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The
manuscript should meet the following criteria: the material is
original, study methods are appropriate, data are sound,
conclusions are reasonable and supported by the data, the
information is important; the topic has general pediatric
interest; and that the article is written in reasonably good
English. Knowledge, attitude, practice (KAP) studies are
generally not accepted. The article should be submitted
strictly in the style of Indian Pediatrics (vide infra).
Manuscripts which do not follow the guidelines are likely to
be sent back to authors without initiating the peer-review
process.
The current
acceptance rate of submitted articles is around 25%. All
accepted manuscripts are subject to editorial modifications to
suit the language and style of Indian Pediatrics. Manuscripts
once accepted will be edited in accordance with ‘AMA Manual of
Style’ and returned to author for approval. Rejected
manuscripts are retained for three months to answer any
queries, followed by shredding. Indian Pediatrics reserves the
right to analyze the information obtained from submitted
manuscripts as a part of editorial research to improve the
peer-review process; this does not include use of the
manuscript data.
Unauthorized use:
The copyright of all accepted and published manuscripts is
with Indian Pediatrics; these can not be reproduced elsewhere
or distributed in any form, in whole or part, without the
written permission from the Editor-in-Chief. Mass photocopying
of published article would also amount to copyright violation.
The name, logo, thumbnail, or contents of Indian Pediatrics
cannot be used to promote commercial goods, in any form,
without prior permission. Unauthorized use will attract legal
action.
Review
process:
About one-tenth of the manuscripts are rejected after an
initial in house review. The usual reasons for rejection at
this stage are insufficient originality, serious scientific
flaws, major ethical issues, absence of a message, article not
related to children or adolescents, not submitted in desired
format,
not
of interest to majority of readers, or not in accordance with
the current priorities of the journal. Decision on such papers
is communicated to authors within two weeks. Remaining
articles are sent to two or more reviewers, having sufficient
experience on the subject in a ‘masked fashion’. Manuscripts
are reviewed with due respect for authors’ confidentiality.
The peer reviewer identity is also kept confidential. Period
of decision making process varies from 6-10 weeks depending on
timely response from
reviewers,
revision by the author(s), and reappraisal on revisions(2).
Duplicate
submission and Plagiarism:
Manuscripts are considered with the understanding that they
have not been published previously in print or electronic
format and are not under consideration by another publication
or electronic medium. The author should alert the editor if
the work includes subjects about which a previous report has
been published. A paper submitted to the Indian Pediatrics
should not overlap by more than 10% with previously published
work, or work submitted elsewhere. If in doubt, authors may
submit copies of earlier published work or material submitted
elsewhere to the editorial board of Indian Pediatrics to take
the decision. If plagiarism or duplicate publication is
attempted or occurs without such notification, authors should
expect prompt rejection/retraction and editorial board’s
action such as barring the author from submitting articles in
future, notification in the journal/website, informing the
other medical editors etc.
An article
which has been already rejected should not be resubmitted
again under the original or modified title, especially if the
content remains substantially same. Author should provide
full information regarding previous submission, if any, as
such violations are viewed seriously.
Previous
publication:
Indian
Pediatrics would not publish material that has already
appeared elsewhere; but could accept some papers that have
been published as abstracts or have been partially reported by
the media at scientific meetings, and some that have already
appeared in non-English language journals.
Embargo
policy:
Authors need to maintain confidentiality of
contents of their manuscript, once accepted for publication.
Information contained in or about the accepted articles should
not be released in print/electronic form to any
individual/media/agency, till the manuscript is published in
print or electronic form in Indian Pediatrics.
Proofs and Reprints:
The corresponding author of the accepted article shall be
supplied the printers’ proofs. Corrections on the proof should
be mainly restricted to printers’ errors only. No addition,
deletion, alteration in the sequence of authors or change of
corresponding authorship is permissible at this stage.
Reprints may be ordered on payment.
Articles can be submitted as Research Papers, Short
Communications, Reviews, Perspective, Images, Case Reports,
Research Letters and Correspondence.
Research Papers: These
articles should report research relevant to clinical
pediatrics including randomized clinical trials, intervention
studies, studies of screening and diagnostic tests, cohort
studies, cost-effectiveness analyses, case control studies and
cross-sectional studies. For reporting research, the
authors are expected to comply with the ‘Uniform Requirements
for Manuscripts Submitted to Biomedical Journals’ prepared by
the International Committee of Medical Journal Editors
(ICMJE)(3). Additionally, authors need to adhere to the
standard recommended reporting guidelines (Table I)
depending on the study design of the submitted article.
TABLE 1
Details of Reporting Guidelines
for Different Study Designs
Clinical trial.
A clinical trial is any study that prospectively assigns human
subjects to some intervention (with or without a comparison
group) to evaluate the relationship between a medical
intervention and a health outcome. In randomized controlled
clinical trials, individuals are randomly allocated to receive
or not receive a preventive, therapeutic, or diagnostic
intervention and then followed up to determine the effect of
the intervention. Manuscripts reporting the results of a
randomized controlled trial (RCT) should include the CONSORT
flow diagram showing the progress of patients throughout the
trial (see Figure 1). The
CONSORT checklist
(4,5) also should be completed and submitted with the
manuscript.
Trial registration:
We urge the authors to register their clinical trials
involving human subjects in CTRI (Clinical Trials Registry of
India) available at
www.ctri.in, hosted by the Indian Council of Medical
Research(10). Preference will be accorded to registered
clinical trials. Registration in one of the following trial
registers is also acceptable:
http://www.actr.org.au;
http://www.clinicaltrials.gov;
http://isrctn.org;
http://www.trialregister.nl/trialreg/index.asp; and
http://www.umin.ac.jp/ctr.
