Under-recognition of Low Blood Pressure Readings in Patients with Duchenne Muscular Dystrophy
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  • 作者:Syed Asif Masood ; Suhaib Kazmouz ; Peter Heydemann ; Hong Li…
  • 关键词:Duchenne muscular dystrophy ; Blood pressure ; Under ; recognition ; Heart failure therapy
  • 刊名:Pediatric Cardiology
  • 出版年:2015
  • 出版时间:October 2015
  • 年:2015
  • 卷:36
  • 期:7
  • 页码:1489-1494
  • 全文大小:352 KB
  • 参考文献:1.Andersson DC, Meli AC, Reiken S, Betzenhauser MJ, Umanskaya A, Shiomi T, D’Armiento J, Marks AR (2012) Leaky ryanodine receptors in β-sarcoglycan deficient mice. Skelet Muscle 2(1):9. doi:10.-186/-044-5040-2-9 PubMed Central CrossRef PubMed
    2.Casey DP, Hart EC (2008) Cardiovascular function in humans during exercise: role of the muscle pump. J Physiol 586(Pt 21):5045-046PubMed Central CrossRef PubMed
    3.Fleming S, Thompson M, Stevens R, Heneghan C, Plüddemann A, Maconochie I, Tarassenko L, Mant D (2011) Normal ranges of heart rate and respiratory rate in children from birth to 18?years of age: a systematic review of observational studies. Lancet 377(9770):1011-018PubMed Central CrossRef PubMed
    4.Gillett C, Wong A, Wilson DG, Wolf AR, Martin RP, Kenny D (2011) Underrecognition of elevated blood pressure readings in children after early repair of coarctation of the aorta. Pediatr Cardiol 32(2):202-05CrossRef PubMed
    5.Haque IU, Zaritsky AL (2007) Analysis of the evidence for the lower limit of systolic and mean arterial pressure in children. Pediatr Crit Care Med 8(2):138-44CrossRef PubMed
    6.Ito K, Kimura S, Ozasa S, Matsukura M, Ikezawa M, Yoshioka K, Ueno H et al (2006) Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice. Hum Mol Genet 15(14):2266-275CrossRef PubMed
    7.Judge DP, Kass DA, Reid Thompson W, Wagner KR (2011) Pathophysiology and therapy of cardiac dysfunction in duchenne muscular dystrophy. Am J Cardiovasc Drugs 11(5):287-94CrossRef PubMed
    8.Kuan SC, Chen KM, Wang C (2012) Effectiveness of Qigong in promoting the health of wheelchair-bound older adults in long-term care facilities. Biol Res Nurs 14(2):139-46CrossRef PubMed
    9.Lang RM, Bierig M, Devereux RB, Flachskampf FA, Foster E, Pellikka PA (2005) Recommendations for chamber quantification. American Society of Echocardiography’s Nomenclature and Standards Committee; Task Force on Chamber Quantification; American College of Cardiology Echocardiography Committee; American Heart Association; European Association of Echocardiography, European Society of Cardiology. J Am Soc Echocardiogr 18(12):1440-463CrossRef PubMed
    10.Lanza GA, Dello Russo A, Giglio V, De Luca L, Messano L, Santini C, Ricci E, Damiani A, Fumagalli G, De Martino G, Mangiola F, Bellocci F (2001) Impairment of cardiac autonomic function in patients with Duchenne muscular dystrophy: relationship to myocardial and respiratory function. Am Heart J 141(5):808-12CrossRef PubMed
    11.Low blood pressure (hypotension). http://?www.?mayoclinic.?org/?diseases-conditions/?low-blood-pressure/?basics/?causes/?con-20032298 . Accessed April 17, 2014
    12.Miller G, D’Orsogna L, O’Shea JP (1989) Autonomic function and the sinus tachycardia of Duchenne muscular dystrophy. Brain Dev 11(4):247-50CrossRef PubMed
    13.National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The Fourth Report on the Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents. (2004) Pediatrics 114(Suppl 2):555-76
    14.O’Brien T, Harper PS, Newcombe RG (1983) Blood pressure and myotonic dystrophy. Clin Genet 23(6):422-26CrossRef PubMed
    15.Piepoli M, Clark AL, Coats AJ (1995) Muscle mechanoreceptors in hemodynamic, autonomic, and ventilatory responses to exercise in men. Am J Physiol 269:H1428–H1436PubMed
