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關于研究文獻透明化的聲明
——一種克服不充分研究報告的方法

2014-02-09 09:40:23DouglasAltmanDavidMoher
中國全科醫學 2014年2期
關鍵詞:報告信息研究

Douglas G.Altman,David Moher

Douglas G.Altman,David Moher.關于研究文獻透明化的聲明——一種克服不充分研究報告的方法[J].中國全科醫學,2014,17(2):119-122.[www.chinagp.net]

Douglas G.Altman(道格拉斯G.沃特曼):英國牛津大學生物統計學教授、生物統計中心主任;國際著名方法學家,Cochrane協作網方法學組負責人,曾任內科學年鑒主編,現任國際方法學專業雜志Trials主編;隨機對照試驗報告指南(CONSORT)工作組負責人之一;國際促進衛生研究質量與透明化協作網(EQUATOR)主要負責人;國際期刊編輯倫理委員會(COPE)成員。

David Moher(大衛.墨赫爾):加拿大渥太華大學公共衛生流行病學教授,臨床試驗中心主任,世界衛生組織國際臨床試驗注冊平臺專家組成員。國際著名臨床研究方法學家,CONSORT工作組負責人之一,Cochrane協作網替代醫學組首席方法學家,EQUATOR特邀專家,COPE成員。

“確保所發表的報告無偏倚、準確地重現研究是每一位參與者的責任”[1]。

研究記錄常常會做簡化處理,但卻存在對患者不利的風險。因此,醫學研究界需要變革來保證讀者獲得所有研究的真相,特別是隨機對照試驗報告,具有解答什么是對患者最有利治療的作用。

如果不發表所有研究特別是隨機對照試驗的結果,將嚴重地誤導循證臨床決策。最近一項關于瑞波西汀治療抑郁的系統評價發現約有四分之三參與研究的患者未在發表試驗中[2]。904項治療缺血性卒中(1955—2008年)的已完成試驗中,有五分之一沒有被適當地發表,“其中有的大到足以影響臨床實踐以及系統評價和Meta分析的結果”[3]。

與不發表一樣惡劣的是,不完整或誤導發表導致的問題更大。發表在同行評審刊物的臨床試驗結果可能與之前呈報到管理機構的不同[4-6],陽性結果可能更多。主要測量指標常與研究者在研究計劃[7-8]或注冊機構[9-10]中所描述的不一樣。選擇性地不發表不利的有統計學意義的結果,使文獻產生偏倚[11-12]。更有甚者,作者常歪曲表述和解釋他們的研究結果。一項研究發現,72個主要測量指標差異無統計學意義的隨機對照試驗都存在同樣問題[13]。在診斷準確性試驗研究中也有相似的發現[14]。

同行專家評審不能保證雜志發表的文章包含有讀者需要的詳細的臨床和方法學的關鍵內容。對已發表的隨機對照試驗報告的評估發現,其常缺乏對干預措施的評估[15-16]、患者納入標準[17]和結果[18-19]的詳細信息;研究方法的詳細信息也不充分,特別是關于分組的信息。一項2006年的研究發現,僅三分之一的研究報告描述了隨機序列的產生方法、僅四分之一充分描述了隱蔽分組方法[20]。一項包含357個Ⅲ期腫瘤臨床試驗的綜述總結道:“大量的內容在許多試驗中都沒有報告”[21]。不利事件也常常報告不充分[22-23]。

其他類型研究在結果和報告中的問題可能較隨機對照試驗更嚴重。雖然集中研究較少,相似觀點已經在有關的流行病學[24-25]、藥物流行病學[26]、診斷性研究[27]、預后研究[28]和臨床前研究[29-30]中表達過。當然,高質量報告并不等于有同樣高質量的研究。但是,完整和清楚的報告可讓讀者判斷研究的可靠性,獲取所需的相關信息。有人認為商業資助的研究可能更多地不被發表[2,31],一旦發表這些試驗報告則更加完整[32]。

那么,什么是必須的?報告應該對研究者如何實施其研究及研究結果進行清楚和透明地描述。忽略方法學或研究實施的重要細節應被認為是不可接受的,期刊不應發表這樣的報告。雖然找到一些缺失信息需要額外的途徑(例如從試驗注冊機構或研究計劃獲得信息),多數缺失信息在稿件中都很明顯并能檢測出來,盡管報告指南如CONSORT[33]容易獲得,但這種狀況的改善仍然緩慢[34]。

