EMQs in MRCOG P1
EMQs in MRCOG P1
EMQs in MRCOG P1
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10.1576/toag.9.3.189.27340 www.rcog.org.uk/togonline
2007;9:189194
Education
Key content:
Extended Matching Questions (EMQs) are going to be introduced into the Part 1
MRCOG examination from September 2007.
One of the main aims is to direct the learning of aspects of biological sciences that
are relevant to the clinical practice of obstetrics and gynaecology.
The advantages of the EMQ format over the multiple-choice format include the
ability to test a candidates understanding of the relationship between facts.
Learning objectives:
To understand how the EMQ format can lead to better testing of knowledge of
basic and clinical sciences and increased examination validity.
To be aware of the additional discrimination EMQs have demonstrated in the first
Part 2 paper.
To be aware of the new bioscience and curriculum context of the MRCOG
examinations.
Ethical issues:
Improving the reliability and validity of the Part 1 MRCOG examination
contributes to setting standards in women's health.
Keywords EMQs / MCQs / Part 1 MRCOG
Please cite this article as: Duthie S, Fiander A, Hodges P. EMQs: a new component of the MRCOG Part 1 examination. The Obstetrician & Gynaecologist 2007;9:189194.
Author details
Suresh Duthie FRCOG
Consultant Obstetrician and
Gynaecologist
Blackpool, Fylde and Wyre Hospitals NHS
Trust, Blackpool Victoria Hospital, Whinney
Heys Road, Blackpool FY3 8NR, UK
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Introduction
What is the best way to prepare a doctor to become
a specialist obstetrician and gynaecologist in this
new century? Clinical and medical science is
growing faster than ever and investigations and
treatments derived from the new bioscience of the
1980s and 1990s are now having an impact on
clinical practice. Clinical consultants are being
asked to use these tools properly and to advise
women of their use. Senior clinicians need to be
able to engage with scientific innovations,
understand the opportunities and limitations of
new techniques and tools introduced into medicine
and to be confident when appraising new
technologies. This confidence can only follow from
an adequate grounding in clinical science.
Ultrasound, laparoscopy, in vitro fertilisation, fetal
blood sampling and prenatal diagnosis are now all
used in day-to-day clinical practice. Molecular
biology and genetics have clinical applications in
prenatal diagnosis, gynaecological oncology and
reproductive medicine. Advances in gene therapy
and stem cell science will, undoubtedly, be
translated into practice in the next decade. Clinical
epidemiology, statistics and an understanding of
clinical risk are other relatively new concepts that
are becoming increasingly deeply embedded within
clinical practice. In contrast, some subjects that the
doctor in training needs to know are unchanging,
such as embryology and the surgical anatomy of the
pelvis. Knowledge continues to be the single best
determinant of expertise in a subject1 and it
remains essential that a doctor in training
understands, assimilates and retains knowledge of
the basic and clinical sciences. The aim of the Part 1
MRCOG is, therefore, to direct the learning of
aspects of biological science that are relevant to the
clinical practice of obstetrics and gynaecology.
The new Core Curriculum allows the MRCOG
examinations to be blueprinted2 and maps the
Part 1 MRCOG as a component part of the overall
process of assessment for future consultants in the
specialty.3 The Part 1 and Part 2 MRCOG
examinations will, from September 2007, form a
single integrated and blueprinted examination of
relevant factual knowledge and clinical skills in the
specialty. Various preparations have been made for
this endpoint, including the ending of the
exemption scheme for Part 1.
The new syllabus will be clearer, better defined and
less broad than that currently in place. However, as
mentioned above, the syllabus has been updated to
include important new bioscience topics.4 This is so
throughout the syllabus and is made particularly
explicit in the Core Curriculum Matrix. Topic areas
included as distinct areas for the first time include:
virology, clinical trial design and analysis,
molecular and cell biology, genomics and
regulation of gene expression.
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a list of options
a lead-in statement
items (questions).
In the examination a single EMQ will consist of a
list of options with one to four items or questions,
avoiding overemphasis on a single subject. In
answering EMQs, candidates are advised not to
read through the list of options first to avoid being
wrongly cued by distractors among them. The leadin statement and then the items or questions should
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Table 1
Discrimination
descriptor
Overall point
biserial figure
range
Percentage of MCQ
format questions
achieving
Percentage of
EMQ format
questions
achieving
Moderate to high
High
Very high
0.10.3
0.30.4
0.4
50.4
4.4
1.3
57.5
27.5
10.0
TRUE/FALSE
Figure 1
Figure 2
Options
Example 2 (EMQ 1)
Maternal disease
Type
Babesiosis
Protozoan
No
Babesiosis
Protozoan
Yes
Coccidioidomycosis
Fungus
No
Coccidioidomycosis
Fungus
Yes
Malaria
Bacterium
Yes
Malaria
Protozoan
No
Malaria
Protozoan
Yes
Malaria
Virus
Yes
Fever
Rickettsia
Yes
Q fever
Virus
Yes
Schistosomiasis
Helminth
Yes
Schistosomiasis
Protozoan
Yes
Syphilis
Protozoan
Yes
Syphilis
Spirochete
No
Syphilis
Spirochete
Yes
Syphilis
Virus
Yes
Tuberculosis
Bacterium
No
Tuberculosis
Bacterium
Yes
Tuberculosis
Fungus
No
Tuberculosis
Protozoan
No
Instructions: The options above refer to different maternal diseases caused by micro-organisms, the type of organism and
whether there is a risk of transplacental infection. Select the single correct profile for each of the micro-organisms in the items
below. Each option may be used once, more than once or not at all.
ITEM 1
Treponema pallidum
Answer
O. Syphilis; Spirochete; Yes
ITEM 2
Mycobacterium tuberculosis
Answer
R. Tuberculosis; Bacterium; Yes
ITEM 3
Plasmodium falciparum
Answer
G. Malaria; Protozoan; Yes
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Options
A
Embryological origin
Endoderm epithelium
Catecholamines
Neural crest
Catecholamines
Mesonephric duct
Neural crest
Catecholamines
Paramesonephric duct
Endoderm epithelium
Cortisol
Instructions: The list of options describes the profile of human organs in terms of embryological origin, the substances that are produced at that particular site and the
arterial blood supply. Select the most closely matching profile for each of the structures in the items below from the list of options. Each option may be used once, more
than once or not at all.
ITEM 1
Adrenal cortex
Answer
B
ITEM 2
Adrenal medulla
Answer
D
Figure 3
Example 3 (EMQ 2)
Figure 4
Example 4 (EMQ 3)
3-hydroxyisovaleric acid
17 -hydroxyprogesterone
17 -hydroxyprogesterone
17 -hydroxyprogesterone
Acetic acid
Adrenocorticotrophic hormone
Bilirubin
Ceramide trihexoside
Citrulline
Cortisol
K`
Cystine
Galactitol
Glutaric acid
Insulin
Methylmalonic acid
Succinylacetone
ITEM 1
Congenital adrenal hyperplasia
Answer
B.
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17 -hydroxyprogesterone
Examples
Example 1 (Figure 1) is a typical true/false MCQ
Part 1 question, which most candidates should be
able to answer successfully. Those who do not
know the answer have a 50:50 chance of guessing
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Options
A
Ovarian cancer
Retinoblastoma
Education
Figure 5
Example 5 (EMQ 4)
ITEM 2
BRCA2
Answer
C.
ITEM 3
Answer
Hereditary retinoblastoma
T.
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Figure 6
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Conclusion
The key points are:
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