Preparing a research
paper: Each manuscript should be
accompanied with a structured
Abstract in not
more than 250 words using the following headings: Objective,
Design, Setting, Participants/patients, Intervention (if any),
Main Outcome Measures, Results, and Conclusions (See under
heading ‘Preparing the Manuscript’). Four to five key words to
facilitate indexing should be provided in alphabetical order
below the abstract. The text should be arranged in sections on
Introduction, Methods,
Results and
Discussion. Key Message should be provided at the end
of the manuscript in a box
under
2
headings: ‘What
is Already Known’ and ‘What
this Study Adds’. As
far as possible, authors should restrict to a one line answer
for each of these two queries. Number of tables and figures
should be limited to a maximum of 4 and 2 respectively. Extra
tables and figures, subject to clearance by editorial review
process, can be allowed on payment. The typical text length
for such contributions is 1500-2000 words (excluding
title page, abstract, tables, figures, acknowledgments, key
messages and references). Number of references should be
limited to 25.
Short Communications:
Brief accounts of descriptive, observational studies,
epidemiological assessments, and surveys are published as
Short Communications. A series of cases can also be considered
as Short Communication. Abstract should be unstructured,
limited to 100 words; and highlight the aims, methods and main
results. Provide 2-3 key words. The text should contain no
more than 1000 words, two illustrations/tables and up to
15 references, preferably recent publications. The text should
be arranged in order of
Introduction, Methods, Results and
Discussion. Also
include a box entitled ‘What
this Study Adds’,
highlighting the main result of the study. The number of
authors should be limited to five.
Review Article:
State-of-the-art review articles or systematic, critical
assessments of literature are also published. The authors may
consult the Editor-in-Chief before submitting such articles as
similar reviews may be already in submission. Normally a
review article on a subject already published in Indian
Pediatrics in last 3 years is not accepted. The typical length
for review articles is 2500-3000 words (excluding
tables, figures, and references). Authors submitting review
manuscripts should include an abstract of around 200 words
describing the need and purpose of review, methods used for
locating, selecting, extracting and synthesizing data, and
main conclusions. Number of authors should be limited to
three. The number of references should be limited to 50.
Drug Review: Indian
Pediatrics publishes state of the art reviews on the
drugs/agents meant for therapeutic or prophylactic use in
children. It is expected that the authors have sufficient
credible experience in the related field. The following
guidelines should be adhered to when preparing a drug review:
-
Drug should
be recently developed and should be available commercially
for use in human subjects. The reviews related to agents
under research and development, are generally not accepted.
-
Drug should
preferably belong to a new class of drugs or having
substantial difference in properties and not just an
addition to the existing drugs having many similar
properties/actions in that class/group of compounds.
-
The drug
should have the potential to be used on a large scale for
pediatric conditions. Drugs primarily catering to other
medical fields (e.g. adult medicine, dermatology or surgical
specialities) are not preferred.
-
The drug and
related review should have the potential to influence
practice, policy and research related issues.
-
The review
should be a systematic, critical assessment of the
literature and not just an elaboration of the information
already provided by pharmaceutical companies.
Perspective: Articles
published under this heading intend to cover challenging and
controversial topics of current interest in pediatric health
care and the intersection between medicine and society. The
related issues could be national, regional (South East Asia)
or global. Though the articles are usually solicited, we
welcome submissions and proposals from researchers and opinion
makers provided they have sufficient credible experience and
recognition on the subject for giving opinions. Some of the
manuscripts submitted as ‘Review Articles’ may also be
considered for publication under this section at the
discretion of editors. The following guidelines need to be
followed:
1.
The number of
authors should be limited to maximum of three.
2. The
topic should be specific and related to child health in
general.
3. Word
limit: 2500 words and may include one figure and one Table.
4. Unstructured
abstract of up to 150 words.
5. The
views should be supported by appropriate evidence and
references. Number of references should be limited to a
maximum of 30.
Clinical Practice
Guidelines/Recommendations: In order to streamline the
diagnosis, management or prevention of various childhood
problems, Indian Pediatrics periodically publishes Guidelines
and Recommendations formulated by various Chapters and Task
Forces constituted by Indian Academy of Pediatrics (IAP) or a
similar National association/society. The 8 desirable
attributes of practice guidelines are validity, reliability
and reproducibility, clinical applicability, flexibility,
clarity, documentation, development by a multidisciplinary
process, and plans for review(11). In order to maintain
uniformity of reporting and improve readability and
applicability of these practice guidelines, the following
10-point policy should be followed:
-
The Guideline/Recommendation
should have been formalized through a consultative
meeting/conference/workshop having a National representation
approved by Indian Academy of Pediatrics (IAP) or a similar
society. The Guidelines emerging out of one such meeting
should be preferably presented in a single paper.
-
The date(s) and place of such
meeting should be clearly mentioned in the Introduction. The
names of the chairperson, convener and participants should
be listed as ‘Annexure’ at the end of the draft.
-
For indexing purposes, the
author of the guidelines would be the name of the
organization/working group e.g., Indian Academy of
Pediatrics: Nephrology Group. However, names of up to six
persons as writing committee may be placed at the end of the
manuscript before ‘References’.
-
The final guidelines should be
cleared by the related Society/Chapter. A letter to this
effect should be enclosed. It is presumed that the
corresponding author has obtained permission from all
members of the committee/expert group to act in this
capacity.
-
The manuscript should consist of
an Abstract (250-300 words), Text (3000-4000 words), and
References (limited to 50). The number of figures and tables
should be limited to maximum of 5 each.
-
Abstract: Should be structured
as Justification, Process, Objectives, and Recommendations.
-
Text should be arranged in
headings of Introduction, Aims and Objectives, and
Recommendations.
-
Introduction: Justify the need
of formulating the guidelines/recommendations in a brief
paragraph followed by the process of arriving at the
guidelines/recommendations. Describe the methods used to
search the literature, and criteria used to grade the
quality of evidence.
-
Aims and Objectives: Should
clearly state (in doable terms, using action verbs) the
terms of reference of the consultative meeting/
conference/ workshop. List 2-3 main objectives only.
-
The main text of the
Guidelines/Recommendations should be mentioned under the
same terms of reference as per aims and objectives
outlined earlier. Preferably, provide level of evidence
for each major recommendation.
-
The Recommendations should not
provide ‘Review of literature’ or ‘What is already known’
For example, if the guidelines pertain to management of
Dengue fever, there is no point in writing about the
epidemiology, clinical features, differential diagnosis,
etc. of Dengue fever. Background material on the concerned
subject will not be published.