由于研究者對信息的刻意隱瞞使試驗結果不易獲得,這與赫爾辛基宣言相違背,不僅不符合當前研究的道義和科學性,而且浪費了大量稀缺資源、降低了研究的社會價值[35]。由于誤導或不充分地發表研究結果使研究者和資助組織失去了公眾的信任。從科學的角度,這不利于系統評價研究者匯集所有的證據,與使用所有信息的評估比較,只評估部分內容會對有效性和安全性的評估產生偏倚,降低準確性,不利于找到最利于患者的措施。

有一個幾乎立刻就能實施的計劃:我們建議每本雜志在作者投稿時都增加一個所有作者簽署的發表透明化聲明,在為其他目的提交報告時,如對監管機構,也需做類似的聲明(見下文示例)。

透明化聲明:負責作者*證明,本文對研究所做的報告是誠實、準確和透明的;沒有遺漏重要的內容,對與研究計劃(如果有,與所注冊的信息)的任何不一致均做了解釋。

注:*指文稿的保證人

編輯和編輯團隊可以通過更新其“作者須知”來支持本倡議,將完整的發表透明化保證作為投稿程序的一部分。我們認為這與當前廣泛實施的要求作者做“利益沖突聲明”相似,具有科學上的必要性。采用這樣的措施之后還有隱瞞或發表不正確信息的報告,將作為制裁學術不端行為的證據。我們希望此措施將鼓勵作者更加仔細地撰寫論文,并鼓勵他們按照相關報告指南審核自己的文稿。BMJ,我們中的一人(Douglas G.Altman)是其高級統計學編輯,和BMJ開放版(BMJOpen)正在帶頭實施這項政策。我們邀請其他雜志也實行這項政策,并支持EQUATOR網站(www.equator-network.org)的透明化聲明。

科學界和公眾對準確和完整的研究報告寄予厚望,我們需要變革來給以保障。廣泛認可和實行的發表透明化聲明是幫助實現醫學研究最大價值的一條途徑,然而其影響不了未發表的研究,這仍然是一件恥辱。

DeclarationofTransparencyforEachResearchSrticle

"Itistheresponsibilityofeveryoneinvolvedtoensurethatthepublishedrecordisanunbiased,accuraterepresentationofresearch."1

The research record is often manipulated for short term gain but at the risk of harm to patients.The medical research community needs to implement changes to ensure that readers obtain the truth about all research,especially reports of randomised trials,which hold a special place in answering what works best for patients.

Failure to publish the findings of all studies,especially randomised trials,seriously distorts the evidence base for clinical decision making.A recent systematic review of reboxetine for treating depression found that almost three quarters of included patients were in unpublished trials2.Of 904 completed trials of interventions for acute ischaemic stroke (1955—2008),a fifth were not properly published,"several of which may be large enough to influence clinical practice and the findings of systematic reviews and meta-analyses"3.

Bad as non-publication is,incomplete or misleading publications cause greater problems.Results of clinical trials published in peer reviewed publications may differ from what was previously submitted to regulatory agencies4-6,with the published data being more positive.The primary outcome often differs from what the researchers had stated in the trial protocol7-8or clinical trial registry9-10.Selective non-publication favours statistically significant findings,biasing the literature11-12.Furthermore,authors often distort the presentation and interpretation of their findings.One study found that such "spin" was common in 72 reports of randomised controlled trials with statistically non-significant primary outcomes13.Similar findings have been reported recently for studies of the accuracy of diagnostic tests14.Peer review is failing to ensure that journal articles contain the key clinical and methodological details that readers need.Reviews of published reports of randomised trials have found common deficiencies in the details of the interventions being evaluated15-16,participant eligibility criteria17,and outcomes18-19.Details of study methods are also often inadequate,especially in relation to allocation.A 2006 study found that only a third of trial reports described how the randomisation sequence was generated and only a quarter described an adequate method of allocation concealment20.A review of 357 phase Ⅲ oncology trials concluded that "numerous items remained unreported for many trials"21.Harms too are poorly reported22-23.

The problems associated with publishing and reporting other types of research may be worse than for randomised trials.Although less intensively studied,similar concerns have been expressed in relation to epidemiology24-25,pharmacoepidemiology26,diagnosis research27,prognosis research28,and preclinical research29-30.Of course,good reporting is not the same as high quality research.But a full and clear report allows readers to judge a study′s reliability and relevance.There are concerns that commercially sponsored research may be more likely to remain unpublished2,31,but when published these trials are reported more fully32.

So what is needed? Published research articles should provide a clear and transparent description of how researchers conducted their study and what they found.Omission of important details of methods or study conduct should be deemed unacceptable,and journals should not publish them.Although detection of some deficiencies requires external information (for example,from a trials register or protocol),most deficiencies are inherent in a submitted manuscript and should be detected.Despite the availability of reporting guidelines such as CONSORT33,improvements are slow to materialise34.

