INTRODUCTION
The first dorsal compartment of the wrist, also known as first extensor compartment of the wrist, includes tendons of abductor pollicis longus (APL) and of extensor pollicis brevis (EPB). APL tendon inserts into the radial side of the base of the first metacarpal bone but also into the trapezium bone, allowing abduction and extension in the carpometacarpal joint of the thumb. EPB tendon inserts into the base of the first phalanx of the thumb, allowing extension in the metacarpophalangeal join of the thumb. However, many studies have showed multiple anatomical variations in the first dorsal compartment. Most frequently reported anomalies are multiple APL tendons, multiple EPB tendons and the presence of the intercompartmental fibro-osseus septum [3, 8, 25, 41, 48]. Unfortunately, studies describing those variations are not consistent. Awareness of anatomical anomalies in the first dorsal compartment is highly significant during both conservative and surgical treatment of de Quervain’s disease. Usually, first method used in clinical treatment of de Quervain’s disease are corticosteroid injections into the first dorsal compartment of the wrist [49]. Knowledge of anatomical conditions in the first dorsal compartment may increase chances of successful steroid treatment [49]. During surgical treatment of de Quervain’s disease, anatomical orientation may prevent potential misinterpretations, which may lead to failure to decompress the compartment [16]. Therefore, the aim of this study was to provide most accurate data about these anatomical variations in the population, using systematic review and meta-analysis.
MATERIALS AND METHODS
Search strategy
Data collection was performed in January 2022 using either leading databases such as PubMed, Scopus, Web of Science and Embase but also number of minor online libraries. Search was made for publications referring to anatomical variations in the first dorsal compartment of the wrist, especially number of APL tendons, number of EPB tendons and presence of intercompartmental fibro-osseous septum. Search was ended in February 2022. Searched phrases were made according to Boolean search terms. In each database we used the following scheme: (first) AND ((dorsal) OR (extensor)) AND ((compartment) OR (slot)) AND ((anatomy) or (anatomic) or (anatomical) OR (variations) OR (variant) OR (anomalies)). We also used terms like “de Quervain’s”, “Quervain”, “APL”, “abductor pollicis longus”, “EPB”, “extensor pollicis brevis”, “septum”, “extensor retinaculum” in many variations. Neither date, language, article type or text availability conditions were applied. During our study we followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Furthermore, the Critical Appraisal Tool for Anatomical Meta-analysis (CATAM) was used to provide the highest quality findings [13].
Eligibility criteria
A total of 1629 articles were initially evaluated including the main search and search through the references of the classified articles. After removing duplicates, 1248 publications were enrolled. Each article which included exact data about number of APL tendons or number of EPB tendons or a presence of intercompartmental septum was qualified for a more precise evaluation. Studies showing incomplete data, conference abstracts, letter to the editors or case reports were excluded. Subsequently, 101 articles were extracted, of which 33 were excluded due to its irrelevance or incomplete data. Finally, 68 articles were included in this meta-analysis. To minimise bias of included studies, we used the AQUA Tool which was specifically designed for anatomical meta-analyses. Process of collecting data is imaged in Figure 1.
Data extraction
Data from qualified studies were extracted manually by two independent researchers. Numerical and categorical data including number of APL tendons, number of EPB tendons, presence of septum, number of individuals, number of wrists, sex of subjects and geographic location were extracted.
Statistical analysis
In order to perform those meta-analysis we used STATISTICA version 13.1 software (StatSoft Inc., Tulsa, OK, USA) and MetaXL version 5.3 (EpiGear International Pty Ltd, Wilston, Queensland, Australia) to calculate the pooled prevalence. We performed a random-effects model in all analyses. Heterogeneity among the studies was assessed, using both the Chi-squared test and I-squared statistic [23]. A p value less than 0.05 was considered to be statistically significant. We interpretate the I-squared statistic as follows: 0–40% as “might not bed important”; 30–60% as “may represent moderate heterogeneity; 50–90% as “may represent substantial heterogeneity”; 75–100% as “may represent considerable heterogeneity”. In order to determine statistically significant differences between studied groups, we used confidence intervals (CIs). If the CIs between groups overlapped, we considered the differences insignificant, while in the reverse situation, we considered the differences statistically significant.
