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Program of combined physical exercise reduces the perception of pain in a patient with sickle cell anemia. Case report

ABSTRACT

BACKGROUND AND OBJECTIVES:

Sickle cell anemia is one of the most common hereditary hematological disease in the world. Among many clinical manifestations, the main characteristic of this disease is the painful crises. Considering the increasing number of individuals with sickle cell anemia in Brazil, the increase in life expectancy of these individuals, who are advised to restrict physical activity, it is important to investigate this subject since exercises have been listed as relevant in health promotion. The objective of this study was to analyze the perception of pain, some physiological responses and the quality of life of a patient with sickle cell anemia undergoing a program of physical exercises (aerobic and resistance).

CASE REPORT:

Female patient, 56 years old, diagnosed with sickle cell anemia as a child, and in the course of this research did not make routine use of drugs in the control of the disease. On physical and ergo-spirometric examination, and during four-month of combined exercise, she did not present critic clinical condition, only some characteristic difficulties such as musculoskeletal pain, low cardiorespiratory resistance, and early fatigue.

CONCLUSION:

The results suggested that a program of combined and regular exercises produced important changes in the patient, in several aspects related to her health, including the reduction of musculoskeletal pain and increased general physical fitness, contributing to the improvement of the perception of quality of life.

Keywords:
Health promotion; Musculoskeletal pain; Physical exercise; Physiology; Quality of life; Sickle cell disease

RESUMO

JUSTIFICATIVA E OBJETIVOS:

A anemia falciforme é uma das doenças hematológicas hereditárias mais frequentes no mundo. Dentre as diversas manifestações clínicas, a principal característica dessa doença são as crises dolorosas. Considerando o crescente número de indivíduos com anemia falciforme no Brasil, o aumento da expectativa de vida desses indivíduos, e que ainda recebem orientação para restringirem práticas de esforços físicos, investigações sobre o tema se tornam relevantes, uma vez que o exercício físico tem sido elencado como estratégia na promoção da saúde. O objetivo deste estudo foi analisar a percepção da dor, algumas respostas fisiológicas e a qualidade de vida de uma portadora de anemia falciforme submetida a um programa de exercício físico combinado (aeróbio e resistido).

RELATO DO CASO:

Paciente do sexo feminino, 56 anos de idade, diagnosticada com anemia falciforme quando criança, e no decorrer desta pesquisa não fez uso rotineiro de fármacos para o controle da doença. No exame físico e ergoespirométrico, e durante o período de intervenção de quatro meses de exercício físico combinado, não apresentou quadro clínico crítico, apenas algumas dificuldades características, como: dores osteomusculares, baixa resistência cardiorrespiratória e fadiga precoce.

CONCLUSÃO:

Os resultados sugeriram que um programa de exercício físico combinado e regular produziu alterações importantes para a paciente, em diferentes aspectos relacionados à sua saúde, dentre elas destacam-se a diminuição da dor osteomuscular e aumento da aptidão física geral, contribuindo para a melhora da percepção da qualidade de vida.

Descritores:
Anemia falciforme; Dor musculoesquelética; Exercício físico; Fisiologia; Promoção da saúde; Qualidade de vida

INTRODUCTION

Sickle cell anemia (SCA) is a hemoglobinopathy arising from the replacement of a glutamic acid by a valine at the sixth position of the beta globin, giving rise to hemoglobin S (HbS). The gene responsible for encoding this protein is located on chromosome 11. In the case of absence or decreased oxygen tension, HbS undergoes polymerization, changing the morphology of the red blood cells (sickling), carrying less oxygen and having difficulties to properly circulate through the small blood vessels, resulting in the obstruction of the capillary blood flow and their early destruction11 Steinberg MH. Pathophysiologically based drug treatment of sickle cell disease. Trends Pharmacol Sci. 2006;27(4):204-10..

