Example of Drug and Therapeutics Bulletin format
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Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format
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Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format Example of Drug and Therapeutics Bulletin format
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open access Open Access

Drug and Therapeutics Bulletin — Template for authors

Categories Rank Trend in last 3 yrs
Pharmacology (medical) #205 of 246 down down by 10 ranks
journal-quality-icon Journal quality:
Low
calendar-icon Last 4 years overview: 214 Published Papers | 86 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 04/07/2020
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Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

A measure of average citations received per peer-reviewed paper published in the journal.

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.4

33% from 2019

CiteRatio for Drug and Therapeutics Bulletin from 2016 - 2020
Year Value
2020 0.4
2019 0.3
2018 0.3
2017 0.3
2016 0.3
graph view Graph view
table view Table view

0.147

11% from 2019

SJR for Drug and Therapeutics Bulletin from 2016 - 2020
Year Value
2020 0.147
2019 0.132
2018 0.124
2017 0.117
2016 0.119
graph view Graph view
table view Table view

0.263

116% from 2019

SNIP for Drug and Therapeutics Bulletin from 2016 - 2020
Year Value
2020 0.263
2019 0.122
2018 0.04
2017 0.022
2016 0.032
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 33% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased by 11% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 116% in last years.
  • This journal’s SNIP is in the top 10 percentile category.
Drug and Therapeutics Bulletin

Guideline source: View

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BMJ Publishing Group

Drug and Therapeutics Bulletin

For nearly 50 years, DTB has provided rigorous and independent evaluations of, and practical advice on, individual treatments and the overall management of disease for doctors, pharmacists and other healthcare professionals. DTB was started in 1962. From the outset, it has pro...... Read More

Medicine

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Last updated on
04 Jul 2020
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ISSN
0012-6543
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Impact Factor
Low - 0.254
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Open Access
No
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
unsrt
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Citation Type
Numbered
[25]
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Bibliography Example
C. W. J. Beenakker. Specular andreev reflection in graphene. Phys. Rev. Lett., 97(6):067007, 2006.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1136/DTB.2019.000008
How to communicate evidence to patients.
Alexandra L. J. Freeman1

Abstract:

All medical treatments have potential harms as well as benefits, and it is vital that everyone has a good understanding of what these might be, how dramatic they might be and how likely. In fact, in the UK, the Montgomery judgement in the supreme court in 2015 (see Box 1) has made it a legal necessity for patients to be given... All medical treatments have potential harms as well as benefits, and it is vital that everyone has a good understanding of what these might be, how dramatic they might be and how likely. In fact, in the UK, the Montgomery judgement in the supreme court in 2015 (see Box 1) has made it a legal necessity for patients to be given comprehensible, personally relevant information about all reasonable treatment options, including none.1 So, how should we ensure good, clear communication of relevant evidence? Box 1. ### The Montgomery judgement In 1999, Nadine Montgomery was preparing for the birth of her son Sam. She was of small stature, with diabetes, and was concerned about being able to give birth naturally. Unfortunately, difficulties did arise during birth, and Sam suffered brain damage as a result. Her obstetrician had not discussed the risk of this particular complication occurring, deeming it best Nadine attempted a vaginal birth. On appeal at the supreme court, Nadine Montgomery won her case. This laid down a new legal basis for informed consent, in line with the General Medical Council guidelines;1 > “The doctor is therefore under a duty to take reasonable care to ensure that the patient is aware of any material risks involved in any recommended treatment, and of any reasonable alternative or variant treatments.” > > “The test of materiality is whether, in the circumstances of the particular case, a reasonable person in the patient's position would be likely to attach significance to the risk, or the doctor is or should reasonably be aware that the particular patient would be likely to attach significance to it. ” > > “The assessment of whether a risk is material cannot be reduced to percentages. The significance of a given risk is likely to reflect a variety of factors besides its magnitude” > > “The doctor’s advisory role involves dialogue, … read more read less

Topics:

Reasonable person (53%)53% related to the paper
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33 Citations
Journal Article DOI: 10.1136/DTB.2018.000035
Central sensitisation: another label or useful diagnosis?

