Abstracts
Objective:
To study the self-medication for pain among students of medicine and nursing of the PUCSP compared with students from other knowledge areas.
Material and methods:
Data were obtained in two groups: A - students from the health knowledge area, and B - students of law and engineering. It was used a questionnaire developed by the authors. Statistical analysis used the Chi-square test and the Fischer.
Results:
In relation to gender, there is a predominance of women in the health group and a male majority in other one. In the health group there was a greater number of medical students, and in the control group of engineering. It is observed a high degree of selftreatment in both groups. It appears that participants in the health group have used more anti-inflammatory drugs and opioid than the others subjects studied.
Conclusion:
The frequency of medication for pain is higher in the group of health students, and self-medication is equally practiced among students of health and other areas.
Pain; Analgesics; Self-medication
Objetivo:
Estudar a automedicação para dor entre estudantes de cursos de medicina e enfermagem da PUCSP em comparação com estudantes das outras áreas de conhecimento.
Material e métodos:
Esses dados foram obtidos em dois grupos: A - estudantes da área da saúde e B - estudantes da área de ciências humanas e exatas. Utilizou-se um questionário elaborado pelos autores. A análise estatística usou o teste do qui-quadrado e de Fischer.
Resultados:
Na área de saúde há um predomínio do gênero feminino, e nas outras áreas um predomínio masculino. Na área de saúde a maior parte dos estudantes cursa medicina, e nas outras áreas engenharia. Observa-se um alto índice de automedicação em ambos os grupos, constatando-se que os participantes do grupo da área de saúde usam significativamente mais opioides e anti-inflamatórios que os demais estudados.
Conclusão:
A frequência do uso de medicamentos para dor é maior no grupo de estudantes da área de saúde, e a automedicação é praticada igualmente entre estudantes da área de saúde e das demais áreas.
Dor; Analgésicos; Automedicação
Introduction
Pain is defined as "a sensory and emotional experience associated with existing or potential tissue damage, reported as if the injury already existed." Pain is classified as acute or chronic. The occurrence of acute pain indicates injury and exhibits a physiological factor of defense. On the other hand, chronic pain in general has no physiological value and corresponds to an adaptation mechanism.11. Fink Jr WA. The pathophysiology of acute pain. Emerg Med Clin N Am. 2005;23: 77-284.
2. Porth CM. Fisiopatologia. 6ª ed. Rio de Janeiro: Guanabara Koogan, 2004; Cap. 48.
3. Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.-44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006. Moreover, Woolf55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451. divides pain in adaptive pain, associated with the protection of the body and with promotion of wound healing (nociceptive and/or inflammatory origin), and maladaptive pain, which is related to pathological CNS activity (neuropathic and/or functional origin).
Pain should be treated with analgesics and non-pharmacological measures. Among these, we emphasize healthcare education, exercise, and physical medicine. According to Teixeira,44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006. physical medicine provides comfort, cures physical dysfunctions, normalizes physiological dysfunctions and reduces the fear associated with the mobilization or immobilization of body parts. The modalities used in physical medicine are acupuncture, thermotherapy, massotherapy, mobilization, electroanalgesia and psicoprophylaxis (meditation, hypnosis, relaxation, etc.).33. Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.,44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006.,66. Sousa AC, Lopes MJM. Práticas terapêuticas entre idosos de Porto Alegre: uma abordagem qualitativa. Rev Esc Enferm. USP. 2007;41:52-56.
Pharmacological therapy is aimed at treating short-term pain, enabling the individual to achieve mobility.33. Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.,44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006. Analgesia obtained through drugs does not eliminate the cause of pain, but its proper use may lead to an improved quality of life since it facilitates the treatment of the causal factor, and possibly prevents the acute to chronic pain progression.44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006. The drugs used include analgesics, nonsteroidal anti-inflammatory drugs (NSAIDs), opioids and possibly antidepressants and anticonvulsants as adjuvants.33. Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.
4. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006.-55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.
8. Perrot S, Maheu E, Javier RM, Eschalier A, Coutaux A, Le Bars M, et al. Guidelines for the use of antidepressants in painful rheumatic conditions. Eur J Pain. 2006;10:185-92.
9. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.-1010. Ardoin SP, Sundy JS. Update on nonsteroidal antiinflammatory drugs. Curr Opin Rheumatol 2006; 18: 221-226. The indiscriminate use of these drugs should be avoided, because of its adverse effects. One of the central aspects regarding the appropriate use of drugs involves self-medication. Arrais et al.1111. Arrais PSD, Coelho HLL, Bastita MCDS, Carvalho ML, Righi RE, Arnau JM. Perfil da automedicação no Brasil. Rev Saúde Pública. 1997;31:71-7.refer to self-medication as a procedure characterized by the initiative of a patient, or of his (hers) parents, to obtain or produc,e and use a product which, he (she) believes, will benefit the treatment of diseases or for relieving the symptoms.1212. Vitor RS, Lopes CP, MenezesHS, Kerkhoff CE. Padrão de consumo de medicamentos sem prescrição médica na cidade de Porto Alegre, RS. Ciênc. Saúde coletiva. 2008;13;suppl:737-43. Another term used, according to Bestane et al.,1313. Bestane WJ, Meira AR, Krasucki MR. Alguns aspectos da prescrição de medicação para o tratamento de gonorreia em farmácias de Santos (SP). Rev Assoc Med Bras. 1980;26:2-3.is "oriented self-medication", which refers to the reuse of old prescriptions not intended for continuous use.
Theoretically, healthcare professionals and students know the medications and their risks, so they should avoid self-medication. The aim of this study was to evaluate the proper use of pain medication for pain management by healthcare students, compared to students from other knowledge areas.
Material and methods
1) Patients: 247 medicine and nursing students at the Pontifícia Universidade Católica de São Paulo (PUC-SP) were studied.
2) A control group of 252 law and engineering students was also studied.
3) Study Design: A cross-sectional descriptive cohort study.
4) Elaboration and application of a questionnaire containing the following variables: demographic data, student data, number of analgesics used in the last year, presence or absence of medical indication, incidence in both groups of drugs', with and without prescription, adverse effects.
5) Statistical analysis: chi-square or Fisher's exact test were applied (Siegel, 2006), aiming to compare groups A and B in relation to percentage of use, prescriptions obtained, appearance of adverse effects and type of drug used. The level of significance was p < 0.05%, or 5%.
6) Ethical aspects: This project and the obtained informed consent were approved by the Ethics in Research Committee of Faculdade de Ciências Médicas e da Saúde, PUC-SP.
Results
Table 1 shows the distribution of subjects according to gender, age and area of knowledge. Regarding gender, in group A (healthcare subjects) there is a predominance of females; in group B there is a male predominance. In group A, most students pertained to medicine area; in group B, there was a predominance of subjects in the engineering field.
Table 2 shows the frequency and percentage of analgesics used in the last year. More individuals in group A used analgesics, compared to group B.
Table 3 shows the origin of the pharmacological indication, with or without prescription. A high rate of self-medication in both groups was observed, without statistically significant difference.
Table 4 shows the frequency of reported adverse effects after the use of analgesics in both groups.There is a low incidence of adverse effects in both groups, without a statistically significant difference.
Table 5 shows the distribution of analgesics use in relation to pharmaceutical specialties. In group A, analgesics (45.5%) and anti-inflammatory drugs (55.3%) intake was significantly higher than opioids (4.4%), and antidepressants (4.0%) consumption. In group B (control), the chi-square test showed that analgesic consumption (43.2%) was significantly higher than all other drugs. This test also revealed that anti-inflammatory drugs (23.0%) were more used than opioids (1.6%) and antidepressants (2.8%). Comparing the two groups, the statistical analysis showed that the use of anti-inflammatory drugs in group A (55.3%) was significantly higher than the control group (23%). As well as with opioids, the results were not significant, but suggest greater use in group A (4.4%). In relation to analgesics and antidepressant drugs, no significant difference between the two groups was observed.
