Impact of Medical Conditions Flashcards

1
Q

Give examples of medically compromising conditions? (7)

A
  • Cardiovascular (& down’s syndrome)
  • Respiratory
  • Childhood cancer
  • Chronic renal failure
  • Diabetes mellitus
  • Epilepsy
  • Common coagulation defects
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2
Q

Give examples of the aetiology of cardiovascular conditions? (5)

A
  • Maternal rubella
  • Maternal diabetes
  • Maternal drugs - alcohol, phenytoin
  • Foetal chromosome abnormality - Down’s syndrome
  • Foetal inborn errors of metabolism and connective tissue disorder - William’s syndrome
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3
Q

How many people per 1000 have congenital heart disease?

A

1-8 per 1000

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4
Q

Give examples of congenital heart diseases?

A

Cyanotic:

  • Fallot tetralogy
  • Transposition great arteries TGA

Acyanotic:
- VSD, PDA, S, ASD, CoA, AS

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5
Q

What do we need to consider when giving dental treatment to someone with a congenital heart defect? (4)

A
  • Importance of good oral hygiene in preventing infective endocarditis
  • Follow NICE guidelines, any doubt consult cardiologist
  • Anticoagulant medication
  • Treatment under sedation
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6
Q

CHD can have a huge impact. Where can children contact to get more information and support? (4)

A
  • If they are under 11 years old their parents or guardians might find understanding your child’s heart books helpful
  • If they are 13-19 years old they might like to get involved in our meet@teenheart programme that supports young heart patients
  • If they are over 19 we have lots of information on out main website about living with a heart condition and the tests and treatments they might need
  • Anyone can call our heart helpline for information and support. Phone lines are open 9am-5pm Monday to Friday
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7
Q

How should we NOT describe a person with Down’s syndrome? (5)

A
  • Suffers from OR is a victim of DS
  • A Down’s baby/person/child
  • Retarded/mentally handicapped/backward/mental disability
  • Disease/illness/handicap
  • The risk of a baby having down’s syndrome (in relation to pre-natal screening and probability assessments)
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8
Q

How SHOULE we describe a person with Down’s syndrome? (5)

A
  • Has down’s syndrome
  • A person/baby/child with down’s syndrome or who has down’s syndrome
  • Learning disability
  • Condition OR genetic condition
  • The chance of a baby having down’s syndrome
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9
Q

What are myths of people with Down’s syndrome? (5)

A
  • People with DS don’t live very long
  • Only older mothers have babies with DS
  • People with DS cannot achieve normal life goals
  • People with DS all look the same
  • People with DS are always happy and affectionate
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10
Q

What age are people with Down’s syndrome commonly living to currently?

A
  • Today, people with Down’s syndrome are living into their 50’s and 60’s with a small number living into their 70’s and beyond
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11
Q

Why is the statement ‘only older mother’s have babies with DS’ not true?

A
  • Although older mothers have a higher individual chance of having a baby with DS, are are born to younger mothers, reflecting the high birth rate in this group
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12
Q

Why is the statement ‘People with down’s syndrome cannot achieve normal life goals’ not true?

A
  • With the right support, they can. Small but increasing numbers of people with DS are leaving home and living with support in their communities. They are gaining employment, meeting partners and getting the best out of life
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13
Q

Why is the statement ‘People with DS all look the same’ not true?

A
  • There are certain physical characteristics that can occur. Each person will have a number of the more common physical characteristics. A person with DS will always look more like his or her close family than someone else with the condition
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14
Q

Why is the statement ‘People with DS are always happy and affectionate’ not true?

A
  • We are all individuals and people with DS are no different to anyone else in their character traits and have varying moods
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15
Q

How many people with DS tend to have a congenital heart lesion?

A
  • Found in 50%

- ASD, VSD, AV canal

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16
Q

People with DS are more likely to suffer from duodenal atresia. What is this?

A
  • Duodenal atresia is a rare condition that’s present at birth. It is a malformation of the duodenum , which is the section of the small intestine that receives food directly from the stomach. The condition can cause severe vomiting in newborns, and it can also cause some signs during pregnancy, including large amounts of fluid surrounding the growing baby.
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17
Q

People with DS are at a higher risk of atlantoaxial instability. What is this?

