1 / 54

Palliative Care For Children

Palliative Care For Children. General Overview. Mike Harlos MD, CCFP, FCFP. Professor, Faculty of Medicine, University of Manitoba Medical Director, Winnipeg Regional Health Authority Palliative Care Program Co-Chair, Canadian Network of Palliative Care for Children

russell
Download Presentation

Palliative Care For Children

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Palliative Care For Children General Overview Mike Harlos MD, CCFP, FCFP Professor, Faculty of Medicine, University of Manitoba Medical Director, Winnipeg Regional Health Authority Palliative Care Program Co-Chair, Canadian Network of Palliative Care for Children Physician Consultant, Canadian Virtual Hospice

  2. Objectives • To consider the definition of pediatric palliative care • To consider where pediatric palliative care may fit in the care of seriously ill children • To consider similarities/differences with palliative care for adults • To review the prevalence and management of symptoms in children living with life-threatening illness

  3. Prognostic Uncertainty Pediatric Palliative Care services providers must acknowledge the uncertainty involved in determining if a specific circumstance or condition is life-limiting / life-threatening

  4. Common Trajectory Of Decline In Progressive Life-Limiting Illness In Children From presentation by Joanne Wolfe at the 16th International Congress on the Care of The Terminally Ill Functional Status Decline Crises (“Scary Dips”) Death Time

  5. “Prognostic Irrelevance” • In the view of patient, family, and/or care team, there may be unwillingness to even consider the possibility of death • Service availability should not only accommodate prognostic uncertainty, but should not require acceptance of a threatened life

  6. “What if…? Palliative Care… The “What If…?” Tour Guides • What would things look like? • Time frame? • Where care might take place • What should the patient/family expect (perhaps demand?) regarding care? • How might the palliative care team help patient, family, health care team? Disease-focused Care (“Aggressive Care”)

  7. Addressing The “What-Ifs…”Silence Is Not Golden • Children (even young children) are very perceptive, and can tell when something serious is happening • Even when pursuing cure for their child, parents are often aware in their “heart of hearts” that things may not unfold as hoped for • Palliative Care has a role in: • helping families navigate through difficult decisions, at times conflicted about which course is best for their child… “path of least regret” • ensuring that comfort and quality of life are minimally affected by the impact of illness, tests, and treatments • facilitating communication about fears and worries, and open dialogue about what to expect

  8. n = 147 (34 %) n = 282 (66 %) Yes No Do you regret not having done so? Do you regret having done so? No parents regretted having talked with their children about dying Yes No Identify and facilitate communication Talking about Death with Children … ctd Kreicbergs et al NEJM 2004; 351(12):1175-1186. Did you talk about death with your child at any time? Overall: 27% 73% Sensed Child Aware Of Dying: 47% 53% Did Not Sense Child Aware: 87% 13%

  9. What Symptoms Do Children With Advanced Illness Experience?

  10. The Measurement Of Symptoms In Children With CancerCollins JJ, Byrnes ME, Dunkel IJ, Lapin J, Nadel T, Thaler HT et al. J Pain Symptom Manage 2000; 19(5):363-377. • n = 160 cancer patients receiving treatment • aged 10 – 18 yo • 30-item patient-rated instrument (MSAS 10-18) • Inpatients averaged 13 symptoms, outpatients 6.5 • Patients who had recently received chemotherapy had more than double the symptoms of those who had not

  11. Symptoms At The End of Life in Children With Cancer Wolfe J. et al, NEJM 2000; 342(5) p 326-333 80 70 % 60 50 40 30 20 Successfully Treated (% Of Affected Children) 10 27 % 16 % 10 % Nausea And Vomiting Dyspnea Pain

  12. Pain In Advanced Childhood Illness Symptom Prevalence At Study Entry And In Last Month Of LifeUK Children’s Cancer Study Group/Paediatric Oncol Nurses Forum SurveyGoldman A et al; Pediatrics 2006; 117; 1179-1186 Abstract from the 7th International Symposium on Pediatric Pain Stenekes S, Hughes A, Grégoire MC, Frager G 2006 Breau LM, Camfield CS, McGrath PJ, Finley GA. The incidence of pain in children with severe cognitive impairments. Arch Pediatr Adolesc Med 2003; 157(12):1219-1226. Engel JM, Jensen MP, Hoffman AJ, Kartin D. Pain in persons with cerebral palsy: extension and cross validation Arch Phys Med Rehabil 2003; 84(8):1125-1128.

