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Behind the scenes, your phone has to work hard to process and display your videos within the app. Because of this, our app isn't compatible with all operating systems and devices.

Minimum System Requirements For iOS

  • iOS 10 or newer

iOS Devices Compatible With Rylo

Rylo is compatible with all of the devices below, but for the best results, we recommend using our app oniPhone® 5s or newer.

  • iPhone 5s or newer
  • iPad® (5th generation, 2017)
  • iPad Air® 2
  • iPad mini™ 4
  • iPad Pro® (1st generation) or newer
  • iPod Touch® (6th generation)

Minimum System Requirements For Android

Android Devices That Won't Work With Rylo

The following devices have been tested and will not work with Rylo because they don’t have the hardware to decode 4K videos for playback. This is not a comprehensive list. To check whether your device is compatible download the Rylo app from the Monte Carlo surf suit Blue Duskii Free Shipping Excellent Sale Browse On16xBY
. Once downloaded, our app will notify you if your device is compatible or not.

  • Asus Zenfone 3 Zoom
  • Asus Zenpad 8
  • BlackBerry Keyone
  • BlackBerry Motion
  • BLU Vivo V5
  • Huawei Honor
  • HTC Desire 12+
  • Lenovo P2
  • LG Nexus 5
  • LG Stylo 3 Plus
  • Motorola Moto G4
  • Motorola Moto G5 Plus
  • Motorola Moto G5S Plus
  • Nexus 7
  • Samsung Galaxy C5 Pro
  • Samsung Galaxy C7 Pro
  • Samsung Galaxy J7 (2015)
  • Samsung Galaxy J7 Prime
  • Samsung Galaxy J7v
  • Vivo V5 Plus
  • Vivo V7
  • Vivo V7 Plus
  • Vivo V9
  • Vivo V9 Youth
  • Xiaomi Redmi 4X
  • Xiaomi Redmi 5
  • Xiaomi Redmi 5 Plus
  • Xiaomi Redmi Y2

Important Note: Rylo's hardware is compatible with both iOS and Android and you canuse your compatible Android and iOS devices interchangeably with your camera so long as you have the appropriate sync cables .

An even higher dosage may be necessary if amikacin regimen is calculated by using DW or in underweight patients (BMI <20) to avoid underdosage

Therapeutic drug monitoring is mandatory, as no clinical or biologic variable can predict amikacin pharmacokinetics in this population

Acute Physiology and Chronic Health Evaluation

area under the curve

body mass index

clearance

creatinine clearance

C-reactive protein

corrected body weight

ideal body weight

minimum inhibitory concentration

pharmacokinetic

sequential organ failure assessment

total body weight

volume of distribution

total volume of distribution.

Acknowledgements

We thank all the nurses and doctors who contributed to this study. The study was supported by grants from AstraZeneca, Wyeth Pharmaceuticals, GlaxoSmithKline Pharmaceuticals, and Bristol-Myers Squibb.

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The authors declare that they have no competing interests.

FJ conceived the study protocol. FST, FJ, PFL, TD, and HS participated in the design and coordination of the study. FST, JLV, and FJ drafted the present manuscript. All authors read and approved the final manuscript.

Department of Intensive Care, Erasme Hospital, Université Libre de Bruxelles, Bruxelles, Belgium
Department of Intensive Care, Cliniques Universitaires, Bruxelles, Belgium
Department of Intensive Care, Universitair Ziekenhuis Brussel, Bruxelles, Belgium
Department of Intensive Care, St-Pierre Hospital, Ottignies, Belgium
Department of Clinical Biochemistry and Pharmacokinetics, Cliniques Universitaires, Bruxelles, Belgium
Department of Infectious Diseases, Erasme Hospital, Université Libre de Bruxelles, Bruxelles, Belgium
Classification, incidence, and outcomes of sepsis and multiple organ failure. Inadequate antimicrobial treatment of infections: a risk factor for hospital mortality among critically ill patients. The influence of inadequate empirical antimicrobial treatment on patients with bloodstream infections in an intensive care unit. Old antibiotics for infections in critically ill patients. Empirical antibiotic therapy for patients with severe sepsis and septic shock. Does combination antimicrobial therapy reduce mortality in gram-negative bacteraemia? A meta-analysis. Beta lactam antibiotic monotherapy versus beta lactam-aminoglycoside antibiotic combination therapy for sepsis. The association of aminoglycoside plasma levels with mortality in patients with gram-negative bacteremia.
ARUP Laboratories
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DFA
2004598
Ordering Recommendation

Use for the rapid identification of ; sensitivity is dependent on patient population and specimen type. Molecular testing is generally preferred; refer to Legionella Species by Qualitative PCR ( 2010125 ).

Mnemonic
LEGIONFA
Methodology
Direct Fluorescent Antibody Stain
Performed
Sun-Sat
Reported
Within 24 hours
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult ®
Disease Topics
Example Reports
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Specimen Required
Fluid: Tissue: Fluid or Tissue Slides
Reference Interval
Negative
Interpretive Data
Note
A negative stain result does not exclude the possibility of infection. False-negative results may occur due to sampling errors or a low number of organisms in the specimen. DFA is not recommended for diagnosing -caused infections. For diagnosing -caused infections, refer to Species, Culture (ARUP test code 0060113), Species by Qualitative PCR (ARUP test code 2010125) for amplified DNA testing of respiratory specimens, or Antigen, Urine (ARUP test code 0070322) for urine specimens.
Hotline History
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CPT Code(s)
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2004598 - Interface Map

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New York Specimen Requirements Default Option

Certain tests have specimen requirements that differ for specimens shipped from New York state.

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