-
If guidelines are adapted from
statement of some other society or from earlier
recommendations, only changes need to be highlighted
(preferably in a tabular form) without repeating the
detailed guidelines. However, if there is a pressing need
to repeat the recommendations, it should be done after
taking permission from the parent society/journal (as
applicable) clearly mentioning and citing the source.
-
State, whether or not there is a
plan to review these guidelines and an expiration date for
this version of the guideline.
-
Any competing interest including
funding support should be declared.
-
We encourage the authors to
attach a COGS (Conference on Guidelines Standardization)
checklist for reporting clinical practice guidelines(12).
Case Reports: Clinical
cases highlighting some unusual or new but clinically relevant
aspects of a condition are published as Case Reports. Single
case reports are not accepted, unless some new or unusual
aspect regarding etiopathogenesis, diagnosis or management is
brought out that adds to the existing body of knowledge.
Genetic syndromes without a major phenotypic reporting will be
sent back to authors without initiating the peer review
process. Minor or clinically insignificant variations of rare
but well-known disorders are also not preferred. Rarity of the
reported condition alone also will not be a criterion for
acceptance.
The text should not exceed 1000
words and is arranged as introduction, case report and
discussion. Include a brief Abstract of about 50 words. Number
of tables/figures should be limited to 2. Include up to 10
most recent references. Photographs should be in black and
white only. For details, see below under Figures and
Illustrations. A maximum of three authors are permitted from
a single department. Case Reports involving more than one
department can have a maximum of four authors. The patient's
written consent, or that of the next of kin, to publication
must be obtained. The authors would be asked to submit a
signed consent form before publication for all Case Reports
and Images.
Research Letters: Under
this heading, short correspondence pertaining to research
would be included. Research Letters reporting original
research should not exceed 500 words of text and 10
references. They may have no more than 4 authors; other
persons who have contributed to the study may be indicated in
an Acknowledgment, with their permission. An abstract of up to
50 words reporting the key findings should also be included.
Letters must not duplicate other material published, submitted
or planned to be submitted for publication. In general, the
matter of the letter should be unstructured but should follow
the general sequence of introduction, methods, results and
discussion and all other guidelines in ‘Preparing the
Manuscript’.
Correspondence: Letters
commenting upon recent articles in Indian Pediatrics are
welcome. Such letters should be received within 3 months of
the article’s publication. At the Editorial board’s
discretion, the letter may be sent to the authors for reply
and the letter alone or letter and reply together may be
published after appropriate review. Letters may also relate to
other topic of interest to pediatricians, or useful clinical
observations. Letters should not have more than 400 words;
contain not more than one Figure/Table and 5 most recent
references. The text need not be divided into sections. The
number of authors should not exceed two, including the
authors’ reply in response to a letter commenting upon an
article published in Indian Pediatrics. In the later case,
inclusion of only one of the authors (of the article in
question) is permissible, besides the corresponding author.
The corresponding author shall remain the first author for
such reply. Names of additional persons who have helped in
data acquisition can be mentioned in the 'Acknowledgment'
section.
Reader Forum: Readers may
send questions of common interest. Editorial board will try to
elicit answers from the experts; and publish them, if found
suitable.
Images:
Only clinical photographs with/without accompanying skiagrams
or pathological images are considered for publication. Image
should clearly identify the condition and have the classical
characteristics of the clinical condition. Clinical photograph
of condition which are very common, extremely rare, where
diagnosis is obvious (e.g., penile agenesis), or where
diagnosis is not at all possible on images alone would not be
considered. Photographs should be of high quality, usually 127
x 173 mm (5 x 7 in) but no larger than 203 x 254 mm (8 x 10
in). A short text of about 150 words depicting the condition
is needed. The number of authors should not exceed two. Images
are to be sent as hard copies only by surface/air mail. An
electronic submission for this section is not acceptable. The
authors should ensure that images of similar nature have not
been published earlier. Authors must obtain signed informed
consent from the patient.
Manuscripts
should be prepared in accordance with the ‘Uniform
Requirements for Manuscripts Submitted to Biomedical
Journals’(3). A summary of technical requirements for
preparing the manuscript is provided below:
· Three copies of the
manuscript should be submitted.
·
Use 1 side of
standard size 21.6 x 27.9 cm (8˝ ×11 inch) A4, white bond
paper, with margins of at least 2.5 cm (1 inch) on each side.
· Use American (US)
English throughout.
·
Double-space
throughout including title page, abstract, text,
acknowledgements, key messages, references, figure legends and
tables. Start each of these sections (in same order) on a new
page, numbered consecutively in the upper right hand corner,
beginning with the title page.
·
Use at least 12
point font size (Times New Roman or Arial).
· Submit photographs
in a separate heavy paper envelope (enclosed in cardboard, to
prevent bending during mail handling).
·
Units of
measure: Conventional units are
preferred. The metric system is preferred for the expression
of length, area, mass and volume.
· Use nonproprietary
names of drugs, devices and other products.
·
All accepted
manuscripts should be finally accompanied by a signed
statement by all authors regarding authorship criteria,
responsibility, financial disclosure and acknowledgement, as
per standard format (See Annexure I) of the journal.
Those sending their manuscript through e-mail are also
required to submit this form by post with original signatures.
·
Checklist:
All manuscripts should be accompanied with a "Manuscript
submission checklist" duly completed as per
Annexure
II.
Manuscripts not fulfilling the
technical requirements shall be returned to the authors
without initiating the peer-review process.
Title Page
The page should contain (i)
the title of the article: which should be concise but
informative (simpler the title the better; preferably it
should contain all the key words to help electronic retrieval
reliably); (ii) a short running title of not more than
40 characters placed at the foot end of the title page; (iii)
initials and surname (both are essential) of each author with
the highest academic degree(s) and designation at the time
when the work was done; Initials will not be accepted for
surnames. For example; ‘Vidya K’: here, ‘K’ will be considered
as the Initial and ‘Vidya’ will be indexed as surname; (iv)
details of the contribution of each author; (v) name of
department(s) and institution(s) to which the work should be
attributed; (vi) disclaimers, if any; (vii)
name, address, telephone, fax, e-mail address of the
corresponding author, (viii) source(s) of support in
the form of grants, equipment, drugs or all of these; and (ix)
declaration on competing interests; and (x) word count
(not including abstract, tables, figures, acknowledgments,
key messages and references). Also, indicate on top the
category (i.e. Research Paper, Short Communications, Review,
Case Report, Images, Correspondence etc.), for which
the article is being submitted.
