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Efficiency of Pulmonary Administration of Tobramycin Solution for

Inhalation in Cystic Fibrosis Using an Improved Drug Delivery System --

Chest

http://www.pulmonologylinx.com/thearts.cfm?artid=491492 & specid=14

Conclusion: Compared with the standard nebulizer, the AeroDose safely

achieved an approximately threefold greater efficiency in the delivery

of TSI to the lungs in less than half the time...

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Factors Influencing Outcomes in Cystic Fibrosis -- Chest

http://www.pulmonologylinx.com/thearts.cfm?artid=491491 & specid=14

Conclusion: We found substantial differences in lung health across

different CF care sites. We found that frequent monitoring and increased

use of appropriate medications in the management of CF are associated

with improved outcomes...

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GI Complications After Lung Transplantation in Patients With Cystic

Fibrosis -- Chest

http://www.pulmonologylinx.com/thearts.cfm?artid=491493 & specid=14

Conclusion: GI complications after lung transplantation are common in

patients with CF, and attention should be paid to the risk for DIOS in

the early postoperative period. Prevention and early medical treatment

are important in order to avoid acute surgery. ...

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Pneumothorax in Cystic Fibrosis -- Chest

http://www.pulmonologylinx.com/thearts.cfm?artid=491518 & specid=14

Conclusion: The following is a review of what has been published

regarding the incidence and management of pneumothorax in this

population, with some comment on the pathogenesis of the complication...

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Questions on Life Satisfaction for Adolescents and Adults With Cystic

Fibrosis -- Chest

http://www.pulmonologylinx.com/thearts.cfm?artid=491494 & specid=14

Conclusion: The FLZM-CF is a reliable and valid instrument, and it is

short enough to be used as screening instrument. The combination of

generic and disease-specific scales within the FLZM allows comprehensive

measurement of life satisfaction for patients with CF who are > 15 years

old... ________________________________

Acute neurological deficits in a young adult with cystic fibrosis --

Pediatric Pulmonology

http://www.pulmonologylinx.com/thearts.cfm?artid=491981 & specid=14

We conclude that paradoxical embolism should be in the differential

diagnoses of CF patients who have indwelling intravenous catheters and

who develop an unexplained stroke. An extensive investigation to rule

out intracardiac abnormalities and thrombophilia should be considered.

The risks and benefits of PFO closure vs. prophylactic anticoagulant and

antiplatelet aggregation treatment in this group of patients should be

carefully weighed...

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Antimicrobial susceptibility profile of molecular typed cystic fibrosis

Stenotrophomonas maltophilia isolates and differences with noncystic

fibrosis isolates -- Pediatric Pulmonology

http://www.pulmonologylinx.com/thearts.cfm?artid=491973 & specid=14

Conclusion: Susceptibility analysis demonstrated higher resistance rates

among CF S. maltophilia isolates when compared with respiratory isolates

from non-CF patients. Moreover, persistently recovered CF S. maltophilia

isolates were more resistant than sporadic non-CF isolates...

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Three-minute step test to assess exercise capacity in children with

cystic fibrosis with mild lung disease -- Pediatric Pulmonology

http://www.pulmonologylinx.com/thearts.cfm?artid=491974 & specid=14

Conclusion: 15c did not discriminate between a maximal and a submaximal

test, and was less useful than VAS. Important information may be missed

by the step test which is detected by more complex exercise tests...

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Validation of shuttle tests in children with cystic fibrosis --

Pediatric Pulmonology

http://www.pulmonologylinx.com/thearts.cfm?artid=491978 & specid=14

We conclude that when formal exercise testing with treadmill or cycle

ergometer cannot be performed, the shuttle tests provide a reproducible

and valid alternative...

Becki

YOUR FAVORITE LilGooberGirl

YOUNGLUNG EMAIL SUPPORT LIST

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Pediatric Interstitial Lung Disease Society

http://groups.yahoo.com/group/InterstitialLung_Kids/

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