Discussion
Self-medication can induce harmful consequences, regardless of disease, symptom or medication used. In the case of pain, this is even truer.The need for quick relief and the negative impact that pain causes in quality of life imply that the rate of self-medication in this area is quite notorious.
Analgesics and NSAIDs have a similar mechanism of action; both are cyclooxygenase (COX) inhibitors. These en-zymes are classified into: (1) COX-1, a constitutional enzyme expressed in most tissues including circulating platelets and is involved in tissue homeostasis; and (2) COX-2, induced by activated inflammatory cells (IL-1 and TNF-α-mediators), is responsible for the production of prostanoid mediators of inflammation, and it is also a CNS constitutive enzyme.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.,1010. Ardoin SP, Sundy JS. Update on nonsteroidal antiinflammatory drugs. Curr Opin Rheumatol 2006; 18: 221-226. Recently the existence of COX-3 was described, but its actions are not yet fully understood.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Analgesics exert their function mainly by inhibiting COX-2 by reducing the production of prostaglandins, bradykinins and serotonin, which are the main nociceptor stimulants, thus leading to analgesia.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.
NSAIDs, however, have analgesic, antipyretic and anti-inflammatory effects.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The analgesic effect is similar to that quoted as the mechanism of action of analgesic drugs.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The antipyretic effect is result of COX-2 inhibition in the central nervous system, which prevents the set point rise of the hypothalamic thermostat.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Finally, the antiinflammatory effect occurs by COX inhibition which interrupts the production and activation process of inflammatory mediators.55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.,1010. Ardoin SP, Sundy JS. Update on nonsteroidal antiinflammatory drugs. Curr Opin Rheumatol 2006; 18: 221-226.
Both analgesics and NSAIDs have similar adverse effects, due to their mechanisms of action. For NSAIDs, these effects involve gastrointestinal disorders (dyspepsia, diarrhea, nausea, vomiting, gastric ulceration and bleeding),77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.,1010. Ardoin SP, Sundy JS. Update on nonsteroidal antiinflammatory drugs. Curr Opin Rheumatol 2006; 18: 221-226.allergic skin reactions77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. and renal effects,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.(chronic nephritis, papillary necrosis, and acute reversible renal insufficiency).
Drugs characterized as opioids are used as analgesic, antitussive and antidiarrheal agents.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The opioid receptors are: μ (mu), κ (kappa) and δ (delta).77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Each of these receptors is involved with specific effects of opioids, and the μ and δ receptors have similar actions in the same regions.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The analgesia is produced at central level through interaction with opioid receptors present in the CNS, because these have the ability to directly inhibit the ascending transmission of nociceptive information coming from the dorsal horn of the spinal cord, and also have the ability to activate pain inhibitory descending pathways.55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The interaction of receptors with their agonists leads to a reduction of cyclic-AMP (cAMP) within neurons, inhibiting the opening of calcium channels in the presynaptic neuron, thereby inhibiting the release of neurotransmitters.55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.Moreover, the decrease of intracellular cAMP stimulates the opening of potassium channels in the postsynaptic neuron, causing a hyperpolarization that prevents the passage of nerve impulses by the ascending nociceptive pathway; thus, analgesia is produced.55. Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Furthermore, the μ/δ receptors produce analgesia within the descending circuits of pain control partly by removing the inhibition mediated by gamma-aminobutyric acid (GABA) neurons that project to the rostral ventromedial (RVM) part of medulla in the gray periaqueductal (PA) substance, as well as of neurons projecting from the RVM to the spinal cord.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007. The modulatory effects of pain by κ agonists in the brain stem seem to antagonize the effects of μ receptor agonists.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Opioid drugs can produce many adverse effects such as sedation, euphoria, dysphoria, constipation, nausea, vomiting, pruritus, dizziness and respiratory depression, along with causing tolerance and dependence.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.
Antidepressant agents can be used as adjuvant medication in the treatment of pain.33. Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.,44. Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006.,77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.