Authorship Criteria
All persons designated as
authors should qualify for the authorship. Authorship credit
should be based on substantial contributions to (i)
concept and design, or acquisition of data, or analysis and
interpretation of data; (ii) drafting the article or
revising it critically for important intellectual content; and
(iii) final approval of the version to be published.
Conditions (i), (ii) and (iii) must be
met, for all authors, individually. Participation solely in
the acquisition of funding or the collection of data does not
justify authorship. All such people who contributed to the
work but do not satisfy all the conditions should be named in
the acknowledgements. Authors are responsible for obtaining
written permissions from everyone acknowledged by name. One of
the authors shall act as guarantor of the paper and he/she
should take the responsibility for the integrity of the work
as a whole, from its inception to published article. Guarantor
should also take responsibility for obtaining permission from
appropriate authority, if any material (including tables,
figures or text) is used in the article from another
publication. Copyright violations by authors will be viewed
seriously; and all authors will be equally responsible for
such acts. Authors should provide a description of what each
author contributed on the title page. Indian Pediatrics
reserves the right to satisfy itself regarding the specific
role of each listed author to justify authorship. All authors
must give signed consent to publication (Annexure I).
Example of citing
contributors’ credit i.e. specific contribution of each
author is given below:
Contributors:
KDP concieved and designed the study and revised the
manuscript for important intellectual content. He will act as
guarantor of the study. AI, and AK collected data and drafted
the paper. AI also conducted the laboratory tests, and
interpreted them. SK analysed the data and helped in
manuscript writing. The final manuscript was approved by all
authors.
Group Authorship.
All members of the Group (e.g., Pediatric Nephrology
Subchapter of IAP) must meet the criteria of authorship as
described above.
Competing Interest
Competing interest for a given
manuscript exists when the author has ties to activities that
could inappropriately influence his or her judgment, whether
or not judgment is in fact affected(13). Financial
relationships with industry—for example, through employment,
consultancies, stock ownership, honoraria, grant, expert
testimony, either directly or through immediate family, are
usually considered to be the most important competing
interests. However, conflicts can occur for other reasons,
such as personal relationships, academic competition and
intellectual passion. If any of the authors have accepted
reimbursement for attending symposium, a fee for speaking, fee
for organizing educational activities, funds for research,
funds for a member of the staff or consultation fees from an
organization that may in any way gain or lose financially from
the results of the study, review, editorial or letter, a
competing interest would be deemed to exist. If any of the
authors had been employed by an organization that may in any
way gain or lose financially from the publication, or if any
of them hold stocks or shares in such an organization,
competing interest would be deemed to exist. If competing
interest exists, the author(s) must disclose them while
submitting the manuscript.
Funding
Authors are also required to
report all financial and material support for the research and
work.
Abstract and Key words
The second page should carry an
abstract in case of research papers (250 words), review
articles (200 words), perspective (150 words), short
communications (100 words), research letter (50 words), and
case report (50 words), respectively. For research papers, the
abstract should be structured using the following headings:
Objective, Design, Setting, Methods, Results, and Conclusions.
For brevity, parts of the abstract may be written as phrases
rather than complete sentences. Each section should include
the following content:
Objective:
State the precise objective or study question addressed in the
paper. If more than one objective is addressed, the main
objective should be indicated and only key secondary
objectives stated.
Design:
Describe the basic design of the study (eg. randomized
controlled trial, case-control study, prospective, cross
sectional etc.).
Setting:
Describe the study setting to assist readers to determine the
applicability of the report to other circumstances, for
example, general community, a primary care or referral center,
private or institutional practice, or ambulatory or
hospitalized care. State the years of the study and the
duration of follow-up.
Participants/patients:
State the numbers of participants, eligibility criteria, and
the selection process. For selection procedures, these terms
should be used, if appropriate: random sample (where random
refers to a formal, randomized selection in which all eligible
individuals have a fixed and usually equal chance of
selection); population-based sample; referred sample;
consecutive sample; volunteer sample; or convenience sample.
Include the number of otherwise eligible individuals who were
approached but refused. If matching is used for comparison
groups, characteristics that are matched should be specified.
Provide key sociodemographic features of participants. In
follow-up studies, indicate the proportion of participants who
completed the study. For intervention studies, mention the
number of patients withdrawn because of adverse effects.
Intervention:
The essential features of any interventions should be
described, including their method and duration of
administration. The intervention should be named by its most
common clinical name, and nonproprietary drug names should be
used. Include any co-intervention.
Main Outcome Measure(s):
Indicate the primary study outcome measurement(s) as planned
before data collection began. If the manuscript does not
report the main planned outcomes of a study, this fact should
be stated and the reason indicated. State clearly if the
hypothesis being tested was formulated during or after data
collection. Explain outcomes or measurements unfamiliar to a
general medical readership.
Results:
The main outcomes of the study should be reported and
quantified, and must include measures of absolute risks (such
as increase/decrease or absolute differences between groups),
along with 95% confidence intervals or P values.
Measures of relative risk also may be reported (eg, relative
risk, hazard ratios) and should include confidence intervals.
Studies of screening and diagnostic tests should report
sensitivity, specificity, and likelihood ratio. All randomized
controlled trials should include the results of
intention-to-treat analysis, and all surveys should include
response rates.
Conclusions:
Provide only conclusions of the study directly supported by
the results, along with implications for clinical practice.
Avoid speculation and overgeneralization of the results.
Emphasize equally the important positive and negative
findings.
Abstract for Short
Communications. The abstract
should be unstructured and state the purpose of the study,
basic methodology, main findings (giving specific data and
statistical significance) and key conclusion(s), within 100
words. Below the abstract, authors should provide 3-5 key
words for indexing; terms from the Medical Subject Headings
(MESH) list of Index Medicus should be used.
