图书馆主页
数据库简介
最新动态
联系我们



返回首页


 刊名字顺( Alphabetical List of Journals):

  A|B|C|D|E|F|G|H|I|J|K|L|M|N|O|P|Q|R|S|T|U|V|W|X|Y|Z|ALL


  检 索:         高级检索

期刊名称:ANAESTHESIA

ISSN:0003-2409
版本:SCI-CDE
出版频率:Monthly
出版社:BLACKWELL PUBLISHING LTD, 9600 GARSINGTON RD, OXFORD, ENGLAND, OX4 2DG
  出版社网址:http://www.blackwellpublishing.com/
期刊网址:http://www.blackwellpublishing.com/journal.asp?ref=0003-2409&site=1
影响因子:2.178(2008)
主题范畴:ANESTHESIOLOGY

期刊简介(About the journal)    投稿须知(Instructions to Authors)    编辑部信息(Editorial Board)   



About the journal

 

Print ISSN: 0003-2409
Online ISSN: 1365-2044
Issues per Volume: Monthly

Anaesthesia is the official journal of the Association of Anaesthetists of Great Britain and Ireland and is international in scope and comprehensive in coverage. It publishes original, peer-reviewed articles on all aspects of general and regional anaesthesia, intensive care and pain therapy, including research on equipment.

Review articles up to 10,000 words, special articles , case reports and historical notes are welcome. Also published are editorials, book reviews and obituaries of eminent anaesthetists; there is an active correspondence section in each issue and an online correspondence website. The Annual Report of Council is published each year.


Instructions to Authors

 

Anaesthesia is the official journal of the Association of Anaesthetists of Great Britain and Ireland and is published monthly. It is international in scope and comprehensive in coverage. It publishes original, peer-reviewed articles on all aspects of general and regional anaesthesia, intensive care and pain therapy, including research on equipment.

The editors regret that failure to comply with the following requirements may result in a delay in publication of accepted papers.

Submission of Manuscripts and Covering Letter

Manuscripts should be double-spaced with adequate margins (at least 2 cm) and page numbers at the bottom of each page. Use Times New Roman in 11 or 12 point. Please send ONE printed copy plus a disk (Word for Windows or rich text format), which should EXACTLY match the printed version, to:

Professor M. Harmer,
Editor, Anaesthesia,
Department of Anaesthetics,
University of Wales College of Medicine,
Heath Park,
Cardiff,
CF14 4XN,
UK.

Email: anaesthesia@cf.ac.uk

Covering Letter

The covering letter must be signed by all the authors and should include the following points:

  • Confirmation that the paper itself or the data upon which it is based have not been published or accepted for publication elsewhere other than as an abstract or as part of a thesis for a higher degree.
  • Confirmation that the paper is not currently under consideration for publication by any other journal.
  • Confirmation that all authors have made a substantial contribution to the conduct of the study and/or preparation of the manuscript in keeping with the guidelines published by the International Committee of Medical Journal Editors (Annals of Internal Medicine 1988; 108: 258-65). Corresponding authors may be asked to provide details of individual contributions during the editorial process.
  • Mention of any prior or forthcoming presentation of the data in the form of an abstract/free paper/poster at a scientific meeting.
  • Details of any competing interests amongst the authors relating to publication of the data. If there are no such competing interests, this should be stated. For guidance, see the BMJ web-site.

Types of Manuscript

Anaesthesia has the following regular sections: Editorials, Main Articles, Case Reports, Apparatus, Forum, Correspondence and Book Reviews. Reviews, Historical Articles or Special Articles may also be included. Although Editorials and Reviews are usually commissioned, authors may contact the Editor if they wish to discuss potential topics.

Content of Manuscripts

A typical manuscript will have the following sections in the following order, each section starting on a new page:

Title page
The name and address (including email address) of the corresponding author should appear in the top left-hand corner. The rest of the page should be as follows:
Title of paper: as short as possible but capturing the essence of the paper without stating the conclusion or posing a question*
A. B. Author1 and C. D. Author2
1  Position/designation of 1st author, with full postal address.
2  Position/designation of 2nd author with full postal address.

