12 research outputs found
Black Phosphorus Radio-Frequency Transistors
Few-layer
and thin film forms of layered black phosphorus (BP) have recently
emerged as a promising material for applications in high performance nanoelectronics and infrared
optoelectronics. Layered BP thin films offer a moderate bandgap of
around 0.3 eV and high carrier mobility, which lead to transistors
with decent onβoff ratios and high on-state current densities.
Here, we demonstrate the gigahertz frequency operation of BP field-effect
transistors for the first time. The BP transistors demonstrated here
show respectable current saturation with an onβoff ratio that
exceeds 2 Γ 10<sup>3</sup>. We achieved a current density in
excess of 270 mA/mm and DC transconductance above 180 mS/mm for hole
conduction. Using standard high frequency characterization techniques,
we measured a short-circuit current-gain cutoff frequency <i>f</i><sub>T</sub> of 12 GHz and a maximum oscillation frequency <i>f</i><sub>max</sub> of 20 GHz in 300 nm channel length devices.
BP devices may offer advantages over graphene transistors for high
frequency electronics in terms of voltage and power gain due to the
good current saturation properties arising from their finite bandgap,
thus can be considered as a promising candidate for the future high
performance thin film electronics technology for operation in the
multi-GHz frequency range and beyond
Image_3_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.TIFF
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Image_4_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.TIF
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_3_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_5_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_2_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_1_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_4_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Image_1_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.TIFF
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p
Table_6_Dynamic increase in myoglobin level is associated with poor prognosis in critically ill patients: a retrospective cohort study.docx
BackgroundMyoglobin is an important biomarker for monitoring critically ill patients. However, the relationship between its dynamic changes and prognosis remains unclear.MethodsWe retrospectively enrolled 11,218 critically ill patients from a general and surgical intensive care unit (ICU) of a tertiary hospital between June 2016 and May 2020. Patients with acute cardiovascular events, cardiac and major vascular surgeries, and rhabdomyolysis were excluded. To investigate the early myoglobin distribution, the critically ill patients were stratified according to the highest myoglobin level within 48βh after ICU admission. Based on this, the critically ill patients with more than three measurements within 1βweek after ICU admission were included, and latent class trajectory modeling was used to classify the patients. The characteristics and outcomes were compared among groups. Sensitivity analysis was performed to exclude patients who had died within 72βh after ICU admission. Restricted mean survival time regression model based on pseudo values was used to determine the 28-day relative changes in survival time among latent classes. The primary outcome was evaluated with comparison of in-hospital mortality among each Trajectory group, and the secondary outcome was 28-day mortality.ResultsOf 6,872 critically ill patients, 3,886 (56.5%) had an elevated myoglobin level (β₯150βng/mL) at admission to ICU, and the in-hospital mortality significantly increased when myoglobin level exceeded 1,000βΞΌg/mL. In LCTM, 2,448 patients were unsupervisedly divided into four groups, including the steady group (n =β1,606, 65.6%), the gradually decreasing group (nβ=β523, 21.4%), the slowly rising group (nβ=β272, 11.1%), and the rapidly rising group (nβ=β47, 1.9%). The rapidly rising group had the largest proportion of sepsis (59.6%), the highest median Sequential Organ Failure Assessment (SOFA) score (10), and the highest in-hospital mortality (74.5%). Sensitivity analysis confirmed that 98.2% of the patients were classified into the same group as in the original model. Compared with the steady group, the rapidly rising group and the slowly rising group were significantly related to the reduction in 28-day survival time (Ξ²β=ββ12.08; 95% CI β15.30 to β8.86; Ξ²β=ββ4.25, 95% CI β5.54 to β2.97, respectively).ConclusionElevated myoglobin level is common in critically ill patients admitted to the ICU. Dynamic monitoring of myoglobin levels offers benefit for the prognosis assessment of critically ill patients.</p