Abstract for Reviews:
Review articles should include an abstract of no more than 250
words with the following sections: Context (describing the
clinical question or issue and its importance in clinical
practice or public heath), Evidence acquisition (describing
the data sources used, including the search strategies, years
searched, and other sources), Results (major findings of the
review with the greatest emphasis laid on the findings based
on highest quality evidence), and Conclusions (emphasize how
clinicians should apply current knowledge).
Introduction
The introduction must clearly
justify and state the question that the author(s) tried to
answer in the study. It may be necessary to briefly review the
relevant literature. Cite only those references that are
essential to justify the proposed study.
Methods
The methods section should
describe, in logical sequence, how the study was designed (e.g.
how randomization was done), carried out (e.g. how
subjects were chosen or excluded, ethical considerations,
accurate details of materials used, exact drug dosage and form
of treatment etc.) and data were analyzed (e.g.
an estimate of the power of the study, exact test used for
statistical analysis etc.). For standard methods,
appropriate references are sufficient, but if standard methods
are modified these should be clearly brought out. Authors
should provide complete details of any new methods or
apparatus used (manufacturer's name and address in
parentheses).
Ethics:
All studies involving human subjects
must address the ethical issues. When reporting experiments on
human subjects, indicate whether the procedures followed were
in accordance with the ethical standards of the responsible
committee on human experimentation (institutional or regional)
and with the Helsinki Declaration of 1964, as revised in
2004(14). All such studies should have obtained ethical
clearance in writing from a formally constituted Research
Ethics Committee or Institutional Review Board as the case may
be. Indian Pediatrics reserves the right to demand a copy of
the relevant document whenever necessary. Even when a study
has been approved by a research ethics committee or
institutional review board, editors may be worried about the
ethics of the work. Editors may then ask authors for more
detailed information and ask them how they justified the
ethical and moral basis of the work. Editors may also ask
authors to provide the contact details of the research ethics
committee that reviewed the work, so that the journal can
request further information and justification from that
committee. For studies that have not been reviewed by research
ethics committees or institutional review boards editors may
ask authors to explain what ethical issues they considered and
how they justified their work. Editors may consult other
editorial colleagues, association of medical editors or more
commonly the “Ethical Committee” of Indian Pediatrics to
evaluate the ethical aspects of any article, and reserve the
right to reject a manuscript on ethical grounds, on the basis
of recommendations of its “Ethical Committee”, even if the
research was cleared by the institutional research board.
Besides rejecting the manuscript, Indian Pediatrics reserves
the right of explaining such concerns to the head of the
authors’ institution or medical council in order to prevent
unethical practice and to protect patients.
Informed consent must
be obtained in writing from all human participants of a trial.
Indian Pediatrics reserves the right of seeking from the
authors the details of the information given to subjects about
the deviations from the normal, the risks involved and the
potential benefits to the society. Authors should not use
patients' names, initials, or hospital numbers, especially in
illustrative material. Written consent must be obtained from
patients or caregivers for publication (in print or electronic
form) of clinical details or/and clinical photographs in all
‘Case Reports’, ‘Images’ and qualitative research reports. The
identity of the patient in clinical photographs should be
masked by suitable methods.
Statistics:
Describe statistical methods with
enough detail to enable a knowledgeable reader with access to
the original data to verify the reported results. When
possible, quantify findings and present them with appropriate
indicators of measurement error or uncertainty (such as
confidence intervals). Provide actual P values, rather
than stating as just < 0.05 or > 0.05 etc. References for the
design of the study and statistical methods should be to
standard works when possible (with pages stated) rather than
to papers in which the designs or methods were originally
reported. Specify any general-use computer programs used.
Define statistical terms, abbreviations, and most symbols.
Results
This section should include only
relevant, representative data and not all information
collected during the study. Major findings should be presented
clearly and concisely. Text, tables, and illustrations should
be used sensibly. Avoid repeating in the text all the data
depicted in the tables or illustrations; emphasize or
summarize only important observations. Restrict tables and
figures to those needed to explain the argument of the paper
and to assess its support. Cite the tables in the text and
type them on separate sheets. It may also be useful to mention
what the study did not find.
Discussion
Discussion ordinarily should not
be more than one third of the total length of the manuscript.
Do not attempt a detailed review of literature. This section
should include, in the order specified: (i) a summary of the
major findings, (ii) their relationship to other similar
studies, (iii) strength and limitations of methods and (iv)
implications of these findings in future research. Conclusions
should be linked to the goals of the study. Avoid unqualified
statements and conclusions not completely supported by the
data. Authors should also refrain from making statements on
economic benefits and costs unless their manuscript includes
economic data and analyses.
Acknowledgments
List all contributors who do not
meet the criteria for authorship, such as a person who
provided purely technical help, writing assistance, or a
department head who provided only general support. Financial
and material support should also be acknowledged. Groups of
persons who have contributed materially to the paper but whose
contributions do not justify authorship may be listed under a
heading such as “clinical investigators” or “participating
investigators,” and their function or contribution should be
described – for example, “served as scientific advisers,”
“critically reviewed the study proposal,” “collected data,” or
“provided and cared for study patients.” A written consent is
required from all the persons acknowledged, indicating their
acceptance for the same.
References
Authors need to be accurate in
citing and quoting references(15). References should be
numbered consecutively in the order in which they are first
mentioned in the text. Identify references in text, tables,
and legends by Arabic numerals in curved parentheses.
References cited only in tables or in legends to figures
should be numbered in accordance with the sequence established
by the first identification in the text of the particular
table or figure.
Use the style of the examples
below. The titles of journals should be abbreviated according
to the style used in Index Medicus. Do not use
abstracts, unpublished observations and personal
communications as references. References to papers accepted
but not yet published should be designated as "in press";
authors should obtain written permission to cite such papers
as well as verification that they have been accepted for
publication.
The references must be verified by
the author against the original documents. The Uniform
Requirements style (the Vancouver style) is based
largely on an American National Standards Institute (ANSI)
standard style adapted by the NLM for its databases.
Article in journals
List all authors when six or less.
When seven or more, list only first six and add et al.
Swaminathan S, Datta M, Radhamani MP, Mathew S, Reetha AM,
Rajajee S, et al. A profile of bacteriologically
confirmed pulmonary tuberculosis in children. Indian Pediatr
2008; 45: 743-747.
