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Opis fizyczny
Skład produktu
publikacja
Forma
forma podstawowa
książka
Forma produktu
Broszura
Opis bibliograficzny
Tytuł
Cystic Fibrosis : a multisystem disease
Twórca
redaktor naukowy
Sands, Dorota
ISNI 0000000370358668
Wydanie
typ wydania
Wydanie
numer wydania
1
miejsce wydania
Warszawa
Język
język publikacji
polski
Wydawca
imprint
Instytut Matki i Dziecka
pełna nazwa wydawcy
INSTYTUT MATKI i DZIECKA
adres siedziby
ul. M. Kasprzaka 17 A
01-211 Warszawa
01-211 Warszawa
adres www
numer telefonu
Data
data wydania
2024-12-31
data upublicznienia metadanych
2024-12-12
Opis marketingowy
Spis treści
C ONTENT S
CONTRIBUTING AUTHORS 9
PREFACE 13
PART I
EPIDEMIOLOGY AND PATHOPHYSIOLOGY OF CYSTIC FIBROSIS 15
CHAPTER 1
Epidemiology and organization of medical care in Poland according
to European standards 17
Dorota Sands, Andrzej Pogorzelski, Anna Skoczylas-Ligocka, Łukasz Woźniacki
CHAPTER 2
Organization of work at the cystic fibrosis treatment center
and management of patient care 25
Łukasz Woźniacki, Dorota Sands, Szczepan Cofta
CHAPTER 3
Genetic background of cystic fibrosis 33
Katarzyna Wertheim-Tysarowska, Agnieszka Sobczyńska-Tomaszewska, Jerzy Bal
CHAPTER 4
Pathophysiological bases of disorders in cystic fibrosis 41
Katarzyna Wertheim-Tysarowska, Jerzy Bal
PART II
DIAGNOSIS OF CYSTIC FIBROSIS 47
CHAPTER 5
Diagnosis of cystic fibrosis 49
Katarzyna Zybert, Anna Nowakowska, Dorota Sands
CHAPTER 6
Newborn screening 59
Katarzyna Zybert, Dorota Sands
CHAPTER 7
Molecular diagnostics 67
Agnieszka Sobczyńska-Tomaszewska, Kamila Czerska, Katarzyna Wertheim-Tysarowska
CHAPTER 8
Male infertility and CFTR gene mutation carrier status 79
Jan Karol Wolski
CHAPTER 9
Genetic counseling 83
Tadeusz Mazurczak, Anna Kutkowska-Kaźmierczak
CHAPTER 10
Pulmonary function tests 87
Łukasz Woźniacki, Magdalena Postek, Katarzyna Walicka-Serzysko
CHAPTER 11
The role of imaging studies in the diagnosis and monitoring
of cystic fibrosis 107
Maria Uliasz, Joanna Jaworska
PART III
CLINICAL ASPECTS OF CYSTIC FIBROSIS – RESPIRATORY SYSTEM 201
CHAPTER 12
Respiratory infections – the role of cross-infection 203
Justyna Milczewska, Wojciech Skorupa, Katarzyna Walicka-Serzysko
CHAPTER 13
Management of chronic lung disease 225
Katarzyna Walicka-Serzysko, Wojciech Skorupa
CHAPTER 14
The role of physiotherapy in cystic fibrosis 233
Teresa Orlik, Natalia Jeneralska, Aleksandra Cichocka
CHAPTER 15
Pulmonary exacerbation 245
Wojciech Skorupa, Justyna Milczewska, Katarzyna Walicka-Serzysko
CHAPTER 16
Chronic rhinosinusitis in patients with cystic fibrosis 251
Tomasz Gotlib
CHAPTER 17
Noninfectious complications 259
Katarzyna Walicka-Serzysko, Wojciech Skorupa
CHAPTER 18
CFTR variant-specific therapy 273
Dorota Sands, Anna Wołkowicz
CHAPTER 19
Respiratory failure 283
Katarzyna Walicka-Serzysko, Joanna Jaworska
CHAPTER 20
Lung transplantation in cystic fibrosis 291
Katarzyna Walicka-Serzysko, Maria Piotrowska, Bartosz Kubisa
CHAPTER 21
Palliative care of children with cystic fibrosis 309
Marek Karwacki
PART IV
CLINICAL ASPECTS OF CYSTIC FIBROSIS – EXTRAPULMONARY MANIFESTATIONS OF THE DISEASE AND MULTIDISCIPLINARY CARE 331
CHAPTER 22
Nutritional management in cystic fibrosis 333
Monika Mielus, Małgorzata Surowiecka
CHAPTER 23
Gastrointestinal, pancreatic, and liver problems in children
with cystic fibrosis 361
Marek Woynarowski, Beata Oralewska, Michał Szczepański, Mikołaj Teisseyre
CHAPTER 24
Meconium ileus 401
Ewa Sawicka
CHAPTER 25
Abnormal glucose tolerance and cystic fibrosis-related diabetes 413
Katarzyna Walicka-Serzysko, Monika Mielus, Małgorzata Surowiecka, Edyta Jabłońska-Wypustek
CHAPTER 26
Other complications in patients with cystic fibrosis 427
Justyna Milczewska, Monika Mielus, Tomasz Rawo
CHAPTER 27
Gynecological and obstetric care for patients with cystic fibrosis 437
Monika Hanyż, Joanna Jaworska
CHAPTER 28
