PRADER-WILLI SYNDROME

67
PRADER-WILLI SYNDROME Presented by: The Prader-Willi Syndrome Project for New Mexico

description

PRADER-WILLI SYNDROME. Presented by: The Prader-Willi Syndrome Project for New Mexico. HISTORY. 1956 3 Doctors from Switzerland A syndrome is a set of characteristics Incidence Rate: 1:12-15,000 live births. Paternal Deletion A band of genes - PowerPoint PPT Presentation

Transcript of PRADER-WILLI SYNDROME

Page 1: PRADER-WILLI SYNDROME

PRADER-WILLI SYNDROME

Presented by:

The Prader-Willi Syndrome Project

for New Mexico

Page 2: PRADER-WILLI SYNDROME

HISTORY

1956 3 Doctors from

Switzerland

A syndrome is a set of

characteristics

Incidence Rate:

1:12-15,000 live births

Page 3: PRADER-WILLI SYNDROME

GENETICS15th chromosome from

father Paternal Deletion

A band of genes 15q11-q13 is missing from the 15th chromosome coming from the father

75% of people with PWS

Maternal Dysomy the genetic material

on the mother’s 15th chromosome duplicates onto the father’s chromosome

25% of people with PWS

Page 4: PRADER-WILLI SYNDROME

INHERITED PWS

• Incidence – less than 1/10 of 1%

• Mutation on father’s 15th chromosome

• Child can inherit the mutation

• Mosaic PWS

Page 5: PRADER-WILLI SYNDROME

MORE ON GENETICS

• In Paternal Deletion there can be micro and macro deletions

• Deletions may be influencing the other genes on chromosome 15

• Genes on chromosome 15 may be influencing a tendency toward depression and bi-polar disorders

Page 6: PRADER-WILLI SYNDROME

AND MORE

• In Maternal Dysomy the child receives a “double dose” of the mother’s genetic inheritance residing on chromosome 15

• Angelman’s Syndrome is a mirror image of PWS where deletions and duplications occur on the mother’s 15 chromosome - manifests as a different syndrome

• Genetic research continues including treatment with gene therapy

Page 7: PRADER-WILLI SYNDROME

DIAGNOSIS

• PWS can now be diagnosed with a blood test called a protein mythelation assay.

• Results can be obtained in a couple of weeks.

• Test is 99% accurate.

Page 8: PRADER-WILLI SYNDROME

HYPOTHALAMUS

Regulates Regulates

Body Secretion

Processes of

& Hormones

Functions

Page 9: PRADER-WILLI SYNDROME

HYPOTONIA

. Delayed fetal movement

. Weak cry & lethargy

. Feeding difficulties

. Delayed motor skills

. Speech difficulties

. Scoliosis/Hip Dysplasia

. Myopia/Strabismus

. Unbalanced , uncoordinated gait

Page 10: PRADER-WILLI SYNDROME

HYPOTONIAChildren

• Orthopedic evaluation• Strabismus sometimes

requiring surgery• Vision screening• Monitoring for

scoliosis (surgery)• Monitoring for hip

dysplasia (surgery)

Page 11: PRADER-WILLI SYNDROME

HYPOTONIA & OBESITY

• The complications of morbid obesity (30% or more overweight) happen sooner for persons with PWS because of the hypotonia

