SciELO - Scientific Electronic Library Online

 
vol.13 issue3Prevalence of temporomandibular joint dysfunction and different levels of anxiety among college studentsPrevious face-to-face information and pain control for third molar extraction author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Revista Dor

Print version ISSN 1806-0013

Rev. dor vol.13 no.3 São Paulo July/Sept. 2012

http://dx.doi.org/10.1590/S1806-00132012000300009 

ORIGINAL ARTICLE

 

Evaluation of intestinal habits of cancer patients under morphine for pain control*

 

 

Michela Cynthia da Rocha MarmoI; Eliana Maria Monteiro CaranII; Fabiola Castelo Branco PutyIII; Mauro Batista de MoraisIV

IStudents of Biomedicine, Federal University of Alfenas (UNIFAL-MG). Alfenas, MG. Brazil
IIProfessor of Anatomy, School of Dentistry, FOP-UNICAMP and Senior Guest Professor of Capes, Federal University of Alfenas (UNIFAL-MG). Alfenas, MG. Brazil
IIIAssistant Professor Doctor of Basic Statistics, Federal University of Alfenas (UNIFAL-MG). Alfenas, MG. Brazil
IVAssistant Professor Doctor, Department of Anatomy (DAnat), Federal University of Alfenas (UNIFAL-MG). Alfenas, MG. Brazil

Correspondence to

 

 


SUMMARY

BACKGROUND AND OBJECTIVES: There are few data in the literature on intestinal constipation secondary to morphine in cancer patients. This study aimed at evaluating intestinal habits of cancer patients under morphine.
METHOD: This is a prospective non-randomized study carried out from February to November 2007. All patients had cancer, over 4 years of age and were under morphine for pain control. Patients received laxatives 24 hours after starting with morphine. Intestinal habits were evaluated through a structured questionnaire. When needed, feces were rectally or orally desimpacted.
RESULTS: Twenty-two cancer patients aged between 5 and 35 years (mean 16.7 years) were admitted, of whom 63.6% were under palliative care. During the first week under morphine and lactulose, 40.9% of patients were constipated. In the second and third weeks, constipation was present in 38.8% and 16.6% of patients, respectively. Treatment was able to control constipation in 50% of cases.
CONCLUSION: Constipation was frequent however the specific attention to their intestinal habits has increased adherence to laxatives and has decreased the formation of fecal impaction.

Keywords: Intestinal constipation, Pain, Morphine, Neoplasia.


 

 

INTRODUCTION

Pain is common in cancer patients and is considered the most prevalent and disabling symptom in this population, especially in case of metastases or relapses1,2. The World Health Organization (WHO) indicates morphine to treat moderate to severe pain of cancer patients3. However, although effective, the treatment with morphine is often associated to side effects, such as constipation4,5.

There are few data in the literature about constipation secondary to morphine among pediatric cancer patients. This symptom is more commonly studied in adults6. However, after studying adverse morphine effects in 122 Brazilian cancer children7, authors have observed that 72.9% of cases had constipation. Although being a relatively common manifestation in patients under opioids, it is worsened by several other factors such as malnutrition, dehydration and simultaneous use of other drugs, which are especially present in metastatic oncologic patients under palliative care8.

Constipation is a challenge for the oncologic practice because it is often neglected by health professionals and caregivers, although being associated to several other symptoms, such as discomfort, abdominal pain, nausea, vomiting, fecal impaction with or without anal injury4,5, which invariably impact global health and quality of life of cancer patients, in addition to increasing the use of other drugs for relief or symptomatic treatment of symptoms and the rate of complications and costs related to such interventions.

Considering the relevance of the subject and that experience in the treatment of opioid-induced constipation in children is scarce, this study aimed at evaluating intestinal habits of cancer patients under morphine.

