gms | German Medical Science

68. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC)
7. Joint Meeting mit der Britischen Gesellschaft für Neurochirurgie (SBNS)

Deutsche Gesellschaft für Neurochirurgie (DGNC) e. V.

14. - 17. Mai 2017, Magdeburg

The administration of gelatine based colloids is safe in patients with signs of hypovolemia after elective intracranial surgeries

Meeting Abstract

  • Helene Hurth - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland
  • Ulrich Birkenhauer - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland
  • Jochen Steiner - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland
  • Dennis Schlak - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland
  • Marcos Tatagiba - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland
  • Florian H. Ebner - Neurochirurgie, Universitätsklinikum Tübingen, Tübingen, Deutschland

Deutsche Gesellschaft für Neurochirurgie. Society of British Neurological Surgeons. 68. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 7. Joint Meeting mit der Society of British Neurological Surgeons (SBNS). Magdeburg, 14.-17.05.2017. Düsseldorf: German Medical Science GMS Publishing House; 2017. DocDI.28.06

doi: 10.3205/17dgnc350, urn:nbn:de:0183-17dgnc3506

Veröffentlicht: 9. Juni 2017

© 2017 Hurth et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Objective: To evaluate adverse effects of administering gelatin to neurosurgical patients with postoperative signs of hypovolemia after elective intracranial surgeries being monitored at a neurosurgical intensive care unit (ICU).

Methods: We performed a retrospective study in our department on 100 consecutive patients operated electively on an intracranial pathology and showing postoperatively clinical signs of hypovolemia. All patients were treated with intravenous colloid fluids containing gelatin and monitored at the neurosurgical ICU. Since former studies have reported severe adverse effects of gelatin in intensive care patients we analyzed the ICU charts for anaphylaxis, renal failure, respiratory distress, bleeding complications and hypercoagulation. Pre-existing pulmonary, renal, thromboembolic conditions and history of bleeding complications or cardiac failure were compiled. In addition vital parameters, blood gas analyses, central venous pressure and the need of catecholamine therapy were compared before administration of gelatin, after 2 hours, after 6 hours and after 24h hours. Blood laboratory findings including blood count, clotting as well as renal parameters were compared postoperatively before administration of gelatin with the findings after one day.

Results: None of the patients presented with severe adverse effects such as anaphylaxis, the need of renal replacement therapy or prolonged ventilation time due to pulmonary edema. One patient presented with multiple thromboembolic complications. Due to extremely elevated D-dimer levels immediately after the operation the presence of thrombosis before gelatin administration was highly suspective. One patient required another surgery due to a major bleeding in the area of operation after initiation of preterm postoperative low-dose heparin therapy. There was no significant difference in laboratory findings before gelatin administration and after one day. Thirtythree percent of the patients were suffering from a preoperatively known minor limitation of their pulmonary, renal and/or cardiac function and/or had a history of thromboembolism. There was no difference in findings between patients with and without preexisting conditions.

Conclusion: Based on our findings we conclude that the use of gelatin based colloids in neurosurgical patients undergoing elective intracranial surgeries is safe even in patients with a history of minor respiratory, renal and/or cardiac disease and/or former thromboembolism.