- Department of Surgery, Section of Neurosurgery, Aga Khan University Hospital, Karachi, Pakistan
Correspondence Address:
Muhammad Shahzad Shamim
Department of Surgery, Section of Neurosurgery, Aga Khan University Hospital, Karachi, Pakistan
DOI:10.4103/2152-7806.85055
Copyright: © 2011 Sobani ZA. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.How to cite this article: Sobani ZA, Shamim MS, Zafar SN, Qadeer M, Bilal N, Murtaza SG, Enam SA, Bari ME. Cranioplasty after decompressive craniectomy: An institutional audit and analysis of factors related to complications. Surg Neurol Int 17-Sep-2011;2:123
How to cite this URL: Sobani ZA, Shamim MS, Zafar SN, Qadeer M, Bilal N, Murtaza SG, Enam SA, Bari ME. Cranioplasty after decompressive craniectomy: An institutional audit and analysis of factors related to complications. Surg Neurol Int 17-Sep-2011;2:123. Available from: http://sni.wpengine.com/surgicalint_articles/cranioplasty-after-decompressive-craniectomy-an-institutional-audit-and-analysis-of-factors-related-to-complications/
Abstract
Background:Although a relatively simple procedure, cranioplasties have been associated with high complication rates. Keeping this in perspective, we aimed to determine the factors associated with immediate and long-term complications of cranioplasties at our institution.
Methods:A retrospective review of patient records was carried out for patients having undergone reconstructive cranioplasties at our institution during the last 10 years (2001-2010). All case notes, records, and investigations were reviewed and the data were recorded in a predesigned questionnaire. Complications were recorded along with existing comorbids and measures taken for their prevention and management. Univariate and multivariate logistic regression analysis was performed to determine possible predictors of complications.
Results:A total of 96 patients with a mean age of 33 + 15 years were included in the study. Of the sample, 76% (n = 73) had no comorbids. The leading primary pathology was blunt traumatic brain injuries in 46% (n = 44), followed by cerebrovascular incidents in 24% (n = 23), penetrating traumatic brain injuries in 12% (n = 11), and tumors in 10% (n = 10) of cases, with 41% (n = 39) of patients requiring multiple craniotomies. In a mean follow-up of 386 ± 615 days, complications were noted in 36.5% (n = 35) of the patients. Twenty six percent of patients (n = 25) had minor complications which included breakthrough seizures (15.6%, n = 15), subgaleal collections (3.1%, n = 3), and superficial wound infections (3.1%, n = 3), whereas major complications (10.4% n = 10) included hydrocephalus (3.1%, n = 3), transient neurological deficits (3.1%, n = 3), and osteomyelitis (2.1%, n = 2). Univariate and multivariate analysis revealed External Ventricular Drain (EVD) placement and parietal flaps to be associated with complications. This could be explained by the fact that the patients requiring EVD usually have relatively severe head injuries, increasing the possibility of hydrocephalus.
Conclusion:We have found a higher risk of complications of cranioplasty in patients who had EVD placement and removal prior to their constructive surgery. We however did not find any association between risks of complications in any other studied variable. We also did not find any association between intraoperative placement of subgaleal drains and postoperative risk of subgaleal fluid collections. Overall, our results are comparable with other reported series on cranioplasties.
Keywords: Decompressive craniectomy [E04.188.200], reconstructive cranioplasty
INTRODUCTION
Decompressive craniectomies have been demonstrated as an effective modality in reducing intracranial pressure (ICP) in emergency situations involving severe head injuries,[
However, in the long run, alterations in hemodynamics, venous drainage, cerebrospinal fluid (CSF) dynamics, and general metabolic function have been demonstrated along with gradual neurological decline.[
MATERIALS AND METHODS
A retrospective review of patient records was carried out for patients having undergone reconstructive cranioplasties at our institution during the last 10 years (2001-2010). Patients of all age groups undergoing cranioplasty procedures following decompressive craniectomy for intractable intracranial hypertension were included in the study. The cases were included regardless of the material used for cranioplasty, i.e., patients having undergone cranioplasties with autologous bone, polymethylmethacrylate (PMMA), autologous bone with PMMA, and autoclaved autologous bone were included in the study. Cranioplasties performed for infected post-craniotomy bone flaps, post-trauma cranial defects, bone involved with tumors, and those done for cosmetic reasons, not preceded by a decompressive surgery, were not included. In cases where autologous bone flaps were used, the bone flaps were either stored in an anterior abdominal wall subcutaneous pocket or in a -26°C freezer. All cranioplasties were performed by either senior residents or chief residents, supervised by one of five credentialed neurosurgeons. The technique remained largely same over the study period with only minor variations depending upon surgeons’ preferences and individual cases.