 

METHOD

Prospective, cohort, non randomized, single-armed study carried out from February to November 2007 with cancer patients followed by the pain outpatient clinic, Pediatric Oncology Institute (IOP), Federal University of São Paulo-SP. Participated in this study cancer patients under morphine for at least one week, indicated to control baseline cancer-related pain, with at least four years of age. Patients with clinical instability were excluded. The Free and Informed Consent Term was obtained from all patients/ guardians.

The intestinal habit of patients included in the study was evaluated before admission to the study, 72 hours after admission and then in weeks 1, 2 and 3, depending on the time they remained under the analgesic.

According to literature criteria, constipation was considered when: hard stools elimination, in the shape of cymbals, pebbles, cylindrical or with cracks; difficulty or pain to evacuate; or decreased number of evacuations per week (< 3 times) or elimination of bulky stools which clog the toilet; or evidences of fecal impaction.

Indications for morphine use and withdrawal, initial doses and dose adjustments were established according to the pain treatment protocol used for IOP's routine. Initial morphine dose was oral 0.3 mg/kg every 4 hours.

Patients started treatment with osmotic laxative 24 hours after starting with morphine: syrup lactulose solution in the presentation of 667 mg/mL, in the dose of 1 mL/kg/day until the maximum of 60 mL/day.

Fecalomas were systematically investigated through physical evaluation or, when needed, with plain abdominal X-rays. Treatment of fecaloma by fecal desimpaction was oral with 3350 polyethylene glycol (PEG 3350 Muvinlax®), 1.5 g/kg/day for three days (maximum dose of 100 g/day), or rectal using 10% glycerin solution (10 mL/day). Rectal desimpaction was indicated when oral route was unfeasible due to suspended diet or intolerance to oral PEG 3350. To be submitted to rectal desimpaction, patients had to have platelet counts above 50,000
/µL and more than 500 granulocytes /µL.

Laxative intervention outcomes were: 1) evacuation at least every two days, with no pain or difficulty to evacuate and 2) lack of fecal impaction during morphine use. Efficacy analyses were carried out weekly, according to the time patients remained in the study. Patients with unsatisfactory therapeutic response received therapeutic options, such as the association of other laxatives or replacement of morphine by different opioids.

This study was approved by the Ethics Committee, Federal University of São Paulo (UNIFESP) under number 1502/2006.

 

RESULTS

Participated in this study 22 patients under morphine and meeting eligibility criteria. Mean age of patients was 16.7 years (5 to 35 years), being 54% males. From evaluated patients, 63.6% (14/22) had no possibility of being cured and were receiving palliative chemotherapy (Table 1).

At admission, 27.2% of patients had constipation, being recommended the use of lactulose (1 mL/kg/day) for all cases. Two patients needed bisacodyl due to intolerance to lactose. After 72 hours, all patients were under laxatives; however, two out of 22 cases had fecaloma needing rectal desimpaction with glycerin solution and maintenance with bisacodyl (10 mg/day), which stimulates bowel movements.

During the first week, 40.9% of patients had constipation being two with fecalomas. Four out of these nine patients did not adhere to prescription and had lower lactulose doses. For patients with poor adhesion to treatment, lactulose dose was maintained and medical recommendations were reinforced. For the other four patients evolving with constipation, lactulose dose was increased to 2 mL/kg/day.

In the second week, four out of 22 patients left the study because morphine was withdrawn. Seven out of 18 remaining patients (38.8%) had constipation and four of them presented fecaloma, which was desimpacted with oral PEG 3350 in two cases and with rectal glycerin solution in two patients. One of these two patients died due to progression of baseline disease.

In the third week, morphine was withdrawn for six patients. From the 12 patients remaining in follow up, 83% remained without constipation and 16.6% of them had constipation signs.

One refractory patient was identified as not adhering to the lactulose treatment and maintenance with PEG 3350 (0.5 g/kg/Day) was started with good acceptance and favorable response in future evaluations. The other patient had fecal impaction resolved with rectal glycerin solution. Constipation in this case was considered refractory to normal treatment being necessary to replace the opioid. Patient's intestinal habit was normalized with intradermal fentanyl. One patient died in the third week due to baseline disease progression.