Organization as author
Working Group on Management of
Congenital Heart Diseases in India. Consensus on timing of
intervention for common congenital heart disease. Indian
Pediatr 2008; 45: 117-126.
Polio Eradication Committee,
Indian Academy of Pediatrics (PEC,IAP), Vashishtha VM, John
TJ, Agarwal RK, Kalra A. Universal immunization program and
polio eradication in India. Indian Pediatr 2008; 45: 807-813.
Personal author
Singh M. Care of the Newborn, 5th
ed. New Delhi: Sagar publications; 1999.
Chapter in a book
Gupta P, Shah D, Ghai OP.
Micronutrients in health and disease. In: Ghai
OP, Gupta P, Paul VK, editors. Ghai Essential
Pediatrics. 6th ed. New Delhi: CBS Publishers & Distributors;
2004. p. 119-135.
Conference proceedings
Kimura J, Shibasaki H, editors.
Recent advances in clinical neurophysiology. Proceedings of
the 10th International Congress of EMG and Clinical
Neurophysiology; 1995 Oct 15-19; Kyoto, Japan. Amsterdam:
Elsevier; 1996.
Conference paper
Mukherjee DK, Chowdhury BH, Das
MM. Intrauterine growth of low birth weight babies and its
relation to various placental and maternal factors- A
multifaceted study. In: Choudhury P, Sachdev HPS, Puri RK,
Verma IC, editors. 8th Asian Congress of
Pediatrics; 1994 Feb 6-11; New Delhi, India. New Delhi: Jaypee
Brothers; 1994. p. 36.
Newspaper article
Bacteria boost. Hindustan Times
2008 Nov 23; New Delhi: p.19 (col 1-4).
Dictionary and similar
references
Stedman's medical dictionary. 26th
ed. Baltimore: Williams & Wilkins; 1995. Apraxia; p. 119-120.
Unpublished accepted material
Gupta N, Shah D, Singh U, Tiwari
A. Antenatal diagnosis of large sacro-coccygeal teratoma with
fetal cardiomegaly and hydrops. Kathmandu Univ Med J. In press
2008.
Material from Internet
The IMRAD Research Paper Format.
FIN-1 Finnish Institutions Research Paper (Hopkins),Department
of Translation Studies, University of Tampere. Available from:
URL: http://www.uta.fi/FAST/FIN/RESEARCH/imrad.html. Accessed
November 24, 2008.
International Committee of Medical
Journal Editors. Sponsorship, Authorship, and Accountability.
Available from: URL: http://www.icmje.org/sponsor.htm.
Accessed November 24, 2008.
Electronic material
Neonatal Resuscitation Program
(NRP) Training Aids [on CD-ROM]. National Neonatology Forum,
New Delhi, 2006.
Hemodynamics III: the ups and
downs of hemodynamics [computer program]. Version 2.2. Orlando
(FL): Computerized Educational Systems; 1993.
Tables
Type each table with
double-spacing on a separate sheet of paper. Do not submit
tables as photographs. Number tables consecutively (Roman
numerals) in the order of their first citation in the text,
and supply a brief but self-explanatory title for each. Tables
with only two columns should be avoided. Give each column a
short or abbreviated heading. Place explanatory matter in
footnotes, not in the heading. Explain in footnotes all
nonstandard abbreviations that are used in each table. For
footnotes use the following symbols, in this sequence:
*, † , ‡, §, ||, ¶, **,††, ‡‡, §§ and so
on. Identify statistical measures of variations such as
standard deviation and standard error of the mean. Do not use
internal horizontal and vertical rules. Be sure that each
table is cited in the text. If data is used from another
published or unpublished source, obtain permission and
acknowledge them fully.
Figures and Illustrations
Figures should be professionally
drawn and photographed; freehand or typewritten lettering is
unacceptable. Instead of original drawings, x-ray films, and
other material, send sharp, glossy, black-and-white
photographic prints of high quality, usually 127 x 173 mm (5 x
7 in) but no larger than 203 x 254 mm (8 x 10 in). For color
illustrations, provide negatives or positive transparencies,
along with color prints. Except for images section, color
photographs are not accepted, except for images section. It is
preferable to have the photograph in portrait form rather than
in landscape form to fit easily into one column. Letters,
numbers, and symbols in photographs should be clearly legible.
Each figure should have a label
pasted on its back indicating the number of the figure,
author's name, and an arrow to mark the top and left side of
the figure. Do not write on the back of figures or
scratch or mar them by using paper clips. Do not bend
figures or mount them on cardboard.
If photographs of
individual/people are used, either the subjects must not be
identifiable or their pictures must be accompanied by written
permission to use the photograph. It is advisable to cover the
eyes unless specifically need to be shown. If a figure has
been published, acknowledge the original source and submit
written permission from the copyright holder to reproduce the
material. Figures should be numbered consecutively (Arabic
numerals) according to the order in which they have been first
cited in the text.
Legends for Illustrations
Type or print out legends for
illustrations using double-spacing, starting on a separate
page, with Arabic numerals corresponding to the illustrations.
When symbols, arrows, numbers, or letters are used to identify
parts of the illustrations, identify and explain each one
clearly in the legend. Explain the internal scale and identify
the method of staining in photomicrographs.
Units of Measurement
Measurements of length,
height, weight, and volume should be reported in metric units,
i.e. meter(m), gram(g), or liter(L) or their decimal
multiples. Milliliter or deciliter should be expressed as mL
or dL and not ml/dl. Red and White blood cell counts are to be
expressed as ´106/mL
and ´103/mL
respectively. Temperatures should be given
in degrees Celsius. Blood pressures should be given in
millimeters of mercury (mm Hg). All hematological and clinical
chemistry measurements should be reported in the conventional
system or in terms of the International System of Units (SI)
(See Annexure III).
Abbreviations and Symbols
Use only standard abbreviations.
Avoid abbreviations in the title and abstract. The full term
for which an abbreviation stands should precede its first use
in the text unless it is a standard unit of measurement. Year,
month, day, hour, minute and second should be abbreviated as
yr, mo, d, h, min, and s respectively.
