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DOI: 10.1055/s-0035-1549061
Step-Ladder Expansive Cranioplasty after Decompressive Craniotomy and Expansive Duraplasty: Discussing Possibilities on a Mathematical Model
Abstract
Background Role of decompressive craniectomy in reducing intracranial pressure is well established. However, it comes with a cost of requiring a second surgery in the form of cranioplasty without which unacceptable hemodynamic consequences occur. It is generally felt that a credible alternative is required.
Objective The aim of the study is to devise a mathematical model, which closely represents the cranium and intracranial contents, on which various alternatives can be evaluated with reproducible results, and to work out the effects of a novel technique of expansive cranioplasty on that model.
Methods A mathematical model was designed based on the presumption that dura forms a watertight bag-containing brain, floating in cerebrospinal fluid (CSF). A model for an expansive cranioplasty was designed, and its ability to provide the space required to allow volume expansion and to achieve adequate reduction in intracranial pressure (ICP) was evaluated on this model.
Results The mathematical model could closely reproduce the surface area–volume relationships in the published literature. Based on the calculations on the model, it was found that a projection of dural outpouching of 0.83 cm beyond the craniectomy margin on either side of a bilateral 12 × 15 cm elliptical craniectomy defect is required to achieve and accommodate a volume expansion of 157 cm3, which was recorded to be the maximum volume expansion in the reviewed literature. A two-step step-ladder cranioplasty can be constructed to achieve an increase in cranial width by 1.1 to 1.3 cm on each side.
Conclusion Calculations based on the present model indicate that a two-step expansive cranioplasty can accommodate adequate volume expansion while alleviating the ill effects of a craniectomy and necessity of a second surgery. However, these are discussions on mathematical model, based on multitude of assumptions and approximations, and hence these discussions require clinical trials to validate the findings.
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Introduction
Raised intracranial pressure (ICP) and the resultant decrease in cerebral perfusion pressure is the root cause of deterioration in various clinical settings of brain injury, which include those inflicted by traumatic and ischemic insults. Role of decompressive craniectomy in reducing ICP is well established.[1] [2] [3] However, it often requires a second surgery in the form of cranioplasty. Bone removal is known to give rise to complications in the form hydrocephalus and “syndrome of trephined.”[4] There is a felt necessity to look for other alternatives.
A mathematical model was designed, based on the laws of physics and solid geometry, to simulate the intracranial compartment and discuss the various effects of volume and pressure changes occurring in the event of craniectomy performed in the face of a raised ICP. Some of the observations of existing studies, which have been accepted universally and incorporated in neurosurgical practice, were studied on this model to derive certain relevant data, which are not available at present but are required to formulate new treatment strategies.
The volume expansion required to achieve adequate pressure reduction was noted from the existing widely accepted studies[5] [6] and a novel design of expansive craniectomy was assessed for its ability to accommodate the volume, thereby allowing a possibility of doing away with the second surgery for replacing the bone flap and avoiding the complications of sunken flap syndrome.
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Methods
The Mathematical Model to Represent the Intracranial Compartment
A mathematical model was designed, based on the presumption that dura forms a watertight bag-containing brain floating in CSF, which is again reconstituted once a dural closure has been achieved. For this study, the dural bag has been presumed to be hemispherical in shape, with the flat circular surface of the hemisphere lying over the base of the skull ([Fig. 1A]). Volume of a hemisphere is ⅔ πR 3, where R is the radius of the sphere, of which the hemisphere has been carved out. Considering the intracranial volume to be approximately of 1,500 mL,[7] [8] R would work out to be 8.945 cm (a value of 9 cm has been used for the subsequent calculations).
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On the basis of Pascal law, it can be stated that the ICP is exerted equally on the dural bag tangentially all over its wall, always trying to expand it outward ([Fig. 1A]). Any expansion in the size of the dural bag is, however, prevented by the intact rigid cranium around it. A craniectomy defect can be circular, rectangular, or oval in shape. The defect with a given surface area, of any shape, has been represented in the model by a circular area of equal surface area, having a radius r 1 ([Fig. 1B]). The maximum distance of the imaginary horizontal line drawn at the level of the craniectomy defect to the normal location of the dura in unoperated skull, obtained by drawing a perpendicular from the center of the imaginary sphere representing the craniectomy defect to the pole, is represented in the model by h 1.
h 1 = R − √(R 2 − r 1 2) (1)
The volume of the part of the dural sac (E), without any stretching, calculated from the edge of the defect is
2/3 πr 1 2 h 1 (2)
The outpouching of the dural bag, after a dural closure has been achieved ([Fig. 1C]), has been considered to be represented by a section of an imaginary sphere with a radius r ([Fig. 1D]). The maximum distance of the dural outpouching from the craniectomy margin is represented by h.