During the study period, nine fecaloma episodes were diagnosed. Four patients using oral PEG 3350 for fecal desimpaction had favorable response before the third day of medication and no side effects were observed. With regard to oral lactulose used for maintenance, two patients had nausea and the drug was replaced. Table 2 shows intestinal habits and presence of fecalomas.

 

DISCUSSION

Constipation diagnosis and treatment of cancer patients have major peculiarities. In these cases, several factors may change intestinal habits, such as poor food acceptance, dehydration, walking difficulties, use of numerous drugs, and clinical and emotional instability. Among drugs, opioids play a relevant role on constipation8-10. These aspects make cancer patients a group with differentiated attention needs and any sign or symptom of constipation should be considered11,12. The complex clinical situation of cancer patients impairs the collection of information to diagnose the cause of intestinal habit changes as well as to determine the effective treatment.

Our study group was heterogeneous with different types of cancer, different evolution times, simultaneous drugs, dose and duration of morphine treatment. Most patients (63.6%) had no possibility of being cured and presented a large number of intercurrences during the evaluation of intestinal habits, such as infections, tumor progression, and loss of anal sphincter control. It has to be stressed that the clinical status of cancer patients is dynamic, both with regard to baseline disease and to existing comorbidities7. Constipation secondary to morphine is not exception to this rule and our study has observed the need for regular and frequent intestinal habit follow up.

The incidence of constipation is high (40% to 60%) after starting with opioids, regardless of the type of morphine prescribed, be it immediate or slow release12. However, in spite of the frequency and the difficulty of treating it, constipation secondary to morphine is poorly valued by health professionals13,14. No studies were found in the Brazilian literature systematically evaluating the presence of constipation and the effectiveness of its treatment in children under opioids. Studies with adult patients are useful15, however they cannot simply be extrapolated as paradigm for children and adolescents with their own physical, physiological and psychological characteristics.

Although the pain control protocol used in this study recommended laxatives when starting with morphine, we have observed that only 36.4% of patients adhered to prescription. In practice, there has been poor adhesion to laxatives probably due to dysgeusia caused by cancer treatment and the need for several simultaneous drugs. After the beginning of this study, the adhesion to recommended laxatives was very satisfactory and in the second and third study weeks only one case of non-adhesion was detected. This result reinforces the need for health professionals careful attention to diagnose, follow up and treat morphine-induced constipation.

Drugs used in this study (laxatives and fecal desimpaction) have followed the recommendations for the treatment of children with chronic severe functional constipation according to approaches normally adopted in Brazil, which are in line with the North-American therapeutic guidelines16.

Studies have found that constipation is present between the 4th and the 8th day under morphine12. However, in our study, probably due to the small sample size, there has been no relationship between constipation and the time morphine was been used. Constipation secondary to morphine was observed in 40.9% of patients in the first week, in 38.8% in the second week and in 16.6% in the third week.

In spite of the small number of patients, these results may be considered similar to the international literature17,18 and are attributed, in addition to the drugs, to the fact that the study was prospective and that specific attention was given to constipation.

It is worth reminding that, according to the literature, constipation secondary to morphine affects 70% to 80% of terminal patients and is difficult to control7,13,14,19. Our study has shown that it was possible to control constipation for most patients. However, the effectiveness of the therapy should be analyzed with caution considering that, for ethical reasons, it would be impossible to have a control group. In addition, 40% of patients had constipation in spite of preventive measures, suggesting the need for studies with laxatives acting on specific intestinal receptors with higher effectiveness and few side effects20-22.

During the study, nine clinical fecaloma were diagnosed and fecal desimpaction was a difficult stage of patients' management, generating pain and discomfort. The elimination of impacted stools was achieved with rectal drugs or high dose oral laxatives. The acceptance and the efficacy of this procedure are critical for the evolution of the maintenance treatment with oral laxatives.