Sickle cell anemia is one of the most common hereditary hematological disease in the world. In Brazil, it has a significant epidemiological importance due to its prevalence; 2 to 8% of the population and its morbidity and mortality, therefore it has been singled out as a public health issue22 Fernandes AP, Januário JN, Cangussu CB, Macedo DL, Viana MB. Mortality of children with sickle cell disease: a population study. J Pediatr. 2010;86(4):279-84. English, Portuguese.. However due to the advances in treatment, the infant mortality rate has decreased significantly in recent decades, however, the number of adults with SCA with late complications increased33 McGann PT, Ware RE. Hydroxyurea therapy for sickle cell anemia. Expert Opin Drug Saf. 2015;14(11):1749-58..

The pathophysiological mechanism of the disease can cause several acute and chronic clinical manifestations, such as acute chest syndrome, pulmonary hypertension, heart failure and stroke44 Mya ST, Norris EI, Swee LT. Sickle cell disease in the older adult. Pathology. 2017;49(1):1-9.. Among the characteristic manifestations of the disease, vaso-occlusive crises are frequent, causing pain in bones, muscles, and joints as a result of the obstruction of the microcirculation of the sickled erythrocytes55 Stettler N, McKiernan CM, Melin CQ, Adejoro OO, Walczak NB. Proportion of adults with sickle cell anemia and pain crises receiving hydroxyurea. JAMA. 2015;313(16):1671-2..

The intense physical effort is one of the factors that can contribute to this process66 Ballas SK, Gupta K, Adams-Graves P. Sickle cell pain: a critical reappraisal. Blood. 2012;120(18):3647-56. which can worsen the complications and cause sudden death of these patients. However, Harmon et al.77 Harmon KG, Drezner JA, Klossner D, Asif IM. Sickle cell trait associated with a RR of death of 37 times in National Collegiate Athletic Association football athletes: a database with 2 million athlete-years as the denominator. Br J Sports Med. 2012;46(5):325-30. found that the absolute number of deaths in people with SCA due to physical exercise (PE) is small and that mortality occurred with practitioners of intense physical exercise. Thus, there are some recommendations for the practice of physical exercises in order to reduce the risks and injuries of the disease, such as: control the intensity and duration of exercises and hydration during the performance88 Ethical guidelines for publication in clinical hemorheology and microcirculation. Clin Hemorheol Microcirc. 2010;44(1):1-2.,99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63.. Following the recommendations, the study of Barbeau et al.1010 Barbeau KF, Woods LT, Ramsey MS, Litaker DM, Pollock JS, Pollock LA, et al. Exercise in sickle cell anemia: Effect on inflammatory and vasoactive mediators. Endothelium. 2008;8(2):147-55. showed that regular exercise with moderate intensity (60-75%) can decrease the risk of the inflammatory reaction related to exercise and increase the vasodilator reserve, decreasing the risk of vaso-occlusive crisis.

Systemic deficiencies caused by the disease can lead to a more sedentary lifestyle, which in turn may result in an overall loss of muscle strength and cardiorespiratory capacity. Ivo and de Carvalho1111 Ivo ML, de Carvalho EC. [Nursing care for patients with sickle cell disease, in the light of Roy' model. Rev Lat Am Enfermagem. 2003;11(2):192-8. Portuguese. reported that patients with SCA had dyspnea when walking, climbing stairs or ramps, or performing vigorous physical activities, which indicates a loss of functional capacity in this population. As a result of these alterations, limitations, and pain, it is also common to see a variable impact on the quality of life (QoL) of these patients1212 Braga JA. Medidas gerais no tratamento das doenças falciformes. Rev Bras Hematol Hemoter. 2007;29(3):233-8..

As a consequence of the inherent risks in the practice of misguided physical exercises and incipient information in the scientific literature, professionals are still reluctant to recommend physical exercises. Studies on the effects of physical exercises in patients with SCA showed beneficial effects on pain, strength and QoL in children1313 Alcorn R, Bowser B, Henley EJ, Holloway V. Fluidotherapy and exercise in the management of sickle cell anemia. A clinical report. Phys Ther. 1984;64(10):1520-2.,1414 Tinti G, Somera R, Valente FM, Domingos CR. Benefits of kinesiotherapy and aquatic rehabilitation on sickle cell anemia. Genet Mol Res. 2010;9(1):360-4.. However, little is known about the possible effects on adults, especially, the combined physical exercise. Considering the increasing number of cases of SCA in Brazil, the increase in life expectancy of these individuals and the progressive reduction in functional capacity due to complications, specifically the painful crises, investigations on the subject become relevant, both for patients who will directly benefit from the effects of physical exercises and for health professionals, who can identify therapeutic strategies for these patients.