Page 12: PRADER-WILLI SYNDROME

HYPOGONADISM

• Small genitals

• Low levels of sexual hormone

• Incomplete puberty due to hypothalamus not triggering the pituitary gland

• Risk for premature osteoporosis

• Low levels of Growth Hormone

Page 13: PRADER-WILLI SYNDROME

MALE HYPOGONADISM

• Undescended testes• Small penis• Lack of growth spurt• Lack of secondary

sexual characteristics• Infertility usual

Page 14: PRADER-WILLI SYNDROME

FEMALE HYPOGONADISM

• Small genitalia• Absent/irregular

menses• Lack of growth spurt• Lack of secondary

sexual characteristics• Infertility usual

Page 15: PRADER-WILLI SYNDROME

HYPOMENTIA

• All have Learning Disabilities

• Mental Retardation

• IQ scores range from 35-110, most testing around 70

Page 16: PRADER-WILLI SYNDROME

HYPOMENTIACognitive Strengths

• Fine Motor Skills

• Long Term Memory

• Visual Perceptional Skills

• Verbal Skills/Receptive Language

• Artistic Abilities

Page 17: PRADER-WILLI SYNDROME

HYPOMENTIACognitive Challenges

• Abstract/Conceptual Thinking

• Auditory Short Term Memory

• Loss of Learned Information

• Set of Specific Learning Disabilities

. Sequencing . Generalizing

. Social Context . Meta-Cognition

Page 18: PRADER-WILLI SYNDROME

LYING & PWS

• Lying to get out of trouble

• Lying to manipulate • Confabulations – the

telling of tall tales for no apparent reason

• Type of lying determines the response

Page 19: PRADER-WILLI SYNDROME

BEST PRACTICES FOR THE CLASSROOM

• Structure & consistency – is essential for management of PWS & needs to be visually presented

• Activities – a full day moving from one to another with no “hanging out”

• Individual attention – as much as possible• Positive reinforcement – as much as possible• Peer relationships – need to be encouraged• Visual learners

Page 20: PRADER-WILLI SYNDROME

MORE BEST PRACTICES

• Some children with PWS are easily over- stimulated and have short attention spans – may need to make environmental accommodations

• Concrete, hands-on learning style – learn by doing• Need to be weighed and measured weekly, same

time and same scale • Therapies – often OT, SLP and PT

Page 21: PRADER-WILLI SYNDROME

HYPERPHAGIA the food problem

• Non-functioning Hypothalamus• No feeling of fullness – satiety• Always feeling hungry – insatiable appetite• Slower metabolism – up to 1/3 slower• Gain weight 3 times faster; need 1/3 fewer calories• Can’t raise basal metabolic rate – little weight loss

with exercise• Too much adipose tissue and not enough lean

muscle mass – making them feel “mushy”

Page 22: PRADER-WILLI SYNDROME

FOOD SEEKING

• Incessant hunger makes person constantly think about food and how to get it

• Body thinks it’s starving – survival instinct is stuck on ON

• Person does whatever they have to do to obtain food

• Out of their control – like you holding your breath and then body takes over and breathes for you

Page 23: PRADER-WILLI SYNDROME

FOOD SEEKING AT SCHOOL

• Should be expected• Most of it is opportunistic – result of failure

of caretakers to follow rules• Forgive yourself & start again• Successful food stealing encourages food

seeking• If occurring weekly, food security not

established

Page 24: PRADER-WILLI SYNDROME

FOOD STEALING

• Ask for food – do not take it – let family know if child chooses to eat it

• Establish consequence ahead of time – may require searches

• Respond matter- of-factly

• Do not be angry, lecture or apologize

• Once it’s over, it’s over

Page 25: PRADER-WILLI SYNDROME

DANGERS OF MORBID OBESITY

• Cardio-pulmonary Disease

• Hypertension• Obstructive Sleep

Apnea• Pickwickean

Syndrome• Incontinence

• Type II Diabetes – as early as 6 years old

• Edema• Skin sores• Yeast Infections• Inability to walk• Right side heart failure

Page 26: PRADER-WILLI SYNDROME

MORBID OBESITY

Page 27: PRADER-WILLI SYNDROME

MORBID OBESITYMedical Implications

• Growth charts with children• Regular weighing • Pulmonary functioning exams sometimes leading

to sleep studies• Regular screening for Type II diabetes• Echocardiograms- right side heart

failure• Care of skin and effects of self-abuse

Page 28: PRADER-WILLI SYNDROME

MANAGING an INSATIABLE APPETITE at SCHOOL

• ENVIRONMENTAL CONTROLS – keep the environment clear of food

• Out of sight; out of mind• Locking food sources• Not eating in front of

person• Managing classroom

parties & food sales• Not using food as a

reward

• SUPERVISION OF THE PERSON - keep the person in sight

• In the cafeteria• In the classroom• Changing classes• At recess• On the bus

Page 29: PRADER-WILLI SYNDROME

DIETARY MANAGEMENT

• Supervision around food & no food around

• Modified lunch menus

• No money at school

• Pre-plan parties & treats – do not exclude

• Watch for food trading & the generosity of children

Page 30: PRADER-WILLI SYNDROME

SECONDARY MANIFESTATIONS

• Almond-shaped eyes• Tented upper lip• Narrow temples• Narrow jaw• Larger space between

nose and mouth• Straight ulnar border

• Smaller hands & feet• “Pear-shaped”torso• Short stature• Hypo pigmentation• Thicker saliva leading