8. Perrot S, Maheu E, Javier RM, Eschalier A, Coutaux A, Le Bars M, et al. Guidelines for the use of antidepressants in painful rheumatic conditions. Eur J Pain. 2006;10:185-92.-99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The classes of antidepressant agents used are: monoamine oxidase inhibitors (MAOIs), tricyclic antidepressants (TCAs) and selective serotonin re-uptake inhibitors (SSRIs).77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. MAOIs inhibit the action of the enzyme monoamine oxidase (MAO), which is responsible for the degradation of monoamines (dopamine, norepinephrine and serotonin, for instance), thereby maintaining a high concentration of monoamines of inhibitory pain pathways in the synaptic cleft.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. TCAs and SSRIs decrease the neurotransmitter re-uptake in inhibitory pain pathways at the synaptic clefts, thus increasing the concentration of these peptides in the synapses and thereby increasing the stimulus in the postsynaptic neuron.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.Antidepressants increase the efferent pathway of pain inhibition, producing analgesia.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.,99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Furthermore,TCAs are weak agonists of μ opioid receptors, helping to obtain an analgesic effect.99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. Antidepressants can cause several adverse effects such as sedation, anticholinergic effects (dry mouth, constipation, blurred vision, urinary retention, etc.), postural hypotension, convulsions, impotence, weight gain, liver damage (rare), nausea and agitation.77. Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.
8. Perrot S, Maheu E, Javier RM, Eschalier A, Coutaux A, Le Bars M, et al. Guidelines for the use of antidepressants in painful rheumatic conditions. Eur J Pain. 2006;10:185-92.-99. Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007. The analgesic effect of TCAs is well documented; however, the analgesia produced by the use of MAOIs and SSRIs needs further studies.88. Perrot S, Maheu E, Javier RM, Eschalier A, Coutaux A, Le Bars M, et al. Guidelines for the use of antidepressants in painful rheumatic conditions. Eur J Pain. 2006;10:185-92.
The degree of knowledge on this topic can generate an awareness of the risk of self-medication but, on the other hand, can cause a false sense of security in the use of these drugs, since access to such information is more expressive. Although healthcare students have greater knowledge, it is known that even experienced professionals are cautious about the use and prescription of these medications.
Among lay population, Pereira et al.1414. Pereira FSVT, Bucaretchi F, Stephan C, Cordeiro R. Automedicação em crianças e adolescentes. J Pediatr. 2007;83:453-458.reported that 51% of drugs were indicated by mothers and 7.8% by fathers; 20.1% by pharmacy employees, 15.3% resulted from the use of old prescriptions for the child or other family member, and 1.8% by media influence. According to the article "Prevalence and factors associated with self-medication: results from the Bamburgh project",1515. Loyola Filho AI, Uchoa E, Guerra HL, Firmo JOA, Costa MFL. Prevalência e atores associados à automedicação: resultados do projeto Bambuí. Rev Saúde Pública. 2002;36:55-62. the 16 non-prescription drugs more commonly consumed by self-medication were analgesics/ antipyretics (47.6%), followed by drugs acting on the digestive tract, that is, antispasmodics, antidiarrheals, and antacids (8.5%); antibiotics or chemotherapeutic agents (6.2%) and vitamins, tonics or anti-anemic drugs (4.7%).
On the other hand, among healthcare professionals, Hem et al.,1616. Hem E, Stokke G, Tyssen R, Gronvold NT, Vaglum P, Ekeberg O. Self-prescribing among young Norwegian doctors: a nine-year follow-up study of a nationwide sample. BMC Med.2005;3:16. in a cohort composed by young Norwegian doctors, found a prevalence of 54% between the fourth and fifth year after graduation; and among those who used drugs in the year prior to the interview, 90% were self-prescriptions. Now Tomasi et al.1717. Tomasi E, Sant'Anna GC, Oppelt AM, Petrini RM, Pereira IV, Sassi BT. Condições de trabalho e automedicação em profissionais da rede básica de saúde da zona urbana de Pelotas, RS. Rev Bras Epidemiol. 2007;10:66-74. in their cross-sectional study found that 47% of healthcare workers reported drug using in the last 15 days, especially analgesics (27%), regardless of having, or not, a health problem. Moreover, these authors observed that self-medication was common practice since one fourth of the respondents stated that most drugs used had no prescription. Also in this work, 43% of physicians reported self-medication.