The objective of this study was to analyze the perception of pain, some physiological responses and the QoL of an SCA patient undergoing a combined physical exercise program.

CASE REPORT

Female patient, 56 years old, diagnosed with SCA as a child. She underwent a multidisciplinary treatment with the family, to better understand the disease, signs of severity, and proper measures to prevent and treat her crises. During this survey, and in the six previous months, she did not take any drugs routinely to control the disease, only when she had the painful crises. Her hemoglobin test showed a moderate anemia (9.7 g/dL), according to the World Health Organization (WHO)1515 WHO. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. Vitamin and Mineral Nutrition Information System. Geneva: World Health Organization; 2011.. In the physical examination and ergospirometry test, she did not present critical clinical conditions (ulcers, bacterial infections or any other renal, ophthalmologic, neurologic, cardiovascular and pulmonary complications)1616 Azar S, Wong TE. Sickle cell disease: a brief update. Med Clin North Am. 2017;101(2):375-93., only some difficulties characteristic of the disease as musculoskeletal pain (mainly in the lower limbs and the lumbar region), low cardiorespiratory resistance and early fatigue in the ergospirometry test. Apart from that, she had a physically active life according to the data obtained by the International Physical Activity Questionnaire (IPAQ).

Before the beginning of the activities, it was applied the pain questionnaires (Brief Pain Inventory - BPI)1717 Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer. 2011;19(4):505-11. and level of physical activity by IPAQ, brief forms1818 Pardini R, Matsudo SM, Matsudo VK, Araujo T, Andrade E, Braggion GF, et al. Validation of international physical activity questionnaire (IPAQ): pilot study in Brazilian young adults. Med Sci Sports Exerc.1997;29(6):5-9.. Also, we had anthropometric evaluations (body mass, height, and body mass index - BMI), and physical fitness test (flexibility of upper/lower limbs, motor coordination, agility, upper and lower limbs and abdominal strength, and static balance1919 Clark BA. Tests for fitness in older adults: AAHPERD Fitness Task Force. J Phys Educ Recreat Dance. 1989;60(3):66-71.. The ergospirometry test was performed on a treadmill to measure the cardiorespiratory capacity, using the Bruce Protocol adapted, with progressive load until maximum voluntary exhaustion. During the test, the heart rate (HR) was monitored using a frequency counter (POLAR® T31), blood pressure (Premium sphygmomanometer and stethoscope) and the subjective perceived exertion (The Borg Rating of Perceived Exertion scale - RPE)2020 Borg GA. Psychophysical bases of perceived exertion. Med Sci Sports Exerc. 1982;14(5):377-81.. During the assessment, the level of hemoglobin was also measured by capillary blood collection and by hemoglobinometer (Agabe®).

In addition, for the analysis of the effect of the physical exercise pre-and post-program on the patient›s QoL (qualitative character), a semi-structured interview was elaborated aiming at the self-perception of the improvement or worsening in relation to: pain, sleep, mood, self-esteem, health, pleasure, stimulation, posture and exercises.

The physical exercise program adopted lasted for four months (48 sessions). The training was a combined approach (aerobic and resisted in the same session)2121 Kraemer WJ, Keuning M, Ratamess NA, Volek JS, McCormick M, Bush JA, et al. Resistance training combined with bench-step aerobics enhances women's health profile. Med Sci Sports Exerc. 2001;33(2):259-69., and the overload was applied in accordance with the results obtained in the tests and by the RPE during the program. Three weekly sessions of 60 minutes each, consisting of 30 minutes of aerobic training (at HR between the anaerobic threshold 1 and the anaerobic threshold 2 [110-125 bpm]) and 30 minutes of resisted exercise, with three sets of 10 to 12 repetitions, for the large muscle groups, alternating exercises for the lower and upper members. The sequence adopted throughout the experiment was aerobic followed by resisted training, and the subject accomplished the 48 scheduled sessions of physical exercises (100% attendance).