References
1.
Gupta P, Choudhury
P. Impact factor and Indian Pediatrics. Indian Pediatr 2006;
43: 107-110.
2.
Gupta P, Kaur G,
Sharma B, Shah D, Choudhury P. What is submitted and what gets
accepted in Indian Pediatrics: Analysis of submissions, review
process, decision making, and criteria for rejection. Indian
Pediatr 2006; 43: 479-489.
3.
International
Committee of Medical Journal Editors. Uniform Requirements for
Manuscripts Submitted to Biomedical Journals. Ann Intern Med
1997; 126: 36-47. (Updated October 2007 version Available
from: URL: http://www.icmje.org. Accessed November 22, 2007).
4.
Moher M, Schulz KF,
Altman DG, for the CONSORT Group. The CONSORT Statement:
revised recommendations for improving the quality of reports
of parallel group randomized trials. Lancet 2001; 357:
1191-1194. (Also available from: URL:
http://www.consort-statement.org. Accessed November 21, 2007).
5.
Altman DG, Schulz
KF, Moher D, Egger M, Davidoff F, Elbourne D, et al.
for the CONSORT Group. The revised CONSORT statement for
reporting randomized trials: explanation and elaboration. Ann
Intern Med 2001; 134: 663-694. (Also available from: URL:
http://www.consort-statement.org. Accessed November 21, 2007).
6.
Bossuyt PM, Reitsma
JB, Bruns DE, Gatsonis CA, Glasziou PP, Irwig LM, et al.
for the STARD Group. Towards complete and accurate reporting
of studies of diagnostic accuracy: The STARD Initiative. Clin
Chem 2003; 49: 1-6.
7.
STROBE statement:
Checklist of essential items Version 3 (Sept 2005). Available
from: URL: http://www.equator-network.org/index.aspx?o=1051.
Accessed November 21, 2007.
8.
Moher D, Cook DJ,
Eastwood S, Olkin I, Rennie D, Stroup DF. Improving the
quality of reports of meta-analyses of randomised controlled
trials: The QUOROM statement. Quality of Reporting of
Meta-Analyses. Lancet. 1999; 354: 1896–1900.
9.
Stroup DF, Berlin
JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al.
for the Meta-analysis of observational studies in epidemiology
(MOOSE) Group. Meta-analysis of observational studies in
epidemiology: a proposal for reporting. JAMA 2000; 283:
2008-2012.
10.
Clinical Trials
Registry - India. National Institute of Medical Statistics
(ICMR). Available from: URL:
http://www.ctri.in/Clinicaltrials/trials_jsp/index.jsp.
Accessed November 18, 2008.
11. Institute
of Medicine. Guidelines for Clinical Practice: From
Development to Use. Washington
DC: National Academy Press; 1992.
12. Shiffman RN,
Shekelle P, Overhage JM, Slutsky J, Grimshaw J, Deshpande AM.
Standardized Reporting of Clinical Practice Guidelines: A
proposal from the Conference on Guideline Standardization. Ann
Intern Med 2003; 139: 493-498.
13.
Gupta P, Choudhury
P. Declaring competing interests. Indian Pediatr 2003; 40:
3-6.
14.
52nd WMA
General Assembly. World Medical Association Declaration of
Helsinki. Ethical principles for medical research involving
human subjects. Adopted 1964. Updated 2004. Available from:
URL: http://www.wma.net/e/policy/b3.htm. Accessed October 11,
2006.
15.
Gupta P, Yadav M, Mohta A, Choudhury P. References in Indian
Pediatrics: Authors need to be accurate. Indian Pediatr 2005;
42: 140-145.
Authorship Criteria and Responsibility, Financial Disclosure,
Acknowledgment, and Copyright Transfer Form
Manuscript no. IP/200 /
Manuscript Title
I/We certify that the manuscript
represents valid work and that neither this manuscript nor one with
substantially similar content under my/our authorship has been published
or is being considered for publication elsewhere. For papers with more
than 1 author, We agree to allow the corresponding author to serve as
the primary correspondent with the editorial office, to review the
edited typescript and proof.
I/We have seen and approved
the submitted manuscript. All of us have participated sufficiently in
the work to take public responsibility for the contents. All the authors
have made substantial contributions to the intellectual content of the
paper and fulfil at least 1 condition for each of the 3 categories of
contributions: i.e., Category 1 (conception and design, acquisition of
data, analysis and interpretation of data), Category 2 (drafting of the
manuscript, critical revision of the manuscript for important
intellectual content) and Category 3 (final approval of the version to
be published).
I/We also certify that all
my/our affiliations with or financial involvement with any organization
or entity with a financial interest in or financial conflict with the
subject matter or materials discussed in the manuscript are completely
disclosed on the title page of the manuscript. My/our right to examine,
analyze, and publish the data is not infringed upon by any contractual
agreement.
I/We certify that all persons who have made substantial contributions to
the work reported in this manuscript (e.g., data collection, writing or
editing assistance) but who do not fulfill the authorship criteria are
named along with their specific contributions in an acknowledgment
section in the manuscript. If an acknowledgment section is not included,
no other persons have made substantial contributions to this manuscript.
I/We also certify that all persons named in the acknowledgment section
have provided written permission to be named.
The author(s) undersigned hereby transfer(s), assign(s),
or otherwise convey(s) all copyright ownership, including any and all
rights incidental thereto, exclusively to the Indian Pediatrics, in the
event that such work is published in Indian Pediatrics.
Authors’ name(s) in order of appearance in the manuscript
Signatures (date)
1.
2.
3.
4.
Manuscript Submission Checklist
Submitted by: Email/post/both
Covering Letter and Submission
1. Covering letter (in original)
2. Copyright transfer form (in original)
3. Illustrations (in original)
4. Manuscript (E-mail/original)
5. Category for which submitted
6. Number of authors restricted as per instructions
7. Word count restricted as per instructions.
Presentation and Format
1. Printed on A4 paper with 1” margins on all sides in double space
2. Abstract, text, acknowledgement, what is already known and what
this study adds, references, legends, tables starting on a new page.