Abstract:

### Key learning points Chronic pain affects up to 30% of the Western population with a prevalence higher than any other chronic disease.1 Chronic pain is often of a non-specific nature, implying that there is no tissue damage, or that tissue damage is not severe enough to explain the pain experience and/or related symptoms.... ### Key learning points Chronic pain affects up to 30% of the Western population with a prevalence higher than any other chronic disease.1 Chronic pain is often of a non-specific nature, implying that there is no tissue damage, or that tissue damage is not severe enough to explain the pain experience and/or related symptoms. This non-specific nature accounts for non-cancer pain as well as post-cancer pain (ie, pain in cancer survivors). Chronic pain has a significant personal and socioeconomic impact: among long-term conditions, it is responsible for the highest number of years lived with disability and is the most expensive cause of work-related disability.2–4 Chronic pain also decreases life expectancy, in part due to excess deaths from cancer and cardiovascular disease.5–7 Over the past decades, neuroscience has advanced our understanding about pain, including the role of CNS sensitisation—more briefly termed central sensitisation (CS). The original definition for CS—‘an amplification of neural signaling within the CNS that elicits pain hypersensitivity’—originated from laboratory research, but nowadays the chronic pain management field has more or less … read more read less

Topics:

Chronic pain (74%)74% related to the paper, Population (51%)51% related to the paper
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19 Citations
Journal Article DOI: 10.1136/DTB.2018.000028
Overview of Gilbert's syndrome.
D King1, Matthew J. Armstrong1

Abstract:

### Key learning points Gilbert’s syndrome (GS) is a benign hereditary disorder of bilirubin conjugation resulting in an isolated, elevated blood level of unconjugated bilirubin.1 GS affects 2%–10% of the Caucasian population in the Western world.2,3 The inheritance pattern for GS is commonly autosomal recessive, but can be ... ### Key learning points Gilbert’s syndrome (GS) is a benign hereditary disorder of bilirubin conjugation resulting in an isolated, elevated blood level of unconjugated bilirubin.1 GS affects 2%–10% of the Caucasian population in the Western world.2,3 The inheritance pattern for GS is commonly autosomal recessive, but can be dominant as well; however, genetic counselling is not necessary as there is no impact on life expectancy. For the patient, however, the condition may be an initial cause for concern as they commonly present with painless, non-pruritic jaundice or an incidental finding of hyperbilirubinaemia on routine blood testing. Episodes of jaundice may be exacerbated by heavy physical exertion, fasting, sleep deprivation, alcohol, dehydration, surgery and concurrent illness. Patients will have normal liver enzymes, normal liver synthetic function (clotting, albumin) and a negative haemolysis screen. GS is a diagnosis of exclusion. The primary care practitioners’ main aim is to confirm the diagnosis, reassure the patient and clarify any concerns related to the condition. GS does not require secondary care referral and is largely asymptomatic. Observational studies highlight that the antioxidant effect of unconjugated bilirubin may confer a survival benefit to patients,4,5 and indeed, the greatest risk to those with the condition is in pursuit of an alternative diagnosis. Patients should … read more read less

Topics:

Gilbert's syndrome (57%)57% related to the paper, Jaundice (55%)55% related to the paper, Haemolysis (52%)52% related to the paper, Diagnosis of exclusion (52%)52% related to the paper
19 Citations
open accessOpen access Journal Article DOI: 10.1136/DTB.2018.000009
Stopping, rationalising or optimising antipsychotic drug treatment in people with intellectual disability and/or autism.
Rohit Shankar1, Michael Wilcock, Katy Oak, Paula McGowan, Rory Sheehan2

Abstract:

### Key learning points Intellectual disability (ID; also known as learning disability) is characterised by significant impairment of both cognitive functioning and adaptive behaviours, and an onset in early childhood. People with ID experience a different pattern of morbidity to the general population and die considerably y... ### Key learning points Intellectual disability (ID; also known as learning disability) is characterised by significant impairment of both cognitive functioning and adaptive behaviours, and an onset in early childhood. People with ID experience a different pattern of morbidity to the general population and die considerably younger than their counterparts without ID.1 Autism is a neurodevelopmental disorder characterised by troubles with social interaction and communication, and by restricted and repetitive behaviour. In both conditions, complex mental and physical health problems, as well as social issues, are common and are associated with communication difficulties that can result in maladaptive behavioural patterns (often referred to as ‘behaviour that challenges’). Ideally, all people presenting with behaviour that challenges should be assessed by a specialist multidisciplinary team (comprising psychiatrists, psychologists, speech and language therapists, occupational therapists) to develop an understanding of the behaviour and an appropriate support plan with tailored treatment strategies and specialist follow-up.2 Non-pharmacological interventions for challenging behaviour, such as positive behavioural support or cognitive–behavioural therapy and manipulation of environmental triggers, are preferred to psychotropic medication. However, antipsychotic medication is often prescribed to adults with ID and/or autism to manage behaviour that challenges in the absence of severe mental illness, despite there being little research evidence that antipsychotics are effective in this context.3 There … read more read less

