Abrasions, lacerations, and foreign body penetration are common in the manus of dogs, particularly in working dogs. Reports1,2 suggest that 35% to 52% of search-and-rescue and police dogs have had cuts, abrasions, or punctures during deployment, and 50% to 70% of those injuries were on the distal aspect of the limbs. In those reports, there were > 9 events/1,000 dog deployment hours, which represents the highest system-specific disease incidence rate among deployed dogs.
Even when manus wounds are treated, chronic infection can develop, and the prolonged illness can cause loss of function, requiring rehabilitation. Exploratory surgery and debridement of affected tissues are commonly required in situations of chronic manus infection, but it is often difficult to achieve a cure with a single procedure, and multiple surgeries may be required.3 Surgical exploration generally must be extensive because infection typically extends beyond the site of initial injury. The requirement of a large surgical field and the common need for multiple procedures often result in prolonged patient illness. A method for predicting the likely path of extension of a pathological process from a given injury site could help surgeons more efficiently plan their approaches and therefore minimize damage to unaffected anatomic structures.
Soft tissue spaces and myofascial compartments in the human hand4–7 and foot8–10 are important in confining disease processes such as inflammation, infection, and neoplasia.11–14 Because inflammation generally does not extend beyond the boundaries of such anatomic structures, surgical intervention can be directed at the affected space or compartment, and complete exploration of the hand or foot is usually unnecessary.12,14,15 We recently identified soft tissue spaces and myofascial compartments in the canine manus that are similar to those in humans.16 However, to our knowledge, distribution of infection from the interdigital spaces has not been described.
The purpose of the study reported here was to test the hypothesis that fluid injected into different interdigital spaces as a model of infection will extend into and be confined differently by the surrounding soft tissues. We anticipated that this model would yield a predictable path of disease based on the site of initial injury, with different sites of injury leading to spread of disease into different regions.
Materials and Methods
Sample collection—Forelimbs were removed from 23 medium- to large-breed dogs euthanized for reasons unrelated to forelimb disease and were frozen at −8°C immediately after removal. Limbs were to be excluded when there was evidence of orthopedic or soft tissue abnormalities; however, no such abnormalities were identified. Once frozen, the 46 limbs were separated into 5 batches of 9 or 10 limbs for imaging, and each batch was allowed to thaw in a walk-in cooler for approximately 16 hours before imaging. This thawing time allowed the limbs to be easily manipulated and injected during the imaging phase of the study.
Contrast medium preparation—Contrast medium components were mixed immediately prior to the first injections of each batch of limbs. The contrast medium mixture included 5 mL of iopromidea and 2 mL of indigo blue acrylic inkb diluted in 45 mL of 0.9% NaCl solution. The mixture was shaken approximately every 5 minutes to keep the blue pigment in suspension.
CT scanning and injection protocol—All limbs in each batch were imaged simultaneously with a 16-slice helical CT scanner.c Three forelimbs were positioned on the couch side-by-side, in an extended position, as for a patient positioned head-first in sternal recumbency. Cardboard platforms were used to support 2 additional layers of 3 or 4 limbs on top of the 3 forelimbs placed directly on the couch; the positioning of the limbs in the upper 2 rows was the same as that for the limbs in the lower row. Limb location was determined randomly. Before injection of contrast medium (precontrast), CT scans of the forelimbs were obtained from the distal aspect of the digits through the distal antebrachium with helical acquisitions of 0.5-mm slice thickness by use of a modified carpus protocol (0.5-second rotation, 300 mA, 120 kVp, 0.688 pitch factor, 250-mm field of view, and 512 × 512 matrix, with bone and soft tissue reconstruction algorithms).
Afterward, 1 of the 3 interdigital web spaces in each manus was injected with 3 mL of the contrast medium with a 22-gauge needle. The interdigital web space was defined as the skin and connective tissue between adjacent digits near the metacarpophalangeal joints; the 3 web spaces were referred to as medial (between digits II and III), central (between digits III and IV), and lateral (between digits IV and V). In preliminary tests, the amount of contrast medium administered yielded repeatable marked distention of the interdigital web space and extension of the contrast medium into the surrounding tissues in all specimens. The injection site for each limb was determined by random drawing. One limb in the first scan group (the group of 10 limbs) was not injected; thus, a total of 45 limbs were injected. After injection of the contrast medium, the limbs were returned to their previous positions on the CT couch and CT scans of the limbs (postcontrast) were repeated with the same protocol as was used for the precontrast scan.