Whenever a craniectomy is done, the vector of forces become free to stretch the dural bag over the portion of the craniectomy defect ([Fig. 2]). Because the pressure exerted at each point is equal, this is expected to cause a spherical outpouching. It is the volume of this outpouching that will determine the volume expansion achieved and will require to be accommodated by an expansive craniectomy technique.
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For a circular craniectomy defect ([Fig. 1]) of known size (r 1) and volume (V), maximum distance of the sac from the craniectomy margin (h) can be calculated by the formula
h = 3V/2πr 1 2 (3)
The projection of the dural bag beyond the preoperative dural limit
(H) = h − h 1 (4)
The relationship of r 1 to the r (the radius of the sphere of which this outpouching is a part) is given by the formula
r = (r 1 2 + h 1 2)/2h 1 (5)
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Designing Expansive Cranioplasty
A craniectomy procedure aims to increase the available intracranial volume, thereby reducing the ICP. Literature review was done to find out the median volume expansion achieved after craniectomy in series with satisfactory ICP reduction and maximum volume expansion achieved among all the studies in which volume expansion has been documented after craniectomy procedures. To accommodate this additional volume, the projection of the dural bag required to take place, beyond the preoperative state, was calculated for different craniotomy size. A step-ladder pattern cranioplasty technique, in which the free bone flap and the craniectomy edge are fixed on two opposite surfaces of titanium miniplates ([Fig. 3]), was evaluated for its applicability.
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#
Results
Considering the volume of the cranial contents to be 1,500 cm3, it can be represented by a hemisphere of 9 cm radius.
The results have been summarized in [Table 1].
Sl. no. |
Ref. |
No. of cases in the study |
Surgery performed |
Size of craniectomy |
Volume expansion (cm3) |
Height of the dural outpouching (cm) |
||||
---|---|---|---|---|---|---|---|---|---|---|
Surface area recorded in the study (cm2) |
Corresponding diameter in our model (2 × r 1) (cm) |
As recorded in the study |
From the craniectomy margin |
Depth till inner table as on the model (h 1) |
From the level of inner table (h − h 1) calculated on the model |
|||||
Recorded in the study |
Calculated in the model based on vol expansion (h) |
|||||||||
1 |
Munch et al |
49 |
Unilateral FTP D/C with Exp duraplasty |
67.9 ± 15.5 Mean 67.9 Maximum 83.4 |
9.296 10.302 |
92.6 ± 65 92.6 157.6[a] |
0.790 2.045 2.834 |
1.29 1.62 |
2.045 2.834 |
|
2 |
Cavuşoğlu et al |
33 |
FTP D/C with Exp duraplasty |
Median 67.9 Maximum 113 |
9.295 11.992 |
67.5 107.2 |
2.85 3.80 |
2.78 3.70 |
1.29 2.28 |
1.492 1.423 |
3 |
Olivecrona et al |
93 21 underwent D/C |
Unilateral D/C 88 ± 7 |
Median 88 Maximum 95 |
10.582 10.994 |
98 109 |
1.720 1.874 |
1.670 1.721 |
||
Bilateral D/C 116 ± 11 |
Median 116 Maximum 127 |
12.15 12.71 |
124[b] 138 |
2.360 2.629 |
1.603 1.630 |
|||||
Calculations on the mathematical model |
||||||||||
Surgery performed |
Surface area |
Diameter of equivalent circular defect |
Desired volume expansion |
|||||||
1 |
Unilateral FTP D/C 12 × 15 cm oval craniectomy |
141.42 cm2 |
13.4 cm |
157.6 cm3 |
3.0 |
1.67 |
||||
124 cm3 |
1.31 |
|||||||||
2 |
Unilateral FTP D/C 12 × 8 cm oval craniectomy |
75.42 cm2 |
9.79 cm |
124 cm3 |
1.45 |
1.37 |
Abbreviations: D/C, decompressive hemicraniectomy; Exp, expansive; FTP, frontotemporoparietal.
