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Anorectal Manometry in 3D NEW! - Swiss-knife.org

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plantation. With the <strong>in</strong>troduction of voriconazole and other new antifungal agents the mortality of IPA<br />

dropped but rema<strong>in</strong>s still high, especially for patients with prolonged neutropenia. Surgical resection <strong>in</strong><br />

addition to antifungal therapy is an option for selected cases with IPA. However this approach is often<br />

feared due to the fact that the patients are immunocompromised.<br />

Methods: We analysed the perioperative outcome of 69 hematological patients (mean age 43 years)<br />

undergo<strong>in</strong>g surgery for aspergillosis over a period of 25 years at our <strong>in</strong>stitution.<br />

Results: 48 patients suffered from leukemia, 2 from myelodysplastic syndrome, 8 from aplastic anemia,<br />

3 from lymphoma, 1 from melanoma and 7 from other hematologic diseases. 42 underwent<br />

high dose chemotherapy, 18 stem cell transplantation, 6 antilymphocyte globul<strong>in</strong>e and 3 patients no<br />

specific therapy. On the day of surgery 42 patients were neutropenic. The mean platelet count was 87<br />

x 109/L. Lung resection consisted of wedge resections <strong>in</strong> 42, lobectomy <strong>in</strong> 25 and enucleation <strong>in</strong> 2<br />

cases. Fungal <strong>in</strong>fection was documented histologically <strong>in</strong> 51 patients. Reoperation was performed <strong>in</strong> 4<br />

cases: bronchial stump dehiscence, persistent airleak, chylothorax and seroma. M<strong>in</strong>or complications<br />

at the site of surgery occurred <strong>in</strong> 12 cases (6 pleural effusion, 2 hematothorax; 2 seroma; 2 prolonged<br />

airleak). In only two cases there was an uncontrolled dissem<strong>in</strong>ated fungal <strong>in</strong>fection (pleural aspergillosis;<br />

cerebral aspergillosis). The overall mortality at 30 days was 7.2% (5/69). Medium and longterm<br />

survival was ma<strong>in</strong>ly <strong>in</strong>fluenced by progression or reoccurrence of the underly<strong>in</strong>g hematologic disease<br />

and neither by the surgical procedure nor by unsuccessful resection of the fungus.<br />

Conclusion: Lung resection is a therapeutic option for patients with hematologic diseases suffer<strong>in</strong>g<br />

from pulmonary fungal <strong>in</strong>fection. Despite the immunocompromised status of these patients the perioperative<br />

morbidity and mortality is acceptable and the prognosis is more determ<strong>in</strong>ed by the underly<strong>in</strong>g<br />

hematologic disease than the surgical <strong>in</strong>tervention itself.<br />

35.5<br />

Prolonged amelioration of acute lung allograft rejection by sequential overexpression of human <strong>in</strong>terleuk<strong>in</strong>-10<br />

and hepatocyte growth factor <strong>in</strong> rats<br />

R. Fak<strong>in</strong>, J. Hamacher, M. Gugger, A. Gazdhar, R. A. Schmid (Berne)<br />

Objective: The effect of prolonged electroporation-mediated human <strong>in</strong>terleuk<strong>in</strong>-10 (hIL-10) overexpression<br />

24 hours before transplantation, comb<strong>in</strong>ed with sequential human hepatocyte growth factor<br />

(HGF) overexpression <strong>in</strong>to skeletal muscle on day 5 on rat lung allograft rejection was evaluated.<br />

Methods: Left lung allotransplantation was performed from Brown-Norway to Fischer-F344 rats. Gene<br />

transfer <strong>in</strong>to skeletal muscle was enhanced by electroporation. Three groups were studied: Group I<br />

animals (n=5) received 2.5μg pCIK-hIL-10 on day -1 and 80μg pCIK-HGF on day 5. Group II animals<br />

(n=4) received 2.5μg pCIK-hIL-10 and pUbC-hIL-10 on day -1. Control Group III animals (n=4) were<br />

treated by sham electroporation on days -1 and 5. All animals received daily non-therapeutic <strong>in</strong>traperitoneal<br />

dose of Cyclospor<strong>in</strong>-A (2.5 mg/kg) and were sacrificed on day 15. Graft oxygenation and<br />

allograft rejection were evaluated.<br />

Results: Significant differences were found between study groups <strong>in</strong> graft oxygenation (PaO2)<br />

(p=0.0028 Group I vs. II and III). PaO2 was low <strong>in</strong> Group II (31±1 mmHg) and <strong>in</strong> Group III controls<br />

(34±10 mmHg), without statistically significant difference between these two groups (p=0.54). In contrast,<br />

<strong>in</strong> Group I PaO2 of recipients sequentially transduced with IL-10 and HGF plasmids was much<br />

improved with 112±39 mmHg (p

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