to dental problems

Page 31: PRADER-WILLI SYNDROME

FACIAL FEATURES

Page 32: PRADER-WILLI SYNDROME

BODY FEATURES

Page 33: PRADER-WILLI SYNDROME

HYPOTHALAMUS DYSFUNCTION

• Brain arousal

• Internal body temperature

• Pain sensitivity

• Difficulty with or inability to vomit

• Reactions to medications is different

• Symptoms of illness

Page 34: PRADER-WILLI SYNDROME

EXPERIENCE OF ILLNESS

• The body registers the pain or illness but the mind does not perceive it

• The person acts out the pain or illness

. Disorientation .Vomiting

. Confusion . Memory loss

. Fatigue . Odd behaviors

. Loss of appetite . Loss of interest

Page 35: PRADER-WILLI SYNDROME

RECENT MEDICAL ISSUES

• Gorging• Water Intoxication• Rectal Digging• Hernias• Gastro-Intestinal

Complaints• Aspiration• Thyroid Problems• Acute Idiopathic Gastric

Dilation

Page 36: PRADER-WILLI SYNDROME

CHECK THE BODY FIRSTINTERNALLY

• X-RAYS

• ULTRASOUNDS

• LAB WORK

Page 37: PRADER-WILLI SYNDROME

THE HYPOTHALAMUS&

EMOTIONS

• Mood Swings

• Disproportionate emotional responses

• Longer calming time

• Temper tantrums

• Clinical depression

• Psychosis

Page 38: PRADER-WILLI SYNDROME

THE HYPOTHALAMUS&

BEHAVIOR• Obsessive/compulsive

• Inflexibility

• Perseveration

• Stubbornness

• Hoarding

• Aggression/violence

• Self-trauma

Page 39: PRADER-WILLI SYNDROME

STRESS & BEHAVIOR

• Due to genetic reality people with PWS more vulnerable to stress

• PWS itself is a stressor• Access to food and food itself is a stressor• Too much independence can be a stressor• Crisis for persons with PWS is the conflict

between environment and their personalities and coping mechanisms

Page 40: PRADER-WILLI SYNDROME

STRESS, BEHAVIOR & FOOD

• Lack of food security = Hope = Disappointment = Stress = Behaviors

• Food security = No hope = No disappointment = No stress = No behaviors

Page 41: PRADER-WILLI SYNDROME

DEVELOPMENTAL DELAYS

AND BEHAVIOR• Delay at the

narcissistic stage of development – around 3 years of age

• Delay at around 12 years of age in judgment

Page 42: PRADER-WILLI SYNDROME

BEHAVIOR APPROACH

• Look at underlying stressors not each individual behavior

• Often stressors can be modified with environmental modifications

• Reduction of stressors often leads to diminishment of behaviors without the need for medication

Page 43: PRADER-WILLI SYNDROME

A WAY OF LOOKING AT BEHAVIOR

When behaviors occur look at:

1. Physical illness

2. Stressors

3. Medications – SSRI’s can trigger the mood instability

Page 44: PRADER-WILLI SYNDROME

3 MAIN WAYS TO MANAGE PWS BEHAVIORS

• STRUCTURE

• CONSISTENCY

• PREDICTABILITY

Page 45: PRADER-WILLI SYNDROME

THE THERAPEUTIC MILIEU

• Structured daily plan• Rules• Reward Management

System• Consequence System

• Environmental Controls

• Communication• Staff Supervision• Food Security

Page 46: PRADER-WILLI SYNDROME

REWARD MANAGEMENT SYSTEM

• Defined system of daily rewards & weekly reinforcers• Visual reminders – point sheet or chart• Reinforcers must be varied & interesting to the person• Individual needs to be involved in choosing reinforcers• Frequent random praise• Data sheets to document progress

Page 47: PRADER-WILLI SYNDROME

BEHAVIOR CONTRACTS

• Identify target behaviors – around 3 or 4• Write out what is expected• Write out consequence• Have person & team sign contract• Give points on a set time frame for absence

of target behaviors – differential reinforcement

• Points translate into tokens

Page 48: PRADER-WILLI SYNDROME

CONSEQUENCE SYSTEM

• Defined system of consequence – initially thoroughly presented to person & then given low attention