RESULTS
Due to diversity of studied groups we decided to divide the extracted data into three categories — cadavers, patients with the de Quervain’s disease and patients without the de Quervain’s disease. Each category includes meta-analysis of data considering quantity of APL tendons, EPB tendons and presence of septum in the first dorsal compartment. Sets of characteristics from each study that has been included in this meta-analysis are presented in Table 1. Summarised geographic features of admitted articles can be found in Table 2.
Author, year |
Continent |
Country |
Affiliation* |
Number of studied wrists |
Roy et al., 2016 |
Asia |
India |
1 |
86 |
Gao et al., 2017 |
Asia |
China |
1 |
40 |
Aktan et al., 1998 |
Asia |
Turkey |
1, 2 |
69 |
Hazani et al., 2008 |
North America |
USA |
1 |
32 |
Sugiura et al., 2017 |
Asia |
Japan |
1 |
45 |
Nam et al., 2018 |
Asia |
South Korea |
1 |
40 |
Xu et al., 2018 |
Asia |
China |
1 |
2 |
Jackson et al., 1986 |
North America |
USA |
1, 2 |
340 |
Shiraishi and Matsumura, 2005 |
Asia |
Japan |
1 |
60 |
Takahashi et al., 1994 |
Asia |
Japan |
1, 2 |
267 |
Kutsumi et al., 2005 |
North America |
USA |
1 |
15 |
Bernstein et al., 2019 |
North America |
Texas |
1, 2 |
181 |
Mahakkanukrauh and Mahakkanukrauh, 2000 |
Asia |
Thailand |
1 |
200 |
Gurses et al., 2015 |
Asia |
Turkey |
1 |
50 |
Alemohammad et al., 2009 |
Asia |
Iran |
1, 2 |
233 |
Kang et al., 2017 |
Asia |
South Korea |
1 |
30 |
Nayak et al., 2009 |
Asia |
India |
1 |
156 |
Kulthanan and Chareonwat, 2007 |
Asia |
Thailand |
1, 2 |
148 |
Ravi et al., 2019 |
Asia |
India |
1 |
77 |
Mirzanli et al., 2012 |
Asia |
Turkey |
1 |
150 |
Rousset et al., 2010 |
Europe |
Paris |
1 |
40 |
Opreanu et al., 2010 |
North America |
USA |
1 |
50 |
Tripathy et al., 2015 |
Asia |
India |
1 |
50 |
Motoura et al., 2010 |
Asia |
Japan |
1 |
246 |
Minamikawa et al., 1991 |
North America |
USA |
1, 2 |
141 |
Sugiura et al., 2019 |
Asia |
Japan |
1 |
24 |
Leslie et al., 1990 |
North America |
USA |
1 |
100 |
Gonzalez et al., 1995 |
North America |
USA |
1 |
66 |
Leversedge et al., 2016 |
North America |
USA |
1 |
50 |
Kutsikovich and Merrell, 2018 |
North America |
USA |
1 |
43 |
Öztürk et al., 2021 |
Asia |
Turkey |
1 |
86 |
Güleç et al., 2016 |
Asia |
Turkey |
1 |
48 |
Suhani et al., 2012 |
Asia |
India |
1 |
73 |
Abdel-Hamid et al., 2013 |
Africa |
Egypt |
1 |
95 |
Leao, 1958 |
South America |
Brazil |
1 |
50 |