A
  • Atlantoaxial instability, clinically referred to as AAI, is defined by the excessive movement at the intersection of the atlas, the first cervical vertebra (C1) and the axis, the second cervical vertebra (C2).
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18
Q

Give a few other things that people with DS are at increase risk of? (3)

A
  • Umbilical hernia +/- absence of a rib
  • Immunological defects affecting the skin, GIT, RespTracts e.g. periodontal destruction seen in the mouth
  • Increased risk of hypothyroidism and Alzheimer’s
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19
Q

All of the clinical features discussed above are more common in a person with DS. How many times more common are these features in a person with DS?

A
  • 20x more common
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20
Q

Give examples of clinical features of a person with Down’s syndrome? (14)

A
  • Ageing and its consequences
  • Alzheimer’s disease
  • Bereavement
  • GI problems in children
  • Managing sleep problems in children
  • Diabetes
  • Eye problems in children
  • Oral health care
  • Continuing pregnancy with a diagnosis of down’s
  • Depression
  • Thyroid disorder
  • Neck instability
  • Epileptic spasms in children
  • Sexual health
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21
Q

What are oral manifestations of a person with Down’s syndrome? (7)

A
  • Mouth (small, open lip posture)
  • Tongue (protrusive, fissured tongue. Circumvallate papillae may be enlarged and filiform absent)
  • Lips (thick, dry, fissured)
  • Occlusion (AOB, post x-bite, Class III)
  • Palate (high. Bifid uvula and CLP more common)
  • Teeth (eruption delayed, hypodontia, microdontia, hypoplasia, low caries incidence)
  • Periodontium (immunological defect of white cell chemotaxis may cause severe early onset disease)
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22
Q

What oral and dental management would we implement for a person with Down’s syndrome? (5)

A
  • Preventive protocol
  • OH - modify toothbrush handle or electric?
  • Advice about oral hygiene reiterated in congenital heart disease
  • Treat under LA if compliance allows
  • Chlorhexidine gel or mouthwash specifically for periodontal disease
23
Q

What can a person with Down’s syndrome struggle with (what is the impact of DS)? (6)

A
  • Development (like all children they benefit from high expectations, social inclusion is key)
  • Speech and language - delayed speech, easy read resources
  • Motor skills
  • Social development -
  • Memory skills
  • Education - most benefit from being in mainstream school, everyone will have some degree of learning disability
24
Q

Give examples of medically compromising conditions? (7)

A
  • Cardiovascular (inc downs syndrome)
  • Respiratory (Asthma and CF)
  • Childhood cancer
  • Chronic renal failure
  • Diabetes mellitus
  • Epilepsy
  • Common coagulation defects
25
Q

What % of the population has asthma?

A

2-5%

26
Q

What % of children in the UK have asthma?

A

7-19%

27
Q

What % of 13 year olds in Scotland have Asthma?

A

37%

28
Q

What does asthma consist of? (3)

A
  • Excess mucous production
  • Inflammation of epithelial lining of airways
  • Increased bronchial smooth muscle tone
29
Q

What are the risks and considerations we need to make with a person with asthma? (7)

A
  • Anxiety and stress can precipitate
  • Asthma medication side effects
  • Adrenal suppression
  • Avoid aspirin and other NSAID’s such as ibuprofen or Diclofenac for pain relief
  • Allergy to penicillin more common
  • IS (mild/mod) rather than IV sedatives (resp failure)
  • GA risk
30
Q

If giving GA to a patient with mild asthma what would they be referred for?

A
  • Outpatient GA

- (ASA II)

31
Q

If giving GA to a patient with moderate asthma what would they be referred for?

A
  • Inpatient GA

- (ASA III)

32
Q

If giving GA to a patient with severe asthma what would they be referred for?

A
  • Inpatient GA

- (ASA IV)

33
Q

What are the oral implications of asthma? (4)

A
  • Acidic inhalers - palatal erosion (not proven)
  • Dryness of mouth - increased intake of acidic beverages
  • Laxity of lower oesophageal sphincter - reflux of gastric acid
  • Chronic cough at night - reflux of gastric acid
34
Q

What is a possible treatment of palatal erosion in a person with asthma? (2)

A
  • Palatal metal shims

- Composite resin

35
Q

What are allergies that are common in a person with asthma?