By not making results of their research easily accessible,researchers are withholding knowledge,in contravention of the Declaration of Helsinki.Not only are current practices questionable on moral and scientific grounds,failure to publish all research findings is a massive waste of scarce resources and diminishes the social value of the research35.Researchers and funding organisations also fail the public when research findings are published in a misleading or inadequate way.Scientifically,this harms systematic reviewers who want to aggregate all of the evidence.Reviewing a partial picture provides biased and less precise estimates of effectiveness and safety than when the full information is used,and it may compromise the identification of what works best for patients.

We have a proposal that can be acted on almost immediately.We suggest that authors should sign a publication transparency declaration (box) as part of every journal submission.The same declaration could be appropriate for submissions in other contexts-for example,to regulatory agencies.

Transparencydeclaration:Theleadauthor*affirmsthatthismanuscriptisanhonest,accurate,andtransparentaccountofthestudybeingreported;thatnoimportantaspectsofthestudyhavebeenomitted;andthatanydiscrepanciesfromthestudyasplanned(and,ifrelevant,registered)havebeenexplained.

*Themanuscript′sguarantor.

Editors and editorial groups can support this initiative by updating their instructions to authors so that a completed publication transparency pledge is required as part of the submission process.We see this action as a necessary scientific analogue of the current widespread practice of asking authors about conflicts of interest.Subsequent revelation of withheld or incorrect information would be evidence of scientific misconduct for which various actions could be taken.We hope that this step will encourage authors to reflect more carefully on how they write their article and encourage them to check that they have adhered to relevant reporting guidelines.TheBMJ,for which one of us (DGA) is the senior statistics editor,andBMJOpenare leading the way by implementing this policy immediately.We invite other journals to do likewise and support the transparency declaration on the EQUATOR website (www.equator-network.org).

The scientific community and the public at large deserve an accurate and complete record of research;we need to make changes to ensure that we will get one.Widespread endorsement and implementation of a publication transparency declaration is one way to help to get the maximum value from medical research.It will,however,have no influence on the non-publication of studies,which is a continuing disgrace.

1 PLoS Medicine Editors.An unbiased scientific record should be everyone′s agenda[J].PLoS Med,2009,24(6):e1000038.

2 Eyding D,Lelgemann M,Grouven U,et al.Reboxetine for acute treatment of major depression:systematic review and meta-analysis of published and unpublished placebo and selective serotonin reuptake inhibitor controlled trials[J].BMJ,2010,341:c4737.

3 Gibson LM,Brazzelli M,Thomas BM,et al.A systematic review of clinical trials of pharmacological interventions for acute ischaemic stroke (1955—2008) that were completed,but not published in full[J].Trials,2010,11:43.

4 Turner EH,Knoepflmacher D,Shapley L.Publication bias in antipsychotic trials:an analysis of efficacy comparing the published literature to the US Food and Drug Administration database[J].PLoS Med,2012,9(3):e1001189.

5 Turner EH,Matthews AM,Linardatos E,et al.Selective publication of antidepressant trials and its influence on apparent efficacy[J].N Engl J Med,2008,358(3):252-260.

6 Vitry AI.Reporting of studies on new medicines in major medical journals:a case study in breast cancer[J].Clin Pharmacol Ther,2010,87(4):398-400.

7 Dwan K,Altman DG,Cresswell L,et al.Comparison of protocols and registry entries to published reports for randomised controlled trials[J].Cochrane Database Syst Rev,2011(1):MR000031.

8 Nankervis H,Baibergenova A,Williams HC,et al.Prospective registration and outcome-reporting bias in randomized controlled trials of eczema treatments:a systematic review[J].J Invest Dermatol,2012,132(12):2727-2734.

9 Mathieu S,Boutron I,Moher D,et al.Comparison of registered and published primary outcomes in randomized controlled trials[J].JAMA,2009,302(9):977-984.

10 Rosenthal R,Dwan K.Comparison of randomized controlled trial registry entries and content of reports in surgery journals[J].Ann Surg,2013,257(6):1007-1015.

11 Song F,Parekh S,Hooper L,et al.Dissemination and publication of research findings:an updated review of related biases[J].Health Technol Assess,2010,14(8):1-193.

12 Dwan K,Kirkham JJ,Williamson PR,et al.Selective reporting of outcomes in randomised controlled trials in systematic reviews of cystic fibrosis[J].BMJ Open,2013,3(6):e002709.

