Clinical features of adverse reactions associated with telbivudine
AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of e...
Saved in:
Published in | World journal of gastroenterology : WJG Vol. 14; no. 22; pp. 3549 - 3553 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China
14.06.2008
The WJG Press and Baishideng |
Subjects | |
Online Access | Get full text |
ISSN | 1007-9327 2219-2840 |
DOI | 10.3748/wjg.14.3549 |
Cover
Abstract | AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.
METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.
RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.
CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. |
---|---|
AbstractList | AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.
METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.
RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.
CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.AIMTo analyze the clinical features and risk factors of adverse reactions associated with telbivudine.Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.METHODSClinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.RESULTSOut of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions.CONCLUSIONThe adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. R5; AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis.RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high.CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. RESULTS: Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. CONCLUSION: The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. Clinical data were collected from cases that presented with serious adverse reactions to telbivudine. We analyzed general information and medicine status, clinical features, results of examination, and misdiagnosis. Out of 105 patients who were treated with telbivudine for hepatitis B in an outpatient department from January, 2007 to January, 2008, five presented with serious adverse drug reactions. Most of these five patients had used other nucleoside analogues in the past. Four were treated with a combination of telbivudine and interferon or another nucleoside analogue, while the other received an increased dose of telbivudine. The main adverse reactions were myalgia and general weakness. This was accompanied by cardiac arrhythmia in one patient, and nervous symptoms in three. Serum creatine kinase was elevated. The rate of misdiagnosis was high. The adverse reactions were related to telbivudine, but the biological mechanism of the reactions is not yet clear. Combination therapy with interferon or another nucleoside analogue and a high dose may increase the risk of adverse reactions. |
Author | Xue-Song Zhang Rui Jin Shi-Bin Zhang Ming-Ling Tao |
AuthorAffiliation | Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China |
AuthorAffiliation_xml | – name: Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China |
Author_xml | – sequence: 1 givenname: Xue-Song surname: Zhang fullname: Zhang, Xue-Song – sequence: 2 givenname: Rui surname: Jin fullname: Jin, Rui – sequence: 3 givenname: Shi-Bin surname: Zhang fullname: Zhang, Shi-Bin – sequence: 4 givenname: Ming-Ling surname: Tao fullname: Tao, Ming-Ling |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18567085$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kUmPEzEQhS00iMkMnLijFkJcUAdv7eUyEkRs0khc4Gy53dWJQ8eesd2J-Pc4SlglTj74q_fqvbpCFyEGQOgpwUsmuXp92K6XhC9Zx_UDtKCU6JYqji_QgmAsW82ovERXOW8xpox19BG6JKoTEqtugd6uJh-8s1Mzgi1zgtzEsbHDHlKGJoF1xceQG5tzdN4WGJqDL5umwNT7_Tz4AI_Rw9FOGZ6c32v09f27L6uP7e3nD59Wb25bx1lXWjFSTC2MPZcDB64k567HWAgOgEfNpCBABFWYEitcL6SSoCiV2nZaC8DsGt2cdO_mfgeDg1CSncxd8jubvptovfn7J_iNWce9oZIIQXQVeHESONgw2rA22zinUFc2tUKKcXXDRFbs5dknxfsZcjE7nx1Mkw0Q52yEpkxKxSr47M-Ffm3ys90KvDoBLsWcE4y_EWyOtzsaG8LN8XaVJv_Qzhd7rL-m8dN_Zp6fZzYxrO99DdVb9230E9TYoianhP0Afkmn8A |
