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Orthopaedic Proceedings
Vol. 91-B, Issue SUPP_II | Pages 320 - 320
1 May 2009
González G Cáceres E Monllau JC
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Introduction and purpose: One of the complications observed after meniscal transplant is allograft shrinkage. Amongst the proposed causes are both a subtle immunological rejection, and an alteration of meniscal permeability leading to nutritional deficit. The purpose of this study was to asses freezing, one of the most frequently used processes to preserve menisci, and provide evidence either in favor of those articles in the literature that claim that freezing does not affect the collagen network, or against it.

Materials and methods: Twenty-six lateral menisci were obtained during total knee replacement. Thirteen were frozen at −80° and the rest were used as a control group. The menisci were analyzed with Transmission Electronic Microscopy. According to the periodicity and degree of disruption of the collagen, loss of band pattern and intrafibrillar edema, each meniscus was scored from 0 to 7 points. Subsequently the menisci were classified by degrees from normal (grade I, 0 to 2 points) to severely altered (grade III, 5 to 7 points).

Results: Collagen fibers in longitudinal sections averaged 14.26 nm in previously frozen menisci and 17.28 in the control group (p=0.019), whereas in cross sections they averaged 13.14 nm. vs. 16.93 nm. respectively (p=0.003)..

Eight of the 13 frozen menisci were classified as grade III (61.54%) and 5 as grade II. In the control group 6 were classified as grade I (46.15%) and 7 as grade II (53.85%). Frozen menisci averaged 4.85 points and the control menisci 2.46 (p< 0.001).

Conclusions: The freezing process to −80°C seems to alter both each fiber of collagen as well as its spatial position. We have presented a new qualitative/quantitative assessment scale for meniscal status.


Orthopaedic Proceedings
Vol. 87-B, Issue SUPP_I | Pages 84 - 84
1 Mar 2005
Gelber P Reina F Soldado F Monllau JC
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Introduction and purpose: Different neurovascular structures may be damaged when making arthroscopic portals to the shoulder joint. The description of new portals poses new challenges. The goal of the present study is to provide an update on the anatomic vasculonervous responses of the current approaches to shoulder arthroscopy.

Materials and methods: 16 fresh cadavers were systematically dissected. The most usual arthroscopic portals were marked and, then, the dissection started on a plane-to-plane basis. Relationships were identified and distances were measured to the most important neurovascular elements with a standard caliber (accuracy: 0.5mm).

Results: The portals studied and the structures at risk were the following:

* Posterior portal: anterior branch of the axillary nerve and posterior circumflex artery 3.4 cm (range: 1.4 – 5); cutaneous branch of the axillary nerve 6.3 cm (range: 3.8 – 8.3), suprascapular nerve 2.8 cm (range: 2.1–3.3).

* Anterosuperior portal: main branch of the musculocutaneous nerve 6.5 cm (range: 3.8 – 11).

* Lateral subacromial portal: axillary nerve and posterior circumflex artery 3.7 cm (range: 2– 5.5).

* Anteroinferior subaxillary portal 4 cm (range: 3.1 –6).

* Supraspinatus portal: suprascapular nerve 3.2 cm (range: 2.4 – 4).

Conclusions: Although the crucial elements at risk when performing a shoulder arthroscopy are multiple, the axillary and suprascapular nerves were the most vulnerable structures to the different approaches. In spite of the presence of the “safe areas” described above, the neurovascular bundle was frequently affected by passage through the anteroinferior subaxillary portal. The results suggest that the use of this portal is not safe for routine arthroscopic practice.