Kistik Fibrozis
Özet
Referanslar
Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. J Pediatr. 1998;132(2):255– 259.
Rohlfs EM, Zhou Z, Heim RA, Nagan N, Rosenblum LS, Flynn K, et al. Cystic fibrosis carrier testing in an ethnically diverse US population. Clin Chem. 2011;57(6):841-848.
Wagener J, Zemanick E, Sontag M. Newborn screening for cystic fibrosis. Curr Opin Pediatr. 2012;24(3):329–335.
Gürson CT, Sertel H, Gürkan M, Pala S. Newborn screening for cystic fibrosis with the chloride electrode and neutron activation analysis. Helv Pediatr Acta. 1973;28:165-174.
Gibson LE, Cooke RE. A Test for Concentration of Electrolytes in Sweat in Cystic Fibrosis of the Pancreas Utilizing Pilocarpine by Iontophoresis. Pediatrics. 1959;23(3):545–549.
CFTR2@Johns Hopkins. Home page [Internet]. Http://cftr2.org/. Updated August 2016. Accessed July 31, 2019
McCague AF, Raraigh KS, Pellicore MJ, Davis-Marcisak EF, Evans TA, Han ST, et al. Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis. Am J Respir Crit Care Med. 2019;199(9):1116–1126.
Irish MS, Ragi JM, Karamanoukian H, Borowitz DS, Schmidt D, Glick PL. Prenataldiagnosis of the fetus with cystic fibrosis and meconium ileus. Pediatr Surg Int Berl. 1997;12(5-6):434–436.
De Oronzo MA. Hyperechogenic fetal bowel: An ultrasonographic marker for adverse fetal and neonatal outcome? J Prenat Med. 2011;5(1):9–13.
Rentea RM, St Peter SD. Pediatric Rectal Prolapse. Clin Colon Rectal Surg. 2018;31(2):108–116.
Özçelik U. Kistik fibrozis. In: Yurdakök M. (Ed). Yurdakök Pediatri. Güneş Tıp Kitapevi Yayıncılık. 2017:2885-97.
Paranjape SM, Mogayzel PJ. Cystic Fibrosis. Pediatr Rev.2014;35(5):194–205.
De Boeck K, Vermeulen F, Dupont L. The diagnosis of cystic fibrosis. Presse Med. 2017;46:e97-e108.
https://www.uptodate.com/contents/cystic-fibrosis-clinical-manifestations-and-diagnosis
Southern KW, Noone PG, Bosworth DG, Legrys VA, Knowles MR, Barker PM. A modified technique for measurement of nasal transepithelial potential difference in infants. J Pediatr. 2001;139(3):353-8.
Toraks Derneği Kistik Fibrozis Tanı ve Tedavi Rehberi. Türk Toraks Dergisi 2011;12:1-140.
Özkan T, Kasırga E, Ecevit Ç. Kistik Fibrozisli Çocuğa Yaklaşım Rehberi. Türk Çocuk Gastroenteroloji, Hepatoloji ve Beslenme Derneği. 2020.
Wallis C. Diagnosis of cystic fibrosis. In: Hodson M, Geddes DM, Bush A (ed). Cystic fibrosis (3rd ed). London: Edward Arnold, 2007: 99-108.
Soares R, Neto P, Pereira N, Cunha C, Pinto C, Fonseca M, et al. Dilated fetal bowel as indication for prenatal diagnosis of cystic fibrosis. BMJ Case Rep. 2010.
Mogayzel PJ, Naureckas ET, Robinson KA, Mueller G, Hadjiliadis D, Hoag JB, et al. Cystic Fibrosis Pulmonary Guidelines: Chronic Medications for the Maintenance of Lung Health. Am J Respir Crit Care Med. 2013;187(7):680– 689.
Flume PA, Robinson KA, O'Sullivan BP, Finder JD, Vender RL, Willey-Courand DB, et al. Clinical Practice Guidelines for Pulmonary Therapies Committee. Cystic fibrosis pulmonary guidelines: airway clearance therapies. Respir Care. 2009 Apr;54(4):522-37.
