Depuis les dernières années, la prévalence de personnes souffrant de dégénérescence des cartilages articulaires, communément appelée ostéoarthrite (OA), ne cesse d’augmenter. Les douleurs articulaires et les raideurs musculaires associées à cette pathologie mènent à des limitations des capacités fonctionnelles, à une perte de mobilité et d’autonomie affectant grandement la qualité de vie de ces personnes. Afin de soulager les personnes souffrant de cette pathologie, l’arthroplastie de la hanche est une procédure chirurgicale fréquemment utilisée. À la suite de cette chirurgie, une amélioration de la qualité de vie et une reprise des capacités fonctionnelles sont souvent observées. Cependant, comparativement à des sujets sains, la vitesse de marche est diminuée, une faiblesse des muscles abducteurs de la hanche est constatée et des mouvements compensatoires au niveau du tronc sont persistants. L’objectif de cette thèse est d’évaluer le patron locomoteur chez des patients qui subiront une arthroplastie de la hanche. Plus spécifiquement, les adaptations locomotrices pré et post-opératoires seront quantifiées dans le but d’apporter des modifications aux programmes de réhabilitation pour ainsi favoriser un patron locomoteur sans déficit. Afin de répondre à cet objectif, trois études distinctes ont été effectuées. Dans le cadre de la première étude, l’impact de l’implantation d’une prothèse totale de la hanche avec une tête fémorale de large diamètre et une prothèse de resurfaçage a été évalué par rapport aux sujets sains lors de la locomotion. Au cours de cette étude, le contrôle du tronc a été analysé en utilisant la distance entre le centre de masse corporel et le centre articulaire de la hanche opérée. Suite aux résultats obtenus, aucune différence majeure n’existe entre les deux types de prothèses en ce qui a trait au contrôle du tronc et ce, à un an post-opératoire. Lors de la deuxième étude, la symétrie des paramètres biomécaniques des membres inférieurs lors de la locomotion chez des patients ayant bénéficié de l’implantation d’une prothèse de la hanche a été caractérisée suite à un programme d’exercices péri-opératoires (pré et post-opératoire). Lors de cette étude, le programme d’exercices péri-opératoires était complémentaire au protocole de réadaptation du centre hospitalier. D’après les résultats obtenus lors de cette étude exploratoire, ce programme d’exercices péri-opératoires semble permettre d’améliorer la symétrie de la puissance et du travail musculaire au niveau de la hanche, du genou et de la cheville favorisant ainsi un patron de marche avec de minimes compensations. Finalement, dans le cadre de la troisième étude, l’approche prédictive et l’approche fonctionnelle, utilisées pour localiser le centre articulaire de la hanche, ont été comparées aux mesures radiographiques, chez des patients à la suite d’un remplacement articulaire de la hanche. À la suite de cette étude, les résultats démontrent que l’utilisation de l’approche fonctionnelle est plus appropriée chez des patients ayant bénéficié d’une arthroplastie de la hanche. En effet, cette approche individualisée est plus précise ce qui, par conséquent, permettra d’obtenir des résultats de plus grande qualité lors d’analyses biomécaniques de la locomotion. / In recent years, the prevalence of people suffering from joint cartilage degeneration, called osteoarthritis (OA), still increases. The joint pain and muscle stiffness related to this pathology have an impact on patients’ quality of life by limiting their functional capacities, mobility and autonomy. In order to relieve these patients, hip arthroplasty is a frequently used surgical procedure. Even if there is an improvement in quality of life and a restoration of functional capacities in these patients, some impairment seem to persist during the post-operative period. The walking velocity is slower when compared to healthy subjects, a hip abductor muscle weakness is observed and trunk compensations lasted during the post-operative period. The aim of this thesis is to evaluate patients undergoing hip arthroplasty during locomotion. More specifically, gait pattern adaptations will be quantified pre and post-operatively to revise rehabilitation programs in order to promote a healthy gait pattern. Three separate studies were conducted to meet this objective. The first study compared the effect of a large femoral head hip prosthesis and a hip resurfacing prosthesis to healthy subjects. During this study, the trunk control was analyzed using the distance between the body center of mass and the hip prosthetic joint center. The results obtained show no major difference between the two types of prosthesis and the healthy control one year post-operatively. During the second study, biomechanics parameter symmetry of the lower limb of gait pattern in patients undergoing hip arthroplasty was characterized following a peri-operative (pre and post-operatively) exercise program. The exercise program was complementary to the medical center standard rehabilitation program. Based on the results of this exploratory study, the peri-operative exercise program seems to improve the symmetry of the muscular power and work of the hip, knee and ankle which promote a healthy gait pattern without compensations. Finally, for the third study, the predictive and the functional approaches, used to locate the hip joint center, were compared to radiographic measurements in patients undergoing hip arthroplasty. The results of this study demonstrated that the functional approach was more appropriate for these patients. This individualized approach is more accurate which leads to quality improvement during biomechanical analysis of gait pattern.