CitedBy_id | crossref_primary_10_1371_journal_pone_0165416 crossref_primary_10_5144_0256_4947_2013_169 crossref_primary_10_1097_MCG_0b013e31821f8bdf crossref_primary_10_6064_2012_478631 crossref_primary_10_4166_kjg_2013_61_1_30 crossref_primary_10_1007_s11901_010_0039_1 crossref_primary_10_1111_1751_2980_12173 crossref_primary_10_1007_s00228_024_03674_w crossref_primary_10_1517_17425255_4_10_1351 crossref_primary_10_1517_13543780903241599 crossref_primary_10_4254_wjh_v9_i5_227 crossref_primary_10_1586_eri_09_6 crossref_primary_10_1021_tx200458s crossref_primary_10_1016_j_jhep_2010_03_006 crossref_primary_10_3350_cmh_2013_19_1_82 crossref_primary_10_1093_jac_dkr388 crossref_primary_10_1016_j_jhep_2009_04_019 crossref_primary_10_1002_pds_1493 crossref_primary_10_1186_1743_422X_7_323 crossref_primary_10_1016_j_nbd_2018_11_025 crossref_primary_10_1002_14651858_CD007003_pub2 crossref_primary_10_1007_s10157_020_01850_7 crossref_primary_10_1002_14651858_CD007003_pub3 crossref_primary_10_1111_j_1365_2893_2010_01412_x crossref_primary_10_4155_fmc_2020_0123 |
Cites_doi | 10.1128/AAC.48.4.1300-1306.2004 10.1128/AAC.01313-05 10.1177/0091270005284849 10.1177/095632020701800103 10.1053/j.gastro.2008.02.017 10.1080/028418602317314064 10.1056/NEJMoa066422 10.1042/cs0920225 10.2174/092986706778521995 10.1212/WNL.41.7.1053 10.1128/AAC.50.3.874-879.2006 10.1111/j.1872-034X.2007.00106.x 10.1093/brain/118.2.339 10.1002/hep.22075 10.1016/j.gastro.2005.05.053 10.7326/0003-4819-147-11-200712040-00183 10.1074/jbc.M106743200 10.1128/AAC.45.1.229-235.2001 10.1016/j.clinthera.2007.12.032 |
ClassificationCodes | R5 |
ContentType | Journal Article |
Copyright | Copyright © Wanfang Data Co. Ltd. All Rights Reserved. 2008 The WJG Press and Baishideng. All rights reserved. 2008 |
Copyright_xml | – notice: Copyright © Wanfang Data Co. Ltd. All Rights Reserved. – notice: 2008 The WJG Press and Baishideng. All rights reserved. 2008 |
DBID | 2RA 92L CQIGP W91 ~WA AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 2B. 4A8 92I 93N PSX TCJ 5PM |
DOI | 10.3748/wjg.14.3549 |
DatabaseName | 维普期刊资源整合服务平台 中文科技期刊数据库-CALIS站点 中文科技期刊数据库-7.0平台 中文科技期刊数据库-医药卫生 中文科技期刊数据库- 镜像站点 CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic Wanfang Data Journals - Hong Kong WANFANG Data Centre Wanfang Data Journals 万方数据期刊 - 香港版 China Online Journals (COJ) China Online Journals (COJ) PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 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: 2 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 |
DocumentTitleAlternate | Clinical features of adverse reactions associated with telbivudine |
EISSN | 2219-2840 |
EndPage | 3553 |
ExternalDocumentID | PMC2716619 wjg200822017 18567085 10_3748_wjg_14_3549 27627121 |
Genre | Journal Article |
GroupedDBID | --- 123 29R 2B. 2C~ 2RA 2WC 36B 53G 5VR 8WL 92F 92I 92L 93N 93R AAKDD ACGFO AENEX AFUIB ALMA_UNASSIGNED_HOLDINGS CCEZO CDYEO CHBEP CIEJG CQIGP CS3 CW9 DIK DU5 E3Z EBS EJD EMB F5P FA0 FRP GX1 HYE M~E OK1 P2P RNS RPM SV3 TCJ TGQ TR2 W91 WFFXF XSB ~WA AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 4A8 PSX 5PM |
ID | FETCH-LOGICAL-c435t-6f202aefb47d4e48744cb00664ee0f93761e1628021a6cb6787e82279a5996e03 |
ISSN | 1007-9327 |