    16.Sorel JE, Ragland DR, Syme SL (1991) Blood pressure in Mexican Americans, Whites, and Blacks. Am J Epidemiol 134(4):370-78PubMed
    17.Yotsukura M, Fujii K, Katayama A et al (1998) Nine-year follow-up study of heart rate variability in patients with Duchenne-type progressive muscular dystrophy. Am Heart J 136:289-96CrossRef PubMed
  • 作者单位:Syed Asif Masood (1)
    Suhaib Kazmouz (1)
    Peter Heydemann (3)
    Hong Li (4)
    Damien Kenny (2)

    1. Department of Congenital and Pediatric Cardiology, Rush University Medical Center, Chicago, IL, USA
    3. Departments of Pediatrics and Neurology, Rush University Medical Center, Chicago, IL, USA
    4. Department of Preventive Medicine, Rush University Medical Center, Chicago, IL, USA
    2. Department of Congenital and Pediatric Cardiology, Rush Center for Congenital Heart Disease, Rush University Medical Center, 1653W Congress Pkwy, Chicago, IL, 60612, USA
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Cardiology
    Cardiac Surgery
    Vascular Surgery
  • 出版者:Springer New York
  • ISSN:1432-1971
文摘
Duchenne muscular dystrophy (DMD), a recessive sex-linked hereditary disorder, is characterized by degeneration, atrophy, and weakness of skeletal and cardiac muscle. The purpose of this study was to document the prevalence of abnormally low resting BP recordings in patients with DMD in our outpatient clinic. The charts of 31 patients with DMD attending the cardiology clinic at Rush University Medical Center were retrospectively reviewed. Demographic data, systolic, diastolic, and mean blood pressures along with current medications, echocardiograms, and documented clinical appreciation and management of low blood pressure were recorded in the form of 104 outpatient clinical visits. Blood pressure (BP) was classified as low if the systolic and/or mean BP was less than the fifth percentile for height for patients aged ?7 years (n = 23). For patients ?8 years (n = 8), systolic blood pressure (SBP) <90 mmHg or a mean arterial pressure (MAP) <60 mmHg was recorded as a low reading. Patients with other forms of myopathy or unclear diagnosis were excluded. Statistical analysis was done using PASW version 18. BP was documented at 103 (99.01 %) outpatient encounters. Low systolic and mean BP were recorded in 35 (33.7 %) encounters. This represented low recordings for 19 (61.3 %) out of a total 31 patients with two or more successive low recordings for 12 (38.7 %) patients. Thirty-one low BP encounters were in patients <18 years old. Hispanic patients accounted for 74 (71.2 %) visits and had low BP recorded in 32 (43.2 %) instances. The patients were non-ambulant in 71 (68.3 %) encounters. Out of 35 encounters with low BP, 17 patients (48.6 %) were taking heart failure medication. In instances when patients had low BP, 22 (66.7 %) out of 33 echocardiography encounters had normal left ventricular ejection fraction. Clinician comments on low BP reading were present in 11 (10.6 %) encounters, and treatment modification occurred in only 1 (1 %) patient. Age in years (p = .031) and ethnicity (p = .035) were independent predictors of low BP using stepwise multiple regression analysis. Low BP was recorded in a significant number of patient encounters in patients with DMD. Age 17 years or less and Hispanic ethnicity were significant predictors associated with low BP readings in our DMD cohort. Concomitant heart failure therapy was not a statistically significant association. There is a need for enhanced awareness of low BP in DMD patients among primary care and specialty physicians. The etiology and clinical impact of these findings are unclear but may impact escalation of heart failure therapy. Keywords Duchenne muscular dystrophy Blood pressure Under-recognition Heart failure therapy
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