Notes: All entries in red represent calculations made over the mathematical model. Entries in black represent findings in various published studies.
a Maximum volume expansion for unilateral D/C in reviewed literature.
b Median volume expansion in a study with positive outcome.
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Conversion of elliptical craniectomy defects of different surface area in the published studies to equivalent circular defects in the present model.
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An elliptical craniectomy defect of 12 × 15 cm has a surface area of 141.42 cm2; an equivalent circular defect of equal surface area will have a diameter of 13.4 cm.
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An elliptical craniectomy defect of 12 × 08 cm has a surface area of 75.42 cm2; an equivalent circular defect of equal surface area will have a diameter of 9.79 cm.
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A craniectomy defect of 67.9 cm2 will be represented by a circular defect of 9.29 cm diameter.
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Measurements of dural sac at the craniectomy site.
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Maximum distance from the line joining the craniectomy margins to the outer margin of unexpanded dura (h 1):
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For a 13.4-cm diameter circular (equivalent to 12 × 15 cm elliptical) craniectomy defect: 3.00 cm.
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For a 9.79-cm diameter circular (equivalent to 12 × 08 cm elliptical) craniectomy defect: 1.45 cm.
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For a 67.9-cm2 (9.29-cm diameter circular) craniectomy defect: 1.3 cm.
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For an additional volume of 124 cm3, to be accommodated, the required increase in the height of the dural pouch projecting from craniectomy defects (h − h 1):
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For a 13.4-cm diameter circular (equivalent to 12 × 15 cm elliptical) craniectomy defect: 1.32 cm.
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For a 9.79-cm diameter circular (equivalent to 12 × 08 cm elliptical) craniectomy defect: 2.47 cm.
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For a 67.9-cm2 (9.29 cm diameter circular) craniectomy defect: 2.74 cm
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For an additional volume of 157.6 cm3, to be accommodated, the required increase in the height of the dural pouch projecting from craniectomy defects (h − h 1):
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For a 13.4-cm diameter circular (equivalent to 12 × 15 cm elliptical) craniectomy defect: 1.67 cm.
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For an additional volume of 157.6 cm3, to be accommodated in a bilateral hemicraniectomy, in which each side has to accommodate a volume expansion of 78.8 cm3, the required increase in the height of the dural pouch projecting from craniectomy defects (h − h 1):
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For a 13.4-cm diameter circular (equivalent to 12 × 15 cm elliptical) craniectomy defect: 0.83 cm.
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For an additional volume of 124 cm3, to be accommodated in a bilateral hemicraniectomy, in which each side has to accommodate a volume expansion of 62 cm3, the required increase in the height of the dural pouch projecting from craniectomy defects (h − h 1):
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For a 9.79-cm diameter circular (equivalent to 12 × 8 cm elliptical) craniectomy defect: 1.23 cm
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For a 67.9-cm2 (9.29 cm diameter circular) craniectomy defect: 1.37 cm.
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If an expansive cranioplasty is constructed, widening the craniectomy site by 1 cm, it can allow a volume expansion of:
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For a 13.4-cm diameter circular (equivalent to 12 × 15 cm elliptical) craniectomy defect: 94 cm3.
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For a 9.79-cm diameter circular (equivalent to 12 × 8 cm elliptical) craniectomy defect: 50 cm3.
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-
#
Discussion
Raised ICP and the resultant decrease in cerebral perfusion pressure is the root cause of deterioration in various clinical settings of brain injury. The fact that decompressive craniectomy effectively reduces ICP is well established.[1] [2] [3] [9]
Some of the problems that crop up after craniectomy, which offset the obvious advantages of the procedure, thereby annulling the benefits accrued by opening the cranium and reduction in ICP, are postcraniectomy cerebral edema,[10] [11] derangements of cerebral autoregulation, infarct of the prolapsed brain parenchyma, intracerebral hemorrhages,[12] and sunken flap syndrome.