All case notes, records, and investigations were reviewed and the data were recorded in a predesigned questionnaire. Follow ups including complications were recorded along with the measures taken for their management. Descriptive analysis was performed by calculating means and standard deviations for continuous variables and proportions for categorical ones. All major complications (Subdural Hematoma [SDH], Extradural Hematoma [EDH], Osteomyelitis, Neurological deficits) were clumped into a binary variable, i.e., yes/no. To determine factors associated with the occurrence of complications, we first performed univariate analysis using logistic regression and tabulated odds ratios with 95% confidence intervals. A multivariate logistic regression model was then constructed including all variables with P values <0.25 upon univariate analysis and clinically relevant variables which were determined a priori by the authors. The data were analyzed using Statistical Package for Social Sciences version 17 (International Business Machines, Armonk, New York).
RESULTS
A total of 96 patients met the above criteria and were included in the study. Analysis of the data revealed a mean age of 33 ± 14.8 years, 72.9% (n = 70) of our patients were males, 27.1% (n = 26) were females. Of the sample, 76% (n = 73) had no known comorbids, the rest had one or two comorbids, and seven patients had multiple (>2) comorbidities. The leading primary pathology was blunt traumatic brain injuries in 45.8% (n = 44), followed by cerebrovascular incidents in 23.95% (n = 23), penetrating traumatic brain injuries in 11.5% (n = 11), and tumors in 10.4% (n = 10) of cases, with 40.6% (n = 39) of patients requiring more than one cranial procedures. Nearly all (97.9%, n = 94) index surgeries were performed at our center and the rest were performed elsewhere and referred to us for further management. The various flaps used included standard trauma (59.4%, n = 57), frontal (16.7%, n = 16), parietal (13.5%, n = 13), and temporal (9.4%, n = 9) flaps. Of these, 82.3% (n = 79) were unilateral and the rest (15.6%, n = 15) were bilateral. The craniotomy bone flaps were preserved in 85.4% (n = 82) of cases using cryopreservation in 76% (n = 73) and subcutaneous preservation in 9.4% (n = 9), whereas 14.6% (n = 14) were damaged or discarded.
Reconstructive cranioplasties were performed as a separate hospital admission in 79.2% (n = 76) of the patients, whereas in 20.8% (n = 20) patients, it was carried out during the same admission. The reconstructive procedure was performed after a mean delay of 90 ± 116 days. Mean preoperative Glasgow coma scale (GCS) score of the patients undergoing cranioplasties was 12 ± 3.06 and they were operated at mean hemoglobin of 12 ± 1.32 mg/dl. At the time of the cranioplasty, 31.2% (n = 30) patients had their airway maintained through tracheostomies, 11.5% (n = 11) were receiving nutrition through gastrostomy tubes, and 2.1% (n = 2) patients had ventriculoperitoneal (VP) shunts placed. Intravenous cefazolin (first generation cephalosporin) was the most commonly administered prophylactic antibiotic, administered to 87.5% (n = 84) of the patients, while the remaining received other antibiotics depending on their pre-existing regimens. Perioperatively, 34.4% (n = 33) were already on antiepileptics for post-traumatic seizures. Phenytoin was the most commonly administered perioperative antiepileptic in 20.8% (n = 20) of the patients. Drug levels were checked and brought to therapeutic levels in all patients prior to surgery.
The defect was reconstructed using saved autologous bone in 67.7% (n = 65) of the patients, 15.6% (n = 15) had a bone fashioned using PMMA, 11.5% (n = 11) had their autologous bone used along with PMMA, and 5.2% (n = 5) had their bone flap autoclaved prior to replacement. The flaps were secured using silk sutures (33.3%, n = 32), vicryl sutures (27.1%, n = 26), titanium plates (19.8%, n = 19), or wires (18.8%, n = 18). Galeal closures were done using absorbable vicryl in all patients and skin was closed using either sutures (69.8%, n = 67) or staples (30.2%, n = 29) depending upon the surgeons’ preference. Subgaleal drains were placed prior to closure in 28.1% (n = 27) of the patients and no patient underwent placement of an epidural or subdural drain. The mean duration of surgery was 185.2 ± 67.3 minutes, resulting in an average blood loss of 365 ± 263 ml. Seventeen patients (17.7%) required intraoperative blood transfusions and mean duration of hospital stay was 12 ± 17 days.