Psychological issues associated with cystic fibrosis 447
Urszula Borawska-Kowalczyk
ANNEX 463
CONTRIBUTING AUTHORS 9
PREFACE 13
PART I
EPIDEMIOLOGY AND PATHOPHYSIOLOGY OF CYSTIC FIBROSIS 15
CHAPTER 1
Epidemiology and organization of medical care in Poland according
to European standards 17
Dorota Sands, Andrzej Pogorzelski, Anna Skoczylas-Ligocka, Łukasz Woźniacki
CHAPTER 2
Organization of work at the cystic fibrosis treatment center
and management of patient care 25
Łukasz Woźniacki, Dorota Sands, Szczepan Cofta
CHAPTER 3
Genetic background of cystic fibrosis 33
Katarzyna Wertheim-Tysarowska, Agnieszka Sobczyńska-Tomaszewska, Jerzy Bal
CHAPTER 4
Pathophysiological bases of disorders in cystic fibrosis 41
Katarzyna Wertheim-Tysarowska, Jerzy Bal
PART II
DIAGNOSIS OF CYSTIC FIBROSIS 47
CHAPTER 5
Diagnosis of cystic fibrosis 49
Katarzyna Zybert, Anna Nowakowska, Dorota Sands
CHAPTER 6
Newborn screening 59
Katarzyna Zybert, Dorota Sands
CHAPTER 7
Molecular diagnostics 67
Agnieszka Sobczyńska-Tomaszewska, Kamila Czerska, Katarzyna Wertheim-Tysarowska
CHAPTER 8
Male infertility and CFTR gene mutation carrier status 79
Jan Karol Wolski
CHAPTER 9
Genetic counseling 83
Tadeusz Mazurczak, Anna Kutkowska-Kaźmierczak
CHAPTER 10
Pulmonary function tests 87
Łukasz Woźniacki, Magdalena Postek, Katarzyna Walicka-Serzysko
CHAPTER 11
The role of imaging studies in the diagnosis and monitoring
of cystic fibrosis 107
Maria Uliasz, Joanna Jaworska
PART III
CLINICAL ASPECTS OF CYSTIC FIBROSIS – RESPIRATORY SYSTEM 201
CHAPTER 12
Respiratory infections – the role of cross-infection 203
Justyna Milczewska, Wojciech Skorupa, Katarzyna Walicka-Serzysko
CHAPTER 13
Management of chronic lung disease 225
Katarzyna Walicka-Serzysko, Wojciech Skorupa
CHAPTER 14
The role of physiotherapy in cystic fibrosis 233
Teresa Orlik, Natalia Jeneralska, Aleksandra Cichocka
CHAPTER 15
Pulmonary exacerbation 245
Wojciech Skorupa, Justyna Milczewska, Katarzyna Walicka-Serzysko
CHAPTER 16
Chronic rhinosinusitis in patients with cystic fibrosis 251
Tomasz Gotlib
CHAPTER 17
Noninfectious complications 259
Katarzyna Walicka-Serzysko, Wojciech Skorupa
CHAPTER 18
CFTR variant-specific therapy 273
Dorota Sands, Anna Wołkowicz
CHAPTER 19
Respiratory failure 283
Katarzyna Walicka-Serzysko, Joanna Jaworska
CHAPTER 20
Lung transplantation in cystic fibrosis 291
Katarzyna Walicka-Serzysko, Maria Piotrowska, Bartosz Kubisa
CHAPTER 21
Palliative care of children with cystic fibrosis 309
Marek Karwacki
PART IV
CLINICAL ASPECTS OF CYSTIC FIBROSIS – EXTRAPULMONARY MANIFESTATIONS OF THE DISEASE AND MULTIDISCIPLINARY CARE 331
CHAPTER 22
Nutritional management in cystic fibrosis 333
Monika Mielus, Małgorzata Surowiecka
CHAPTER 23
Gastrointestinal, pancreatic, and liver problems in children
with cystic fibrosis 361
Marek Woynarowski, Beata Oralewska, Michał Szczepański, Mikołaj Teisseyre
CHAPTER 24
Meconium ileus 401
Ewa Sawicka
CHAPTER 25
Abnormal glucose tolerance and cystic fibrosis-related diabetes 413
Katarzyna Walicka-Serzysko, Monika Mielus, Małgorzata Surowiecka, Edyta Jabłońska-Wypustek
CHAPTER 26
Other complications in patients with cystic fibrosis 427
Justyna Milczewska, Monika Mielus, Tomasz Rawo
CHAPTER 27
Gynecological and obstetric care for patients with cystic fibrosis 437
Monika Hanyż, Joanna Jaworska
CHAPTER 28
Psychological issues associated with cystic fibrosis 447
Urszula Borawska-Kowalczyk
ANNEX 463
Tekst promocyjny
Dear Readers,
We were very pleased with the positive response to the first edition of our monograph, and that it sold out very quickly. We were delighted to learn that the book is being used both by physicians dealing with cystic fibrosis on a daily basis and those preparing for their specialty examinations. It is also being used by dieticians, physiotherapists, and psychologists involved in the treatment of patients as members of multidisciplinary teams.