Mogayzel PJ, Naureckas ET, Robinson KA, Brady C, Guill M, Lahiri T, et al. Cystic Fibrosis Foundation Pulmonary Guideline. Pharmacologic Approaches to Prevention and Eradication of Initial Pseudomonas aeruginosa Infection. Ann Am Thorac Soc. 2014;11(10):1640–1650.
Stevens DA, Moss RB, Kurup VP, Knutsen AP, Greenberger P, Judson MA, et al. Allergic bronchopulmonary aspergillosis in cystic fibrosis-state of the art: Cystic Fibrosis Foundation Consensus Conference. Clin Infect Dis. 2003(37 Suppl 3):225–264.
Dinwiddie R. Anti-inflammatory therapy in cystic fibrosis. J Cyst Fibros. 2005 (2):45–8.
Lands LC, Stanojevic S. Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis. Cochrane Database of Syst Rev. 2019 Sep 9;9(9):CD001505.
Southern KW, Barker PM, Solis-Moya A, Patel L. Macrolide antibiotics for cystic fibrosis. Cochrane Database Syst Rev. 2004;(2)
Martiniano SL, Elbert AA, Farrell PM, Ren CL, Sontag MK, Wu R, et al. Outcomes of infants born during the first 9 years of CF newborn screening in the United States: A retrospective Cystic Fibrosis Foundation Patient Registry cohort study. Pediatr Pulmonol. 2021 Dec;56(12):3758-3767.
Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41(6):583–591.
Borowitz D, Grand R, Durie P. Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy. J Pediatr. 1995;127(5):681–684.
Grasemann H CFTR Modulator Therapy for Cystic Fibrosis. N Engl J Med. 2017;377(21):2085– 2088.
Cystic Fibrosis Foundation; Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, Spear SL, Michel SH, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr. 2009 Dec;155(6 Suppl):S73-93.
Ramos KJ, Smith PJ, McKone EF, Pilewski JM. Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines. J Cyst Fibros. 2019;18(3):321–333.
Referanslar
Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. J Pediatr. 1998;132(2):255– 259.
Rohlfs EM, Zhou Z, Heim RA, Nagan N, Rosenblum LS, Flynn K, et al. Cystic fibrosis carrier testing in an ethnically diverse US population. Clin Chem. 2011;57(6):841-848.
Wagener J, Zemanick E, Sontag M. Newborn screening for cystic fibrosis. Curr Opin Pediatr. 2012;24(3):329–335.
Gürson CT, Sertel H, Gürkan M, Pala S. Newborn screening for cystic fibrosis with the chloride electrode and neutron activation analysis. Helv Pediatr Acta. 1973;28:165-174.
Gibson LE, Cooke RE. A Test for Concentration of Electrolytes in Sweat in Cystic Fibrosis of the Pancreas Utilizing Pilocarpine by Iontophoresis. Pediatrics. 1959;23(3):545–549.
CFTR2@Johns Hopkins. Home page [Internet]. Http://cftr2.org/. Updated August 2016. Accessed July 31, 2019
McCague AF, Raraigh KS, Pellicore MJ, Davis-Marcisak EF, Evans TA, Han ST, et al. Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis. Am J Respir Crit Care Med. 2019;199(9):1116–1126.
Irish MS, Ragi JM, Karamanoukian H, Borowitz DS, Schmidt D, Glick PL. Prenataldiagnosis of the fetus with cystic fibrosis and meconium ileus. Pediatr Surg Int Berl. 1997;12(5-6):434–436.
De Oronzo MA. Hyperechogenic fetal bowel: An ultrasonographic marker for adverse fetal and neonatal outcome? J Prenat Med. 2011;5(1):9–13.
Rentea RM, St Peter SD. Pediatric Rectal Prolapse. Clin Colon Rectal Surg. 2018;31(2):108–116.
Özçelik U. Kistik fibrozis. In: Yurdakök M. (Ed). Yurdakök Pediatri. Güneş Tıp Kitapevi Yayıncılık. 2017:2885-97.
Paranjape SM, Mogayzel PJ. Cystic Fibrosis. Pediatr Rev.2014;35(5):194–205.