CT data recording—Computed tomographic scans of the forelimbs were reviewed by 2 board-certified veterinary radiologists (CPO and JCJ) with the aid of a remote diagnostic workstation and commercially available DICOM viewing software.d Extension of the contrast medium at 8 predetermined CT slice locations was recorded through line drawings, and contrast medium dispersion was also described relative to recognizable anatomic structures such as individual phalanges.
Agreement between CT and anatomic findings—The forelimbs were refrozen after CT scanning. After freezing, 9 limbs were removed from the freezer for transverse sectioning with a band saw. The remaining specimens were later rethawed for conventional dissection. Manus selection for transverse sectioning and dissection was determined by random drawing, and all injection sites were represented by multiple specimens in each of the 2 sectioning methods. Extent of the blue-staining contrast medium was examined for correspondence with imaging findings.
Statistical analysis—Outcome was defined as extension of the contrast medium into any of 5 regions associated with each of the 4 digits (axial digit, abaxial digit, palmar digit, dorsal digit, or dorsal subcutaneous space of the metacarpus) or into any of the 3 web spaces (lateral, central, or medial; Figure 1). Thus, presence or absence of contrast medium within each of the 23 regions was considered for each injection. Subsequently, data regarding presence or absence of contrast medium were summarized in contingency tables of injection site (lateral, medial, or central) by digit region or web space. To test the null hypothesis that there was no association between site of injection and contrast medium migration to any of the digit regions or to any of the interdigital web spaces, the Fisher exact test was used. Statistical significance was set at a value of P ≤ 0.05. All analyses were performed by use of commercially available statistical software.e
Results
CT scanning and injection protocol—Use of our CT scanning protocol allowed good visualization of all forelimbs. The contrast medium could be easily differentiated from the surrounding tissues, and the spatial resolution was sufficient to determine the extent of the contrast medium.
Sixteen injections were made into the medial interdigital web space, 15 into the central web space, and 14 into the lateral web space. Marked distention of the injected interdigital spaces resulting in displacement of the associated digits away from the web space was evident for all injections, and increasing resistance to injection was evident during each injection of contrast medium.
CT data recording—No difficulties in identifying the contrast medium were noticed during the recording of data. Skin contamination with contrast medium was identified on 2 limbs, and there was a focus of soft tissue mineralization that was not continuous with the contrast medium in 1 digit; however, neither of these situations hindered interpretation of contrast medium distribution. Gas bubbles were noticed as incidental findings at 2 injection sites.
Agreement between CT and anatomic findings—Computed tomographic findings and anatomic descriptions were nearly identical in all limbs. No discrepancies were evident between CT and anatomic descriptions of the transverse sections. However, in some situations of conventional manus dissection, it was difficult to determine whether the contrast medium extended into an adjacent interdigital web space or remained within the soft tissues of a digit. Evaluation of this contrast-agent distribution was much easier when a manus was viewed transversely (by means of CT or transverse sectioning).
Pattern of contrast medium extension—Repeatable and predictable patterns of contrast medium extension were observed with injection of the interdigital web spaces. In nearly all situations, injection of a web space caused filling of that web space and the adjacent margins of the associated digits (Table 1). For example, injection of the medial interdigital web space caused filling of that web space, the axial soft tissues of digit II, and the abaxial soft tissues of digit III. The contrast medium also commonly extended into the palmar and dorsal soft tissues of those digits. However, in all instances of dorsal extension, there was a filling defect immediately dorsal to the phalanges in the location of the digital extensor tendons, and in all instances of palmar extension, there was a filling defect immediately palmar to the phalanges in the location of the digital flexor tendons. When a soft tissue region was involved for a given digit, the region adjacent to the proximal phalanx was almost invariably affected (98% of instances), the region adjacent to the middle phalanx was relatively commonly affected (71%), and the contrast medium uncommonly extended to the level of the distal phalanx (17%).
Percentage of specimens with extension of contrast medium into the soft tissues of specific regions of the manus (n = 45) of the forelimbs of cadavers of healthy dogs, by injection site and as determined via CT.