Rectal desimpaction should not be done under certain clinical conditions, such as leucopenia, low platelet count, anal injury, severe immunodepression and without patients' previous consent. In these cases, the option is high-dose oral laxative which, in our study, was successfully used for three times. The effectiveness of oral desimpaction with PEG 3350 has been described in the literature23. In 2006, the American Society for Pediatric Gastroenterology, Hepatology and Nutrition has recommended the use of oral laxatives in high doses for fecal desimpaction, however stressing the need for further studies in the pediatric age group.

In one patient, constipation was refractory to treatment and morphine had to be replaced by intradermal fentanyl in the third week. The replacement of one opioid by another should be considered to control refractory or unbearable side effects24. The choice of the drug to replace morphine varies according to the experience and the availability of different medical centers. µ receptor agonist opioids have the same action mechanism; however, they are different in pharmacodynamics and in the affinity for the receptor, which could explain differences in analgesia and side effects25.

Nevertheless, the regular use of osmotic and stimulating laxatives in adequate doses has improved constipation-related symptoms in 50% of patients, which is in line with the literature26,27. In three weeks of follow up it was possible to evaluate the intestinal habit profile of patients under morphine, confirming the high incidence of constipation, its difficult control and the need for an organized multidisciplinary protocol to diagnose, prevent and treat constipation secondary to morphine.

Early preventive treatment with laxatives, guidance and regular follow up may decrease the incidence of severe constipation with fecal impaction. Further controlled studies with a higher number of cases are needed to develop effective multiprofessional therapeutic practices to decrease the distress of cancer patients under morphine.

 

CONCLUSION

Constipation was frequent in patients under morphine, however, the protocol with specific attention to constipation has increased patients' adhesion to laxatives and, as a consequence, has decreased the incidence of fecalomas.

 

REFERENCES

1. Donnelly S, Davis MP, Walsh D, et al. Morphine in cancer pain management: a practical guide. Support Care Cancer. 2002;10(1):13-35.         [ Links ]

2. Portenoy RK, Lesage P. Management of cancer pain. Lancet. 1999;353(9165):1695-700.         [ Links ]

3. World Health Organization, International Association for the Study of Pain. Cancer pain relief and palliative care in children. Geneva: Switzerland: WHO; 1998. p. 76.         [ Links ]

4. De Schepper HU, Cremonini F, Park MI, et al. Opioids and the gut: pharmacology and current clinical experience. Neurogastroenterol Motil. 2004;16(4):383-94.         [ Links ]

5. Lacy BE, Brunton SA. Partnering with gastroenterologists to evaluate patients with chronic constipation. Med Gen Med. 2005;7(2):19-34.         [ Links ]

6. Glare P, Walsh D, Sheehan D. The adverse effects of morphine: a prospective survey of common symptoms during repeated dosing for chronic cancer pain. Am J Hosp Palliat Care. 2006;23(3):229-35.         [ Links ]

7. Monteiro Caran EM, Dias GG, Seber A, et al. Clinical aspects and treatment of pain in children and adolescents with cancer. Pediatr Blood Cancer. 2005;45(7):925-32.         [ Links ]

8. McNicol E, Horowicz-Mehler N, Fisk RA, et al. Management of opioid side effects in cancer-related and chronic noncancer pain: a systematic review. J Pain. 2003;4(5):231-56.         [ Links ]

9. Ross GR, Gabra BH, Dewey WL, et al. Morphine tolerance in the mouse ileum and colon. J Pharmacol Exp Ther. 2008;327(2):561-72.         [ Links ]

10. Sahinler BE. A review of pediatric pain management in acute and chronic setting. Pain Pract. 2002;2(2):137-50.         [ Links ]

11. Rasquin A, Di Lorenzo C, Forbes D, A et al. Childhood functional gastrointestinal disorders: child/adolescent. Gastroenterology. 2006;130(5):1527-37.         [ Links ]

