| Anesthesiology and Intensive Care ¹4 2009 E.
V. Suborov, E. A. Postnikova, A. A. Kapinos, V. V. Kuzkov, A. A. Smetkin, M.
Yu. Kirov
Use of microstream capnography and alveolar recruitment during off-pump
coronary artery bypass grafting
The aim of the study was to investigate changes in EtCO2 and its correlation
with PaCO2, and cardiac function during off-pump coronary artery bypass
grafting (OPCAB) and to evaluate whether the recruitment maneuver was
effective in improving gas exchange after OPCAB. Twenty adult patients
scheduled for elective OPCAB were enrolled in a prospective randomized study.
Anesthesia was maintained with midazolam, propofol, and fentanyl. After
OPCAB, the patients were randomized to a control group receiving
conventional ventilation (n = 10) or to a RM group (n = 10) having
ventilation and RM. RM was performed at min 15 after transfer to an ICU, by
increasing airway pressure to 40 cm H2O for 40 sec subsequently adjusting
PEEP to a level of 2 cm H2O above the lower inflection point of the
pressure-volume curve. The measurements included hemodynamics, microstream
capnography, respiratory parameters, and blood gasses. The baseline EtCO2 correlated with PaCO2 and cardiac index in both groups (r = 0.7 and 0.81,
respectively; p < 0.05). In the control group, OPCAB was followed by a rise
in PaCO2 and worsening of arterial oxygenation (p < 0.05). After recruitment,
EtCO2 increased transiently whereas PaO2/FiO2 returned to the baseline level.
There was a moderate correlation between EtCO2 and PaCO2 before and after RM
(r = 0.7 and 0.8, respectively; p < 0.05). The Bland-Altman analysis has
shown that the difference between PaCO2 and EtCO2 was 1.9±11.4 mm Hg (M±2SD).
Thus, during OPCAB, EtCO2 measured by microstream capnography correlated
well with PaCO2 and cardiac function. The use of RM after OPCAB increases
CO2 elimination and improves arterial oxygenation.
Key words:
capnography, microstream; alveolar mobilization; aortocoronary bypass
surgery
REFERENCES
1. Ãëàíö Ñ. Ìåäèêî-áèîëîãè÷åñêàÿ ñòàòèñòèêà. — Ì., 1999. — Ñ. 12—429.
2. Êîçëîâ È. À., Ðîìàíîâ À. À. // Àíåñòåçèîë. è ðåàíèìàòîë. — 2007. — ¹ 2. —
C. 27—31.
3. Òàæèåâ Ì. Ñ. // Òåð. àðõ. — 2004. — ¹ 1. — C. 33—37.
4. Altman D. G. // J. Epidemiol. Commun. Hlth. — 1986. — Vol. 40. — P.
274—277.
5. Amato M. B., Borges J. B., Okamoto V. N. et al. // Am. J. Respir. Crit.
Care Med. — 2006. — Vol. 174. — P. 268—278.
6. Cheifetz I. M., MacIntyre N. R. // Respir. Care. — 2007. — Vol. 52. – P.
406—407.
7. Colman Y., Krauss B. // J. Clin. Monit. Comput. — 1999. — Vol. 15. — P.
403—409.
8. Domsky M., Wilson R. F., Heins J. // Crit. Care Med. — 1995. — Vol. 23. —
P. 1497—1503.
9. Dubin A., Murias G., Estenssoro E. et al. // Intensive Care Med. — 2000.
— Vol. 26. — P. 1619—1623.
10. Dyhr T., Layrsen N., Larsson A. // Acta Anaesthesiol Scand. — 2002. —
Vol. 46. — P. 717—725.
11. Idris A. H., Staples E. D., O’Brien D. J. et al. // Ann. Emerg. Med. —
1994. — Vol. 23. — P. 568—572.
12. Isserles S. A., Breen P. H. // Anesth. Analg. — 1991. — Vol. 73. — P.
808—814.
13. Jindani A., Aps C., Neville E. et al. // Br. Heart J. — 1993. — Vol. 69.
— P. 59—64.
14. Loeb R. G., Brown E. A. et al. // Anesthesiology. — 1999. — Vol. 91. —
P. A474.
15. Mack M. J., Brown P. P., Kugelmass A. D. et al. — Ann. Thorac. Surg. —
2004. — Vol. 77. — P. 761—768.
16. Magnusson L., Zemgulis V., Tenling A. et al. // Anesthesiology. — 1998.
— Vol. 88. — P. 134—142.
17. Maslow A., Stearns G., Bert A. et al. // Anesth. Analg. — 2001. — Vol.
92. — P. 306—313.
18. Polese G., Lubil P., Mazzuco A. et al. // Intensive Care Med. — 1999. —
Vol. 25. — P. 1092—1099.
19. Suh G. Y., Koh Y., Chung M. P. et al. // Crit. Care Med. — 2002. — Vol.
30. — P. 1848—1853.
20. Tusman G., Böhm S. H., Vazquez de Anda G. R. et al. // Br. J. Anaesth. —
1999. — Vol. 82. — P. 8—13. |