8 research outputs found
Table1_Effect of orthostatic hypotension on long-term prognosis of elderly patients with stable coronary artery disease: a retrospective cohort study.docx
BackgroundThe long-term prognosis of patients with stable coronary artery disease (CAD) combined with orthostatic hypotension (OH) has rarely been reported. This research was designed to examine whether OH increases the risk of all-cause mortality and cardiovascular death among patients with stable CAD.MethodsWe retrospectively analyzed retired military personnel over 65 years of age who were hospitalized at the General Hospital of Southern Theater Command of the Chinese People’s Liberation Army between March and July 2010. A total of 924 patients with stable CAD were included, among whom 263 had OH. The risk of all-cause mortality and cardiovascular death in OH and non-OH groups were analyzed with the Cox proportional hazards models, and restricted cubic spline plots were utilized for subgroup analyses. Furthermore, competing risk models were applied for sensitivity analyses.ResultsThe median age of the patients was 82.00 (80.00–85.00) years. Over 159 months of follow-up, the loss to follow-up rate was 2.27%, and all-cause mortality was observed in 574 (63.57%) patients, including 184 with OH. Moreover, cardiovascular death occurred in 127 patients (13.73%), with 58 cases associated with OH. Although the relationship between OH and all-cause mortality was non-significant [body mass index (BMI) ConclusionOur study, based on retired military personnel with stable CAD, found that OH led to a significantly higher risk of cardiovascular death, but it was not noticeably associated with all-cause mortality on long-term prognosis.</p
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries
In Situ Imaging the Oxygen Reduction Reactions of Solid State Na–O<sub>2</sub> Batteries with CuO Nanowires as the Air Cathode
We
report real time imaging of the oxygen reduction reactions (ORRs)
in all solid state sodium oxygen batteries (SOBs) with CuO nanowires
(NWs) as the air cathode in an aberration-corrected environmental
transmission electron microscope under an oxygen environment. The
ORR occurred in a distinct two-step reaction, namely, a first conversion
reaction followed by a second multiple ORR. In the former, CuO was
first converted to Cu<sub>2</sub>O and then to Cu; in the latter,
NaO<sub>2</sub> formed first, followed by its disproportionation to
Na<sub>2</sub>O<sub>2</sub> and O<sub>2</sub>. Concurrent with the
two distinct electrochemical reactions, the CuO NWs experienced multiple
consecutive large volume expansions. It is evident that the freshly
formed ultrafine-grained Cu in the conversion reaction catalyzed the
latter one-electron-transfer ORR, leading to the formation of NaO<sub>2</sub>. Remarkably, no carbonate formation was detected in the oxygen
cathode after cycling due to the absence of carbon source in the whole
battery setup. These results provide fundamental understanding into
the oxygen chemistry in the carbonless air cathode in all solid state
Na–O<sub>2</sub> batteries