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279 results for “AKI”
Fig. 5 in Molecular Phylogenetic and Morphological Problems of the Aki Salamander Hynobius akiensis: Description of Two New Species from Chugoku, Japan
Fig. 5. Larvae, egg sacs, and habitat at the type locality of Hynobius geiyoensis sp. nov. (A, C, and E, respectively) and H. sumidai sp. nov. (B, D, and F, respectively).
Fig. 1 in Molecular Phylogenetic and Morphological Problems of the Aki Salamander Hynobius akiensis: Description of Two New Species from Chugoku, Japan
Fig. 1. Sampling map of the three Hynobius species used in this study. The enlarged area includes the central to the western part of Hiroshima Prefecture and the northernmost part of Ehime Prefecture. Closed symbols correspond to each of the three species sequenced in the current study. Open symbols correspond to each of the three species sequenced by other studies. The underlined localities show the sampling points of individuals for morphological comparisons: Pops. 1 (18 males) and 2 (1 male) for H. geiyoensis sp. nov.; Pop. 8 (7 males) for H. sumidai sp. nov.; Pops. 14 (3 males), 15 (7 males), 20 (6 males), 29 (3 males), 30 (1 male), 34 (6 males), 39 (1 male), 54 (1 male) for H. akiensis.
Fig. 4 in Molecular Phylogenetic and Morphological Problems of the Aki Salamander Hynobius akiensis: Description of Two New Species from Chugoku, Japan
Fig. 4. Holotype of Hynobius geiyoensis sp. nov. (HMNH-AM-101, adult male, 58.4 mm SVL) from the (A) dorsal and (B) ventral perspective; holotype of H. sumidai sp. nov. (HMNH-AM-102, adult male, 48.2 mm SVL) from the (C) dorsal and (D) ventral perspective; and a specimen from the type locality (topotype) of H. akiensis (KPM-NFA 946, adult male, 55.3 mm) from the (E) dorsal and (F) ventral perspective.
Fig. 3 in Molecular Phylogenetic and Morphological Problems of the Aki Salamander Hynobius akiensis: Description of Two New Species from Chugoku, Japan
Fig. 3. Two-dimensional plots of canonical discriminant analysis in males. The x and y axes show discriminant score 1 (DS1) and discriminant score 2 (DS2), respectively. The contribution ratios of DS1 and DS2 were 88.03 % and 11.97 %, respectively.
Fig. 2 in Molecular Phylogenetic and Morphological Problems of the Aki Salamander Hynobius akiensis: Description of Two New Species from Chugoku, Japan
Fig. 2. Phylogenetic tree produced by Bayesian inference using 630-bp cytochrome b genes. Salamandrella keyserlingii was used as an outgroup. Scale bar shows genetic distance (expected changes per site). Numbers located near the nodes are posterior probabilities (PP) for Bayesian inference and bootstrap (BS) values for maximum likelihood estimation. Values appearing in parentheses after the haplotype names correspond to population localities as indicated in Table 1 and Fig. 1. Asterisks after the parentheses (Pops. 1, 8, and 54) indicate the type locality of the three species. The labels covered by shaded boxes indicate the transition type of Hynobius akiensis.