In a mean follow up of 386 ± 615 days, complications were noted in 36.5% (n = 35) of the patients. The complications were divided into major and minor complications. Minor complications accounted for 29.1% (n = 25) including most notably, breakthrough seizures (15.6%, n = 15), CSF leak (4.1%, n = 4), postoperative subgaleal fluid collections other than that caused by underlying hydrocephalus (3.1%, n = 3), superficial wound infections (SWI) (3.1%, n = 3), and new-onset transient neurological deficits (3.1%, n = 3) [
Univariate regression analysis revealed that External Ventricular Drain (EVD) placement prior to reconstructive cranioplasty was 4.2 (0.98-18.1, P = 0.05) times more likely to be associated with complications. When considering the flap sites, parietal flaps were 6.11 (1.20-31.16) times more likely to be associated with complications compared with frontal flaps. Other factors were not associated with significant odds of complication [
DISCUSSION
It is apparent from the growing body of evidence that decompressive craniectomies will be a significant part of neurosurgical practice and so will be the requirement of cranioplasties. However, integral the reconstructive procedure may be, there have been few studies that have actually addressed the issue and no comprehensive guidelines are available regarding the technique and timing of the procedure, especially with respect to the possible complications.[
We have presented one of the largest series of post-decompressive craniectomy cranioplasties with a mean follow-up of more than one year. To the best of our knowledge, no previous study has analyzed more preoperative variables than ours. Moreover, we have primarily used autologous bone, saved at negative 26°C with acceptable rates of infection, thus supporting recent reports that freezing bone flaps at lower temperatures may not be necessary.[
Our study shows that an EVD placement prior to the reconstructive procedure was more likely to be associated with complications. This can be explained by the fact that the nine patients requiring EVD placement had relatively severe injuries resulting in an increased risk of complications. Further studies on larger cohorts will be required to validate this particular observation before any definite conclusions could be drawn. Our study revealed that parietal bone flaps were associated with higher complications. However, this could be explained by the fact that patients undergoing parietal flaps in our dataset mainly constituted those undergoing index surgeries due to penetrating head trauma or tumor surgeries at the site, which are inherently associated with a higher rate of complications.
A 36.5% risk of complications may appear high but it may be noted that other centers have reported similarly high complication rates ranging between 16.4% and 34%.[
Limitations
The study was carried out as a retrospective.
CONCLUSION
When undergoing a cranioplasty for decompressive craniectomy, we have found a higher risk of complications in patient who had an EVD at the time of decompressive surgery. We however did not find any association between risk of complications and age of patient, presence of comorbids, time interval between the two surgeries, the method of flap preservation, the type of material used for plasty, i.e., autograft vs allograft, or the material used to secure the bone flap, or any of the other variables studied. Overall, our results are comparable with other reported series on cranioplasties. It will therefore suffice to say that in its rich history of nearly 400 years, from the initial gold plates of Fallopius and the first bone graft by Meekeren,[
References
1. Aarabi B, Hesdorffer DC, Simard JM, Ahn ES, Aresco C, Eisenberg HM. Comparative study of decompressivecraniectomy after mass lesion evacuation in severe head injury. Neurosurgery. 2009. 64: 927-39
