S167508
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2018-01-01
PublicationDateYYYYMMDD 2018-01-01
PublicationDate_xml – month: 01
  year: 2018
  text: 2018-01-01
  day: 01
PublicationDecade 2010
PublicationPlace New Zealand
PublicationPlace_xml – name: New Zealand
PublicationTitle Patient preference and adherence
PublicationTitleAlternate Patient Prefer Adherence
PublicationYear 2018
Publisher Dove Medical Press Limited
Dove Medical Press
Publisher_xml – name: Dove Medical Press Limited
– name: Dove Medical Press
SSID ssj0063621
Score 2.4512005
SecondaryResourceType review_article
Snippet Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis (PsO), and...
Purpose: Proper adherence and persistence to medications are crucial for better quality of life and improved outcomes in rheumatoid arthritis (RA), psoriasis...
Mwangi J Murage,1 Vanita Tongbram,2 Steven R Feldman,3 William N Malatestinic,1 Cynthia J Larmore,1 Talia M Muram,1 Russel T Burge,1,4 Charles Bay,2 Nicole...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 1483
SubjectTerms Adalimumab
adherence
Arthritis
Care and treatment
Comorbidity
discontinuation
Diseases
Drugs
Drugstores
Etanercept
Golimumab
Infliximab
Patient compliance
Pharmaceutical industry
Pharmacy
Psoriasis
Psoriatic arthritis
Review
Rheumatoid factor
systematic
Ustekinumab
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9tAEF5KDqWX0neVpu0WAoVSNdqHVlJvbmkIhZRAG_Bt2ZewIcgmtv9Gf3NndmVFoim59GCwveOVPTOe-Xa18w0hx20VPCAFkTPHQy5bJvPGOAiGjZJM-taIWCR2_kOdXcrv83I-avWFZ8ISPXBS3InglZMslCWsO2QhvW1LWwcRkPSkCD7yfELO2y-mUgxWEJZZaqsCl62bearMw548JxcXs08_GeBk7Cg5ykWRsv_vwDzKTNNTk6M0dPqIPOzxI52l7_2Y3AvdE3L_vL9D_pT8TndeUN3U-EUq5qOm83SNO2ObCJHpsqM9oeqG4k4svV6EHWDX1dJTUMkiMh19pOvNCvxzg0_jDPElXPhG5jM19IYMml4NJM001cQ8I5en3359Pcv7ngu5A2yyzWF1JE2jauZaGRoL-IoJqyz3LHiwm-K2rbnjTemMYkbVhTAtryrWuEZZ6QrxnBx0qy68JNR5sFglQwkQSPLWW-Fq8JgWHhBGrMjIh732tesJybEvxpWGhQmaSoOpdG-qjBwPwuvEw3G72Bc04yCC5NnxDXAp3buUvsulMvIWnUCnStQhBOgZVqjV4FLVPyUU50wVkPEz8j5KYJiAH-VMX-0AqkHCrclcd0iO5jyaSEIgcJOJbhseffrd3qc1DuHhui6sdhuN1dOFaGomM_Ii-figQIj_FS65M1JNvH-i4elIt1xEmnIFyBLA8eH_MMkr8gCQap32vo7IwfZ6F14DGtzaN_GP_wdBKly8
  priority: 102
  providerName: Directory of Open Access Journals
Title Medication adherence and persistence in patients with rheumatoid arthritis, psoriasis, and psoriatic arthritis: a systematic literature review
URI https://www.ncbi.nlm.nih.gov/pubmed/30174415
https://www.proquest.com/docview/2099039814
https://pubmed.ncbi.nlm.nih.gov/PMC6110273
https://doaj.org/article/327c41e55717404dbf5b8e3e01460ed3
Volume 12
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3_q9MwEA_PJ4i_iN-dPmeEB4LYZ9OkSSuITPExhMkDHcyfSpqkbjDauW6g_4R_s3dp17fqRH8YbM017e4ud59LchdCTgvlLCAFHjATuUAUTASpNmAMUymYsIXmPkls8lGOp-LDLJ4dkd1hnC0D64OhHZ4nNV0vz75_-_EGBvxr3MbMhHp5cTE6-8QA-WLS71VwSQpH6ER0ywkSrDRrTlmBt0jSWZOo9_vNPdfkK_j_aaf3HFV_E-WeVzq_SW60cJKOGvnfIkeuvE2uTdoF8zvkZ7MQg9yn2s6b3D6qS0tXOFFWe8RMFyVt66vWFCdm6XrutgBlq4WloFpzX_joBV3VFahrjV99D_4nPPiS5hXV9LI2NF12NZtpkyJzl0zP339-Nw7aIxgCA1BlE0CwJHQqE2YK4dIc4Bbjucwjy5wFMcooL5LIRGlstGRaJiHXRaQUS00qc2FCfo8cl1XpHhBqLAQ_SrgYEJGICptzk4ACFfABq5LzAXm-435m2vrkeEzGMoM4BUWVgaiyVlQDctoRr5qyHIfJ3qIYOxKspe0vVOuvWTs0Mx4pI5iLY4hsRShsXsR54rjDsjqhs_BiT1AJsiYxtbMI2QgT1hJQKfVXChlFTIYAAAbkmadAPYY_ZXSb_ACswfpbvb7-QbnX50mPEuyC6XV0qHnv7qc7nc6wCffala7a1hkmU4c8TZgYkPuNjncMBHegMAIfENXT_h6H-y3lYu6rlksAmoCVH_7Hcx-R64BLk2am64Qcb9Zb9xiw3yYfkivhl_HQz5wM_Rj_BQWLWuI
linkProvider Scholars Portal
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=Medication+adherence+and+persistence+in+patients+with+rheumatoid+arthritis%2C+psoriasis%2C+and+psoriatic+arthritis%3A+a+systematic+literature+review&rft.jtitle=Patient+preference+and+adherence&rft.au=Murage%2C+Mwangi+J&rft.au=Tongbram%2C+Vanita&rft.au=Feldman%2C+Steven+R&rft.au=Malatestinic%2C+William+N&rft.date=2018-01-01&rft.issn=1177-889X&rft.eissn=1177-889X&rft.volume=12&rft.spage=1483&rft_id=info:doi/10.2147%2FPPA.S167508&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1177-889X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1177-889X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1177-889X&client=summon