Randomized trial of AKI alerts in hospitalized patients
<p><b>Objective: </b>To determine whether electronic health record (EHR) alerts for Acute Kidney Injury (AKI) would improve patient outcomes of mortality, dialysis and progression of AKI. </p> <p><b>Design: </b>Double-blinded, multicenter, parallel, randomized, controlled trial of an electronic AKI alert versus usual care (no alert). Participants were electronically identified and randomized via a best practice alert build using simple randomization with allocation concealment.</p> <p><b>Setting:</b> Six diverse hospitals (four teaching and two non-teaching) ranging from small community hospitals to large tertiary care centers.</p> <p><b>Participants:</b> 6,030 adult inpatients with AKI, as defined by the Kidney Disease: Improving Global Outcomes (KDIGO) creatinine criteria.</p> <p><b>Interventions:</b> An EHR-based "pop-up" alert for AKI with an associated AKI order set upon provider opening of the patient's medical record.</p> <p><b>Main Outcome Measures: </b>A composite of AKI progression, receipt of dialysis, or death within 14 days of randomization. Pre-specified secondary outcomes included per-hospital outcome rates and rates of various AKI care practices. </p> <p><b>Results: </b>6,030 patients were randomized over 22 months. The primary outcome occurred in 653 (21.4%) patients in the alert group and 622 (20.9%) in the usual care group (relative risk 1.02, 95% confidence interval [CI] 0.93 to 1.13, p=0.67). Per-hospital analysis revealed worse outcomes in the two non-teaching hospitals (N=765, 13%), where alerts were associated with a relative risk of the primary outcome of 1.49 (95% CI, 1.12 to 1.98, p=0.006). More deaths (15.6% in the alert group vs. 8.6% in the usual care group) occurred at these centers (p=0.003). Certain AKI care practices were increased in the alert group but did not appear to mediate these outcomes.</p> <p><b>Conclusions: </b>Alerts did not reduce rates of our primary outcome among hospitalized patients with AKI. The overall lack of clinical benefit and signals of harm in non-teaching hospitals should lead to a re-evaluation of existing AKI alerting systems.</p> <p><b>Trial Registration: </b>ClinicalTrials.gov NCT02753751.</p>
CHIP calls for BioVU cohort – resolving vs. non-resolving AKI analysis
<p>Data for analysis examining clonal hematopoiesis of indeterminate potential (CHIP) and AKI recovery patterns in cohort of individuals from the BioVU biorepository</p>
IMPROVE AKI Cluster-Randomized Trial
ClinicalTrials.gov study NCT03556293. IPD Sharing: YES. Countries: 1. Publications: 2.
NIRS Monitoring to Detect AKI in Preterm Infants
ClinicalTrials.gov study NCT03384173. IPD Sharing: NO. Countries: 1. Publications: 5.
Personalized Recommendations for Acute Kidney Injury (AKI) Care
ClinicalTrials.gov study NCT04040296. IPD Sharing: YES. Countries: 1. Publications: 3.
Standard vs. Accelerated Initiation of RRT in Acute Kidney Injury (STARRT-AKI: Principal Trial)
ClinicalTrials.gov study NCT02568722. IPD Sharing: Not stated. Countries: 15. Publications: 8.
(Revival) Study to Investigate the Efficacy and Safety of Alkaline Phosphatase in Patients With Sepsis-Associated AKI
ClinicalTrials.gov study NCT04411472. IPD Sharing: Not stated. Countries: 15. Publications: 2.
A Safety, Tolerability, Efficacy and QoL Study of Human recAP in the Treatment of Patients With SA-AKI
ClinicalTrials.gov study NCT02182440. IPD Sharing: UNDECIDED. Countries: 11. Publications: 2.
Safety and Efficacy of a Selective Cytopheretic Device (SCD) in Pediatric Patients With Acute Kidney Injury (AKI).
ClinicalTrials.gov study NCT02820350. IPD Sharing: NO. Countries: 1. Publications: 1.
Randomized trial of AKI alerts in hospitalized patients
Open the record for dataset details and reuse information.
Suppl. Data for AKI-to-CKD_human-mouse
<p>Suppl. Data for AKI-to-CKD_human-mouse</p>
FIGURE 15. Hisonotus aky, MCP 41474 in Four new species of Hisonotus (Siluriformes: Loricariidae) from the upper rio Uruguay, southeastern South America, with a review of the genus in the rio Uruguay basin
FIGURE 15. Hisonotus aky, MCP 41474, female, 33.7 mm SL. Rio Forquilha at Espraiado bathing spot on secondary road from Maximiliano de Almeida to Paim Filho, Paim Filho, Rio Grande do Sul, Brazil.
aki_labeled_dataset
<p>Dataset provided by Todd Miano for BMIN5030/EPID6000 class project.</p>
Development and Validation of a Prediction Model for AKI Following Cisplatin-Based HIPEC in Patients With Ovarian Cancer
ClinicalTrials.gov study NCT06697613. IPD Sharing: Not stated. Countries: 1. Publications: 4.
Mehran 2.0 Risk Score for Prediction of CA-AKI After PCI
ClinicalTrials.gov study NCT05132062. IPD Sharing: UNDECIDED. Countries: 1. Publications: 3.
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