De Boeck K, Vermeulen F, Dupont L. The diagnosis of cystic fibrosis. Presse Med. 2017;46:e97-e108.
https://www.uptodate.com/contents/cystic-fibrosis-clinical-manifestations-and-diagnosis
Southern KW, Noone PG, Bosworth DG, Legrys VA, Knowles MR, Barker PM. A modified technique for measurement of nasal transepithelial potential difference in infants. J Pediatr. 2001;139(3):353-8.
Toraks Derneği Kistik Fibrozis Tanı ve Tedavi Rehberi. Türk Toraks Dergisi 2011;12:1-140.
Özkan T, Kasırga E, Ecevit Ç. Kistik Fibrozisli Çocuğa Yaklaşım Rehberi. Türk Çocuk Gastroenteroloji, Hepatoloji ve Beslenme Derneği. 2020.
Wallis C. Diagnosis of cystic fibrosis. In: Hodson M, Geddes DM, Bush A (ed). Cystic fibrosis (3rd ed). London: Edward Arnold, 2007: 99-108.
Soares R, Neto P, Pereira N, Cunha C, Pinto C, Fonseca M, et al. Dilated fetal bowel as indication for prenatal diagnosis of cystic fibrosis. BMJ Case Rep. 2010.
Mogayzel PJ, Naureckas ET, Robinson KA, Mueller G, Hadjiliadis D, Hoag JB, et al. Cystic Fibrosis Pulmonary Guidelines: Chronic Medications for the Maintenance of Lung Health. Am J Respir Crit Care Med. 2013;187(7):680– 689.
Flume PA, Robinson KA, O'Sullivan BP, Finder JD, Vender RL, Willey-Courand DB, et al. Clinical Practice Guidelines for Pulmonary Therapies Committee. Cystic fibrosis pulmonary guidelines: airway clearance therapies. Respir Care. 2009 Apr;54(4):522-37.
Mogayzel PJ, Naureckas ET, Robinson KA, Brady C, Guill M, Lahiri T, et al. Cystic Fibrosis Foundation Pulmonary Guideline. Pharmacologic Approaches to Prevention and Eradication of Initial Pseudomonas aeruginosa Infection. Ann Am Thorac Soc. 2014;11(10):1640–1650.
Stevens DA, Moss RB, Kurup VP, Knutsen AP, Greenberger P, Judson MA, et al. Allergic bronchopulmonary aspergillosis in cystic fibrosis-state of the art: Cystic Fibrosis Foundation Consensus Conference. Clin Infect Dis. 2003(37 Suppl 3):225–264.
Dinwiddie R. Anti-inflammatory therapy in cystic fibrosis. J Cyst Fibros. 2005 (2):45–8.
Lands LC, Stanojevic S. Oral non-steroidal anti-inflammatory drug therapy for lung disease in cystic fibrosis. Cochrane Database of Syst Rev. 2019 Sep 9;9(9):CD001505.
Southern KW, Barker PM, Solis-Moya A, Patel L. Macrolide antibiotics for cystic fibrosis. Cochrane Database Syst Rev. 2004;(2)
Martiniano SL, Elbert AA, Farrell PM, Ren CL, Sontag MK, Wu R, et al. Outcomes of infants born during the first 9 years of CF newborn screening in the United States: A retrospective Cystic Fibrosis Foundation Patient Registry cohort study. Pediatr Pulmonol. 2021 Dec;56(12):3758-3767.
Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol. 1988;41(6):583–591.
Borowitz D, Grand R, Durie P. Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy. J Pediatr. 1995;127(5):681–684.
Grasemann H CFTR Modulator Therapy for Cystic Fibrosis. N Engl J Med. 2017;377(21):2085– 2088.
Cystic Fibrosis Foundation; Borowitz D, Robinson KA, Rosenfeld M, Davis SD, Sabadosa KA, Spear SL, Michel SH, et al. Cystic Fibrosis Foundation evidence-based guidelines for management of infants with cystic fibrosis. J Pediatr. 2009 Dec;155(6 Suppl):S73-93.
Ramos KJ, Smith PJ, McKone EF, Pilewski JM. Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines. J Cyst Fibros. 2019;18(3):321–333.
