語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Pulmonary hypertension in adult cong...
~
Diller, Gerhard-Paul.
Pulmonary hypertension in adult congenital heart disease
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Pulmonary hypertension in adult congenital heart disease/ edited by Konstantinos Dimopoulos, Gerhard-Paul Diller.
其他作者:
Dimopoulos, Konstantinos.
出版者:
Cham :Springer International Publishing : : 2017.,
面頁冊數:
xv, 368 p. :ill., digital ; : 24 cm.;
Contained By:
Springer eBooks
標題:
Pulmonary hypertension. -
電子資源:
http://dx.doi.org/10.1007/978-3-319-46028-4
ISBN:
9783319460284
Pulmonary hypertension in adult congenital heart disease
Pulmonary hypertension in adult congenital heart disease
[electronic resource] /edited by Konstantinos Dimopoulos, Gerhard-Paul Diller. - Cham :Springer International Publishing :2017. - xv, 368 p. :ill., digital ;24 cm. - Congenital heart disease in adolescents and adults,2364-6659. - Congenital heart disease in adolescents and adults..
This book is intended as a comprehensive, practically oriented reference on pulmonary hypertension within the context of adult congenital heart disease (ACHD) After an introductory chapter on pathophysiology, the various types of pulmonary hypertension that may be encountered in ACHD are discussed, highlighting the specifics observed within different patient categories. The diagnostic approach is then addressed in detail, and the last section of the book is devoted to management options, from conservative approaches to interventional treatment and the concept of treat and repair. Management in specific patient subjects, such as pregnant women, Fontan patients, and Down syndrome patients with Eisenmenger syndrome, is fully discussed, and guidance is also provided on palliative care. Pulmonary arterial hypertension related to congenital heart disease (PAH-CHD), despite significant similarities in lung pathohysiology, differs significantly from other types of PAH in terms of mechanism of onset, natural history and management. Mistakes and pitfalls in the management of patients with PAH-CHD are often related to a lack of knowledge or expertise in this condition. Pulmonary Hypertension in Adult Congenital Heart Disease will be a valuable resource and learning tool for all who care for patients with ACHD, both in tertiary practice and general cardiology.
ISBN: 9783319460284
Standard No.: 10.1007/978-3-319-46028-4doiSubjects--Topical Terms:
680747
Pulmonary hypertension.
LC Class. No.: RC776.P87
Dewey Class. No.: 616.132
Pulmonary hypertension in adult congenital heart disease
LDR
:02394nam a2200313 a 4500
001
924375
003
DE-He213
005
20180207134549.0
006
m d
007
cr nn 008maaau
008
190625s2017 gw s 0 eng d
020
$a
9783319460284
$q
(electronic bk.)
020
$a
9783319460260
$q
(paper)
024
7
$a
10.1007/978-3-319-46028-4
$2
doi
035
$a
978-3-319-46028-4
040
$a
GP
$c
GP
041
0
$a
eng
050
4
$a
RC776.P87
072
7
$a
MJD
$2
bicssc
072
7
$a
MED010000
$2
bisacsh
082
0 4
$a
616.132
$2
23
090
$a
RC776.P87
$b
P982 2017
245
0 0
$a
Pulmonary hypertension in adult congenital heart disease
$h
[electronic resource] /
$c
edited by Konstantinos Dimopoulos, Gerhard-Paul Diller.
260
$a
Cham :
$c
2017.
$b
Springer International Publishing :
$b
Imprint: Springer,
300
$a
xv, 368 p. :
$b
ill., digital ;
$c
24 cm.
490
1
$a
Congenital heart disease in adolescents and adults,
$x
2364-6659
520
$a
This book is intended as a comprehensive, practically oriented reference on pulmonary hypertension within the context of adult congenital heart disease (ACHD) After an introductory chapter on pathophysiology, the various types of pulmonary hypertension that may be encountered in ACHD are discussed, highlighting the specifics observed within different patient categories. The diagnostic approach is then addressed in detail, and the last section of the book is devoted to management options, from conservative approaches to interventional treatment and the concept of treat and repair. Management in specific patient subjects, such as pregnant women, Fontan patients, and Down syndrome patients with Eisenmenger syndrome, is fully discussed, and guidance is also provided on palliative care. Pulmonary arterial hypertension related to congenital heart disease (PAH-CHD), despite significant similarities in lung pathohysiology, differs significantly from other types of PAH in terms of mechanism of onset, natural history and management. Mistakes and pitfalls in the management of patients with PAH-CHD are often related to a lack of knowledge or expertise in this condition. Pulmonary Hypertension in Adult Congenital Heart Disease will be a valuable resource and learning tool for all who care for patients with ACHD, both in tertiary practice and general cardiology.
650
0
$a
Pulmonary hypertension.
$3
680747
650
0
$a
Congenital heart disease.
$3
783240
650
1 4
$a
Medicine & Public Health.
$3
593949
650
2 4
$a
Cardiology.
$3
593957
650
2 4
$a
Cardiac Surgery.
$3
673715
650
2 4
$a
Pneumology/Respiratory System.
$3
668561
700
1
$a
Dimopoulos, Konstantinos.
$3
1201328
700
1
$a
Diller, Gerhard-Paul.
$3
1201329
710
2
$a
SpringerLink (Online service)
$3
593884
773
0
$t
Springer eBooks
830
0
$a
Congenital heart disease in adolescents and adults.
$3
1112917
856
4 0
$u
http://dx.doi.org/10.1007/978-3-319-46028-4
950
$a
Medicine (Springer-11650)
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入