dos Remédios et al., 2005 |
Europe |
France |
1 |
31 |
Bharambe et al., 2017 |
Asia |
India |
1 |
100 |
Vollala, 2006 |
Asia |
India |
1 |
100 |
Giles, 1960 |
Europe |
England |
1 |
50 |
Oudenaarde, 1991 |
Europe |
Netherlands |
1 |
84 |
Schulz et al., 2002 |
Europe |
Germany |
1 |
73 |
Palatty et al., 2020 |
Asia |
India |
1 |
50 |
El-Beshbishy and Abdel-Hamid, 2013 |
Asia |
Saudi Arabia |
1 |
50 |
Brunelli and Brunelli, 1992 |
Europe |
Italy |
1 |
52 |
Kulshreshtha et al., 2007 |
Europe |
England |
1 |
44 |
Matzon et al., 2019 |
North America |
USA |
2 |
130 |
Choi et al., 2011 |
Asia |
South Korea |
2 |
15 |
Gousheh et al., 2009 |
Asia |
Iran |
2 |
50 |
Beutel et al., 2020 |
North America |
USA |
2, 3 |
102 |
Bahm et al., 1995 |
Europe |
France |
2 |
10 |
Lee et al., 2014 |
Asia |
South Korea |
2 |
60 |
Chang et al., 2017 |
North America |
USA |
2 |
94 |
Stahl et al., 2015 |
Europe |
Germany |
2 |
77 |
Kwon et al., 2010 |
Asia |
South Korea |
2 |
43 |
Sato et al., 2016 |
Asia |
Japan |
2 |
112 |
McDermott et al., 2012 |
North America |
USA |
2 |
42 |
Bing et al., 2018 |
Asia |
South Korea |
2 |
28 |
Kim et al., 2020 |
Asia |
South Korea |
2 |
29 |
López Mendoza et al., 2011 |
North America |
Mexico |
2 |
32 |
Shiroishi et al., 2002 |
Asia |
Japan |
2 |
158 |
Harvey et al., 1990 |
Australia |
Australia |
2 |
20 |
Yuasa and Kiyoshige, 1998 |
Asia |
Japan |
2 |
22 |
de Keating-Hart et al., 2016 |
Europe |
France |
2 |
41 |
Alexander et al., 2002 |
North America |
USA |
2 |
26 |
Witt et al., 1991 |
North America |
USA |
2 |
30 |
Weiss et al., 1994 |
North America |
USA |
2 |
45 |
Nagaoka et al., 2000 |
Asia |
Japan |
2 |
32 |
Hoch et al., 2004 |
Europe |
Germany |
3 |
14 |
Continent |
Number or studies |
Number of wrists |
Africa |
1 |
95 |
Asia |
36 |
3029 |
Australia |
1 |
20 |
Europe |
11 |
516 |
North America |
18 |
1519 |
South America |
1 |
50 |
Overall |
68 |
5229 |
APL
The quantity of APL tendons in the first dorsal compartment of the wrist was examined in 21 cadaveric studies [3, 8, 14, 16, 17, 22, 25, 26, 30, 32, 47, 51–53, 57, 59, 60, 65–68] including 1749 wrists. Number of APL tendons varied from zero to seven. For a single APL tendon, prevalence was 16.91% (95% CI: 8.96–26.63%). For a double APL tendon, prevalence was 46.04% (95% CI: 36.84–55.38%). For a triple APL tendon, prevalence was 19.19% (95% CI: 13.24–25.92%). Results mentioned above, are all gathered in Table 3.