Background: Patient reports of pain and function are used to inform the need for and timing of total knee replacement (TKR) and evaluate TKR outcomes. This dissertation compared measurement properties of commonly-used patient surveys in TKR and explored ways to develop more efficient knee-specific function measures. Methods: 1,179 FORCE-TJR patients (mean age=66.1, 61% female) completed questionnaires before and 6 months after TKR. Patient surveys included the knee-specific Knee injury and Osteoarthritis Outcome Score (KOOS) and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and generic SF-36 Health Survey. Tests of KOOS and WOMAC measurement properties included evaluations of scaling assumptions and reliability. Item response theory methods were used to calibrate 22 KOOS function items in one item bank; simulated computerized adaptive tests (CAT) then were used to evaluate shorter function scores customized for each patient. Validity and responsiveness of measures varying in attributes (knee-specific versus generic, longer versus shorter, CAT versus fixed-length) were compared. Results: KOOS and WOMAC scales generally met tests of scaling assumptions, although many pain items were equally strong measures of pain and physical function. Internal consistency reliability of KOOS and WOMAC scales exceeded minimum levels of 0.70 recommended for group-level comparisons across sociodemographic and clinical subgroups. Function items could be calibrated in one item bank. CAT simulations indicated that reliable knee-specific function scores could be estimated for most patients with a 55-86% reduction in respondent burden, but one-third could not achieve a reliable (≥ 0.95) CAT score post-TKR because the item bank did not include enough items vi measuring high function levels. KOOS and WOMAC scales were valid and responsive. Short function scales and CATs were as valid and responsive as longer KOOS and WOMAC function scales. The KOOS Quality of Life (QOL) scale and SF-36 Physical Component Summary discriminated best among groups evaluating themselves as improved, same or worse at 6 months. Conclusions: Results support use of the KOOS and WOMAC in TKR. Improved knee-specific function measures require new items that measure higher function levels. TKR outcomes should be evaluated with a knee-specific quality of life scale such as KOOS QOL, as well as knee-specific measures of pain and function and generic health measures.

No description available.

No description available.

