/
Palliative Medicine Doctors’ Meeting____________________________H Palliative Medicine Doctors’ Meeting____________________________H

Palliative Medicine Doctors’ Meeting____________________________H - PDF document

tatiana-dople
tatiana-dople . @tatiana-dople
Follow
391 views
Uploaded On 2017-11-28

Palliative Medicine Doctors’ Meeting____________________________H - PPT Presentation

Case histories contributed by Dr Ng Sheung Ching and Dr Ma Chi Ming The Story of Madam C Madam C a 72year old retired farmer had been suffering from right biliary papillomatosis since 2003 with ID: 610792

Case histories contributed

Share:

Link:

Embed:

Download Presentation from below link

Download Pdf The PPT/PDF document "Palliative Medicine Doctors’ Meetin..." is the property of its rightful owner. Permission is granted to download and print the materials on this web site for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.


Presentation Transcript

Palliative Medicine Doctors’ Meeting____________________________HKSPM Newsletter 2007 Dec Issue 3 p 16 Case histories contributed by Dr Ng Sheung Ching and Dr Ma Chi Ming The Story of Madam C Madam C, a 72-year old retired farmer, had been suffering from right biliary papillomatosis since 2003 with extended right hepatectomy performed. Extensive liver metastases were noted since 2006 and metastatic adenocarcinoma to left lung was detected in improvement in bronchorrhea but were complicated by nausea with erythromycin and impaired renal function with indomethacin. Continuous subcutaneous infusion of hyoscine hydrobromide up to 1.6 mg per day was given with no improvement in sputum volume but resulted in excessive drowsiness. Continuous subcutaneous infusion of fentanyl and midazolam was needed to control her dyspnea and restlessness. second marriage. She was diagnosed to have polymyositis in 1997 presenting with weakness. Multiple immunosuppressive therapies had been tried including glucocorticoids, azathioprine, cyclophosphamide, cyclosporin, intravenous immunoglobulins, mycophenolate mofetil, and rituximab, but her disease progressed. She had an episode of severe pneumonia requiring intubation and subsequent tracheostomy. She was then transferred to the rehabilitation ward for convalescence. to infrequent visits from her family, and anger and frustration about her physical needs not being promptly addressed by staff. She frequently called for help with dramatic gestures and repeated call bells ringing. The multidisciplinary team attempted to address her multiple needs. The physiotherapist performed vigorous chest physiotherapy and hand function enhancement exercises; the occupational therapist designed a special chair and a foot platform to facilitate her sitting out; the Palliative Medicine Doctors’ Meeting____________________________HKSPM Newsletter 2007 Dec Issue 3 p 18 adenocarcinoma of lung at a dose 300-500 micrograms daily. 16 It is postulated to have an inhibitory action on the secretin receptors in the bronchial tree. The patient we presented above further substantiates its potential role in bronchorrhea. The Management of Sialorrhea Normal adults produce 750 to 1500 ml of saliva per day. Unlike bronchorrhea which is usually the result of excessive secretion, sialorrhea is usually due to oropharyngeal dysphagia and impaired cough effort caused by various neurological diseases, or esophageal dysphagia caused by mechanical obstruction or esophageal dysmotility. Sialorrhea may affect feeding, interfere with speech, lead to social embarrassment, induce sense of suffocation with resultant fear, and increase susceptibility to aspiration pneumonia. The management of excessive oropharyngeal secretions comprises of physical modalities, medications, irradiation to salivary glands and various surgical maneuvers. 