In our study the frequency of analgesic use was also significant, and it occurred most often through self-medication. This is true for both groups. The group A used significantly more pain medication than the other students. One aspect that may have reinforced this habit was the low frequency of adverse effects experienced by the subjects.
The group A used proportionately more anti-inflammatory and opioid drugs. We attribute this difference to the greater knowledge and access to these drugs, although they increase the risk of complications.
We can conclude that the frequency of drug use for pain is higher in the group of healthcare students (group A), and self-medication is practiced equally among healthcare students and group B.
REFERÊNCIAS
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1Fink Jr WA. The pathophysiology of acute pain. Emerg Med Clin N Am. 2005;23: 77-284.
-
2Porth CM. Fisiopatologia. 6ª ed. Rio de Janeiro: Guanabara Koogan, 2004; Cap. 48.
-
3Teixeira MJ. Dor: Contexto interdisciplinar. 1ª ed. Curitiba: Ed. Maio, 2003; Cap.17.
-
4Teixeira MJ. Dor: Manual para o clínico. 1ª ed. São Paulo: Atheneu, 2006.
-
5Woolf CJ. Pain: moving from symptom control toward mechanism-specific pharmacologic management. American College of Physicians. 2004;140:441-451.
-
6Sousa AC, Lopes MJM. Práticas terapêuticas entre idosos de Porto Alegre: uma abordagem qualitativa. Rev Esc Enferm. USP. 2007;41:52-56.
-
7Brunton LL, Lazo JS, Parker KL. In: Goodman & Gilman. As Bases Farmacológicas da Terapêutica. 11. ed. Rio de Janeiro: Mc Graw Hill, 2007.
-
8Perrot S, Maheu E, Javier RM, Eschalier A, Coutaux A, Le Bars M, et al. Guidelines for the use of antidepressants in painful rheumatic conditions. Eur J Pain. 2006;10:185-92.
-
9Rang HP, Dale MM, Ritter JM, Flower RJ. Farmacologia. 6ª ed. Rio de Janeiro: Elsevier, 2007.
-
10Ardoin SP, Sundy JS. Update on nonsteroidal antiinflammatory drugs. Curr Opin Rheumatol 2006; 18: 221-226.
-
11Arrais PSD, Coelho HLL, Bastita MCDS, Carvalho ML, Righi RE, Arnau JM. Perfil da automedicação no Brasil. Rev Saúde Pública. 1997;31:71-7.
-
12Vitor RS, Lopes CP, MenezesHS, Kerkhoff CE. Padrão de consumo de medicamentos sem prescrição médica na cidade de Porto Alegre, RS. Ciênc. Saúde coletiva. 2008;13;suppl:737-43.
-
13Bestane WJ, Meira AR, Krasucki MR. Alguns aspectos da prescrição de medicação para o tratamento de gonorreia em farmácias de Santos (SP). Rev Assoc Med Bras. 1980;26:2-3.
-
14Pereira FSVT, Bucaretchi F, Stephan C, Cordeiro R. Automedicação em crianças e adolescentes. J Pediatr. 2007;83:453-458.
-
15Loyola Filho AI, Uchoa E, Guerra HL, Firmo JOA, Costa MFL. Prevalência e atores associados à automedicação: resultados do projeto Bambuí. Rev Saúde Pública. 2002;36:55-62.
-
16Hem E, Stokke G, Tyssen R, Gronvold NT, Vaglum P, Ekeberg O. Self-prescribing among young Norwegian doctors: a nine-year follow-up study of a nationwide sample. BMC Med.2005;3:16.
-
17Tomasi E, Sant'Anna GC, Oppelt AM, Petrini RM, Pereira IV, Sassi BT. Condições de trabalho e automedicação em profissionais da rede básica de saúde da zona urbana de Pelotas, RS. Rev Bras Epidemiol. 2007;10:66-74.
Publication Dates
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Publication in this collection
Mar-Apr 2014
History
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Received
26 July 2012 -
Accepted
26 Aug 2013