This issue only affected users of the LastPass browser extension. Fixed an issue that caused the master password to not be accepted (when making changes in Account Settings) after the user changed their password iteration value and logged out.Fixed an issue in which the user was not prompted to enter the recipient's address to share an item when sharing a vault item via the LastPass browser extension.As a workaround, users could add headers to Keeper's exported CSV file and re-import it successfully. Previously, users would encounter either a blank import screen or "Invalid format" error message upon importing. Fixed an issue in which users were unable to import data (that was exported from Keeper as a CSV file) into LastPass.Fixed an issue that allowed users to generate a secure password for a website, even though that was added to the "Never Generate Password" section of the Never URLs configuration page in Account Settings.V4.109.0 - February 10th 2023 - Chrome, Chromium Edge, Firefox, Opera, Safari, IE Fixed an issue in which the matching sites count in the LastPass browser extension would reflect an incorrect number when switching between sites in two different browsers.Now, Free users encounter a message, "It looks like you don't have permission to write to this shared folder" when attempting to manage a shared folder item. Try again." when attempting to add or update a vault item within a shared folder. Fixed an issue in which Free users would encounter a misleading error message, "LastPass couldn't save your password.Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from.Recent changes to LastPass: v4.110.0 - February 23rd 2023 - Chrome, Chromium Edge, Firefox, Opera, Safari, IE PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. This functionality is provided solely for your convenience and is in no way intended to replace human translation. You have requested "on-the-fly" machine translation of selected content from our databases. Nevertheless, higher rates of small for gestational age neonates (57.1 % versus 33.3 %), neonatal respiratory distress syndrome (39.2 % versus 8.3 %) and neonatal sepsis (34.2 % versus 12.5 %) were noted in the HELLP syndrome group.ĪFLP is associated with a higher rate of multiple organ dysfunction in mothers, whereas HELLP syndrome is associated with a higher rate of neonatal morbidity. However, the AFLP group had more other maternal complications including jaundice (85.7 % versus 13.8 %), acute kidney injury (61.9 % versus 15.0 %), disseminated intravascular coagulopathy (66.7 % versus 8.8 %), and sepsis (47.6 % versus 10.0 %) compared to the HELLP syndrome group. There was a higher rate of preeclampsia (95.0 % versus 23.8 %) in the HELLP syndrome group compared to the AFLP group. Subsequent logistic regression analyses adjusting by potential confounding factors with significant difference were analyzed.ĭuring the study period, 21 women had AFLP and 80 women had HELLP syndrome. We analyzed the categorical variables with Chi-square test or Fisher’s exact test and continuous variables with Student’s t test or Mann-Whitney U test. Maternal characteristics, laboratory data, complications, and neonatal outcomes were compared. We used the Swansea Criteria to diagnose AFLP, and the Tennessee Classification System to diagnose HELLP syndrome. This retrospective cohort study was performed at a tertiary referral center in Taiwan between June 2004 and April 2020. This study aimed to compare maternal and neonatal outcomes between AFLP and HELLP syndrome. Acute fatty liver of pregnancy (AFLP) and hemolysis, elevated liver enzymes and low platelets (HELLP) syndrome are two uncommon disorders that mimic each other clinically, but are distinct pathophysiologically.
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