  13. Symptoms in Children with Neurodegenerative Illness % Hunt and Burne, 1995

  14. 2002 College Of Physicians And Surgeons Of Manitoba Child Health Standards Committee Report 2002 Manitoba Deaths Unlikely role for Palliative Care in symptom management, though potentially in family and staff support Potential role for Palliative Care in symptom management as well as family and staff support

  15. “Palliative in Parallel” • Palliative care for children should not be exclusive of ongoing cure-focused care • Can be involved as a parallel process, with a variable profile depending on goals of care and clinical circumstances • It is not unusual for children/families/clinicians to harbour seemingly conflicting thoughts and contradictory goals • There are some situations where one could argue that the standard of care should require involvement of a palliative service… eg: • Phase One Clinical trials • Organ Transplant waiting lists

  16. Various Patterns Of Pediatric Palliative Care Involvement Cure-Oriented; Disease-Focused Palliative

  17. Group 1 Group 2 Children with progressive life-limiting/life-threatening conditions who are not expected to survive into adulthood, but whose prognosis is anticipated to exceed one year Advanced life-limiting condition from which death within 12 months would not be unexpected Group 1A Comfort-focused approach has been chosen, or disease-focused interventions not possible Group 1B Advanced life-limiting illness with substantial disease and symptom burden for whom cure is nonetheless hoped for, or for whom all aggressive disease-focused and potentially life-sustaining options are being pursued Patient Groups For Pediatric Palliative Care Services

  18. Pediatricians’ Sense Of Preparedness For Practice Lieberman L, Hilliard LI; Medical Education 2006; 40: 539–546 n = 239 pediatricians certified in Canadian training programs between1999 and 2003

  19. Keeping The Momentum – Recent Developments • 2003: Canadian Network of Palliative Care for Children (CNPCC)- see http://cnpcc.ca • March 2006- Pediatric Hospice Palliative Care Guiding Principles And Norms Of Practice, through joint work by the CNPCC and CHPCA • 2006: 1st major clinical textbook in pediatric palliative care, The Oxford Textbook of Palliative Care for Children. • 2006: The Canadian Council on Health Services Accreditation (CCHSA) released in its standards for Hospice and End-of-Life Care • The Royal College of Physicians and Surgeons of Canada is exploring core competencies in Pediatric Palliative Care • There is increasing interest is there amongst physicians training in Pediatrics

  20. Pain Assessment In Children • Pain can be measured by: • self-report (what children say) – “Gold Standard” • biological markers (how their bodies react) • behaviour (what children do) • Biological and behavioural measures tend to habituate over time; parameters may not be specific to pain. • May deny pain if the questioner is a stranger, if they believe they are supposed to be brave, if they are fearful, or if they anticipate receiving an injection for pain. • Much variability in developmental capacity for children to report and describe pain • Questioning should be patient & use words familiar to the child, eg. • "Do you have any hurt?" • "Is there an ‘owie’ or ‘boo-boo’ in your tummy?"