2. Beauchamp KM, Kashuk J, Moore EE, Bolles G, Rabb C, Seinfeld J. Cranioplasty after postinjurydecompressivecraniectomy: Is timing of the essence?. J Trauma. 2010. 69: 270-4
3. Bhaskar IP, Zaw NN, Zheng M, Lee GY. Bone flap storage following craniectomy: A survey of practices in major Australian Neurosurgical centres. ANZ J Surg. 2011. 81: 137-41
4. Bullock MR, Chesnut R, Ghajar J, Gordon D, Hartl R, Newell DW. Surgical management of traumatic parenchymal lesions. Neurosurgery. 2006. 58: S25-46
5. Chang V, Hartzfeld P, Langlois M, Mahmood A, Seyfried D. Outcomes of cranial repair after craniectomy. J Neurosurg. 2010. 112: 1120-4
6. Colohan AR, Ghostine S, Esposito D. Exploring the limits of survivability: Rational indications for decompressivecraniectomy and resection of cerebral contusions in adults. Clin Neurosurg. 2005. 52: 19-23
7. Datti R, Cavagnaro G, Camici S. Stainless steel wire mesh cranioplasty: Ten years’ experience with 183 patients (100 followed up). Acta Neurochir (Wien). 1985. 78: 133-5
8. Dujovny M, Fernandez P, Alperin N, Betz W, Misra M, Mafee M. Post-cranioplasty cerebrospinal fluid hydrodynamic changes: Magnetic resonance imaging quantitative analysis. Neurol Res. 1997. 19: 311-6
9. Gooch MR, Gin GE, Kenning TJ, German JW. Complications of cranioplasty following decompressivecraniectomy: Analysis of 62 cases. Neurosurg Focus. 2009. 26: E9-
10. Jho DH, Neckrysh S, Hardman J, Charbel FT, Amin-Hanjani S. Ethylene oxide gas sterilization: A simple technique for storing explanted skull bone.Technical note. J Neurosurg. 2007. 107: 440-5
11. Juttler E, Schwab S, Schmiedek P, Unterberg A, Hennerici M, Woitzik J. Decompressivesurgery for the treatment of malignant infarction of the middle cerebral artery (DESTINY): A randomized, controlled trial. Stroke. 2007. 38: 2518-25
12. Ma L, Liu WG, Sheng HS, Fan J, Hu WW, Chen JS. Decompressivecraniectomy in addition to hematoma evacuation improves mortality of patients with spontaneous basal ganglia hemorrhage. J Stroke Cerebrovasc Dis. 2010. 19: 294-8
13. Meier U, Grawe A, Konig A. The importance of major extracranial injuries by the decompressivecraniectomy in severe head injuries. Acta Neurochir Suppl. 2005. 95: 55-7
14. Merenda A, DeGeorgia M. Craniectomy for acute ischemic stroke: How to apply the data to the bedside. Curr Opin Neurol. 2010. 23: 53-8
15. Sahuquillo J, Arikan F. Decompressivecraniectomy for the treatment of refractory high intracranial pressure in traumatic brain injury. Cochrane Database Syst Rev. 2006. p. CD003983-
16. Sanan A, Haines SJ. Repairing holes in the head: A history of cranioplasty. Neurosurgery. 1997. 40: 588-603
17. Skoglund TS, Eriksson-Ritzen C, Jensen C, Rydenhag B. Aspects on decompressivecraniectomy in patients with traumatic head injuries. J Neurotrauma. 2006. 23: 1502-9
18. Smith ER, Carter BS, Ogilvy CS. Proposed use of prophylactic decompressivecraniectomy in poor-grade aneurysmal subarachnoid hemorrhage patients presenting with associated large sylvian hematomas. Neurosurgery. 2002. 51: 117-24
19. Stephens FL, Mossop CM, Bell RS, Tigno T, Rosner MK, Kumar A. Cranioplasty complications following wartime decompressivecraniectomy. Neurosurg Focus. 2010. 28: E3-
20. Unterberg A, Juettler E. The role of surgery in ischemic stroke: Decompressivesurgery. Curr Opin Crit Care. 2007. 13: 175-9
21. Vahedi K, Vicaut E, Mateo J, Kurtz A, Orabi M, Guichard JP. Sequential-design, multicenter, randomized, controlled trial of early decompressivecraniectomy in malignant middle cerebral artery infarction (DECIMAL Trial). Stroke. 2007. 38: 2506-17
22. Yadla S, Campbell PG, Chitale R, Maltenfort MG, Jabbour P, Sharan AD. Effect of early surgery, material, and method of flap preservation on cranioplasty infections: A systematic review. Neurosurgery. 2011. 68: 1124-9
23. Yamaura A, Makino H. Neurological deficits in the presence of the sinking skin flap following decompressivecraniectomy. Neurol Med Chir (Tokyo). 1977. 17: 43-53