No / There are few data on the associations between anaemia, allogeneic blood transfusion (ABT), patient blood management, and outcome after arthroplasty in the UK. National agencies nevertheless instruct NHS Trusts to implement blood conservation measures including preoperative anaemia management. Internationally, blood management programmes show encouraging results. METHODS: We retrospectively audited 717 primary hip or knee arthroplasties in a UK general hospital and conducted regression analyses to identify outcome predictors. We used these data to modify previously published algorithms for UK practice and audited its introduction prospectively. The retrospective audit group served as a control. RESULTS: Preoperative haemoglobin (Hb) concentration predicted ABT (odds ratio 0.25 per 1 g dl(-1), P<0.001). It also predicted the length of stay (LOS, effect size -0.7 days per 1 g dl(-1), P=0.004) independently of ABT, including in non-anaemic patients. Patient blood management implementation was associated with lower ABT rates for hip (23-7%, P<0.001) and knee (7-0%, P=0.001) arthroplasty. LOS for total hip replacement and total knee replacement decreased from 6 (5-8) days to 5 (3-7) and 4 (3-6) days, respectively, after algorithm implementation (P<0.001). The all-cause re-admission rate within 90 days decreased from 13.5% (97/717) before to 8.2% (23/281) after algorithm implementation (P=0.02). CONCLUSIONS: We conclude that preoperative Hb predicts markers of arthroplasty outcome in UK practice. A systematic approach to optimize Hb mass before arthroplasty and limit Hb loss perioperatively was associated with improved outcome up to 90 days after discharge.

Every year, about 1 million patients worldwide and 16000 patients in Sweden undergo total hip arthroplasty (THA). This surgical intervention is considered a successful, safe and cost-effective procedure to regain pain-free mobility and restore hip joint function in patients suffering from severe hip joint disease or trauma. Besides relieving the pain, restoration of biomechanical forces around the hip with appropriate femoral offset (FO), leg length and proper component position and orientation are important goals. The radiographic preoperative planning and postoperative evaluation of these parameters require good validity, interobserver reliability and intraobserver reproducibility. It remains controversial as to how much postoperative leg length discrepancy (LLD) and FO change are acceptable. Generally, lengthening of the operated leg ≥ 10mm and FO reduction of the operated hip &gt; 5mm should be avoided by using preoperative radiological templating and intraoperative measurement methods. There is no consensus on the association between LLD and FO and outcome after THA. The aims of this thesis were to: 1. To determine the influence of non-corrected LLD after THA on patients’ reported hip function and quality of life (QoL). 2. To study the association of global FO changes after THA with patients’ reported hip function, QoL and abductor muscle strength. 3. To evaluate the concurrent validity of the Sundsvall method of measuring postoperative global FO by comparing it to a standard method and to evaluate the interobserver reliability and intraobserver reproducibility of measurement of postoperative global FO, LLD and acetabular cup inclination and anteversion. 4. To analyse the postoperative radiographs of THA patients with leg lengthening and FO reduction to determine whether the problem is located in the stem, cup or both. Study I: A prospective cohort study of 174 patients with unilateral osteoarthritis (OA), comparing patients with lengthening ≥ 10mm, restoration (between 9 mm lengthening and 5 mm shortening) or shortening &gt; 5 mm of the operated leg after THA. Follow up was 12–15 months. We found that a LLD of up to 20 mm did not influence the functional outcome (WOMAC) or QoL (EQ-5D). However, the lengthening group showed less improvement in WOMAC and more use of a shoe lift. Study II: A prospective cohort study of 222 patients with unilateral hip OA, comparing patients with decreased global FO (&gt; 5 mm reduction), restored FO (within 5 mm restoration), and increased FO (&gt; 5 mm increment) after THA. Follow up was was 12–15 months. The unadjusted results showed that the decreased FO group had a worse WOMAC index, less abductor muscle strength, and more use of walking aids. When these results were adjusted for possible confounding factors, only global FO reduction was statistically significantly associated with reduced abductor muscle strength. The incidence of residual hip pain and analgesics use was similar in the 3 groups. Study III: A prospective cohort study of 90 patients with primary unilateral OA treated with THA. Global FO using the Sundsvall method, global FO (standard method), LLD, acetabular cup inclination and anteversion were measured on postoperative radiographs. The interobserver reliability and intraobserver reproducibility were tested using three independent observers. We found that the Sundsvall method is as reliable as the standard method and the evaluated radiographic measurement methods have the required validity and reliability to be used in clinical practice. Study IV: A prospective cohort study of 174 patients with unilateral primary OA treated with THA. LLD and global FO were measured on postoperative radiographs. Patients with lengthening of the operated leg ≥ 10mm (n=41) and patients with reduction of global FO &gt; 5mm (n=58) were further studied to investigate the amount of lengthening and global FO reduction that took place in the stem and in the cup compared with the contralateral side. The interobserver reliability and intraobserver reproducibility were tested using two independent observers. We found that post-THA lengthening of the operated leg ≥ 10mm was mainly caused by improper placement of the femoral stem, whereas a decrease of global FO &gt; 5 was caused by improper placement of both acetabular and femoral components. The radiological measurement methods used showed substantial to excellent interobserver reliability and intraobserver reproducibility and are therefore clinically useful. The main conclusions of this thesis are: LLD up to 20 mm and reduced global FO more than 5 mm did not influence the functional outcome or quality of life at 12–15 months postoperatively. Lengthening ≥ 10mm was associated with increased use of a shoe lift. A reduction of global FO more than 5 mm compared to the contralateral hip was associated with weaker hip abductor muscles and more use of walking aids. Therefore both should be avoided. The radiographic measurement methods of LLD, global FO, cup inclination and anteversion have the required validity and reliability to be used in clinical practice. Lengthening of the operated leg is mainly caused by improper femoral stem positioning while global FO reduction results from improper positioning of both acetabular and femoral components. Surgeons should be aware of these operative pitfalls in order to minimize component malpositioning. / Varje år opereras ungefär 1 miljon patienter runt om i världen och 16000 patienter i Sverige med en total höftledsprotes (THA). Operation med höftledsprotes anses vara enav de mest framgångsrika, säkra och kostnadseffektiva kirurgiska åtgärderna med syfte att för att återställa livskvalité. Målet är att smärtlindra och återställa rörligheten i dendestruerade höftleden vid artros, reumatisk destruktion eller men efter exempelvis Perthes sjukdom. Vid operation med THA är det viktigt att återställa de biomekaniskakrafterna runt höftleden med en adekvat så kallad femoral offset (FO), postoperativ benlängdsskillnad (BLS) och ett tillfredsställande komponentläge. Den preoperativaplaneringen och den postoperativa bedömning av dessa parametrar kräver god tillförlitlighet, det vill säga validitet och reproducerbarhet både mellan olika bedömareoch vid upprepade mätningar av samma bedömare. Det är fortfarande inte klarlagt hur mycket postoperativ förändring i FO och BLS som är acceptabla. I dagsläget är detacceptabelt om den postoperativa benförlängningen understiger 1 cm och förändringen i FO är under 5 mm. Det finns ingen konsensus huruvida det föreligger ett sambandmellan BLS, FO och den patientrapporterade höftfunktionen och livskvalitén efter THA. Syftet med denna avhandling var: 1. Att studera effekten av icke-korrigerad BLS efter THA på den patientrapporterade höftfunktionen och livskvalitén. 