Category |
Structure |
Subcategory |
Number of wrists |
Prevalence |
LCI |
HCI |
Cochran’s Q |
I2 (95% CI) |
Cadavers |
APL |
None APL |
1749 |
0.27% |
0.07% |
0.58% |
4.84 |
0.00 (0.00–0.00) |
Single APL |
1749 |
16.91% |
8.96% |
26.63% |
471.02 |
95.75 (94.53–96.70) |
||
Double APL |
1749 |
46.04% |
36.84% |
55.38% |
297.65 |
93.28 (91.01–94.98) |
||
Triple APL |
1749 |
19.19% |
13.24% |
25.92% |
219.99 |
90.91 (87.49–93.39) |
||
Quadruple APL |
1749 |
5.91% |
3.26% |
9.24% |
131.98 |
84.85 (78.07–89.53) |
||
Fivefold APL |
1749 |
1.53% |
0.61% |
2.81% |
62.56 |
68.03 (49.74–79.66) |
||
Sixfold APL |
1749 |
0.65% |
0.28% |
1.16% |
24.17 |
17.25 (0.00–51.02) |
||
Sevenfold APL |
1749 |
0.33% |
0.11% |
0.66% |
17.12 |
0.00 (0.00–38.13) |
||
EPB |
None EPB |
1814 |
1.18% |
0.63% |
1.89% |
28.99 |
27.55 (0.00–57.00) |
|
Single EPB |
1814 |
94.89% |
92.54% |
96.82% |
81.45 |
74.22 (60.85–83.02) |
||
Double EPB |
1814 |
3.47% |
1.85% |
5.55% |
86.94 |
75.85 (63.59–83.98) |
||
Triple EPB |
1814 |
0.49% |
0.21% |
0.87% |
19.22 |
0.00 (0.00–41.21) |
||
Quadruple EPB |
1814 |
0.27% |
0.07% |
0.57% |
5.28 |
0.00 (0.00–0.00) |
||
Septum |
Absent septum |
2635 |
54.26% |
47.25% |
61.18% |
383.58 |
91.92 (89.64–93.69) |
|
Single septum |
2635 |
45.74% |
38.82% |
52.75% |
383.58 |
91.92 (89.64–93.69) |
||
Patients with de Quervain’s disease |
APL |
Single APL |
608 |
23.79% |
15.12% |
33.68% |
54.01 |
85.19 (73.70–91.66) |
Double APL |
608 |
45.33% |
38.88% |
51.86% |
19.12 |
58.16 (12.40–80.02) |
||
Triple APL |
608 |
22.69% |
17.29% |
28.58% |
20.37 |
60.72 (18.49–81.07) |
||
Quadruple APL |
608 |
5.37% |
2.50% |
9.16% |
23.63 |
66.13 (31.32–83.31) |
||
Fivefold ALP |
608 |
1.04% |
0.35% |
2.06% |
8.27 |
3.24 (0.00–65.94) |
||
Sixfold APL |
608 |
0.38% |
0.02% |
1.07% |
2.53 |
0.00 (0.00–0.00) |
||
EPB |
None EPB |
608 |
2.38% |
0.98% |
4.33% |
13.12 |
39.00 (0.00–71.93) |
|
Single EPB |
608 |
92.04% |
89.63% |
94.16% |
8.59 |
6.87 (0.00–67.22) |
||
Double EPB |
608 |
4.65% |
1.90% |
8.44% |
25.88 |
69.09 (38.21–84.54) |
||
Triple EPB |
608 |
0.75% |
0.19% |
1.63% |
3.01 |
0.00 (0.00–6.58) |
||
Septum |
Absent septum |
1592 |
36.37% |
30.98% |
41.94% |
142.47 |
80.35 (72.47–85.97) |
|
Single septum |
1592 |
63.30% |
57.66% |
68.76% |
145.767 |
80.79 (73.15–86.26) |
||
Double septum |
1592 |
0.69% |
0.34% |
1.17% |
28.30 |
1.06 (0.00–41.95) |
||
Patients without de Quervain’s disease |
APL |
Single APL |
14 |
90.26% |
71.79% |
100.00% |
0.00 |
0.00 (0.00–0.00) |
Double APL |
14 |
9.74% |
0.00% |
28.21% |
0.00 |
0.00 (0.00–0.00) |
||
EPB |
None EPB |
56 |
3.58% |
0.06% |
10.47% |
0.00 |
0.00 (0.00–0.00) |
|
Single EPB |
56 |
96.42% |
89.53% |
99.94% |
0.00 |
0.00 (0.00–0.00) |
||
Septum |
Absent septum |
164 |
69.89% |
19.49% |
100.00% |
62.16 |
96.78 (93.42–98.43) |
|
Single septum |
164 |
30.11% |
0.00% |
80.51% |
62.16 |
96.78 (93.42–98.43) |
||
Overall results |
APL |
None APL |
2371 |
0.29% |
0.11% |
0.55% |
7.18 |
0.00 (0.00–0.00) |
Single APL |
2371 |
22.26% |
15.34% |
30.04% |
564.23 |
