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Panduan Case Report Agha2018
Panduan Case Report Agha2018
Guideline
∗
Corresponding author.
E-mail addresses: mimi.r.borrelli@gmail.com, mimi.r.borrelli@gmail.com (M.R. Borrelli).
https://doi.org/10.1016/j.ijsu.2018.10.028
ai
Università di Padova, Italy
aj
Hyderpora, India
ak
King's College London, UK
al
University Medicine Mainz, Germany
am
Nottingham University Hospitals, UK
an
Campus Biomedco University School of Medicine, Italy
ao
Cairo University, Egypt
ap
University of West Indies, Jamaica
aq
Simplemente Evita Hospital, Argentina
ar
University of Tromsø, Norway
as
Turku University Hospital, Finland
at
Banarus Hindu University, India
au
Texas A&M University, USA
av
Richmond, KY, USA
aw
Wolfson Institute of Preventive Medicine, Queen Mary, University of London, UK
ax
University College London, UK
ABSTRACT
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Surgery Case Reports - a key supporter of the guidelines and a journal authors [9].
where they have been implemented as a mandatory requirement for This update to the SCARE guidelines will help further improve the
submission - were also invited to participate. reporting quality of case reports and we encourage authors, reviewers,
editors and journals to adopt them. Authors should cite the guidelines
2.3. Consensus round in their methods section and upload a completed checklist of com-
pliance for reviewers and editors to inspect. Such checklists will be
Potential contributors were contacted via email. Once participation provided in a variety of formats for easy usage on the SCARE website
was confirmed, the Delphi exercise was circulated. In the first consensus www.scareguideline.com. Additionally, we would encourage ongoing
round, the expert group was asked to indicate whether they agree or research to try and gauge the effectiveness of this revised guideline.
disagreed to suggested changes made to each of the 24 SCARE checklist This approach to guideline development has a number of limita-
items, on a scale of 1 (strongly disagree) to 9 (strongly agree). A two- tions. Firstly, there may be overrepresentation of the editors of a single
week period was given for the initial round of responses and a reminder journal – IJS Case Reports. However, this journal has published 3500
email was sent after one week to those who had not yet responded. As case reports and journal editors often work across multiple journals and
per the previous Delphi exercise, consensus was defined as greater than bring a broad breadth of surgical experience. This was also supple-
70% agreement for an item change. If this was not reached, the item mentary to the existing SCARE group – a broad multidisciplinary group
would remain unchanged. representing 21 countries and all ten surgical specialties as well as al-
lied specialties including; dermatology, pathology, oncology, clinical
3. Results pharmacology, acute care surgery, with many participants also occu-
pying positions on journal editorial boards. Secondly, there are likely to
In total, 56 people agreed to participate and 45 (80%) completed be specific surgical scenarios where other information is pertinent that
the Delphi survey. 16 of these were from the original Delphi exercise in may not be captured by a generic checklist, we encourage the devel-
2016. A summary of the scores is shown below (Table 1). Table 2 shows opment of extensions to these guidelines for such scenarios.
the revised SCARE guidelines.
5. Conclusion
4. Discussion
Updated SCARE guidelines are presented which should now be
The SCARE guidelines have provided a useful guidance to those implemented by authors, reviewers, editors and journals with the aim
writing case reports. Research on their implementation found a statis- of improving reporting quality of surgical case reports in the literature.
tically significant 10% increase in reporting completeness when utilised
[8].
Provenance and peer review
Surgical journals have been slow to take up reporting guidelines. We
have previously reported that of the 193 surgical journals listed in the
Not Commissioned, internally reviewed.
surgery category in the Journal Citation Report 2014, the majority
(62%) made no mention of reporting guidelines within their guide for
Funding
Table 1
SCARE 2.0 Delphi scores. Items indicated are changes made to individual sec- None.
tions of SCARE. Score 1 – Strongly disagree Score 9 – Strongly agree.
Scoring (%) Ethical approval
Following the above, the revised SCARE statement is shown below. NA.
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R.A. Agha et al. International Journal of Surgery 60 (2018) 132–136
Table 2
Revised SCARE guidelines.
SCARE Checklist
Title 1 The words “case report” should appear in the title. The title should also describe the area of focus (e.g. presentation, diagnosis,
surgical technique or device or outcome).
Key Words 2 3 to 6 key words that identify areas covered in this case report (include "case report" as one of the keywords).
Abstract 3a Introduction — Describe what is unique or educational about the case (i.e. what does this work add to the surgical literature,
and why is this important?).
3b Presenting complaint and investigations – describe the patient's main concerns and important clinical findings.
3c The main diagnoses, therapeutics interventions, and outcomes.
3d Conclusion — Describe the main lessons to “take-away” from this case study
Introduction 4 Background – summarise what is unique or educational about the case. Give reference to the relevant surgical literature and
current standard of care. The background should be referenced, and 1–2 paragraphs in length.