2. Att studera effekten av förändringen i FO efter THA på den patientrapporterade höftfunktion, livskvalitén och muskelstyrka i abduktion. 3. Att utvärdera validitet och reliabilitet av en så kallad global FO genom att jämföra den med den gällande standard metoden samt studera tillförlitlighet av de radiologiskamätningar av postoperativa BLS, FO, cup inklination och anteversion efter THA. 4. Att radiologiskt undersöka i vilken av komponenterna (stam eller cup) somförändringen i FO och BLS verkar vara förlagd. Studie I: En prospektiv kohortstudie med 174 patienter som behandlats med THA för en primär unilateral koxartros. Patienterna delades in i tre grupper; de som fått en BLSförlängning över 10mm, återställning (mellan 9mm förlängning och 5mm förkortning) eller förkortning &gt;5mm av det opererande benet efter THA. Uppföljning gjordes 12-15månader postoperativt. Vi fann att BLS upp till 20mm påverkade inte höftfunktion (WOMAC) och livskvalité (EQ-5D), men den förlängda gruppen visade en mindreförbättring i WOMAC och rapporterade en mer frekvent användning av skoinlägg. Studie II: En prospektiv kohortstudie med 222 patienter som behandlats med THA för en primär unilateral koxartros. Patienterna delades in i tre grupper; de patienter medförminskad FO (&gt; 5mm minskning), återställd FO (inom 5mm) eller ökad FO (&gt;5mm ökning). Uppföljning genomfördes efter 1 år med WOMAC, styrkemätning av höftensabduktorer och en frågeformulär. En minskad FO var associerade med en minskad styrka i höftens abduktorer. Det var ingen skillnad mellan grupperna gällandekvarstående höftsmärta och användning av analgetika. Studie III: En prospektiv kohortstudie med 90 patienter som behandlats med THA på grund av primär unilateral koxartros. På de postoperativa röntgenbilderna uppmättesglobala FO (Sundsvalls metodologi), globala FO (standard metod), BLS, cup inklination och anteversion. Reliabilitet och reproducerbarhet bedömdes mellan treoberoende observatörer. Vi fann att global FO (enligt Sundsvalls metodologi) är lika tillförlitlig som den nuvarande standardmetoden och de utvärderade radiologiskamätmetoderna har hög validitet och reliabilitet och kan således användas i klinisk praxis. Studie IV: En prospektiv kohortstudie med 174 patienter som behandlats med en THA för en primär unilateral koxartros. På de postoperativa röntgenbilderna uppmättes BLSoch globala FO. Patienter med förlängning ≥ 10mm (n=41) och patienter med minskning av globala FO &gt;5mm (n=58) studerades for att mäta förlängning ochglobala FO minskning som sitter i stammen eller i cup jämfört med kontralaterala sidan. Reliabilitet och reproducerbarhet bedömdes av två oberoende observatörer. Vifann att en BLS över 10mm sitter framför allt i stamkomponenten i lårbenet medan en minskning i FO över 5 mm sitter i båda stam och cup. De radiologiska mätmetodernahar hög reliabilitet och reproducerbarhet och kan således användas i klinisk praxis. De viktigaste slutsatserna i denna avhandling är: 1. BLS med en förlängning upp till 20 mm och en minskning av globala FO mer än 5 mm påverkar inte patientrapporterad höftfunktion eller livskvalitet 1 år postoperativt. 2. BLS med en förlängning mer än 9 mm var associerad med mer användning av skoinlägg. En minskad FO med mer än 5 mm jämfört med den icke opererade höftenvar associerad med en sämre muskelstyrka i abduktion och ökat användning av gånghjälpmedel. 3. De radiologiska mätmetoderna av BLS, FO, acetabulära komponentens inklination och anteversion har hög validitet och reliabilitet, vilket kan användas i klinisk praxis. 4. En förlängning av det opererade benet orsakas främst av en positioneringen av stamkomponenten i lårbenet medan förlust av FO beror på otillfredsställande placeringav både stam och den acetabulära komponenten. Kirurger bör vara medveten om dessa operativa fallgropar för att optimera det kirurgiska resultatet.