The general characteristics of the patient, the absolute results and the respective classifications of the functional tests (physical fitness), before and after the period of the physical exercises can be observed in table 1. It is worth to highlight the increase in the diastolic blood pressure (DBP) after the training protocol and slight decrease in the hemoglobin value. In addition, the results indicated that the patient showed improvement in all the variables after the PE program, except in static balance, which remained the same. The aspects that had higher differences were: flexibility of upper limb, strength resistance of lower limb, abdominal resistance and agility.

Table 1
Values of body mass index, heart rate, blood pressure, biochemical tests, and functional fitness before and after the PE program

The results of the HR, the RPE, maximum consumption of oxygen (VO2max.), and total time during the ergospirometry test are shown in table 2. We can see a decrease in the VO2max results e longer permanence in the test after the PE program. Moreover, for the same workload, the subject had a lower HR and RPE in relation to the initial data.

Table 2
Data obtained in the ergospirometry test: heart rate, Borg scale, VO2 maximum and total time of the test before and after the physical exercise program

In relation to pain, in the BPI, the patient reported that the main sites of pain in both assessments were concentrated in the lower limbs and the lumbar spine. However, in the assessment after the PE program, she reported a decrease in the pain scale intensity and reduction of pain interference in her daily activities to walk, work, in her social activities, sleep, and mood (Table 3).

Table 3
Pain perception-Brief Pain Inventory before and after the physical exercise program

In relation to the qualitative assessment of the QoL, the subject reported pain reduction in the lumbar spine, a significant improvement in her posture, much more disposition in daily activities, and a significant increase in strength or muscle resistance.

“I feel that I am improving, I don’t feel so tired during work or even with the activities at home, and I regret when I do not come to the session because I feel my body heavier”.

DISCUSSION

SCA clinical manifestations vary among patients, while some have severe conditions with several complications, others evolve only with mild symptoms2222 Zago MA, Pinto AC. Fisiopatologia das doenças falciformes: da mutação genética à insuficiência de múltiplos órgãos. Rev Bras Hematol Hemoter. 2007;29(3):207-14.,2323 Ilesanmi OO. Pathological basis of symptoms and crises in sickle cell disorder: implications for counseling and psychotherapy. Hematol Rep. 2010;2(1):2.. In relation to the patient in this case, despite living a physically active life as seen in the IPAQ, the early diagnosis and proper professional and family follow-up were very important and probably contributed to a controlled clinical condition, without the need for routine use of drugs, providing a longer life expectancy. In fact, authors state that the early diagnosis, added to the expertise of a multidisciplinary team and the participation of the family has a crucial role in the reduction of complications associated with the disease, as well as prolonging the life of patients2424 Bender MA, Douthitt Seibel G. Sickle cell disease. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, et al. (editors) Gene Reviews®. Seattle (WA): University of Washington; 1993-2015.,2525 Kanter J, Jordan LB. Improving the healthcare model for management of adults with sickle cell disease in the PPACA Era. J Hematol Transfus. 2015;3(1):1037..

Pain is a common clinical manifestation of SCA and patients usually seek for medical care2626 Smith WR, Penberthy LT, Bovbjerg VE, McClish DK, Roberts JD, Dahman B, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med. 2008;148(2):94-101.. In fact, Martins, Moraes and Silveira2727 Martins PR, Moraes-Souza H, Silveira TB. Morbimortalidade em doença falciforme. Rev Bras Hemoter Hematol. 2010;32(5):378-83. in a study conducted in a blood bank in Brazil, showed that the most prevalent care for patients with SCA is due to pain crises, accounting for a total of 64.4% of the cases.

In this study, the main discomfort related to pain reported by the subject was in the lower limbs and in the lumbar region, corroborating with Taylor et al.2828 Taylor LE, Stotts NA, Humphreys J, Treadwell MJ, Miaskowski C. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease. J Pain Symptom Manage. 2010;40(3):416-35. study on the multiple dimensions of chronic pain in adults with sickle cell disease, being the hip region the most affected by chronic pain, followed by the spine.