94.51 (93.15–95.59) |
||
Double APL |
2371 |
43.45% |
36.77% |
50.26% |
332.66 |
90.68 (87.93–92.81) |
||
Triple APL |
2371 |
19.27% |
14.73% |
24.26% |
258.75 |
88.02 (84.17–90.93) |
||
Quadruple APL |
2371 |
5.67% |
3.67% |
8.06% |
154.82 |
79.98 (72.37–85.49) |
||
Fivefold APL |
2371 |
1.43% |
0.75% |
2.32% |
70.64 |
56.12 (37.79–70.46) |
||
Sixfold APL |
2371 |
0.56% |
0.29% |
0.90% |
27.17 |
0.00 (0.00–31.20) |
||
Sevenfold APL |
2371 |
0.34% |
0.14% |
0.63% |
18.54 |
0.00 (0.00–0.00) |
||
EPB |
None EPB |
2478 |
1.57% |
0.99% |
2.28% |
48.83 |
34.47 (0.00–57.20) |
|
Single EPB |
2478 |
94.11% |
92.28% |
95.70% |
95.46 |
66.48 (51.75–76.71) |
||
Double EPB |
2478 |
3.78% |
2.39% |
5.46% |
117.25 |
72.71 (61.46–80.67) |
||
Triple EPB |
2478 |
0.57% |
0.31% |
0.91% |
23.07 |
0.00 (0.00–15.69) |
||
Quadruple EPB |
2478 |
0.29% |
0.11% |
0.55% |
6.50 |
0.00 (0.00–0.00) |
||
Septum |
Absent septum |
4391 |
47.38% |
42.24% |
52.55% |
751.84 |
91.35 (89.70–92.74) |
|
Single septum |
4391 |
52.62% |
47.45% |
57.76% |
751.84 |
91.35 (89.70–92.74) |
The quantity of APL tendons in the first dorsal compartment of the wrist in patients with de Quervain’s disease was examined in 9 studies [3, 5, 12, 25, 30, 39, 41, 61, 66] including 608 wrists. Number of APL tendons varied from 1 to 6. For a single APL tendon, prevalence was 23.79% (95% CI: 15.12–33.68%). For a double APL tendon, prevalence was 45.33% (95% CI: 38.88–51.86%). For a triple APL tendon, prevalence was 22.69% (95% CI: 17.29–28.58%). Results mentioned above, are all gathered in Table 3.
Overall, the number of APL tendons in the first dorsal compartment of the wrist was analysed in 2371 wrists. The number of APL tendons ranged from 0 to 7. The variation that occurs the most frequently was found to be a double APL tendon with a prevalence of 43.45% (95% CI: 36.77–50.26%). All the results mentioned above and the more detailed ones are gathered in Table 3.
EPB
The quantity of EPB tendons in the first dorsal compartment of the wrist was examined in 22 cadaveric studies [1, 3, 8, 10, 16, 17, 22, 25, 26, 29, 30, 47, 48, 52–54, 56, 57, 60, 63, 66, 71] including 1814 wrists. Number of EPB tendons varied from 0 to 4. For a single EPB tendon, prevalence was 94.89% (95% CI: 92.54–96.82%). Results mentioned above, are all gathered in Table 3.
The quantity of EPB tendons in the first dorsal compartment of the wrist in patients with de Quervain’s disease was examined in 9 studies [3, 5, 12, 25, 30, 39, 41, 61, 66] including 608 wrists. Number of EPB tendons varied from 0 to 3. For a single EPB tendon, prevalence was 92.04% (95% CI: 89.63–94.16%). Results mentioned above, are all gathered in Table 3.
Overall, the number of EPB tendons in the first dorsal compartment of the wrist was analysed in 2478 wrists. The number of EPB tendons ranged from 0 to 4. The variation that occurs the most frequently was found to be a single EPB tendon with a prevalence of 94.11% (95% CI: 92.28–95.70%). All the results mentioned above and the more detailed ones are gathered in Table 3.