Correspondence to: Dr Corresponding Author (incl. email address)

*footnote if presented in part at any national or international meetings, with details including location and date

Summary and keywords
A Summary of fewer than 150 words should state the purpose of the study or investigation, basic procedures, main findings and their statistical significance, and principal conclusions. The summary should not be structured nor in note or abbreviated form. It should not state that 'the results are discussed' or that 'work is presented'. Abbreviations should not be used except for units of measurement.

Up to 10 keywords may be provided below the Summary. Use terms from the Medical Subject Headings list from Medline. The keywords may be modified at proof stage by the Editor.

Introduction
No heading is required for this section. The Introduction should give a concise account of the subject's background. Previously published work should only be quoted if it has a direct bearing on the present study. The Introduction should clearly and explicitly state the aims of the project.

Methods
A statement confirming Local Research Ethics Committee approval and written informed consent should be at the beginning of this section (see Ethical Considerations, below).

The Methods section must describe in sufficient detail the techniques and processes used so that the investigation can be interpreted and repeated by the reader. Any modification of previously published methods should be described and the appropriate reference given. If the methods are commonly used, only a reference to the original source is required. If special equipment is used, then the manufacturer's details should be given in parentheses. Drugs should be given by their international non-proprietary name. Label groups in a way that is easy to follow; thus 'propofol group' and 'thiopental group' instead of 'Group 1' and 'Group 2'. In some circumstances, abbreviated group titles may be better, e.g. 'Group BLEB' instead of 'bupivacaine-lidocaine-epinephrine-bicarbonate group'. Remember to include inclusion/exclusion criteria, a justification of sample size (see Statistics, below) and the method of randomisation and blinding. The statistical methods used to investigate data should be given at the end of the Methods section (see below).

Results
Express results as mean (SD), median (interquartile range [range]) - i.e. use parentheses then square brackets - or number (proportion) as appropriate.

Results must be presented for all measurements detailed in the Methods section, and in the same order. Sufficient raw data should be supplied to allow the reader to repeat the statistical analysis. However, data should not be repeated unnecessarily in the text, Tables and Figures. Results should not be given to an unwarranted number of decimal places and 95% confidence intervals should be used where possible (see Statistics, below).

Discussion
The Discussion should not merely recapitulate the results but should present their interpretation against a background of existing knowledge. Any conclusions must be warranted by the results. In general, avoid a paragraph headed 'Conclusions' which merely repeats a summary of the results. Also avoid ending with 'further work is needed' (it almost always is) unless you have specific areas of research to suggest.

Acknowledgments
The authors should acknowledge those who have made substantial contributions to the study or preparation of the manuscript but whose contributions do not fulfil the requirements for authorship. Sources of funding and potential conflicts of interest should be given here.

Appendices
Information or data not directly a result of the study but necessary for the reader to understand the manuscript should be included as an Appendix. Examples might include copies of questionnaires used, recognised mathematical processes used to generate results or previously published and validated classification systems. All should be appropriately referenced and the authors must obtain permission from the copyright holders if the contents have been previously published.

References
Number references consecutively in the order they appear in the text, using Arabic numerals enclosed in square brackets on the line (not superscript). Use [1-4] instead of [1,2,3,4]. References cited only in Tables or Figures should be numbered in the sequence established by the particular Table's/Figure's position in the text.

All references (including those in press) should be listed at the end of the text in the order they are quoted; when submitting your manuscript please submit copies of any articles accepted for publication but not yet published. Abstracts may be quoted as references so long as they have been published in peer-reviewed journals. Unpublished observations, personal communications and abstracts published only in proceedings of meetings should be quoted within the text of the manuscript, in parentheses. Information from manuscripts submitted but not yet accepted should be cited in the text as unpublished observations.

List all authors unless there are more than six, in which case give the first three followed by 'et al.'. Spell out the names of all journals in full, and give the first and last page number, not just the first.

Examples:

  • Author AB, Author CD. Title of paper. Journal Title Written out in Full in Italics 1999; 12: 123-4.
  • Author AB, Author CD, Author EF et al. Six or more authors - what's the point? (chapter title). In: Editor GH, Editor IJ, eds. Title of Book. Place: Publisher, 1998: 345-67.
  • Author AB. Book Title, 5th edn. Place: Publisher, 2000.