A
  • Asthmatics are atopic individuals and may have other allergies e.g. nuts, latex, drugs
  • Latex is in the rubber bung of most cartridges of LA including lidocaine and lidocaine with adrenaline, The exception is Citanest and Octapressin which can be given safely
  • *think latex has been removed from the rubber bungs
36
Q

What is the impact of asthma on children in nursery and childcare? (3)

A
  • Asthma policy (most children not diagnosed until around 5 years)
  • Avoidance of triggers (animal fur/smoke/pollen)
  • Individual healthcare plans in place
37
Q

What is the impact of asthma on children at primary school? (4)

A
  • Asthma action plan (diagnosis, typical symptoms, ask for help, tummy ache, go silent?)
  • Communication (how serious - 3 children die every year)
  • Where will reliever inhaler be kept (often blue)
  • Asthma UK
38
Q

What is the impact of asthma on children in secondary school? (4)

A
  • Encourage your child to take more control
  • You and your child meet with school (school nurse, sports teacher)
  • Asthma action plan (discuss)
  • The autumn term (rise in children rushed to hospital)
39
Q

What is the impact of asthma on exercise?

A
  • As normal but be prepared with asthma action plan on fridge, your phone and their phone
40
Q

What is the impact of asthma on travel?

A
  • Weather, altitude, physical activity, air travel, accommodation
41
Q

How many live births have cystic fibrosis?

A
  • 1 in 2500
42
Q

What is the aetiology of cystic fibrosis?

A
  • Autosomal recessive long arm chromosome 7
43
Q

What can be affected in a person with Cystic fibrosis? (5)

A
  • Exocrine system affected in respiratory system (thick mucous) and digestive tract (lack of pancreatic lipases)
  • Diabetes, liver cirrhosis, reproductive problems with age
44
Q

A person with CF is at risk of recurrent chest infections. Give 2 examples of these?

A
  • P.aeruginos

- S.aureus

45
Q

People with CF tend to have a decreased exocrine function. What can this cause?

A
  • Malabsorption especially fats
  • So often given pancreatic supplements and vitamins
  • Need 120-150% of normal energy intake
46
Q

What are the oral manifestations of CF? (6)

A
  • Saliva - thickened
  • Caries may be reduced (? higher salivary ammonia)
  • Higher calculus levels
  • Lowe plaque and gingival disease
  • Enamel defects
  • Delayed eruption
47
Q

How would we dentally manage a person with CF? (5)

A
  • GA risk
  • Diabetes and liver disease
  • Sedation contraindicated - resp failure
  • Diet advice (high sugar intake)
  • Sugar free liquid antibiotics
48
Q

Give examples of things that CF can have an impact on? (12)

A
  • Nutrition
  • Treatment
  • Travel
  • Physiotherapy
  • School
  • Higher education
  • Transition
  • Fertility and pregnancy
  • CF at work
  • Cross infection
  • Transplant
  • Combination therapies
49
Q

How many children under 15 years of age have childhood cancer?

A
  • 1 in 600
50
Q

How many new cases of childhood cancer are there per year in under 15’s?

A
  • 1200-1500

- 700 die under 14 yrs of age

51
Q

What are different possible treatments of childhood cancer? (4)

A
  • Chemotherapy
  • Radiotherapy
  • Surgery
  • High dose therapy with bone marrow rescue
52
Q

What are general side effects of chemotherapy? (6)

A
  • Bone marrow suppression: Hb, WCC, PLT
  • Immunosuppression
  • Anorexia
  • Nausea and vomiting
  • Gut mucosal damage
  • Alopecia
53
Q

Give examples of acute complications of chemotherapy? (19)

A
  • Oral mucosa
  • Haemorrhage
  • Infection
  • Saliva
  • Sialasenitis
  • Taste loss
  • Dysphagia
  • Oral flora
  • Gingiva
  • Tooth sensitivity
  • Tooth mobility
  • Toothache, headache, bone pain
  • Trismus
  • Soft palate
  • Dry lips
  • Halitosis Cacogeusia
  • Glossitis
  • Paraesthesia
  • GvHD
54
Q

Oral ulceration and mucositis is a common side effect of radiotherapy and chemotherapy. When is there an onset of this and what does it consist of? (4)

A
  • Onset 12-15 days after RT and 3-10 days after CT
  • Ulcers on all types of mucosa
  • Mucositis often localised to oropharynx
  • Stomatitis develops as burning which within 1-3 days develops into ulceration