The rapid development of new CFTR variant-specific therapies in cystic fibrosis has encouraged us to work swiftly on the second edition, which is supplemented with the latest developments in biotechnology. Responding to the interest in the book among specialists outside the field of pulmonology, we have significantly expanded the sections on gastroenterology, radiology, and physiotherapy. With hospital management staff in mind, we have prepared a practical chapter on how to organize a cystic fibrosis center in accordance with current European standards.
This second edition of the monograph, available as an e-book, has allowed us to overcome the size constraints of a printed book and also to modernize the chapter presenting the results of diagnostic imaging.
We wish you enjoyable reading!
Prof. Dorota Sands Scientific Editor
We were very pleased with the positive response to the first edition of our monograph, and that it sold out very quickly. We were delighted to learn that the book is being used both by physicians dealing with cystic fibrosis on a daily basis and those preparing for their specialty examinations. It is also being used by dieticians, physiotherapists, and psychologists involved in the treatment of patients as members of multidisciplinary teams.
The rapid development of new CFTR variant-specific therapies in cystic fibrosis has encouraged us to work swiftly on the second edition, which is supplemented with the latest developments in biotechnology. Responding to the interest in the book among specialists outside the field of pulmonology, we have significantly expanded the sections on gastroenterology, radiology, and physiotherapy. With hospital management staff in mind, we have prepared a practical chapter on how to organize a cystic fibrosis center in accordance with current European standards.
This second edition of the monograph, available as an e-book, has allowed us to overcome the size constraints of a printed book and also to modernize the chapter presenting the results of diagnostic imaging.
We wish you enjoyable reading!
Prof. Dorota Sands Scientific Editor
Nota biograficzna
Prof. Dorota Sands, MD, PhD, specializes in pediatrics, allergology, pulmonary disorders, and pediatric pulmonary diseases. She has authored over 100 scientific publications. During her extensive tenure at the Institute of Mother and Child in Warsaw, she has completed multiple internships at leading pulmonology centers, including the Royal Brompton Hospital in London and the Division of Pediatric Pulmonology and Allergology at the Medical University of Graz, where she held a scholarship from the American Austrian Foundation. Prof. Sands pursued her postdoctoral research during a fellowship at the University of Leuven in Belgium. She shares the knowledge gained at the pioneering cystic fibrosis treatment center at the Insti- tute of Mother and Child in Warsaw with members of her multidisciplinary team. This team, recognized across Poland, is widely acknowledged internationally for its expertise. Since January 2017, Prof. Sands has been affiliated with the Children’s Hospital in Dziekanów Leśny. In this capacity, she serves as the head of the Cystic Fibrosis Center (CLM). As a researcher at the Institute of Mother and Child in Warsaw, she also heads the Cystic Fibrosis Department. Being a renowned international expert with extensive experience in conducting clinical trials, Prof. Sands has contributed to the development of European cystic fibrosis standards of care and the organization of cystic fibrosis centers. These standards are successfully implemented at the Dziekanów Leśny Cystic Fibrosis Center, which serves as a model center for the treatment of this condition in Poland.
I am dedicating this book to Anna Nowakowska, MD, PhD my invaluable mentor who, in addition to teaching me clinical skills, instilled in me a deep respect for fellow human beings.
I am dedicating this book to Anna Nowakowska, MD, PhD my invaluable mentor who, in addition to teaching me clinical skills, instilled in me a deep respect for fellow human beings.
Kategoria statystyczna Biblioteki Narodowej
Publikacje naukowe
Temat
mukowiscydoza
Temat
cystic fibrosis