Region of manus | Site of injection | ||
---|---|---|---|
Medial web space | Central web space | Lateral web space | |
Digit II | |||
Abaxial | 19A | 0A | 0A |
Palmar | 75A | 0B | 0B |
Dorsal | 75A | 0B | 0B |
Dorsal subcutaneous space | 6A | 0A | 0A |
Axial | 100A | 0B | 0B |
Medial web space | 100A | 53B | 0C |
Digit III | |||
Abaxial | 100A | 20B | 0B |
Palmar | 94A | 87A | 0B |
Dorsal | 38A | 60A | 0B |
Dorsal subcutaneous space | 12A | 0A | 0A |
Axial | 6B | 87A | 0B |
Central web space | 19B | 100A | 21B |
Digit IV | |||
Axial | 0B | 100A | 7B |
Palmar | 0B | 87A | 93A |
Dorsal | 0B | 67A | 79A |
Dorsal subcutaneous space | 0B | 0B | 29A |
Abaxial | 0B | 7B | 100A |
Lateral web space | 0C | 47B | 100A |
Digit V | |||
Axial | 0B | 0B | 93A |
Palmar | 0B | 0B | 71A |
Dorsal | 0B | 0B | 93A |
Dorsal subcutaneous space | 0A | 0A | 0A |
Abaxial | 0A | 0A | 21A |
Within each row, values with different superscript letters differ significantly (P ≤ 0.05).
The contrast medium generally remained confined to the soft tissues of the digits, without extension proximal to the level of the metacarpophalangeal joints. Extension of the contrast medium proximally into the most distal portion of the dorsal subcutaneous space, associated with the distal metacarpal bones and dorsal sesamoid bones, occurred in only 7 regions following 6 injections (13% of limbs; Figure 2). The contrast medium within the web space tapered to a point proximally at approximately the level of the third and fourth metacarpophalangeal joints, although the precise proximodistal location varied with each manus (Figures 3–6).
Contrast medium extended to the next adjacent interdigital web space (ie, from a medial or lateral web space injection to the central web space or from a central web space injection to the medial, lateral, or both web spaces) in several limbs (Figure 7; Table 1). However, in these situations, the contrast medium never extended further to the next adjacent digit. Small tubular structures in the dorsal soft tissues of the manus extended from the most proximal aspect of the injected interdigital web space in all specimens (Figure 8), and these structures were identified as lymphatic vessels after dissection. In 7 of the 45 (16%) limbs, the contrast medium was also evident in dorsal lymphatic vessels extending from a web space adjacent to the injected space. Palmar lymphatic vessels containing the contrast medium were identified extending from the injected space in 2 (4%) limbs and from a noninjected space in 2 other limbs.
Statistical analysis—The distribution of contrast medium differed significantly among injection sites (Table 1). Contrast medium injected into a given web space was significantly (P < 0.003) more likely to be found within that web space and the adjacent margins of the associated digits than with injections at the other 2 interdigital web spaces. Whereas the contrast medium also commonly extended into the dorsal and palmar tissues of the adjacent digits as well, there were no significant (P > 0.28) differences in frequency of extension to these areas when comparing injections made in the 2 web spaces associated with these digits (eg, extension from the medial and central web spaces to the palmar or dorsal aspect of digit III).
Discussion
Results of the study reported here indicated that injection of contrast medium into the interdigital web spaces of the manus in forelimbs obtained from cadavers of healthy dogs resulted in a predictable pattern of extension of the material into the surrounding soft tissues, as was hypothesized. This is important because the interdigital web spaces are among the most common sites for retention of foreign bodies in dogs17; consequently, knowledge of the likely paths of foreign body migration or spread of infection would be beneficial for surgical planning. Although use of imaging techniques would be beneficial for identification of the extent of inflammation or the presence of a foreign body,18,19 this is not always possible, and exploratory surgery based on probable extent of disease may be required.
The findings in the present study suggested that surgical exploration should begin in the affected interdigital web space because the web spaces are able to contain a large amount of material. The proximal extent of the interdigital web space is approximately at the level of the metacarpophalangeal joints. In our model, spread of contrast medium to the immediately adjacent soft tissues of the related digits occurred almost invariably, and these tissues should be considered to be involved as well. Involvement of the dorsal and palmar soft tissues of the adjacent digits was also common, so exploration of these areas may be required in most situations. Whereas there was no infiltration of contrast medium into the digital extensor and flexor tendons, these structures could be secondarily affected by dorsal or palmar inflammation through adhesion formation.
Just as pertinent for surgical planning are those sites that were involved less commonly in our study because failure to recognize spread of disease to such areas would result in continued illness and the requirement for additional surgical intervention. In the present study, there were 21 instances of contrast medium extension to the next interdigital web space in 18 of the 45 (40%) limbs (3 injections of the central web space resulted in extension to both the medial and lateral web spaces). Because the amount of material in many of these instances was small, it could easily be overlooked. Likewise, involvement of the dorsal subcutaneous space adjacent to 7 metacarpal bones occurred after 6 injections (in 13% of limbs). This finding suggested that injury to the distal aspect of a manus could lead to infection in the dorsal aspect of the metacarpus, which is a site that may not commonly be surgically explored in dogs with a more palmar injury.