  21. Pain AssessmentSelf-Reporting and Developmental Stage • Children have words for pain by about 18 months if age; may prefer the word hurt rather than pain; may use idiosyncratic, family words • Most children > 2 yrs can report presence & location of pain • 3 – 4 yrs: cognitive skills to describe pain intensity (eg. “a little”, “a lot”) • 4-5 yrs: can use the Poker Chip scale • Can test ability to use pain-rating tools with simple test of seriation • By about 5 yrs – capacity to provide good qualitative and quantitative information

  22. Pain AssessmentSelf-Reporting and Developmental Stage ctd… • 5+ yrs can usually rate and score pain; the Bieri Faces Pain Scale may be used • Children point to a face on the scale that matches how they feel. • The child should be trained by asking how he or she would feel following some minor pain. The child is asked about how much a more serious pain would hurt. • 7+ yrs: children can rate pain on a 0 (no pain) – 10 (worst possible pain) scale • 8+ yrs are able to describe the quality of the pain experience • Describing how pain affects emotions requires more abstract concepts • Adolescents are quite capable of using scales that use adjectives to describe both affect and sensory intensity

  23. Faces Pain Scale – Revised Children Beginning At 3-4 yo • Avoid affective descriptors (eg. “Point to the face that shows how you are feeling”) • May be misinterpreted as “are you happy/sad?”

  24. General Principles For The Prevention And Management Of Pain In Newborns • Pain often unrecognized and undertreated. Neonates do feel pain, and analgesia should be prescribed when indicated during their medical care. • If something hurts adults, it will hurt newborns, even if they are preterm. • Compared with older age groups, newborns may experience a greater sensitivity to pain and are more susceptible to the long-term effects of painful stimulation. • Adequate treatment of pain may be associated with ↓complications and ↓ mortality. • The appropriate use of environmental, behavioral, and pharmacological interventions can prevent, reduce, or eliminate neonatal pain in many clinical situations. • Sedation does not provide pain relief and may mask the neonate's response to pain. • Health care professionals have the responsibility for assessment, prevention, and management of pain in neonates. • Clinical units providing health care to newborns should develop written guidelines and protocols for the management of neonatal pain. Anand KJ. Consensus statement for the prevention and management of pain in the newborn. Arch Pediatr Adolesc Med 2001; 155(2):173-180.

  25. Approach To Analgesia Use In Pediatric Palliative Care • The oral (enteral) route preferred for most children, most of the time • However… many alternate routes available if needed: • IV (peripheral and central) • Subcutaneous • Transmucosal (nasal, buccal, sublingual) • Transdermal / transcutaneous • Spinal (epidural, intrathecal) • Rectal (usually not well tolerated) • Use adjuvants as appropriate • The W.H.O. ladder is a good template on which to base analgesic use • Virtually always prescribe laxatives with opioid Rx

  26. Weak Opioids Used In Pediatric Palliative Care • Codeine remains the most commonly prescribed weak opioid, however there are considerations: • Codeine is a pro-drug of morphine, from which its analgesic effect is derived • Up to 10% of the Caucasian population lack the enzyme necessary for transformation of codeine to morphine; perhaps up to 47% of those < 12 yrs old • If 1 mg/kg codeine ineffective, switch to morphine or alternative • Oxycodone: • has some κ receptor agonist activity as well as μ • No ceiling dose – can potentially be continued throughout course of illness

  27. STRONG OPIOIDS • Children > 3 months are probably at no greater risk of signif. resp depression than adults; younger infants may have ↑ risk due to metabolic immaturity affecting pharmacokinetics • Morphine elimination t ½ (h): • Preterm infants: 9 – 10 • Term Infants: 7 • Children: 3 – 4(Saaranmaa E, Huttunen P, Leppaluoto J, Meretoja O, Fellman V. Advantages of fentanyl over morphine in analgesia for ventilated newborn infants after birth: A randomized trial. J Pediatrics 134[2], 144-150. 1999)

  28. STRONG OPIOIDS ctd • most commonly use: • morphine • hydromorphone (Dilaudid ®) • fentanyl (IV infusions) • oxycodone • methadone • DO NOT use meperidine (Demerol®) long-term • active metabolite normeperidine→ seizures