• Consequences given non-confrontationally

• Not to be used as a threat

• Must be consistently enforced and cannot be changed arbitrarily

Page 49: PRADER-WILLI SYNDROME

INTERVENTIONS

• Must have pre-planned interventions for the following PWS possibilities:

. Elopement – running away

. Removal to a quiet place to calm

. Ability to have person remain in quiet

place until they do calm down

. Physical aggression against self or

others requiring an intervention

Page 50: PRADER-WILLI SYNDROME

FOOD SECURITY

• All elements of meals need to be set in advance

• No arbitrary changes

• Planned & posted menus

• Limit discussion about food –

DON’T ARGUE

• All staff trained on diet

Page 51: PRADER-WILLI SYNDROME

SUGGESTED INTERVENTIONS FOR

PWS BEHAVIOR• Stubborn Opposition

• Negativism, Arguing, Defiance

• Perseveration

• Temper Tantrums

• Intermittent Explosiveness

• Physical aggression

• Skin Picking

Page 52: PRADER-WILLI SYNDROME

STUBBORN OPPOSITION

• Planned ignoring of harmless negativity and opposition – wait it out

• Give praise immediately for positive behaviors as soon as exhibited

• Do not comfort or cajole

• Briefly restate request and then stop talking

• Remain neutral

Page 53: PRADER-WILLI SYNDROME

NEGATIVISIM, ARGUING & DEFIANCE

• Use prearranged prompts & cues• Use low attention & redirection• Do not continue to respond back• Do not engage in arguing, simply restate the

rule or expectation• Let the person have the last word• Show with your demeanor that you are calm

and not going to change your mind.

Page 54: PRADER-WILLI SYNDROME

PERSEVERATION

• Planned ignoring – answer question once or explain once then STOP – to continue will give negative attention & reinforcement

• Redirection – if person is truly stuck, reduce stimulus in environment & try to redirect

• Give praise as soon as topic of perseveration changes

Page 55: PRADER-WILLI SYNDROME

TEMPER TANTURMS

• Control physical environment to ensure safety

• Ignore behavior completely if actions not immediately dangerous

• Give mild & neutral praise when person is calm and move on

Page 56: PRADER-WILLI SYNDROME

PHYSICAL AGGRESSION

• Control environment – remove objects that might be thrown; secure exits if person elopes

• Give verbal prompts to calm

• Intervene physically if there is imminent

danger to person or others

Page 57: PRADER-WILLI SYNDROME

SKIN PICKING

• Low attention; Redirection• Do not punish – must live with natural consequences• Make a contract about picking . Take a picture of lesion . Put antibiotic on wound 4 or more times a day . Establish a small reward for healing – reward the healing, rather than the not picking . Expect picking at a new area

Page 58: PRADER-WILLI SYNDROME

PWS Case Study:

-Ms. X presented with severe morbid obesity and diagnosis of PWS (1990).

- Sleep apnea requiring oxygen.

- In wheel chair and trouble walking because of weight.

-Her weight was 291# at 54” (BMI = 70).

Page 59: PRADER-WILLI SYNDROME

Intervention• Environmental modifications

and 24-hour supervision. • Nutrition intervention with

appropriate calorie diet (implemented 1200 calorie diet).

• Weight checks (helps with food seeking behaviors)

• Behavioral supports• PWS training for all

individuals involved in care.

Page 60: PRADER-WILLI SYNDROME

OutcomeResulted in 151-

pound weight loss.Weight at 140# and

has maintained for over eight years.

Out of wheel chairOff oxygenBMI: 34 (was 70)

Prevention of death and premature

disability.

Page 61: PRADER-WILLI SYNDROME

Power Point Presentation Medical Advisor

PWS Project’s Medical Advisor is Dr. Carol Clericuzio Her June 17, 2009 presentation on PWS can be found at

www.ARCAOpeningDoors.org

. Click on – Services We Provide . then Prader-Willi Syndrome Project . then – at bottom of page, link to presentation

Page 62: PRADER-WILLI SYNDROME

WELL MANAGED PWS

Page 63: PRADER-WILLI SYNDROME

ANOTHER

Page 64: PRADER-WILLI SYNDROME

A BABY

Page 65: PRADER-WILLI SYNDROME

AND TWO OTHERS

Page 66: PRADER-WILLI SYNDROME

OUT & ABOUT

Page 67: PRADER-WILLI SYNDROME

AT THE PROM