Patient Information 5a Demographic details – include de-identified demographic details on patient age, sex, ethnicity, occupation. Where possible,
include other useful pertinent information e.g. body mass index and hand dominance.
5b Presentation - describe the patient's presenting complaint (symptoms). Describe the patient's mode of presentation (brought in
by ambulance or walked into Emergency room or referred by family physician).
5c Past medical and surgical history, and relevant outcomes from interventions
5d Other histories – Describe the patient's pharmacological history including allergies, psychosocial history (Drug, smoking, and if
relevant, accommodation, walking aids), family history including relevant genetic information.
Clinical Findings 6 Describe the relevant physical examination and other significant clinical findings. Include clinical photographs where relevant
and where consent has been given.
Timeline 7 Inclusion of data which allows readers to establish the sequence and order of events in the patient's history and presentation
(using a table or figure if this helps). Delay from presentation to intervention should be reported.
Diagnostic Assessment 8a Diagnostic methods – describe all investigations taken to arrive at methods: physical exam, laboratory testing, radiological
imaging, histopathology.
8b Diagnostic challenges – describe what was challenging about the diagnoses, where applicable, for example access, financial,
cultural.
8c Diagnostic reasoning – Describe the differential diagnoses and why they were considered.
8d Prognostic characteristics when applicable (e.g. tumour staging or for certain genetic conditions). Include relevant radiological
or histopathological images in this section.
Therapeutic Intervention 9a Pre-intervention considerations – if there were patient-specific optimisation measures taken prior to surgery or other
intervention these should be included e.g. treating hypothermia/hypovolaemia/hypotension in a burns patient, Intensive care
unit treatment for sepsis, dealing with anticoagulation/other medications, etc.
9b Interventions – describe the type(s) of intervention(s) deployed (pharmacologic, surgical, physiotherapy, psychological,
preventive). Describe the reasoning behind this treatment offered. Describe any concurrent treatments (antibiotics, analgesia,
anti-emetics, nil by mouth, Venous thrombo-embolism prophylaxis, etc). Medical devices should have manufacturer and model
specifically mentioned.
9c Intervention details – describe what was done and how. For surgery include details on; anaesthesia, patient position, use of
tourniquet and other relevant equipment, prep used, sutures, devices, surgical stage (1 or 2 stage, etc). For pharmacological
therapies include information on the formulation, dosage, strength, route, duration, etc. Include intra-operative photographs
and/or video or relevant histopathology in this section. Degree of novelty for a surgical technique/device should be mentioned
e.g. "first in human".
9d Who performed the procedure - operator experience (position on the learning curve for the technique if established,
specialisation and prior relevant training). For example, “junior resident with 3 years of specialised training”
9e Changes – if there were any changes in the interventions, describe these details with the rationale.
Follow-up and Outcomes 10a Follow-up – describe 1) When the patients was followed up. 2) Where. 3) How (imaging, tests, scans, clinical examination,
phone call), and 4) whether there were any specific post-operative instructions. Future surveillance requirements - e.g. imaging
surveillance of endovascular aneurysm repair or clinical exam/ultrasound of regional lymph nodes for skin cancer.
10b Outcomes - Clinician assessed and (when appropriate) patient-reported outcomes (e.g. questionnaire details). Relevant
photographs/radiological images should be provided e.g. 12 month follow-up.
10c Intervention adherence/compliance - where relevant how well patient adhered to and tolerated their treatment. For example,
post-operative advice (heavy lifting for abdominal surgery) or tolerance of chemotherapy and pharmacological agents
10d Complications and adverse events – all complications and adverse or unanticipated events should be described in detail and
ideally categorised in accordance with the Clavien-Dindo Classification. How they were prevented, diagnosed and managed.
Blood loss, operative time, wound complications, re-exploration/revision surgery, 30-day post-op and long-term morbidity/
mortality may need to be specified. If there were no complications or adverse outcomes this should also be included.
Discussion 11a Strengths – describes the strengths of this case
11b Weaknesses and limitations in your approach to this case. For new techniques or implants - contraindications and alternatives,
potential risks and possible complications if applied to a larger population. If relevant, has the case been reported to the
relevant national agency or pharmaceutical company (e.g. an adverse reaction to a device)
11c Discussion of the relevant literature, implications for clinical practice guidelines and any relevant hypothesis generation.
11d The rationale for your conclusions.
11e The primary “take-away” lessons from this case report.
Patient Perspective 12 When appropriate the patient should share their perspective on the treatments they received.
Informed Consent 13 Did the patient give informed consent for publication? Please provide if requested by the journal/editor. If not given by the
patient, explain why e.g. death of patient and consent provided by next of kin or if patient/family untraceable then document
efforts to trace them and who within the hospital is acting as a guarantor of the case report.
Additional Information 14 Conflicts of Interest, sources of funding, institutional review board or ethical committee approval where required.
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