Statistical differences in the contrast medium extension based on site of injection also provided possible evidence of necessary sites for surgical exploration in an injured manus. For example, if the abaxial tissues of digit III are known to be infected, involvement of the medial interdigital web space is also highly likely. However, contrast medium rarely extended from the central interdigital web space to the abaxial aspect of digit III, so exploration of the central web space in such a situation may not be as critical. Additionally, the differences in contrast medium extension from the 3 interdigital web spaces and the marked distensibility of these spaces indicated that these 3 structures can likely be considered discrete soft tissue spaces, similar to those identified elsewhere.16 Retention of contrast medium within the web spaces was incomplete because the volume of contrast medium injected was deliberately chosen to simulate disease spread.
The anatomy of the interdigital web spaces in the manus of dogs appears to be analogous to the anatomy of the interdigital web space in human hands. In humans, the interdigital webs are recognized as distinct subcutaneous fascial spaces in which pus may collect.12,20,21 Indeed, it has been reported that the interdigital web spaces are one of the most common sites of pus collection, second only to the pulp spaces of the finger tips.21 Human web spaces are not continuous with each other and are separated by the joint capsule and collateral ligaments of the intervening metacarpophalangeal joints as well as by the digital extensor tendons.22 However, similar to the findings in our model in dogs, web space infections in humans may spread distally into the digits, medially or laterally into an adjacent web space, or proximally to the dorsal aspect of the metacarpus.21 A fourth direction of spread from the interdigital web spaces described for the human hand is proximally, along a lumbrical canal into the midpalmar space.21 We did not recognize this last path of spread in our study, possibly because of the differing anatomy between dogs and humans, including the vestigial nature of the lumbrical muscles in dogs and the association of canine lumbrical muscles with the flexor tendons rather than with the midpalmar space as in humans.23
Although our study provided a model for disease spread in the canine manus, we recognize that additional research involving live dogs and actual infection would be required to better assess patterns of disease extension. Soft tissue structures may tend to confine pathological processes in humans, but this is not always the situation. Depending on the chronicity and severity of infection and the anatomy of the initially affected soft tissue space, the inflammatory process may extend to a neighboring space.24,25 It is understood that cadaver models cannot replace clinical experiments and experience, as the conditions of infection and increased pressure in soft tissue spaces and myofascial compartments cannot be faithfully replicated in cadavers.6,9 Because of the actions of enzymes released during infection, it is not possible to fully evaluate the resistance of barriers to the spread of disease in a cadaver model; structures recognized as discrete compartments anatomically may not confine disease, particularly when an infection is severe or chronic.24,25 Additionally, although injection studies5,10 of the distal aspect of extremities in humans have involved specimens that were frozen and thawed, the effects of freezing could alter the strength or elasticity of the tissues. For example, ex vivo studies26,27 of human tendons have revealed that tendons that were frozen and thawed had increased stiffness and decreased load-bearing before failure, compared with fresh tendons. Thus, it is possible that some fascial planes in our specimens failed prematurely because of the effects of freezing, and in vivo spread of infection would not be as dramatic in fresh tissues as that identified in this study. Nonetheless, findings of studies20,28,29 concerning disease spread in hands from human cadavers appear to correspond well with clinical experience, and we believe our results likewise represent a meaningful depiction of disease spread from the interdigital web spaces in dogs.
ABBREVIATIONS
CT | Computed tomography |
DICOM | Digital Imaging and Communications in Medicine |
Ultravist, Berlex, Montville, NJ.
Super Pigmented Acrylic Ink, Speedball Art Products Co, Statesville, NC.
Aquilion TSX-101A Multislice CT Scanner, Toshiba America Medical Systems, Tustin, Calif.
eFilm Workstation, version 2.1, Merge Healthcare, Milwaukee, Wis.
SAS, version 9.2, SAS Institute Inc, Cary, NC.
References
- 1.
Slensky KA, Drobatz KJ, Downend AB, et al. Deployment morbidity among search-and-rescue dogs used after the September 11, 2001, terrorist attacks. J Am Vet Med Assoc 2004; 225:868–873.
- 2.
Fox PR, Puschner B, Ebel JG. Assessment of acute injuries, exposure to environmental toxins, and five-year health surveillance of New York Police Department working dogs following the September 11, 2001, World Trade Center terrorist attack. J Am Vet Med Assoc 2008; 233:48–59.
- 3.↑
Lamb CR, White RN, McEvoy FJ. Sinography in the investigation of draining tracts in small animals: retrospective review of 25 cases. Vet Surg 1994; 23:129–134.
- 4.
Doyle JR. Anatomy of the upper extremity muscle compartments. Hand Clin 1998; 14:343–364.