Septum
The presence of intercompartmental fibro-osseous septum in the first dorsal compartment of the wrist was examined in 32 cadaveric studies [2, 3, 6, 10, 15, 17, 19, 20, 22, 25, 26, 30–32, 34, 37, 38, 40, 43–45, 47, 48, 50, 54–57, 63, 64, 66, 71] including 2635 wrists. The septum was either present or not (there were no reports of double septum in this group, unlike in the patients with de Quervain’s disease group). For absence of septum, prevalence was 54.26% (95% CI: 47.25–61.18%). For presence of septum, prevalence was 45.74% (95% CI: 38.82–52.75%). Results mentioned above, are all gathered in Table 3.
The presence of intercompartmental fibro-osseous septum in the first dorsal compartment of the wrist in patients with de Quervain’s disease was examined in 29 studies [2–7, 9, 11, 12, 18, 21, 25, 27, 28, 30, 33, 35, 39, 41–43, 46, 58, 61, 62, 66, 69, 70, 72] including 1592 wrists. The septum was either absent, single our double. For absence of septum, prevalence was 36.37% (95% CI: 30.98–41.94%). For a single septum, prevalence was 63.30% (95% CI: 57.66–68.76%). For a double septum, prevalence was 0.69% (95% CI: 0.34–1.17%). Results mentioned above, are all gathered in Table 3.
The presence of intercompartmental fibro-osseous septum in the first dorsal compartment of the wrist in patients without de Quervain’s disease was examined in 3 studies [7, 11, 24] including 164 wrists. The septum was either present or not (there were no reports of double septum in this group, unlike in the patients with de Quervain’s disease group). For absence of septum, prevalence was 69.89% (95% CI: 19.49–100.00%). For presence of septum, prevalence was 30.11% (95% CI: 0.00–80.51%). Results mentioned above, are all gathered in Table 3.
Overall, the presence of the intercompartmental septum in the first dorsal compartment of the wrist was analysed in 4391 wrists. The septum occurred in 52.62% (95% CI: 47.45–57.76%). All the results mentioned above and the more detailed ones are gathered in Table 3.
Comparison between cadavers and patients with de Quervain’s disease
Data regarding cadavers and patients with de Quervain’s disease groups were compared and there are no statistically significant differences between cadavers and patients with de Quervain’s disease when it comes to anatomical variations of APL and EPB tendons in the first dorsal compartment (p > 0.05). Moreover, there is statistically significant difference between cadavers and patients with de Quervain’s disease when it comes to presence of septum in the first dorsal compartment (p < 0.05). Those p-values are gathered in Table 4.
Compared variant |
P |
Single APL |
0.3912 |
Double APL |
0.9131 |
Triple APL |
0.4754 |
Quadruple APL |
0.8463 |
Fivefold APL |
0.5955 |
Sixfold APL |
0.5034 |
None EPB |
0.2058 |
Single EPB |
0.1016 |
Double EPB |
0.6000 |
Triple EPB |
0.6051 |
Absent septum |
0.0002 |
Present septum |
0.0007 |
DISCUSSION
Content of the first dorsal compartment of the wrist shows great anatomical variability. Many studies have described those anomalies, but overall results are inconsistent and some conclusions excludes one another. In clinical practice, anatomy of the first dorsal compartment is essential during treatment of de Quervain’s disease, while its effectiveness may rely on awareness of the contents of patients compartment. Our goal was to provide surgeon’s with the most comprehensive meta-analysis of anatomical variations of the first compartment of the wrist, regarding a total of 5229 studied hands. Our results differ from another systematic-review [36] showing, among others, higher prevalence of double APL variant, lower prevalence of single APL variant, higher prevalence of septum in both cadaveric and de Quervain’s groups etc.