Tables
Do not include Tables in the text. Each Table should be on a separate page and double-spaced. Number the Tables consecutively with Arabic numerals and mark the approximate position of each Table with a highlighted instruction within the text. Each Table should have a brief legend immediately above it; the legend should provide enough information for readers to follow it without having to look through the text. The legend should explain whether the values refer to mean (SD), number (proportion), etc. Abbreviations should not be mentioned in the legend without explanation. Abbreviations used in the body of the Table should be explained as footnotes in the order in which they are first mentioned, using the following symbols (nb not superscript) in the following order: *, ? ? ? ? **, 排, etc. The study groups should form the columns rather than the rows. If statistical comparisons are being made, a separate column with exact p values should appear.

Example:

Table 1 Characteristics of patients receiving rocuronium or vecuronium. Values are median (interquartile range [range]), mean (SD) or number (proportion).


    Rocuronium   Vecuronium
    (n = 36)   (n = 38)

Age; years    24.0 (19-44 [16-52])   26.0 (22-42 [17-67])
 
Weight; kg    64.9 (6.8)   62.1 (5.5)
 
Height; cm    143.3 (12.6)   149.9 (14.4)
 
Sex; M : F    3 : 33   7 : 31
 
ASA Grade;
1    28 (77.8%)   31 (81.6%)
2    7 (19.4%)   4 (10.5%)
3    1 (2.8%)   3 (7.9%)


Legends for figures
Each Legend should provide enough information for readers to follow it without having to look through the text. Thus 'Changes in arterial blood pressure and heart rate in patients given propofol () or thiopental (?' instead of 'Cardiovascular changes'.

Figures
Each Figure should be on a separate page. Number the Figures consecutively with Arabic numerals and mark the approximate position of each Figure with a highlighted instruction within the text. Figures may be included in the disk in separate files and should be placed at the end of the text or collected together in an envelope or folder.

Please ensure related graphs have the same format (fonts, use of symbols, etc). The same requirements for abbreviations and units apply as for those in the text. Plot frames and legends within the graph itself should be removed. Avoid colour and the use of 3-D unless absolutely necessary.

Hard copy Figures should be clearly drawn or printed and should be twice the size of that desired in the published version. Photographs should be glossy black-and-white prints with good contrast. Each hard copy Figure should be identified by its sequential number in pencil on the reverse with the paper's title and authors' names included. Illustrations may also be submitted in electronic form. Ideally, save vector graphics (e.g. line artwork) in Encapsulated Postscript Format (EPS), and bitmap files (e.g. half tones) in Tagged Image File Format (TIFF), at a resolution of 250-300 dpi final size. Excel and Powerpoint files may also be used. Figures may be embedded within the body of the Word document or supplied as separate files. For detailed information on digital illustration standards see www.blackwell-science.com/elecmed/digill.htm.

See notes below for ethical considerations relating to photographs.

Style

In general, we prefer a clear, precise style to jargon. Please avoid long, complicated sentences and the passive voice when the active is more appropriate (e.g. 'We chose epidural anaesthesia because .' instead of 'Epidural anaesthesia was chosen by the authors because .'). Remove unnecessary clutter and focus on the actual message of each sentence; thus 'Hypotension is important because .' instead of 'It would be remiss of us not to mention hypotension because .').

Remember that lungs are ventilated, not patients (nor are they intubated - their tracheas are). Similarly, patients are not induced - anaesthesia is - or put on ventilators. Correct terms are tracheal (not endotracheal) tube and neuromuscular blocking drugs (not muscle relaxants).

For more comprehensive information about use of English and the preferred house style, see the Blackwell Publishing House Style Guide.