Efforts have been made to alleviate some of these problems by resorting to various alternative, novel surgical techniques,[13] [14] [15] and modifications[16] [17] with varied amount of success; however, neither have they gained universal acceptance nor have they been able to take care of all the drawbacks. A wide durotomy and expansive duraplasty have been advocated to accommodate the surplus brain volume caused by the postoperative edema[18] in view of the perceived inevitability of the postcraniectomy cerebral edema.
The postcraniectomy complications can be broadly divided into two groups. First set of complications are due to bone flap removal, namely, sunken flap syndrome and postcraniectomy hydrocephalus. The second set of complications are secondary to the hemodynamic changes brought about by dural opening, namely, postoperative cerebral edema, kinking of cerebral veins, and infarct. First set of complications could be avoided if it was possible to develop a technique of expansive cranioplasty, creating required additional space to accommodate desired volume expansion, while replacing the bone flap on completion of surgery.
Experimenting on these concepts in clinical settings, while established alternatives exist, is unethical at the best. Therefore, a mathematical model was created to juggle with the available information and finally a cranioplasty design was created on this model that would allow adequate volume expansion.
Three studies were found in the literature that compared the craniectomy size with the volume expansion achieved.[5] [6] [18] Although 82 cases of unilateral decompressive craniectomy were reported by Munch et al and Cavuşoğlu et al, 22 operated cases reported by Olivecrona et al underwent either unilateral or bilateral craniectomy based on their computed tomography (CT) findings. The maximum craniectomy size reported for an unilateral surgery was 113 cm2. Largest among the three studies was by Munch et al with 49 cases with a mean craniectomy size of 67.9 cm2 and a mean volume expansion of 92.6 cm3. In their study, the maximum craniectomy size was recorded to be 83.4 cm2 and the maximum volume expansion achieved was 157.6 cm3. The study by Olivecrona et al showed encouraging results with decompressive hemicraniectomy for cases of severe traumatic head injury with resistant raised ICP, a maximum volume expansion of 127 cm3, and an ICP reduction by 41%.
Calculations on the mathematical model showed that a volume expansion of 46.1, 67.5, and 107.2 cm3 achieved over craniectomy defects of 51.5, 67.9, and 113 cm2, respectively, will require the dural outpouchings to project 2.3, 2.78, and 3.70 cm beyond the craniectomy margin. These measurements were similar to the findings recorded in the study by Cavuşoğlu et al.[5]
Mathematical calculations on the model showed that a projection of dural outpouching of 1.32 cm beyond the craniectomy margin of a unilateral 12 × 15 cm elliptical craniectomy defect is required to achieve and accommodate a volume expansion of 124 cm3, which was recorded to be the mean volume expansion in the study published by Olivecrona et al, reporting a positive outcome of the study. A projection of dural outpouching of 0.83 cm beyond the craniectomy margin on either side of a bilateral 12 × 15 cm elliptical craniectomy defect is required to achieve and accommodate a volume expansion of 157 cm3, which was recorded to be the maximum volume expansion in the study published by Munch et al and is by far the maximum volume expansion recorded in any study after a unilateral decompressive hemicraniectomy performed by the standard technique. Considering the thickness of the bones at the anterior and posterior margins of a craniectomy defect to be 5 to 6 mm and the width of the miniplates 0.5 mm, a step-ladder cranioplasty can be constructed to achieve an increase in cranial width by 1.1 to 1.3 cm on each side. The width can be increased further by drilling out a circular area of inner table and dipole from the center of the bone flap by 2 to 3 mm. Performing a three-step step-ladder cranioplasty or leaving a craniectomy defect of 3 cm diameter at the center of the bone flap can also be considered as alternatives. A two-step step-ladder cranioplasty with a gain of 1.0 cm width can, in a bilateral 12 cm × 15 cm elliptical craniotomy and expansive cranioplasty, accommodate 184 cm3 of additional volume, and can effectively allow more ICP reduction by taking the inward pressure of the tensile strength of the scalp flap off the dural pouch.
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Conclusion
Calculations based on the present model indicate that a two-step step-ladder expansive cranioplasty can provide ample space to accommodate the extra volume created by an expansive duraplasty, if the craniectomy is large (12 × 15 cm) and performed bilaterally.