IngestDate | Thu Aug 21 13:48:42 EDT 2025 Thu May 29 04:04:10 EDT 2025 Fri Jul 11 16:29:13 EDT 2025 Wed Oct 16 00:47:27 EDT 2024 Tue Jul 01 03:21:41 EDT 2025 Thu Apr 24 23:03:33 EDT 2025 Thu Nov 24 20:29:41 EST 2022 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | false |
IsScholarly | true |
Issue | 22 |
Keywords | Mitochondria Nucleoside analogue Adverse drug reaction Telbivudine Hepatitis B |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c435t-6f202aefb47d4e48744cb00664ee0f93761e1628021a6cb6787e82279a5996e03 |
Notes | R97 Adverse drug reaction; Hepatitis B;Mitochondria; Nucleoside analogue; Telbivudine Mitochondria Nucleoside analogue 14-1219/R Adverse drug reaction Telbivudine Hepatitis B ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Fax: +86-10-63395319 Correspondence to: Rui Jin, Professor, Department of GI and Hepatology, Beijing Youan Hospital Affiliated to Capital Medical University, Beijing 100069, China. jinrui@public.bta.net.cn Telephone: +86-10-83997117 Author contributions: Jin R designed the research; Zhang SB, Tao ML and Zhang XS performed the research; Zhang SB and Tao ML collected and analyzed the data; and Zhang SB wrote the paper. |
OpenAccessLink | https://www.wjgnet.com/1007-9327/full/v14/i22/3549.htm |
PMID | 18567085 |
PQID | 69237783 |
PQPubID | 23479 |
PageCount | 5 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_2716619 wanfang_journals_wjg200822017 proquest_miscellaneous_69237783 pubmed_primary_18567085 crossref_primary_10_3748_wjg_14_3549 crossref_citationtrail_10_3748_wjg_14_3549 chongqing_backfile_27627121 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2008-06-14 |
PublicationDateYYYYMMDD | 2008-06-14 |
PublicationDate_xml | – month: 06 year: 2008 text: 2008-06-14 day: 14 |
PublicationDecade | 2000 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | World journal of gastroenterology : WJG |
PublicationTitleAlternate | World Journal of Gastroenterology |
PublicationTitle_FL | WORLD JOURNAL OF GASTROENTEROLOGY |
PublicationYear | 2008 |
Publisher | Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China The WJG Press and Baishideng |
Publisher_xml | – name: Department of GI and Hepatology, Beijing Youan Hospital affiliated to Capital Medical University, Beijing 100069, China – name: The WJG Press and Baishideng |
References | ref13 ref12 ref15 ref14 ref31 ref30 ref11 ref10 ref2 ref1 ref17 ref16 ref19 ref18 ref24 ref23 ref26 ref25 ref20 ref22 ref21 ref28 ref27 ref29 ref8 ref7 ref9 ref4 ref3 ref6 ref5 |
References_xml | – ident: ref21 doi: 10.1128/AAC.48.4.1300-1306.2004 – ident: ref3 – ident: ref25 doi: 10.1128/AAC.01313-05 – ident: ref26 doi: 10.1177/0091270005284849 – ident: ref20 doi: 10.1177/095632020701800103 – ident: ref29 – ident: ref28 doi: 10.1053/j.gastro.2008.02.017 – ident: ref24 – ident: ref31 doi: 10.1080/028418602317314064 – ident: ref6 doi: 10.1056/NEJMoa066422 – ident: ref15 doi: 10.1042/cs0920225 – ident: ref4 doi: 10.2174/092986706778521995 – ident: ref12 doi: 10.1212/WNL.41.7.1053 – ident: ref27 doi: 10.1128/AAC.50.3.874-879.2006 – ident: ref19 – ident: ref30 doi: 10.1111/j.1872-034X.2007.00106.x – ident: ref11 doi: 10.1093/brain/118.2.339 – ident: ref17 – ident: ref13 – ident: ref2 – ident: ref5 doi: 10.1002/hep.22075 – ident: ref7 doi: 10.1016/j.gastro.2005.05.053 – ident: ref8 doi: 10.7326/0003-4819-147-11-200712040-00183 – ident: ref23 – ident: ref22 doi: 10.1074/jbc.M106743200 – ident: ref18 – ident: ref1 doi: 10.1128/AAC.45.1.229-235.2001 – ident: ref9 doi: 10.1016/j.clinthera.2007.12.032 – ident: ref16 – ident: ref10 – ident: ref14 |
SSID | ssj0023352 |
Score | 2.0368197 |
Snippet | AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.