13 Boutron I,Dutton S,Ravaud P,et al.Reporting and interpretation of randomized controlled trials with statistically nonsignificant results for primary outcomes[J].JAMA,2010,303(20):2058-2064.

14 Ochodo EA,de Haan MC,Reitsma JB,et al.Overinterpretation and misreporting of diagnostic accuracy studies:evidence of "spin"[J].Radiology,2013,267(2):581-588.

15 Duff JM,Leather H,Walden EO,et al.Adequacy of published oncology randomized controlled trials to provide therapeutic details needed for clinical application[J].J Natl Cancer Inst,2010,102(10):702-705.

16 Glasziou P,Meats E,Heneghan C,et al.What is missing from descriptions of treatment in trials and reviews?[J].BMJ,2008,336(7659):1472-1474.

17 Shapiro SH,Weijer C,Freedman B.Reporting the study populations of clinical trials.Clear transmission or static on the line?[J].J Clin Epidemiol,2000,53(10):973-979.

18 Vera-Badillo FE,Shapiro R,Ocana A,et al.Bias in reporting of end points of efficacy and toxicity in randomized,clinical trials for women with breast cancer[J].Ann Oncol,2013,24(5):1238-1244.

19 Le Cleach L,Chassany O,Levy A,et al.Poor reporting of quality of life outcomes in dermatology randomized controlled clinical trials[J].Dermatology,2008,216(1):46-55.

20 Hopewell S,Dutton S,Yu LM,et al.The quality of reports of randomised trials in 2000 and 2006:Comparative study of articles indexed in PubMed[J].BMJ,2010,340:c723.

21 Peron J,Pond GR,Gan HK,et al.Quality of reporting of modern randomized controlled trials in medical oncology:A systematic review[J].J Natl Cancer Inst,2012,104(13):982-989.

22 Bagul NB,Kirkham JJ.The reporting of harms in randomized controlled trials of hypertension using the CONSORT criteria for harm reporting[J].ClinExp Hypertens,2012,34(8):548-554.

23 Shukralla AA,Tudur-Smith C,Powell GA,et al.Reporting of adverse events in randomised controlled trials of antiepileptic drugs using the CONSORT criteria for reporting harms[J].Epilepsy Res,2011,97(1/2):20-29.

24 Knol MJ,Egger M,Scott P,et al.When one depends on the other:Reporting of interaction in case-control and cohort studies[J].Epidemiology,2009,20(2):161-166.

25 Lee W,Bindman J,Ford T,et al.Bias in psychiatric case-control studies:literature survey[J].Br J Psychiatry,2007,190:204-209.

26 Holmes MV,Shah T,Vickery C,et al.Fulfilling the promise of personalized medicine? Systematic review and field synopsis of pharmacogenetic studies[J].PLoS One,2009,4(12):e7960.

27 Zintzaras E,Papathanasiou A,Ziogas D,et al.The reporting quality of studies investigating the diagnostic accuracy of anti-CCP antibody in rheumatoid arthritis and its impact on diagnostic estimates[J].BMC Musculoskelet Disord,2012,13:113.

28 Kyzas PA,Denaxa-Kyza D,Ioannidis JP.Quality of reporting of cancer prognostic marker studies:association with reported prognostic effect[J].J Natl Cancer Inst,2007,99(3):236-243.

29 Kilkenny C,Parsons N,Kadyszewski E,et al.Survey of the quality of experimental design,statistical analysis and reporting of research using animals[J].PLoS One,2009,4(11):e7824.

30 Dirnagl U,Macleod MR.Stroke research at a road block:the streets from adversity should be paved with meta-analysis and good laboratory practice[J].Br J Pharmacol,2009,157(7):1154-1156.

31 Lundh A,Sismondo S,Lexchin J,et al.Industry sponsorship and research outcome[J].Cochrane Database Syst Rev,2012,12:MR000033.

32 Khan NA,Lombeida JI,Singh M,et al.Association of industry funding with the outcome and quality of randomized controlled trials of drug therapy for rheumatoid arthritis[J].Arthritis Rheum,2012,64(7):2059-2067.

33 Schulz KF,Altman DG,Moher D.CONSORT 2010 Statement:updated guidelines for reporting parallel group randomised trials[J].BMJ,2010,340:c332.

34 Turner L,Shamseer L,Altman DG,et al.Consolidated standards of reporting trials (CONSORT) and the completeness of reporting of randomised controlled trials(RCTs) published in medical journals[J].Cochrane Database Syst Rev,2012,11:MR000030.

35 Chalmers I,Glasziou P.Avoidable waste in the production and reporting of research evidence[J].Lancet,2009,374(9683):86-89.

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