With regard to the hemodynamic variables, the subject had systolic and diastolic blood pressure within the normality limits, however, we noticed an increase in the diastolic blood pressure (DPB) after the PE program. The increase in DPB to 90 mmHg characterizes the cut-off point between normotension and hypertension2929 Malachias MV, Souza WK, Plavnik FL, Rodrigues CI, Brandao AA, Neves MF, et al. 7ª Diretriz Brasileira de Hipertensão. Arq Bras Cardiol. 2016;107(3 Suppl 3):1-82.,3030 National Heart Foundation of Australia. Guideline for the diagnosis and management of hypertension in adults. Melboume: National Heart Foundation of Australia; 2016.. In this case, the proposal for a combined exercise intervention may have been responsible for the increase in DPB (however, within the normal range), at the end of the PF period, probably due to a greater total peripheral vascular resistance and the systolic parietal stress caused by resisted exercise3131 Martins WA, Mesquita ET, Cunha DM, Ferrari AH, Pinheiro LA, Romêo LJ, et al. Alterações cardiovasculares na anemia falciforme. Arq Bras Cardiol. 1998;70(5):365-70..

The results obtained in the ergospirometry confirmed that the cardiorespiratory capacity of the subject, defined by the VO2 peak, was lower when compared to a person without the disease, as in the study of Liem et al.3232 Liem RI, Reddy M, Pelligra SA, Savant AP, Fernhall B, Rodeghier M, et al. Reduced fitness and abnormal cardiopulmonary responses to maximal exercise testing in children and young adults with sickle cell anemia. Physiol Rep. 2015;3(4):1-8.. Van Beers et al.3333 Van Beers EJ, Van Der Plas MN, Nur E, Bogaard HJ, Van Steenwijk RP, Biemond BJ. Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients. Am J Hematol. 2014;89(8):819-24., also affirmed that the cardiorespiratory responses are below average in 83% of patients with SCA. Moreover, the oxygen uptake efficiency seems to be lesser between adults with SCA submitted to sub-maximum effort tests3434 Charlot K, Waltz X, Hedreville M, Sinnapah S, Lemonne N, Etienne-Julan M, et al. Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities. Clin Hemorheol Microcirc. 2014;60(4):413-21..

Some studies analyzed the mechanisms responsible for the intolerance to exercises in patients with SCA and found out that some factors can contribute, such as the reduction of oxygen carrying capacity related with the low hemoglobin level, the functional and structural heart adaptations resulting from the chronic anemia and pulmonary dysfunctions99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63.,3232 Liem RI, Reddy M, Pelligra SA, Savant AP, Fernhall B, Rodeghier M, et al. Reduced fitness and abnormal cardiopulmonary responses to maximal exercise testing in children and young adults with sickle cell anemia. Physiol Rep. 2015;3(4):1-8.,3333 Van Beers EJ, Van Der Plas MN, Nur E, Bogaard HJ, Van Steenwijk RP, Biemond BJ. Exercise tolerance, lung function abnormalities, anemia, and cardiothoracic ratio in sickle cell patients. Am J Hematol. 2014;89(8):819-24..

The patient presented a VO2 max and HR below the expected for her age and physical condition3535 Artur HH, Dorian U. Valores de referência para o teste cardiopulmonar para homens e mulheres sedentários e ativos. Soc Bras Cardiol. 2010;96(1):54-9., both before and after the combined PE intervention. This condition can be attributed, in part, to the left ventricular systolic dysfunction (due to an HR max lower than expected), and/or the decrease in the hemoglobin level. However, despite the decrease in the relative VO2 max, the subject had an increase in the total time of the test (13%), on the same protocol (Bruce adapted). So, one can assume that the low hemoglobin level may have led to the decrease of total oxygen content, but, on the other hand, it may have improved blood flow and, consequently, increased the cardiac output after the training period3636 Lobo C, Marra VN, Silva RM. Crises dolorosas na doença falciforme. Rev Bras Hematol Hemoter. 2007;29(3):247-58..

Regarding the cause of SCA, there are no clear indications in the literature that PE have the potential to change hemoglobin S concentration or to revert the sickling process. In the present study, we found a reduction of 0.3 g/dL in plasma hemoglobin concentration after the PE program. However, such difference does not present great biological relevance. Furthermore, it was not measured if this discrete reduction was on sickle hemoglobin (HbS) or normal hemoglobin (HbAA). However, there was no severe symptom of the disease during the experiment, suggesting that a combined, and guided PE program does not bring risks or harm to patients with SCA.