12. Klepstad P, Kaasa S, Skauge M, et al. Pain intensity and side effects during titration of morphine to cancer patients using a fixed schedule dose escalation. Acta Anaesthesiol Scand. 2000;44(6):656-64.         [ Links ]

13. Woelk CJ. The hand that writes the opioid. Can Fam Physician. 2007;53(6):1015-7.         [ Links ]

14. Woolery M, Carroll E, Fenn E, et al. A constipation assessment scale for use in pediatric oncology. J Pediat Onc Nurs. 2006;23(2):65-74.         [ Links ]

15. Tamayo AC, Diaz-Zuluaga PA. Management of opioid-induced bowel dysfunction in cancer patients. Support Care Cancer. 2004;12(9):613-8.         [ Links ]

16 Evaluation and treatment of constipation in infants and children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr. 2006;43(3):e1-e13.         [ Links ]

17. Michail S, Gendy E, Preud'Homme D, et al. Polyethylene glycol for constipation in children younger than eighteen months old. J Pediatr Gastroenterol Nutr. 2004;39(2):197-9.         [ Links ]

18. Woolery M, Bisanz A, Lyons HF, et al. Putting evidence into practice: evidence-based interventions for the prevention and management of constipation in patients with cancer. Clin J Oncol Nurs. 2008;12(2):317-37.         [ Links ]

19. Droney J, Ross J, Gretton S, et al. Constipation in cancer patients on morphine. Support Care Cancer. 2008;16(5):453-9.         [ Links ]

20. Simpson K, Leyendecker P, Hopp M, J et al. Fixed-ratio combination oxycodone/naloxone compared with oxycodone alone for the relief of opioid-induced constipation in moderate-to-severe noncancer pain. Curr Med Res Opin. 2008;24(12):3503-12.         [ Links ]

21. Akkawi R, Eksborg S, Andersson A, et al. Effect of oral naloxone hydrochloride on gastrointestinal transit in premature infants treated with morphine. Acta Paediatr. 2009;98(3):442-7.         [ Links ]

22. Webster L, Jansen JP, Peppin J, et al. Alvimopan, a peripherally acting mu-opioid receptor (PAM-OR) antagonist for the treatment of opioid-induced bowel dysfunction: results from a randomized, double-blind, placebo-controlled, dose-finding study in subjects taking opioids for chronic non-cancer pain. Pain. 2008;137(2):428-40.         [ Links ]

23. Youssef NN, Peters JM, Henderson W, et al. Dose response of PEG 3350 for the treatment of childhood fecal impaction. J Pediatr. 2002;141(3):410-4.         [ Links ]

24. Radbruch L, Sabatowski R, Loick G, et al. Constipation and the use of laxatives: a comparison between transdermal fentanyl and oral morphine. Palliat Med. 2000;14(2):111-9.         [ Links ]

25. Russell RD, Chang KJ. Alternated delta and mu receptor activation: a stratagem for limiting opioid tolerance. Pain. 1989;36(3):381-9.         [ Links ]

26. Fukshansky M, Are M, Burton AW. The role of opioids in cancer pain management. Pain Pract. 2005;5(1):13-54.         [ Links ]

27. Associação Brasileira de Cuidados Paliativos (ABCP). Consenso Brasileiro de Constipação Intestinal Induzida por Opioides. Rev Bras Cuid Paliat. 2009;2(1):1-34.         [ Links ]

 

 

Correspondence to:
Alessandra Esteves, M.D.
Rua Gabriel Monteiro da Silva, 700 – Centro
37130-000 Alfenas, MG.
Phone: (35) 3299-1302
E-mail: aesteves@unifal-mg.edu.br

Submitted in April 11, 2012.
Accepted for publication in August 26, 2012.

 

 

*Received from the Federal University of São Paulo (UNIFESP). Department of Pediatrics – Institute of Pediatric Oncology. São Paulo, SP.

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License