Thesis (PhD (Industrial Engineering))--University of Stellenbosch, 2011. / ENGLISH ABSTRACT: Back pain is a common concern amongst a growing population of people across the world today, where in most cases the pain can become unbearable resulting in major lifestyle adjustments. Seventy to eighty percent of the population of the Western world experiences low-back pain at one time or another. Pain can be produced as a worn disc becomes thin, narrowing the space between the vertebrae. Pieces of the damaged disc may also break off and cause irritation to the nerves signalling back pain. Depending on the severity of a patient’s condition, and after conservative treatment options have been exhausted, a disc replacement surgery (arthroplasty) procedure may be prescribed to restore spacing between vertebrae and relieve the pinched nerve, while still maintaining normal biomechanical movement. Typical complications that are however still observed in some cases of disc implants include: anterior migration of the disc, subsidence (sinking of disc) and lateral subluxation (partial dislocation of a joint). Issues such as function, correct placement and orientation, as well as secure fixation of such a disc implant to the adjacent vertebrae are highly important in order to replicate natural biomechanical behaviour and minimise the occurrence of the complications mentioned. As various imaging and manufacturing technologies have developed, the option for individual, patientspecific implants is becoming more of a practical reality than it has been in the past. The combination of CT images and Rapid Manufacturing for example is already being used successfully in producing custom implants for maxilla/facial and cranial reconstructive surgeries. There exists a need to formalise a process chain for the design and manufacture of custom-made intervertebral disc implants and to address the issues involved during each step. Therefore this study has investigated the steps involved for such a process chain and the sensible flow of information as well as the use of state-of-the-art manufacturing technologies. Strong emphasis was placed on automation of some of the processes as well as the user-friendliness of software where engineers and surgeons often need to work together during this multi-disciplinary environment. One of the main benefits for customization was also investigated, namely a reduction in the risk and potential for implant subsidence. Stiffness values from pressure tests on vertebrae were compared between customized implants and implants with flat endplate designs. Results indicated a statistically significant improvement of customized, endplate matching implants as opposed to flat implant endplates. Therefore it may be concluded that the use of customized intervertebral disc implants with patient specific endplate geometry may decrease the risk and potential for the occurrence of subsidence. / AFRIKAANSE OPSOMMING: Rugpyn is ‘n algemene bekommernis vir ‘n groeiende populasie van mense in die wêreld vandag, waar in meeste gevalle die pyn ondraagbaar kan raak en groot leefstyl aanpassings vereis. Sewentig tot tagtig persent van die populasie in die Westerse wêreld ondervind lae rugpyn op een of ander stadium. Die pyn kan veroorsaak word deur ‘n intervertebrale skyf wat verweer en dunner word, en veroorsaak dat die spasie tussen die vertebrae vernou. Stukkies van die beskadigde skyf mag ook afbreek en irritasie aan die senuwees veroorsaak wat verdere pyn kan veroorsaak. Afhangende van die ernstigheid van ‘n pasiënt se geval, en nadat opsies vir konservatiewe behandeling uitgeput is, kan ‘n skyf vervangings-prosedure (artroskopie) voorgeskryf word om die spasie tussen die vertebrae te herstel en sodoende die geknypte senuwee te verlos. Die skyf vervanging herstel spasiëring tussen vertebrae terwyl die normale biomeganiese beweging ook behoue bly, in teenstelling met ‘n fusieprosedure wat die betrokke vertebrae aanmekaar vasheg en normale beweging belemmer. Tipiese komplikasies wat egter steeds na ‘n skyf vervanging in sommige gevalle waargeneem word sluit in: anterior migrasie van die inplantaat, insinking, sowel as laterale sublukasie (gedeeltelike dislokasie van ‘n gewrig). Faktore soos funksie, korrekte posisionering en orientasie, sowel as vashegting van so ‘n skyf inplantaat tot die aanliggende vertebrale bene is besonder belangrik om natuurlike biomeganiese beweging te herstel en sodoende bogenoemde komplikasies te verminder. Soos wat verskeie beeldings- en vervaardigingstegnologië verbeter het oor die laaste dekade, het die moontlikheid vir individuele, pasiënt-spesifieke inplantate al hoe meer ‘n praktiese realiteit begin word. Die kombinasie van Gerekenariseerde Tomografie (GT), tesame met Snel Vervaardiging word byvoorbeeld reeds suksesvol aangewend tydens die ontwerp en vervaardiging van pasiënt-spesifieke inplantate vir maksilla- en kraniale rekonstruktiewe chirurgie. Daar bestaan egter ‘n behoefte om ‘n formele prosesketting vir die ontwerp en vervaardiging van pasiënt-spesifieke intervertebrale skyf inplantate te ontwikkel en om belangrike faktore tydens elke stap noukeurig te beskryf. Hierdie studie het na die verskillende stappe in die prosesketting gekyk om ‘n sinvolle vloei van informasie en benutting van hoë gehalte vervaardigingstegnologië saam te snoer. Sterk klem was gelê op outomatisering van prosesse asook gebruikersvriendelikheid van sagteware waar ingenieurs en medici dikwels saam moet werk tydens hierdie kruisdissiplinêre omgewing. Een van die hoof verwagte voordele met die gebruik van pasklaar skyf inplantate, naamlik die vermindering van moontlike insinking van die inplantaat in die been, is ook ondersoek. Die ondersoek het druktoetse behels en die vergelyking van ooreenstemmende styfheid tussen inplantate wat die kontoer van die bene volg teenoor gewone plat eindplate. Die resultate was statisties beduidend in die guns van die pasklaar inplantate wat die beenkontoere gevolg het, en bewys dus dat die risiko vir insinking verminder is.