The functional capacity can influence the performance of daily activities. In this context, the subject reported that most of the time her functional capacity was influenced by pain. Lobo, Marra and Silva3636 Lobo C, Marra VN, Silva RM. Crises dolorosas na doença falciforme. Rev Bras Hematol Hemoter. 2007;29(3):247-58. showed that the results of the physical aspects domain that include the impact of physical health in the performance of daily activities and/or professional were also significantly affected by pain.

In this scope, physical fitness parameters were also assessed, and the absolute values demonstrated that after the PE program there was an improvement in all the variables, except for static balance which remained the same. Moreover, in the strength resistance tests of upper and lower limbs, the classification went from poor to good, and from regular to good, respectively. We did not find studies in the literature that used similar tests in SCA patients. However, the responses found become relevant, especially within the context of the patient’s QoL since it is influenced by physical aspects, as well as emotional and social3737 Strickland OL, Jackson G, Gilead M, McGuire DB, Quarles S. Use of focus groups for pain and quality of life assessment in adults with sickle cell disease. J Natl Black Nurses Assoc. 2001;12(2):36-43..

Therefore, this case demonstrates that although the cardiorespiratory conditions did not improve by the combined PE protocol, it was observed a trend to the improvement in the aspects of physical fitness, pain and in the perception in the QoL. This is an important point to emphasize since this patient was physically active (according to the IPAQ classification), which can lead to the assumption that better results could have been observed in case of sedentary individuals.

It is important to point out the inherent risks of the practice physical exercises not controlled and supervised by qualified professionals, mainly by people with severe SCA complications. The risks go from worsening of disease complications to sudden death, which raise the fear by doctors to recommend physical exercises for SCA patients99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63.. In General, physical exercises induce metabolic changes (production of lactic acid, reactive oxygen species, and other circulating cytokines)3838 Pathare A, Kindi SA, Daar S, Dennison D. Cytokines in sickle cell disease. Hematology. 2003;8(5):329-37.,3939 Wood KC, Granger DN. Metabolites sickle cell disease: role of reactive oxygen and nitrogen. Clin Exp Pharmacol Physiol. 2007;34(9):926-32., changes in temperature and dehydration during exercise, which can stimulate the polymerization of HbS4040 Moheeb H, Wali YA, El-Sayed MS. Physical fitness indices and anthropometrics profiles in school children with sickle cell trait/disease. Am J Hematol. 2007; 82(2):91-7. and trigger the vaso-occlusive crisis99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63..

However, current results support the safety and potential benefits of the practice of PE by SCA patients, as reported by Tinti et al.1414 Tinti G, Somera R, Valente FM, Domingos CR. Benefits of kinesiotherapy and aquatic rehabilitation on sickle cell anemia. Genet Mol Res. 2010;9(1):360-4. and Balayssac-Siransy et al.4141 Balayssac-Siransy EA, Connes P, Tuo N, Danho C, Diaw M, Sanogo I, et al. Mild haemorheological changes induced by a moderate endurance exercise in patients with sickle cell anemia. Br J Haematol. 2011;154(3):398-407., provided that some specific recommendations are followed88 Ethical guidelines for publication in clinical hemorheology and microcirculation. Clin Hemorheol Microcirc. 2010;44(1):1-2.,99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63.. First, before the beginning of PE program, it is recommended to conduct the stress test to identify the intensity of exercise the patient may put up with stand without fatigue, pain or other symptoms. Subsequently, it is recommended to patients to start exercising gradually, avoiding intense efforts and stoping the exercise in the case of fatigue. Also, it is important to pause every 20 minutes for hydration and prevent excessive lactic acid buildup88 Ethical guidelines for publication in clinical hemorheology and microcirculation. Clin Hemorheol Microcirc. 2010;44(1):1-2.,99 Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63..