  29. Using Opioids for Breakthrough Pain • Patient/Family must feel in control, empowered • Use aggressive dose and interval • There should be confidence in the effectiveness of the breakthrough dose; empirically and reliably effective • Patient Taking Short-Acting Enteral Opioids: • 50 - 100% of the q4h dose given q1h prn • Patient Taking Long-Acting Enteral Opioids: • 10 - 20% of total daily dose given q1h prn using short-acting opioid preparation • Patient On Continuous Parenteral Infusion (non-PCA): • 1 – 2 hrs worth of opioid, given q15 minutes prn

  30. PCA Opioids Ref: Pain In Infants, Children, And Adolescents 2nd Ed, 2003; Schechter, Berde, and Yaster Editors • Allows patients to self administer small amounts of opioids when needed • Usually IV or SQ • Most commonly morphine or hydromorphone • May have a continuous background opioid infusion in addition to PCA boluses • A child able to play a video game can also operate a PCA pump (5 – 6 yo) • Varying policies on whether nurse or parent are allowed to initiate a bolus – doing so will lose the inherent safety of being too drowsy to self-overdose

  31. Recommended Opioid Analgesic Doses (> 6 Months Age)* * For infants < 6 months start with ¼ of the pediatric starting dose and titrate

  32. Opioid Side Effects • Constipation – need proactive laxative use • Nausea/vomiting – consider treating with dopamine antagonists and/or prokinetics (metoclopramide, domperidone, prochlorperazine [Stemetil], haloperidol) • Urinary retention • Itch/rash – worse in children; may need low-dose naloxone infusion. May try antihistamines, however not great success • Dry mouth • Respiratory depression – uncommon when titrated in response to symptom • Drug interactions • Neurotoxicity (OIN):delirium, myoclonus ® seizures

  33. Opioid-Induced Pruritus • Not rare; up to 23% in children > 12 yo in one study of long-acting morphine (Zernickow B, Lindena G; Medical and Pediatric Oncology 36:451±458 (2001)) • Pathophysiology unclear • opioid m receptors are relevant to the modulation of pain and itch in the central nervous system. • Opioid peptides may also have a peripheral action potentiating itch due to other agents • Consider switching opioids; may have less pruritus with fentanyl, methadone, oxycodone • Try antihistamines (diphenhydramine, Atarax, trimeprazine) • Naloxone 1 – 2 micrograms/kg/hour as an infusion

  34. Adjuvants Used In Palliative Care • General / Non-specific • corticosteroids • Bone Pain • NSAIDs • bisphosphonates • (calcitonin) • Neuropathic Pain • gabapentin • antidepressants • ketamine • topiramate • clonidine • cannabinoids (not yet commonly used for pain)

  35. Gabapentin For Neuropathic Pain • Common Starting Regimen: • 5 mg/kg hs days 1-3, then • 5 mg/kg bid days 4-6, then • 5 mg/kg tid and slowly titrate up • Usual effective range: 8 – 35 mg/kg/day • Sedation is usual limiting factor. • Doses may need to be rounded of due to the capsule strengths

  36. Reasonable to start with recommended mg/kg for IV dosing and adjust empirically Intranasal Meds * Available to the cerebral cortex 2 – 5 min. after nasal use5 • P. D.Knoester ; Pharmacokinetics and pharmacodynamics of midazolam administered as a concentrated intranasal spray. A study in healthy volunteers; Br J Clin Pharmacol. 2002 May;53(5):501-7 • Rey E. et al; Pharmacokinetics of midazolam in children: comparative study of intranasal and intravenous administration; Eur J Clin Pharmacol 41(4) 1991; 355-357 • Dale O, Hjortkjaer R, Kharasch ED; Nasal administration of opioids for pain management in adults; Acta Anaesthesiol Scand. 2002 Aug;46(7):759-70 • Coda BA, Rudy AC, Archer SM, Wermeling DP; Pharmacokinetics and bioavailability of single-dose intranasal hydromorphone hydrochloride in healthy volunteers; Anesth Analg. 2003 Jul;97(1):117-23 • Fisgin T et al; Effects of intranasal midazolam and rectal diazepam on acute convulsions in children: prospective randomized study; J Child Neurol. 2002 Feb;17(2):123-6