- 5.
DiFelice A Jr, Seiler JG III, Whitesides TE Jr. The compartments of the hand: an anatomic study. J Hand Surg Am 1998; 23:682–686.
- 6.
Guyton GP, Shearman CM, Saltzman CL. Compartmental divisions of the hand revisited: rethinking the validity of cadaver infusion experiments. J Bone Joint Surg Br 2001; 83:241–244.
- 7.
Grodinsky M, Holyoke EA. The fasciae and fascial spaces of the palm. Anat Rec 1941; 79:435–450.
- 8.
Kamel R, Sakla FB. Anatomical compartments of the sole of the human foot. Anat Rec 1961; 140:57–60.
- 9.
Guyton GP, Shearman CM, Saltzman CL. The compartments of the foot revisited: rethinking the validity of cadaver infusion experiments. J Bone Joint Surg Br 2001; 83:245–249.
- 10.
Seidel U, Bade H, Koebke J. Studies of the topography of the compartments of the foot. Fuss Sprunggelenk 2003; 1:191–198.
- 11.
Toomayan GA, Robertson F, Major NM, et al. Upper extremity compartmental anatomy: clinical relevance to radiologists. Skeletal Radiol 2006; 35:195–201.
- 12.
Abrams RA, Botte MJ. Hand infections: treatment recommendations for specific types. J Am Acad Orthop Surg 1996; 4:219–230.
- 13.
Pemberton PA. Infection of fascial spaces of the palm. Am J Surg 1940; 50:512–515.
- 14.
Beye HL. Deep palmar hand infections: a clinical study of the diagnosis and treatment of these conditions. Ann Surg 1918; 67:152–162.
- 15.
Rauwerda JA. Foot debridement: anatomic knowledge is mandatory. Diabetes Metab Res Rev 2000;16(suppl 1):S23–S26.
- 16.↑
Ober CP, Jones JC, Larson MM, et al. Computed tomographic and cross-sectional anatomic characterization of myofascial compartments and soft-tissue spaces in the manus in cadavers of dogs without forelimb disease. Am J Vet Res 2010; 71:138–149.
- 17.↑
Brennan KE, Ihrke PJ. Grass awn migration in dogs and cats: a retrospective study of 182 cases. J Am Vet Med Assoc 1983; 182:1201–1204.
- 18.
Bonatz E, Robbin ML, Weingold MA. Ultrasound for the diagnosis of retained splinters in the soft tissue of the hand. Am J Orthop 1998; 27:455–459.
- 19.
Peterson JJ, Bancroft LW, Kransdorf MJ. Wooden foreign bodies: imaging appearance. AJR Am J Roentgenol 2002; 178:557–562.
- 20.
Hoon LW, Ross GJ. Infections of the hand: a review of 60 cases. Ann Surg 1913; 57:561–568.
- 21.↑
King M, Bewes P, Cairns J, eds. Pus in the hands and feet. In: Primary surgery online. Homberg, Germany: German Society for Tropical Surgery, 2008;8.1–8.10. Available at: www.primary-surgery.org/ps/vol1/ch-8.pdf. Accessed Nov 27, 2009.
- 22.↑
Belcher HJCR, Clare TD. Mini-symposium: the elective hand. IV. Hand infections. Curr Orthop 2003; 17:28–43.
- 23.↑
Hermanson JW, Evans HE. The muscular system. In:Evans HE, ed. Miller's anatomy of the dog. 3rd ed. Philadelphia: WB Saunders Co, 1993;258–384.
- 24.
Goodwin DW, Salonen DC, Yu JS, et al. Plantar compartments of the foot: MR appearance in cadavers and diabetic patients. Radiology 1995; 196:623–630.
- 25.
Ledermann HP, Morrison WB, Schweitzer ME. Is soft tissue inflammation in pedal infection contained by fascial planes? MR analysis of compartmental involvement in 115 feet. AJR Am J Roentgenol 2002; 178:605–612.
- 26.
Clavert P, Kempf J-F, Bonnomet F, et al. Effects of freezing/thawing on the biomechanical properties of human tendons. Surg Radiol Anat 2001; 23:259–262.
- 27.
Giannini S, Buda R, Di Caprio F, et al. Effects of freezing on the biomechanical and structural properties of human posterior tibial tendons. Int Orthop 2008; 32:145–151.
- 28.
Beye HL. Deep palmar hand infections: an experimental and clinical study of the surgical anatomy of these conditions. Ann Surg 1917; 66:24–42.
- 29.
Kanavel AB. Infections of the hand. 4th ed. Philadelphia: Lea & Febiger, 1921.