CONCLUSION

It is expected that the results of this study will contribute to the planning of preventive interventions and promotion of health in patients with SCA through a multi-professional assistance, including the presence of physical education professionals, aiming at the reduction and improvement of pain, improvement of physiological conditions and resistance to efforts, thus improving the perception of the QoL, providing individuals with SCA better conditions to perform daily activities as a result of the practice of PE.

  • Sponsoring sources: none.

REFERENCES

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    Steinberg MH. Pathophysiologically based drug treatment of sickle cell disease. Trends Pharmacol Sci. 2006;27(4):204-10.
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  • 3
    McGann PT, Ware RE. Hydroxyurea therapy for sickle cell anemia. Expert Opin Drug Saf. 2015;14(11):1749-58.
  • 4
    Mya ST, Norris EI, Swee LT. Sickle cell disease in the older adult. Pathology. 2017;49(1):1-9.
  • 5
    Stettler N, McKiernan CM, Melin CQ, Adejoro OO, Walczak NB. Proportion of adults with sickle cell anemia and pain crises receiving hydroxyurea. JAMA. 2015;313(16):1671-2.
  • 6
    Ballas SK, Gupta K, Adams-Graves P. Sickle cell pain: a critical reappraisal. Blood. 2012;120(18):3647-56.
  • 7
    Harmon KG, Drezner JA, Klossner D, Asif IM. Sickle cell trait associated with a RR of death of 37 times in National Collegiate Athletic Association football athletes: a database with 2 million athlete-years as the denominator. Br J Sports Med. 2012;46(5):325-30.
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    Ethical guidelines for publication in clinical hemorheology and microcirculation. Clin Hemorheol Microcirc. 2010;44(1):1-2.
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    Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-63.
  • 10
    Barbeau KF, Woods LT, Ramsey MS, Litaker DM, Pollock JS, Pollock LA, et al. Exercise in sickle cell anemia: Effect on inflammatory and vasoactive mediators. Endothelium. 2008;8(2):147-55.
  • 11
    Ivo ML, de Carvalho EC. [Nursing care for patients with sickle cell disease, in the light of Roy' model. Rev Lat Am Enfermagem. 2003;11(2):192-8. Portuguese.
  • 12
    Braga JA. Medidas gerais no tratamento das doenças falciformes. Rev Bras Hematol Hemoter. 2007;29(3):233-8.
  • 13
    Alcorn R, Bowser B, Henley EJ, Holloway V. Fluidotherapy and exercise in the management of sickle cell anemia. A clinical report. Phys Ther. 1984;64(10):1520-2.
  • 14
    Tinti G, Somera R, Valente FM, Domingos CR. Benefits of kinesiotherapy and aquatic rehabilitation on sickle cell anemia. Genet Mol Res. 2010;9(1):360-4.
  • 15
    WHO. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. Vitamin and Mineral Nutrition Information System. Geneva: World Health Organization; 2011.
  • 16
    Azar S, Wong TE. Sickle cell disease: a brief update. Med Clin North Am. 2017;101(2):375-93.
  • 17
    Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer. 2011;19(4):505-11.
  • 18
    Pardini R, Matsudo SM, Matsudo VK, Araujo T, Andrade E, Braggion GF, et al. Validation of international physical activity questionnaire (IPAQ): pilot study in Brazilian young adults. Med Sci Sports Exerc.1997;29(6):5-9.
  • 19
    Clark BA. Tests for fitness in older adults: AAHPERD Fitness Task Force. J Phys Educ Recreat Dance. 1989;60(3):66-71.
  • 20
    Borg GA. Psychophysical bases of perceived exertion. Med Sci Sports Exerc. 1982;14(5):377-81.
  • 21
    Kraemer WJ, Keuning M, Ratamess NA, Volek JS, McCormick M, Bush JA, et al. Resistance training combined with bench-step aerobics enhances women's health profile. Med Sci Sports Exerc. 2001;33(2):259-69.
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    Zago MA, Pinto AC. Fisiopatologia das doenças falciformes: da mutação genética à insuficiência de múltiplos órgãos. Rev Bras Hematol Hemoter. 2007;29(3):207-14.
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Publication Dates

  • Publication in this collection
    Jul-Sep 2017

History

  • Received
    05 Apr 2017
  • Accepted
    17 July 2017
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