Abbreviations

In general, the Journal does not encourage the use of abbreviations, since their frequent use makes papers difficult to read. However, it will accept abbreviations in the following circumstances:

  • Universal abbreviations that do not need to be written out in full when first mentioned in the text. These include abbreviations that appear in a large proportion of the articles published in the Journal,
    e.g.:
      ECG   SD   SpO2
      BP   SEM   FIO2
      ASA   IQR   F?/SUB>CO2
      pH   ANOVA  
  • Acceptable common abbreviations that can be used but should be written out in full at their first mention,
    e.g.:
      EEG   CNS   ICU   PCA
      PAP   CSF   HDU   CTG
      PCWP   HME   SCBU   ECT
      CVP   PEEP
  • Acceptable abbreviations that do not need to be written out in full when first mentioned in the text but whose use should be restricted to situations where space is limited, e.g. in formulae or in Tables and Figures,
    e.g.:
      O2   CO2   Na+   Ca2+
      N2O   HCO3-   K+   Mg2+

Numbers and Units

Numbers should be spelled out in full when they start a sentence, and when they are less than 10 (unless they are followed by units of measurement). Thus 'Thirteen days later, five patients each received 7 ml solution .' Commas are not used to indicate thousands; thus 2000 and 20 000 instead of 2,000 and 20,000.

Use the format mg.kg-1 not mg/kg.

Use SI units thoughout the text except for vascular pressure measurements (mmHg or cmH2O) and haemoglobin concentration (g.dl-1). Use the 24-hour clock for times.

Ethical Considerations

Whatever their other merits, manuscripts will only be considered for publication in Anaesthesia if they adhere to the highest ethical standards. These are detailed in an editorial (Investigators, Anaesthesia and ethics. Anaesthesia 2000; 55: 521-2) which potential authors are strongly advised to consult.

In brief:

Local or Multicentre Research Ethics Committee (REC) approval must be obtained prospectively for all studies on human subjects. While some audit and epidemiological surveys may be exempt from this stricture, we strongly recommend that authors seek a view from their REC before undertaking such projects.

While an essential preliminary step, REC approval does not guarantee that the ethical standards of a study will meet the requirements of the Editorial Board of Anaesthesia. If authors have any concerns that ethical issues might compromise publication, they are invited to contact the Editor before embarking on the study.

The Editorial Board supports the view of the General Medical Council that full prospective written informed consent should be obtained from all subjects of clinical trials. Authors who do not follow this guidance will need to be able to mount a robust defence of their decision.

In general, submission of a case report should be accompanied by the written consent of the subject to publication; this is particularly important where photographs are to be used or in cases where the unique nature of the incident reported makes it possible for the patient to be identified. While the Editorial Board recognises that it might not always be possible or appropriate to seek such consent, the onus will be on the authors to demonstrate that this exception applies in their case.

In general, authors from outside the United Kingdom are expected to adhere to these same standards, although the Editorial Board will be sympathetic to minor variations.

Statistics

The following guidelines have been prepared by the Editorial Board of Anaesthesia to help authors avoid the common statistical errors that frequently lead to rejection of work submitted for publication. This should not be regarded as an exhaustive list and, of course, the Editorial Board and their reviewers may ask authors for revisions that are not detailed here. However, adherence to these guidelines in a paper that is otherwise acceptable will give researchers a good chance of publication and help ensure that their work is statistically valid. A good overview of the subject can be found in Pocock SJ, Hughes MD, Lee RJ. Statistical problems in the reporting of clinical trials. New England Journal of Medicine 1987; 317: 426-32.

Methods
Randomisation methods must minimize the possibility of predicting / breaking the code [1].

Blinding must be as good as can possibly be achieved.

Where there are several outcomes to be reported, the most important (primary) outcome should be clearly stated.

Power analysis [2]:

  • Justification of sample size should always be performed before randomized controlled trials are started. Details provided should include the power level; the significance level at which a result is sought; and the expected control and study group proportions or mean and pooled SD, in order to allow reviewers and readers to follow the calculation.
  • Power of study should be at least 80% - preferably 90%.
  • The 'clinically important difference' which the study is designed to detect should be clinically relevant and should not be set unreasonably large (sometimes done to justify small sample size).

Descriptive statistics:

  • Use mean (SD) unless:
    • data are discrete (e.g. Apgar scores, sedation scores) or grossly non-normally distributed - use median (IQR [range]).
    • you are interested in the 'true' value for the population (use SE).
  • Visual analogue scores (VAS) for pain may be treated as continuous data and be subjected to parametric tests as long as:
    • the sample size is large (>50).
    • the data appear normally distributed when 'eyeballed'.
  • VAS for other modalities (nausea, drowsiness) have not been so extensively validated and are best treated as ordinal data.