However, it is just a mathematical model, based on multitude of assumptions and approximations, and hence cannot be taken on the face value. If the logics forwarded, after critical review by the neuroscientists, gain some acceptance, various components of the study can be tested in animal models and in suitable, very selective clinical settings.
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Disclosure
None to declare.
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References
- 1 Jiang JY, Xu W, Li WP , et al. Efficacy of standard trauma craniectomy for refractory intracranial hypertension with severe traumatic brain injury: a multicenter, prospective, randomized controlled study. J Neurotrauma 2005; 22 (6) 623-628
- 2 Bao YH, Liang YM, Gao GY, Pan YH, Luo QZ, Jiang JY. Bilateral decompressive craniectomy for patients with malignant diffuse brain swelling after severe traumatic brain injury: a 37-case study. J Neurotrauma 2010; 27 (2) 341-347
- 3 Yoo DS, Kim DS, Cho KS, Huh PW, Park CK, Kang JK. Ventricular pressure monitoring during bilateral decompression with dural expansion. J Neurosurg 1999; 91 (6) 953-959
- 4 Yamaura A, Makino H. Neurological deficits in the presence of the sinking skin flap following decompressive craniectomy. Neurol Med Chir (Tokyo) 1977; 17 (1, Pt 1) 43-53
- 5 Cavuşoğlu H, Kaya RA, Türkmenoğlu ON, Aydin Y. Value of early unilateral decompressive craniectomy in patients with severe traumatic brain injury. Ulus Travma Acil Cerrahi Derg 2010; 16 (2) 119-124
- 6 Münch E, Horn P, Schürer L, Piepgras A, Paul T, Schmiedek P. Management of severe traumatic brain injury by decompressive craniectomy. Neurosurgery 2000; 47 (2) 315-322 , discussion 322–323
- 7 Strik HM, Borchert H, Fels C , et al. Three-dimensional reconstruction and volumetry of intracranial haemorrhage and its mass effect. Neuroradiology 2005; 47 (6) 417-424
- 8 Blatter DD, Bigler ED, Gale SD , et al. Quantitative volumetric analysis of brain MR: normative database spanning 5 decades of life. AJNR Am J Neuroradiol 1995; 16 (2) 241-251
- 9 Whitfield PC, Patel H, Hutchinson PJ , et al. Bifrontal decompressive craniectomy in the management of posttraumatic intracranial hypertension. Br J Neurosurg 2001; 15 (6) 500-507
- 10 Cooper PR, Hagler H, Clark WK, Barnett P. Enhancement of experimental cerebral edema after decompressive craniectomy: implications for the management of severe head injuries. Neurosurgery 1979; 4 (4) 296-300
- 11 Lobato RD, Sarabia R, Cordobes F , et al. Posttraumatic cerebral hemispheric swelling. Analysis of 55 cases studied with computerized tomography. J Neurosurg 1988; 68 (3) 417-423
- 12 Stiver SI. Complications of decompressive craniectomy for traumatic brain injury. Neurosurg Focus 2009; 26 (6) E7
- 13 Schmidt III JH, Reyes BJ, Fischer R, Flaherty SK. Use of hinge craniotomy for cerebral decompression. Technical note. J Neurosurg 2007; 107 (3) 678-682
- 14 Mitchell P, Tseng M, Mendelow AD. Decompressive craniectomy with lattice duraplasty. Acta Neurochir (Wien) 2004; 146 (2) 159-160
- 15 Csókay A, Pataki G, Nagy L, Belán K. Vascular tunnel construction in the treatment of severe brain swelling caused by trauma and SAH. (evidence based on intra-operative blood flow measure). Neurol Res 2002; 24 (2) 157-160
- 16 Alves OL, Bullock R. “Basal durotomy” to prevent massive intra-operative traumatic brain swelling. Acta Neurochir (Wien) 2003; 145 (7) 583-586 , discussion 586
- 17 Wang Y, Wang C, Yang L , et al. Controlled decompression for the treatment of severe head injury: a preliminary study. Turk Neurosurg 2014; 24 (2) 214-220