17 (Table 1) Surgical techniques are limited by its irreversibility and patients’ fitness for surgery. Anticholinergic drugs and antidepressants are limited by their side effects. Radiation to salivary glands may be complicated by development of head and neck malignancies in the long run. There are case reports of the usefulness of local botulinum toxin injection into salivary glands in patients with head and neck cancer, neurodegenerative disorders, and stroke with no reported side effects. 18, 19 Randomized controlled studies have also proven its efficacy. (Table 2) 20 The clinical aspects of botulinum toxin injection have also been reviewed. 20 It can be injected into parotid glands, submandibular glands, or both. The injections can be guided by anatomical landmarks or ultrasound localization of the salivary glands. Use of ultrasound leads to a higher success rate and fewer side effects, and the dose used can be lower. However, it requires certain expertise. The dosages reported varied from 5-75 U into each parotid gland and 5-30 U into each submandibular gland. Usually one to 1.5 milliliters of drugs is injected into each gland, and the effect is achieved by diffusion. The onset of reduced saliva production can be rapid within 1-2 weeks, and the effect can last from a few weeks to several months. The potential side effects are dry mouth, dysphagia, jaw weakness and jaw dislocation. Caution must be exercised in patients with neuromuscular and muscular disease. Its potential indications in palliative care lie in the management of saliva aspiration and drooling in patients with neurological disorders affecting swallowing, surgery involving upper aerodigestive tract, laryngeal and upper Researcher Mancini 21 2003 Lipp 22 2003 Ondo 23 2004 Jongerius 24 2004 Lagalla 25 2006 Patient group Parkinson’s disease Multiple system atrophy Sialorrhea Parkinson’s disease Cerebral palsy Parkinison’s disease N 20 32 16 45 32 Type of study Double blind placebo controlled Dose finding study Double blind placebo controlled Compared with transdermal scopolamine Double blind placebo controlled Outcome Improvement shown at 1 week and 3 months Effect achieved with 75 U into each parotid gland Improved VAS, drooling score and global score Similar effects; fewer side effects Less frequent drooling; less saliva production & improved family and social functioning Table 2: Randomized studies on the use of botulinum toxin in sialorrhea 20 Physical modalities Medications Radiation Surgery Table 1: Management of excessive oropharyngeal secretions 17 Manual suction Various respiratory physical therapy techniques: Postural drainage / Percussion and vibration / Incentive spirometry / Glossopharyngeal breathing / frog breathing / Active cycle of breathing / Forced expiratory maneuvers / Cough assist Anticholinergic dugs Tricyclic antidepressants Botulinum toxin To salivary glands On salivary glands On neural innervation of saliva production Palliative Medicine Doctors’ Meeting____________________________HKSPM Newsletter 2007 Dec Issue 3 p 19 aerodigestive tract tumors, as well as patients with saliva fistula after parotid gland surgery, laryngectomy or pharyngectomy. Conclusion We have reported the usefulness of subcutaneous octreotide infusion and local botulinum toxin injection into submandibular glands in the management of bronchorrhea and sialorrhea respectively, and in both patients, a better symptom control and better quality of life had been achieved. Though these two medications are expensive, its use in selected cases should be carefully considered. References 1. Shimura S, Sasaki T, Sasaki H et al. Viscoelastic properties of bronchorrhea sputum in bronchial asthmatics. Biorheology 1988;25:173-179. 2. Hidaka N, Nagao K. Bronchioloalveolar carcinoma accompanied by severe bronchorrhea. Chest 1996;110: 281-282. 