Topics:

Challenging behaviour (63%)63% related to the paper, Intellectual disability (59%)59% related to the paper, Autism (56%)56% related to the paper, Mental illness (56%)56% related to the paper, Learning disability (55%)55% related to the paper
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16 Citations
open accessOpen access Journal Article DOI: 10.1136/DTB.2018.10.000007
Where now for opioids in chronic pain

Abstract:

Video 1 ### Key learning points Chronic pain has always been and will remain difficult to manage. There have been important developments in our understanding of the neurobiology of pain, but perhaps the greatest advance is our ability to analyse trial data more critically and to realise that we may have been wrongly opti... Video 1 ### Key learning points Chronic pain has always been and will remain difficult to manage. There have been important developments in our understanding of the neurobiology of pain, but perhaps the greatest advance is our ability to analyse trial data more critically and to realise that we may have been wrongly optimistic about the use of some therapies. Although the publication of high-quality literature reviews may have reduced our therapeutic options, it also provides an opportunity to improve patient care by ensuring that we are not exposing patients with pain, whose lives are difficult enough as it is, to the harms of medicines that do not help them. In particular, there is a need to reconsider the place of opioids in the management of chronic pain. This includes the so-called weak opioids (eg, codeine and dihydrocodeine), and strong opioids (eg, morphine, oxycodone, fentanyl and buprenorphine), as well as tramadol (a non-selective agonist at mu, delta and kappa opioid receptors with monoaminergic properties), which should be considered alongside the strong opioids. Opioids emerged into the chronic pain management scene in the 1990s. The recognition of their potent role in the management of acute and end-of-life pain, the inappropriate adoption of WHO analgesic ladder designed for … read more read less

Topics:

Chronic pain (62%)62% related to the paper, Oxycodone (56%)56% related to the paper, Buprenorphine (53%)53% related to the paper
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14 Citations
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Drug and Therapeutics Bulletin format uses unsrt citation style.

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Frequently asked questions

1. Can I write Drug and Therapeutics Bulletin in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Drug and Therapeutics Bulletin guidelines and auto format it.

2. Do you follow the Drug and Therapeutics Bulletin guidelines?

Yes, the template is compliant with the Drug and Therapeutics Bulletin guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Drug and Therapeutics Bulletin?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Drug and Therapeutics Bulletin citation style.

4. Can I use the Drug and Therapeutics Bulletin templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Drug and Therapeutics Bulletin.

5. Can I use a manuscript in Drug and Therapeutics Bulletin that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Drug and Therapeutics Bulletin that you can download at the end.

6. How long does it usually take you to format my papers in Drug and Therapeutics Bulletin?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Drug and Therapeutics Bulletin.

7. Where can I find the template for the Drug and Therapeutics Bulletin?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Drug and Therapeutics Bulletin's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Drug and Therapeutics Bulletin's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Drug and Therapeutics Bulletin an online tool or is there a desktop version?

SciSpace's Drug and Therapeutics Bulletin is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Drug and Therapeutics Bulletin?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Drug and Therapeutics Bulletin?”

11. What is the output that I would get after using Drug and Therapeutics Bulletin?

After writing your paper autoformatting in Drug and Therapeutics Bulletin, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Drug and Therapeutics Bulletin's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Drug and Therapeutics Bulletin?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Drug and Therapeutics Bulletin. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Drug and Therapeutics Bulletin?

The 5 most common citation types in order of usage for Drug and Therapeutics Bulletin are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Drug and Therapeutics Bulletin?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Drug and Therapeutics Bulletin's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Drug and Therapeutics Bulletin in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Drug and Therapeutics Bulletin Endnote style according to Elsevier guidelines.

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