Our results differ from previous major studies regarding prevalence of all APL variations [3, 8, 25, 36, 41, 66]. Our results shows that mostly occurs the double-tendon APL variety with its 43.45% prevalence overall, 46.04% prevalence in cadavers and 45.33% prevalence in patients with de Quervain’s disease. Comparing those and rest of the results in both groups, it may be accompted that there are no statistically significant differences between cadavers and patients with de Quervain’s disease when it comes to anatomical variations of APL tendons in the first dorsal compartment (p > 0.05). Taking into consideration that data showing prevalence of the double APL tendon in cadavers may represent considerable heterogeneity (I2 = 93.28; 95% CI: 91.01–94.98) and the fact that the lower CI value of prevalence of double APL is higher than any higher CI value of any other APL variety, we may acknowledge double APL as a most common variant in the population. In contrast of APL, EPB dominates with its single-tendon variety, both in cadavers and in patients with de Quervain’s disease. Our results differ from previous major studies regarding prevalence of all EPB variations [3, 8, 25, 36, 41, 48, 66]. Comparing other varieties of EPB in both groups, it can also be accompted, that there are no statistically significant differences between cadavers and patients with de Quervain’s disease, when it comes to anatomical variations of EPB in the first dorsal compartment (p > 0.05). Single EPB tendon may be acknowledged as standard in the population because data showing its prevalence may represent substantial heterogeneity (I2 = 74.22; 95% CI: 60.85–83.02) and its prevalence lower CI value is much higher than any other prevalence higher CI value in any other EPB variety in cadaveric studies. In case of the septum, there are statically significant differences between cadaveric and de Quervain’s disease groups (p < 0.05). The presence of the septum is much more common in the de Quervain’s disease group than in the cadaveric group, with its prevalence for a single septum being 63.30% and 45.74%, respectively. We decided not to compare the patients without de Quervain’s disease with other groups due to small amount of studies and lack of data about first dorsal compartment in the no de Quervain’s disease group. Results mentioned above may suggest that presence of the septum in the first dorsal compartment of the wrist may be one of the factors causing de Quervain’s disease. Also it may be that presence of the septum originates this ailment more likely than multiple variations of APL or EPB tendon slips in the compartment. Those suggests can be considered in the further studies.
Clinical treatment of de Quervain’s disease usually starts with a non-surgical approach. Most frequently the first used therapy technique is corticosteroids injection into the first dorsal compartment sheath. Unfortunately, patients experience treatment success after 1 injection only in 51.8% of cases, according to Oh et al. [49]. Anatomical knowledge and awareness of most common variations in the first dorsal compartment may increase chances of successful steroid treatment. We hope that by taking in consideration our results, surgeons will more often perform steroid treatment under the ultrasonography control so the awareness of patients anatomical variation may not be oversight. Especially important factors that may affect results of this treatment are number of APL tendons due to its great diversity in the population and presence of septum, because it creates either fully or partly closed two sub-compartments and injecting steroids into both sub-compartments results with increased chances for successful therapy [27, 42, 73]. During surgical release of the first dorsal compartment, comprehensive anatomical knowledge may prevent potential overlook of the supernumerary tendons, lying in the separate sub-compartment [66]. This knowledge is essential for surgeons while treating de Quervain’s disease, as it may prevent inadequate recognition and in effect, failure to decompress the whole first dorsal compartment [36, 48]. Awareness of anatomical variations in the first dorsal compartment should also be helpful for radiologists who treat and examine wrists. Our results shows that arrangement of 3 tendons (double APL and single EPB) in the first dorsal compartment should be expected most often. This may help to accurately interpretate and describe imaging tests, which may be the base of further diagnostics. Additionally, obtaining an image of intercompartmental septum in the first dorsal compartment, should rise awareness, that this may be the factor causing de Quervain’s disease in the future.
Taking in consideration geographical differences, especially in quantity of carried out research, authors are aware that results included in this meta-analysis might be burdened with a potential bias. Asia dominates with a number of studied wrists, while on the other side, researches realised in Africa, Australia or South America are singular. This may cause our results to reflect more of Asian than global population.
CONCLUSIONS
In conclusion, we believe that it is the most comprehensive analysis of the contents of the first dorsal compartment of the wrist. Double APL and single EPB are the most common variations of tendons in the first dorsal compartment overall and both in cadavers and patients with de Quervain’s disease, with no statistically significant differences between those two groups. Presence of intercompartmental fibro-osseus septum is much more common in patients with de Quervain’s disease than in cadavers, which may be one of the factors evoking de Quervain’s disease. Our results should improve the awareness of anatomical variations in the first dorsal compartment, which in turn should have impact on treatment of de Quervain’s disease in clinical practice.