  37. http://www.wolfetory.com/nasal.html

  38. Management Of: • Nausea And Vomiting • Dyspnea • Secretions In Pediatric Palliative Care

  39. Cortex CTZ GI VOMITING CENTRE Vestibular

  40. Managing Nausea & Vomiting in Palliative Care Some Differences in Children vs. Adults • Assessment, communication challenges • Higher risk of extrapyramidal reactions, akathisia, and somnolence with dopamine antagonists in children than adults • Metoclopramide (Maxeran®) • Prochlorperazine (Stemetil®) • Haloperidol (Haldol®) • Chlorpromazine • If using dopamine antagonists, consider slow administration (45-60 min.), as well as concomitant use of diphenhydramine (Benadryl®) 0.5 – 1 mg/kg q4-6h po/IV continued for additional 24hrs after dopamine antagonist stopped.

  41. D D D 5HT 5HT 5HT 5HT 2 2 2 M M M VOMITING CENTRE H1 H1 CB1 H1 Effector Organs H1 CB1 Muscarinic Cannabinoid Dopamine Serotonin Histamine

  42. Nausea and vomiting associated with cancer chemotherapy: drug management in theory and in practice From: Arch. Dis. Child.2004;89;877-880 E S Antonarakis and R D W Hain

  43. Antinauseants / Antiemetics 1 Komada Y et al. A randomised dose-comparison trial of granisetron in preventing emesis in children with leukaemia receiving emetogenic chemotherapy. Eur J Cancer 1999; 35(7):1095-1101. 2 Principles and Practice of Pediatric Oncology 4th Ed.; Edited by Pizzo & Poplack

  44. Palliative Management of Secretions

  45. Secretions - Prevalence At Study Entry And In Last Month Of LifeUK Children’s Cancer Study Group/Paediatric Oncology Nurses Forum SurveyGoldman A et al; Pediatrics 2006; 117; 1179-1186

  46. Suctioning Increased Secretions Mucosal Trauma Managing Secretions in Palliative Patients • Factors influencing approach management: • Oral secretions vs. lower respiratory • Level of alertness and expectations thereof • Proximity of expected death • “Death Rattle” – up to 50% in final hours of life • At times the issue is more one of creating an environment less upsetting to visiting family/friends • Suctioning: “If you can see it, you can suction it”

  47. Atropine Eye DropsFor Palliative Management Of Secretions • Atropine 1% ophthalmic preparation • Local oral effect for excessive salivation/drooling • Dose is usually 1 – 2 drops SL or buccal q6h prn • There may be systemic absorption… watch for tachycardia, flushing

  48. Glycopyrrolate For Palliative Management Of Secretions • Less sedating than scopolamine (doesn’t cross the blood-brain barrier), longer acting, however not as effective • Useful where patient is still alert; scopolamine will cause sedation and delirium in awake patients Enteral: 40 – 100 micrograms/kg 3 – 4 times daily • 2006 British National Formulary For Children • IWK Health Centre (Halifax) Formulary Refs: Parenteral: 4 – 10 micrograms/kg 3 – 4 times daily (10x the enteral dose) Ref: IWK Health Centre (Halifax) Formulary

  49. ScopolamineFor Palliative Management Of Secretions Ref: 2006 British National Formulary For Children Intermittent SQ/IV: 10 micrograms/kg (max. 600 micrograms) q 4h Continuous SQ/IV: 40-60 microgram/kg/day (1.67 – 2.5 microgram/kg/h) Ref: 2006 Rainbow Hospice Guidelines

  50. DyspneaInPediatric Palliative Care

More Related