Inferential statistics:

  • Use simple tests where possible.
  • Avoid multiple comparisons, especially prevalent with t-tests [3].
  • Reference unusual tests.
  • Include details of computer package/version used.

When looking for relationship between variables [4]:

  • Possible simple descriptive association between two variables - correlation.
  • Possible relationship between two or more variables, especially where one is predictive and other(s) dependent - regression.
  • To compare two methods of measurement - Bland-Altman method [5].

Results
Baseline data (age, ASA status, duration of operation etc.) should not be subjected to statistical comparison, since it is already known that the subjects were randomly allocated and that any difference is therefore due to chance. Describe characteristics and, if possible, allow for differences in the analysis and discussion.

All outcomes mentioned in the Methods section must be reported (in the same order).

The data should look sensible when 'eyeballed'.

The number of decimal places used to describe data should be appropriate to the method of measurement (e.g. mean systolic blood pressure of 124.75 mmHg is too precise).

When reporting differences between groups, 95% confidence intervals should be included as well as p values [6].

95% CI must be used when reporting low or zero incidences (e.g. no headaches after 300 uses of a new spinal needle) [7].

When reporting the effect of an intervention, absolute risk (AR), relative risk (RR) and 'number needed to treat' (NNT) are easily understood by readers and may be preferable to odds ratio (OR) [8, 9].

Post-hoc comparisons should be avoided (comparing or categorising results in ways that were not stated in the original protocol - sometimes called 'data trawling') [10].

Graphs and tables should be appropriate for the data to be displayed. Tables usually convey more precise numerical information; graphs should be reserved for highlighting changes over time or between treatments.

Avoid judgemental terms such as 'highly' significant.

Report actual p values, rather than ranges or limits (e.g. p=0.032, rather than 0.01 < p < 0.05 or p < 0.05).

Conclusions
All conclusions should be warranted by the results and not extend beyond the confines of the study conditions.

A negative result does not mean that there is definitely no difference (confidence in conclusion is dependent upon the power of study).

A positive result does not mean that there definitely is a difference (confidence in conclusion is dependent upon the a-error).

References
1 Altman DG. Randomisation. www.bmj.com/guides/random.shtml
2 Yentis SM. The struggle for power in anaesthetic studies. Anaesthesia 1996; 51: 413-14.
3 Smith DG, Clemens J, Crede W, Harvey M, Gracely EJ. Impact of multpile comparisons in randomized clinical trials. American Journal of Medicine 1987; 83: 545-50.
4 Porter AM. Misuse of correlation and regression in three medical journals. Journal of the Royal Society of Medicine 1999; 92: 123-8.
5 Bland JM, Altman DG. Statistical method for assessing agreement between two methods of clinical measurement. Lancet 1986; 1: 307-10.
6 Gardner MJ, Altman DG. Statistics with Confidence. London: BMJ books, 1989.
7 Hanley JA, Lippman-Hand A. If nothing goes wrong, is everything all right? Interpreting zero numerators. Journal of the American Medical Association 1983; 249: 1743-5.
8 Sackett TR, Cook RJ. Understanding clinical trials. British Medical Journal 1994; 309: 755-6.
9 Laupacis A, Sackett D, Roberts R. An assessment of clinically useful measures of the consequences of treatment. New England Journal of Medicine 1988; 318: 1728-33.
10 Mills JL. Data torturing. New England Journal of Medicine 1993; 329: 1196-9.

Review Process

All papers are reviewed by the Editor and at least one other reviewer, usually an Assistant Editor. External review is used as deemed appropriate. The Editor's verdict on acceptance or rejection is final.

Papers accepted for publication require a Copyright Assignment Form to be signed and returned to the publisher.

Once accepted for publication, the manuscript will be subedited by an Assistant Editor; this usually involves some alterations to clarify points and maintain house style. Rather than be excessively prescriptive, the Editorial team try to be as helpful as possible at this stage - with the aim of improving your paper and its readability. The article is then sent to the publishers who will send a set of proofs to the author, Assistant Editor and finally the Editor. Changes by the authors at proof stage should be kept to a minimum - authors may be charged for excessive alterations.