METHODS: Clinical data were collected from cases that... To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. Clinical data were collected from cases that presented with... To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.AIMTo analyze the clinical features and risk factors of... R5; AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine.METHODS: Clinical data were collected from cases... AIM: To analyze the clinical features and risk factors of adverse reactions associated with telbivudine. METHODS: Clinical data were collected from cases that... |
SourceID | pubmedcentral wanfang proquest pubmed crossref chongqing |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 3549 |
SubjectTerms | Adult Arrhythmias, Cardiac - chemically induced Creatine Kinase - blood Drug Synergism Hepatitis B, Chronic - blood Hepatitis B, Chronic - drug therapy Humans Interferons - adverse effects Interferons - therapeutic use Male Middle Aged Muscle Weakness - chemically induced Neuralgia - chemically induced Nucleosides - adverse effects Nucleosides - therapeutic use Pyrimidinones - adverse effects Pyrimidinones - therapeutic use Rapid Communication Retrospective Studies Risk Factors Telbivudine Thymidine - analogs & derivatives 替比夫定 线粒体 药物反应 |
Title | Clinical features of adverse reactions associated with telbivudine |
URI | http://lib.cqvip.com/qk/84123X/200822/27627121.html https://www.ncbi.nlm.nih.gov/pubmed/18567085 https://www.proquest.com/docview/69237783 https://d.wanfangdata.com.cn/periodical/wjg200822017 https://pubmed.ncbi.nlm.nih.gov/PMC2716619 |
Volume | 14 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELdgCIkXBOIrjEEe9gTKSNLEdh7ZtGmaypCgFX2LnNRuA1MCTcIk_nruYjtp6CQ-XqIqsVzn7nK-O9_9jpBDTmWcqCzzYpWDg0Iz5QnfFx7N_UT6VDC2xNrh95f0fB5dLOLF0MWxqy5psqP85411Jf_DVbgHfMUq2X_gbD8p3IDfwF-4Aofh-lc8PrFljUp2-Jy1OdUHkw67oeiahfqNMCywmeaNvMqKH-3SHqkb21Tn1WxBSaxE3WwqBO3caKQmDB98vui7cfXB5kUrvU-V2QMxHUcDE3xsi9249Lrwjosh-1dUOnm_XHlTu4vaIATHZCld_Gn0JkY8wRRkI8UabQmQrj42anISa5zS3_U3YuEA0a-_rECDH9lRY5Tsyw_p2Xw6TWeni9ltcidkrDue76I0xtHGOrLulNssStdl4uRvt6ZGNI010OY7vN3YKtlxNXYzZu9ei1IB5baMkdkDct94Ee47LRIPyS1ZPiLHVhxcKw5upVwjDm4vDu4gDi6Kg7slDo_J_Ox0dnLumRYZXg52buNRFfqhkCqL2DKSEfYyyFGR0khKX4HpSQMZ0JCDJSdonoFlwiRH0EiBsDzSnzwhe2VVymfEVQmPIxpGjEkKTn8gkjziiQgmVImcc-WQ_Z5cYGLlXxE4LA1hM2VBGDjktSVgmht0eWxycpWCl4mUT4Hy4GemSHmHHPaDv2lQlZuHvbKcSEHp4UmWKGXV1ikFt4QxPnHIU82XYRoeUwZuhEPYiGP9AIRTHz8pi3UHqw7vAcYq_OuB4W1qvrgaFxV2vRFg_3r-x1Xtk3vDN_KC7DWbVh6A6dpkLzs5_QXn8Zzy |
linkProvider | National Library of Medicine |
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+features+of+adverse+reactions+associated+with+telbivudine&rft.jtitle=World+journal+of+gastroenterology+%3A+WJG&rft.au=Zhang%2C+Xue-Song&rft.au=Jin%2C+Rui&rft.au=Zhang%2C+Shi-Bin&rft.au=Tao%2C+Ming-Ling&rft.date=2008-06-14&rft.issn=1007-9327&rft.volume=14&rft.issue=22&rft.spage=3549&rft_id=info:doi/10.3748%2Fwjg.14.3549&rft.externalDBID=NO_FULL_TEXT |
thumbnail_s | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fimage.cqvip.com%2Fvip1000%2Fqk%2F84123X%2F84123X.jpg http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fwww.wanfangdata.com.cn%2Fimages%2FPeriodicalImages%2Fwjg%2Fwjg.jpg |