3. Title page contains the following
- Full title of the paper
- Short running title in 40 characters
- Initials, surname and highest degree of authors, affiliation
- Name of Departments/Institution
- Details of Corresponding Authors including email
- Contributor’s credits
- Source of Funding
- Competing interests
- Word count of the text
4. Abstract and Key
words provided (for research papers, short communications,
Perspective, case reports, research letters and reviews)
5. “What is already known” and “What this
study adds” Boxes (only for research papers and short
communications)
6. References cited in parenthesis
according to journals instructions.
7. Pages numbered consecutively.
Language and Grammar
1. Uniform American English
2. Abbreviations spelt out in full for first time
3. Text arranged as per IMRAD format
4. Follows style of writing in Indian Pediatrics
5. Conventional units used throughout manuscript
Tables and Figures
1. No repetition of data in Table/graphs and in text.
2. Figures are black and white (except Images), good quality; with
labels on back.
3. Table numbers in roman numerals and Figure numbers in Arabic
numerals.
4. Correct symbols used for footnotes to tables
5. Figure legends provided
6.
Patient privacy maintained
Units of Measurements
|
Parameter
|
Conventional
Unit |
SI Unit
|
|
Acid
phosphatase |
units/L |
U/L |
|
Alanine aminotransferase (ALT) |
units/L |
U/L |
|
Albumin |
g/dL |
g/L |
|
Alkaline phosphatase |
units/L |
U/L |
|
Ammonia (as NH3) |
µg/dL |
µmol/L |
|
Amylase |
units/L |
U/L |
|
Aspartate aminotransferase (AST)
|
units/L |
U/L |
|
Bicarbonate |
mEq/L |
mmol/L |
|
Bilirubin |
mg/dL |
µmol/L |
|
Paco2
|
mm Hg |
mm Hg |
|
pH
|
pH units |
pH units |
|
Pao2
|
mm Hg |
mm Hg |
|
Calcium |
mg/dL , mEq/L |
mmol/L |
|
Carbon dioxide |
mEq/L |
mmoI/L |
|
Ceruloplasmin |
mg/dL |
mg/L |
|
Chloride |
mEq/L |
mmol/L |
|
Cholesterol |
mg/dL |
mmol/L |
|
Corticotropin (ACTH) |
pg/mL |
pmol/L |
|
Cortisol |
µg/dL |
nmol/L |
|
Creatine |
mg/dL |
µmol/L |
|
Creatine kinase (CK) |
units/L |
U/L |
|
Creatinine |
mg/dL |
µmol/L |
|
Creatinine clearance |
mL/min |
mL/s |
|
Erythrocyte sedimentation rate |
mm/h |
mm/h |
|
Estradiol |
pg/mL |
pmol/L |
|
Estriol |
ng/mL |
nmol/L |
|
Estrone |
ng/dL |
pmoI/L |
|
Ferritin |
ng/mL |
pmol/L |
|
α
-fetoprotein |
ng/mL |
µg/L |
|
Follicle-stimulating hormone |
mIU/mL |
IU/L |
|
Glucose |
mg/dL |
mmol/L |
|
Hematocrit |
% |
proportion of 1.0 |
|
Hemoglobin (whole blood) |
g/dL |
g/L |
|
Insulin |
µIU/mL |
pmol/L |
|
Iron,
total |
µg/dL |
µmol/L |
|
Lead
|
µg/dL |
µmol/L |
|
Lipids (total) |
mg/dL |
g/L |
|
Lipoprotein (a) |
mg/dL |
µmol/L |
|
Magnesium |
mg/dL mEq/L |
mmol/L |
|
Nitrogen, nonprotein |
mg/dL |
mmol/L |
|
Osmolality |
mOsm/kg |
mmoI/kg |
|
Parathyroid hormone |
pg/mL |
ng/L |
|
Phenobarbital |
mg/L |
µmol/L |
|
Phenytoin |
µg/mL |
µmoI/L |
|
Phosphorus |
mg/dL |
mmol/L |
|
Platelets (thrombocytes) |
×103/µL |
×109/L |
|
Potassium |
mEq/L |
mmoI/L |
|
Progesterone |
ng/mL |
nmol/L |
|
Prolactin |
µg/L |
pmol |
|
Protein, total |
g/dL |
g/L |
|
Prothrombin time (PT) |
s |
s |
|
Protoporphyrin, erythrocyte |
µg/dL |
µmol/L |
|
Red
blood cell count |
×106/µL |
×1012/L |
|
Reticulocyte count |
% of RBCs |
Proportion of 1.0 |
|
Sodium |
mEq/L |
mmol/L |
|
Testosterone |
ng/dL |
nmol/L |
|
Thyroglobulin |
ng/mL |
µg/L |
|
TSH
|
mIU/L |
mIU/L |
|
Thyroxine, free (T4)
|
ng/dL |
pmol/L |
|
Thyroxine, total (T4)
|
µg/dL |
nmol/L |
|
Transferrin |
mg/dL |
g/L |
|
Triglycerides |
mg/dL |
mmol/L |
|
Triiodothyronine Free (T3)
|
pg/dL |
pmol/L |
|
Total
(T3) |
ng/dL |
nmol/L |
|
Urea
nitrogen |
mg/dL |
mmol/L |
|
Uric
acid |
mg/dL |
µmol/L |
|
Vitamin A (retinol) |
µg/dL |
µmoI/L |
|
Vitamin B6 (pyridoxine)
|
ng/mL |
nmol/L |
|
Vitamin B12 (cyanocobalamin)
|
pg/mL |
pmol/L |
|
Vitamin C (ascorbic acid) |
mg/dL |
µmol/L |
|
Vitamin D (1,25-Dihydroxyvitamin D)
|
pg/mL |
pmol/L |
|
Vitamin D (25-Hydroxyvitamin D)
|
ng/mL |
nmol/L |
|
Vitamin E |
mg/dL |
µmoI/L |
|
Vitamin K |
ng/mL |
nmol/L |
|
White
blood cell count |
×103/µL |
×109/L |
|
White
blood cell differential count |
% |
proportion of 1.0 |
|
Zinc
|
µg/dL |
µmoI/L 0 |

Figure 1.
Profile of a Randomized Controlled Trial
|