Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Patricia M Fortin"'
Autor:
Kirstin L Wilkinson, Sally Hopewell, Simon J. Stanworth, Jonathan Huber, Susan J Brunskill, Marialena Trivella, Lise J Estcourt, Carolyn Doree, Patricia M Fortin
Publikováno v:
The Cochrane database of systematic reviews. 11
Background: In the absence of bleeding, plasma is commonly transfused to people prophylactically to prevent bleeding. In this context, it is transfused before operative or invasive procedures (such as liver biopsy or chest drainage tube insertion) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fdc098d7e3d631b96606fe538a063db
https://pubmed.ncbi.nlm.nih.gov/29151811
https://pubmed.ncbi.nlm.nih.gov/29151811
Autor:
Marialena Trivella, Sheila A Fisher, C Doree, Karen V Madgwick, Patricia M Fortin, Lise J Estcourt, Sally Hopewell
Publikováno v:
Europe PubMed Central
The Cochrane Library
The Cochrane Library
Regularly transfused people with sickle cell disease (SCD) and people with thalassaemia (who are transfusion-dependent or non-transfusion-dependent) are at risk of iron overload. Iron overload can lead to iron toxicity in vulnerable organs such as th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262598a3110714c1688f2f9cfbfe4b45
https://doi.org/10.1002/14651858.cd012349.pub2
https://doi.org/10.1002/14651858.cd012349.pub2
Autor:
Noémi B. A. Roy, Lise J Estcourt, Patricia M Fortin, Carolyn Doree, Katherine R. Bull, Marialena Trivella, Sally Hopewell
Publikováno v:
The Cochrane Library
Background Sickle cell disease (SCD) is one of the commonest severe monogenic disorders in the world, due to the inheritance of two abnormal haemoglobin (beta-globin) genes. SCD can cause severe pain, significant end-organ damage, pulmonary complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f20b02405d78b30d374071ba7a2489
https://doi.org/10.1002/14651858.cd012380.pub2
https://doi.org/10.1002/14651858.cd012380.pub2
Autor:
Miguel R. Abboud, Marialena Trivella, Carolyn Doree, Lise J Estcourt, Sally Hopewell, Patricia M Fortin
Publikováno v:
The Cochrane Library
Cochrane Database Syst Rev
Cochrane Database Syst Rev
BACKGROUND: Sickle cell disease (SCD) is one of the commonest severe monogenic disorders in the world, due to the inheritance of two abnormal haemoglobin (beta globin) genes. SCD can cause severe pain, significant end-organ damage, pulmonary complica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::990fba66b115a412963a3549fda6959c
https://pubmed.ncbi.nlm.nih.gov/33533031
https://pubmed.ncbi.nlm.nih.gov/33533031
Publikováno v:
The Cochrane Library
Background Hypertension is a chronic condition associated with an increased risk of mortality and morbidity. Renin is the enzyme responsible for converting angiotensinogen to angiotensin I, which is then converted to angiotensin II. Renin inhibitors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8888d2725f42209b1630fdcfa0f07f7
https://doi.org/10.1002/14651858.cd007066.pub3
https://doi.org/10.1002/14651858.cd007066.pub3
Publikováno v:
Cochrane Database Syst Rev
The Cochrane Library
The Cochrane Library
Background Sickle cell disease is one of the commonest severe monogenic disorders in the world, due to the inheritance of two abnormal haemoglobin (beta globin) genes. Sickle cell disease can cause severe pain, significant end-organ damage, pulmonary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c67d46be8aaa3b34326b53bb8e8a9a82
https://doi.org/10.1002/14651858.cd003146.pub3
https://doi.org/10.1002/14651858.cd003146.pub3
Publikováno v:
The Cochrane Library
Background: Globally, sickle cell disease (SCD) is one of the commonest severe monogenic disorders, due to the inheritance of two abnormal haemoglobin (beta globin) genes. SCD can cause severe pain, significant end‐organ damage, pulmonary complicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7795c85c36282e39ab529e1c0bf5687
http://ora.ox.ac.uk/objects/uuid:c287a018-6947-46c6-947f-4ed3a49a3a7d
http://ora.ox.ac.uk/objects/uuid:c287a018-6947-46c6-947f-4ed3a49a3a7d
Publikováno v:
Journal of Human Hypertension. 23:495-502
We conducted a systematic review and meta-analysis of double-blind randomized controlled trials to quantify the dose-related systolic (SBP) and diastolic blood pressure (DBP) lowering efficacy of renin inhibitors vs placebo in the treatment of adults
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c96944ca70827ff18cb17f3230e9f3f
https://doi.org/10.1038/jhh.2008.162
https://doi.org/10.1038/jhh.2008.162
Autor:
Ian Hambleton, Sally Hopewell, Gavin Cho, Marialena Trivella, Patricia M Fortin, Lise J Estcourt
Publikováno v:
Cochrane Database Syst Rev
The Cochrane Library
The Cochrane Library
BACKGROUND: Sickle cell disease is a genetic haemoglobin disorder, which can cause severe pain, significant end-organ damage, pulmonary complications, and premature death. Sickle cell disease is one of the most common severe monogenic disorders in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::686fdafa8810bbe290e0a957996b0692
https://doi.org/10.1002/14651858.cd008360.pub2
https://doi.org/10.1002/14651858.cd008360.pub2
Publikováno v:
Scopus-Elsevier
The Cochrane Library
The Cochrane Library
Background Intradialytic hypotension (IDH) occurs in 20% to 55% of haemodialysis sessions and is more frequent among patients on long-term haemodialysis. Symptomatic IDH is generally defined as a decrease in systolic blood pressure (BP) of at least 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f359438ace127dcf43c82293fb3464c
https://pubmed.ncbi.nlm.nih.gov/21069691
https://pubmed.ncbi.nlm.nih.gov/21069691