3. Epaulard O, Moro D, Langin T et al. Bronchorrhea revealing cervix adenocarcinoma metastatic to the lung. Lung Cancer 2001; 31:331-334. 4. Shimura S, Takishima T. Bronchorrhea from diffuse lymphangitic metastasis of colon carcinoma to the lung. Chest 1994;105: 308-310. 5. Lembo T, Donnelly TJ. A case of pancreatic carcinoma causing massive bronchial fluid production and electrolyte abnormalities. Chest 1995; 108: 1161-1163. 6. Lundgren JD, Shelhamer JH. Pathogenesis of airway mucus hypersecretion. J Allergy Clin Immunol 1990; 85:399-417. 7. Marom ZM, Goswami SK. Respiratory mucus hypersecretion (bronchorrhea): a case discussion – possible mechanism(s) and treatment. J Allergy Clinic Immunol 1991: 87:1050-1055. 8. Hiratsuka T, Mukae H, Ihiboshi H et al. Severe bronchorrhea accompanying alveolar cell carcinoma: treatment with clarithromycin and inhaled beclomethasone. Nihon Kokyuki Gakkai Zasshi 1998;36(5): 482-487. 9. Nakajima T, Terashima T et al. Treatment of bronchorrhea by corticosteroids in a case of bronchioloalveolar carcinoma producing CA 19-9. Internal Medicine 2002;41(3): 225-228. 10. Tamaoki J, Chiyotani A, Kobayashi K. Effect of indomethacin on bronchorrhea in patients with chronic bronchitis, diffuse panbronchiolitis, or bronchiectasis. Amer Review of Resp Disease 1992;145(3); 548-552. 11. Homma S, Kaukabata M, Kishi K et al. Successful treatment of refractory bronchorrhea by inhaled indomethacin in two atients with bronchioloalveolar carcinoma. Chest 1998;115: 1465-1468. 12. Takeyama K, Dabbagah K, Lee HM et al. Epidermal growth factor system regulates mucin production in airway. Proc Natl Acad Sci USA 1999; 96: 3081-3086 13. Kitazaki T, Soda H, Doi S et al. Gefitinib inhibits MUC5AC synthesis in mucin-secreting non-small cell lung cancer cells. Lung Cancer 2005; 50: 19-24. 14. Milton DT, Kris MG, Gomez JE et al. Prompt control of bronchorrhea in patients with bronchioloalveolar carcinoma treated with gefitinib (Iressa). Support Care Cancer 2005;13:70-72. 15. Kitazaki T, Fukuda M, Soda H et al. Novel effects of gefitinib on mucin production in bronchioloalveolar carcinoma: two case reports. Lung Cancer 2005;49:125-128. 16. Hudson E, Attanoos RL, Byrne A. Successful treatment of bronchorrhea with octreotide in a patient with adenocarcinoma of the lung. J Pain Sympt Manage 2006; 32(3): 200-202. 17. Elman LB, Dubin RM, Kelley M et al. Management of oropharyngeal and tracheobronchial secretions in patients with neurologic diseases. J Pall Medicine 2005; 8(6):1150-1159. 18. Ellies M, Laskawi R et al. Botulinum toxin to reduce saliva flow: selected indications for ultrasound-guided toxin application into salivary glands. The Laryngoscope 2002;112:82-86. 19. Manrique D. Application of botulinum toxin to reduce the saliva in patients with amyotrophic lateral sclerosis. Rev Bras Otorrinolaringo 2005; 71(5):566-569. 20. Tan EK. Botulinum toxin treatment of sialorrhea: comparing different therapeutic preparations. Eur J Neurology 2006;13 (Suppl. 1):60-64. 21. Mancini F, Zangaglia R et al. Double-blind, placebo-controlled study to evaluate the efficacy and safety of botulinum toxin type A in the treatment of drooling in Parkinsonism. Movement Disorder 2006;18:685-688. 22. Lipp A, Trottenberg T et al. A randomized trial of botulinum toxin A for treatment of drooling. Neurology 2003;61: 1279-1281. 23. Ondo WG, Hunter C, Moore W. A double-blind placebo-controlled trial of botulinum toxin B for sialorrhea in parkinson’s disease. Neurology 2004; 62: 37-40. 24. Jongerius PH, van den Hoogen FJ et al. Effect of botulinum toxin in the treatment of drooling: a controlled trial. Pediatrics 2004:114:620-627. 25. Lagalla G, Millevolte M, Capecci M et al. Botulinum toxin type A for drooling in Parkinson’s disease: a double-blind, randomized, placebo-controlled study. Movement Disorder 2006; 21: 704-707.