Time from acceptance to publication is usually under six months.

Checklist for Authors

The following may help authors to check they have met the requirements:

Covering letter:
signed by all authors
confirm no duplicate publication
confirm this paper not submitted elsewhere
confirm all authors have contributed to manuscript
mention abstracts presented at meetings
detail potential conflict of interests
 
Preparation of manuscript:
double-spaced
margins at least 2 cm
page numbers at bottom
one copy on disk (Word for Windows or RTF)
 
Other paperwork:
copyright obtained and submitted if appropriate
papers in-press submitted if appropriate
written consent for subjects of case reports if appropriate
 
Text:
sections in appropriate order
each section mentions points in same order
references checked and in correct format
Tables, Figures and statistics meet above requirements

 

Abstracts presented at specialist societies' meetings

From 2002, the Editorial Board has decided to publish abstracts of free papers/posters that have been presented to national specialist anaesthetic societies based in the UK and Ireland.  Authors should follow the above Instructions for Authors; in general, the following sections should be indicated as appropriate using bold type: Title, Authors, Dept & Institution, Introduction, Methods, Results, Discussion, Acknowledgements, References (maximum 3). Text should be in a fully justified column 8 cm wide and no more than 23 cm high, Times New Roman, size 8 pt. A single Figure or Table (B&W) is allowable but must fit into the allotted space. Abstracts can only be submitted via the appropriate specialist society - do not submit direct to the journal. Further details are available from the relevant specialist society; officers of specialist societies who do not have this information should contact s.yentis@ic.ac.uk.

 


Editorial Board

 

Editor-in-Chief

Dr D Bogod, Department of Anaesthesia, 1st Floor, Maternity Unit, City Hospital, Hucknall Road, Nottingham, NG5 1PB, UK

Tel: +44 115 969 1169
Fax: +44 115 962 7713

e-mail: anaesthesia@nottingham.ac.uk

Editors

Dr W. A. Chambers, Aberdeen Royal Infirmary, Foresterhill, Aberdeen AB25 2ZN, UK

e-mail: Alastair.chambers@btinternet.com

Dr A W Harrop-Griffiths, Department of Anaesthesia, St Mary's Hospital, Praed Street, London, W2 1NY, UK

Tel: +44 207 886 1556
Fax: +44 207 886 6360

e-mail: awhg@btinternet.com

Dr J. A Langton, Plymouth Hospital NHS Trust, Department of Anaesthesia, Critical Care and Pain Management, Plymouth PL6 8DH, UK

Tel: +44 1752 792365
Fax: +44 1752 763287

e-mail: jeremy.langton@phnt.swest.nhs.uk

Dr Michael Nathanson, Department of Anaesthesia, University Hospital, Queen's Medical Centre, Nottingham, NG7 2UH, UK

Tel:  +44 (0)115 970 9195
Fax:  +44 (0)115 978 3891
e-mail:  mike@nathanson.demon.co.uk

Dr S A Ridley, Critical Care Complex, Norfolk and Norwich Hospital, Brunswick Road, Norwich, NR1 2SR, UK

Tel: +44 1603 286199
Fax: +44 1603 287751

e-mail: saxon@domum.globalnet.co.uk

Dr S M Yentis, Magill Department of Anaethesia, Intensive Care and Pain Management, Chelsea and Westminster Hospital, 369 Fulham Road, London, SW10 9NH, UK

Tel: +44 208 746 8026
Fax: +44 208 746 8801

e-mail: s.yentis@ic.ac.uk

Dr P A Clyburn, Department of Anaesthetics and Intensive Care Medicine, University of Wales College of Medicine, Heath Park, Cardiff, CF4 4XN, UK

Tel: +44 2920 744602
e-mail: clyburn@cf.ac.uk

Production Editor

 



 返回页首 


邮编:430072   地址:中国武汉珞珈山   电话:027-87682740   管理员Email:
Copyright © 2005-2006 武汉大学图书馆版权所有