- 18 Olivecrona M, Rodling-Wahlström M, Naredi S, Koskinen LO. Effective ICP reduction by decompressive craniectomy in patients with severe traumatic brain injury treated by an ICP-targeted therapy. J Neurotrauma 2007; 24 (6) 927-935
Address for correspondence
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References
- 1 Jiang JY, Xu W, Li WP , et al. Efficacy of standard trauma craniectomy for refractory intracranial hypertension with severe traumatic brain injury: a multicenter, prospective, randomized controlled study. J Neurotrauma 2005; 22 (6) 623-628
- 2 Bao YH, Liang YM, Gao GY, Pan YH, Luo QZ, Jiang JY. Bilateral decompressive craniectomy for patients with malignant diffuse brain swelling after severe traumatic brain injury: a 37-case study. J Neurotrauma 2010; 27 (2) 341-347
- 3 Yoo DS, Kim DS, Cho KS, Huh PW, Park CK, Kang JK. Ventricular pressure monitoring during bilateral decompression with dural expansion. J Neurosurg 1999; 91 (6) 953-959
- 4 Yamaura A, Makino H. Neurological deficits in the presence of the sinking skin flap following decompressive craniectomy. Neurol Med Chir (Tokyo) 1977; 17 (1, Pt 1) 43-53
- 5 Cavuşoğlu H, Kaya RA, Türkmenoğlu ON, Aydin Y. Value of early unilateral decompressive craniectomy in patients with severe traumatic brain injury. Ulus Travma Acil Cerrahi Derg 2010; 16 (2) 119-124
- 6 Münch E, Horn P, Schürer L, Piepgras A, Paul T, Schmiedek P. Management of severe traumatic brain injury by decompressive craniectomy. Neurosurgery 2000; 47 (2) 315-322 , discussion 322–323
- 7 Strik HM, Borchert H, Fels C , et al. Three-dimensional reconstruction and volumetry of intracranial haemorrhage and its mass effect. Neuroradiology 2005; 47 (6) 417-424
- 8 Blatter DD, Bigler ED, Gale SD , et al. Quantitative volumetric analysis of brain MR: normative database spanning 5 decades of life. AJNR Am J Neuroradiol 1995; 16 (2) 241-251
- 9 Whitfield PC, Patel H, Hutchinson PJ , et al. Bifrontal decompressive craniectomy in the management of posttraumatic intracranial hypertension. Br J Neurosurg 2001; 15 (6) 500-507
- 10 Cooper PR, Hagler H, Clark WK, Barnett P. Enhancement of experimental cerebral edema after decompressive craniectomy: implications for the management of severe head injuries. Neurosurgery 1979; 4 (4) 296-300
- 11 Lobato RD, Sarabia R, Cordobes F , et al. Posttraumatic cerebral hemispheric swelling. Analysis of 55 cases studied with computerized tomography. J Neurosurg 1988; 68 (3) 417-423
- 12 Stiver SI. Complications of decompressive craniectomy for traumatic brain injury. Neurosurg Focus 2009; 26 (6) E7
- 13 Schmidt III JH, Reyes BJ, Fischer R, Flaherty SK. Use of hinge craniotomy for cerebral decompression. Technical note. J Neurosurg 2007; 107 (3) 678-682
- 14 Mitchell P, Tseng M, Mendelow AD. Decompressive craniectomy with lattice duraplasty. Acta Neurochir (Wien) 2004; 146 (2) 159-160
- 15 Csókay A, Pataki G, Nagy L, Belán K. Vascular tunnel construction in the treatment of severe brain swelling caused by trauma and SAH. (evidence based on intra-operative blood flow measure). Neurol Res 2002; 24 (2) 157-160
- 16 Alves OL, Bullock R. “Basal durotomy” to prevent massive intra-operative traumatic brain swelling. Acta Neurochir (Wien) 2003; 145 (7) 583-586 , discussion 586
- 17 Wang Y, Wang C, Yang L , et al. Controlled decompression for the treatment of severe head injury: a preliminary study. Turk Neurosurg 2014; 24 (2) 214-220
- 18 Olivecrona M, Rodling-Wahlström M, Naredi S, Koskinen LO. Effective ICP reduction by decompressive craniectomy in patients with severe traumatic brain injury treated by an ICP-targeted therapy. J Neurotrauma 2007; 24 (6) 927-935
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