Every year 16 000 individuals receive a total hip arthroplasty (THA) in Sweden. Even though THA is a common procedure, adverse events do occur. The most dramatic complication is death in the postoperative phase. The overall aim of this thesis was to describe and investigate early mortality after THA in Sweden. Sweden has an ideal platform for national observational registry studies, thanks to the use of personal identity numbers. Operation-specific information was collected from the Swedish Hip Arthroplasty Register, medical information from the National Board of Health and Welfare, and socioeconomic information was collected from Statistics Sweden. Main outcome was 90-day mortality. Study I was a prospective observational register study investigating the risk of mortality after a simultaneous bilateral THA compared with staged bilateral THA. There was no clinically relevant difference in early postoperative mortality between the two groups. Studies II and III were nation-wide matched cohort studies, with adjustment for comorbidity and socioeconomic background. Adjusted early mortality in femoral neck fracture patients receiving a THA is about double compared with a matched control population. Young (60-69 years) femoral neck fracture patients receiving a THA have a low absolute mortality risk, while those who are older than 80 years with a higher degree of medical comorbidity run a high risk of early death (II). In study III healthier, younger patients with higher socioeconomic status tended to be selected for cementless THA, resulting in selection bias. Even after accounting for this bias, however, there remains a small absolute and adjusted increase in the risk of death within 14 days after elective THA surgery using fully cemented implants. Study IV was a nationwide prospective cohort study comparing different comorbidity measures in terms of predicting early postoperative mortality after THA. A less data-demanding comorbidity measure is better at predicting 90-day mortality than more commonly used coding algorithms. In conclusion, socioeconomic background and the presence of comorbidities have an important influence on early mortality after THA, while the type of fixation is of less importance. Future mortality studies could benefit from the use of data that are routinely collected, and thus avoid the logistically complicated procedure now necessary to merge national databases.

Die Zielsetzung dieser Arbeit besteht darin zu prüfen, ob die Luxationsrate bei Hochrisikopatienten durch den Einsatz von 40-mm- und 44-mm-Köpfen im Vergleich zu Patienten mit maximal 36-mm-Köpfen reduziert werden kann. Hierzu wurden die im Zeitraum von September 2009 bis Mai 2014 hüftendoprothetisch versorgten Patienten mit einem erhöhten Luxationsrisiko erfasst und die Verläufe auf Luxationen überprüft. Zur Risikobewertung diente eine eigens entwickelte Klassifikation. Des Weiteren erfolgte die Analyse der postoperativen Verläufe, der Röntgenbilder und eines Telefoninterviews in den Fällen, in denen Köpfe ≥ 40 mm zum Einsatz kamen. Im Untersuchungszeitraum wurden 288 Hüftendoprotheseneingriffe mit erhöhtem Luxationsrisiko durchgeführt. Bei 278 HTEP-Implantationen erfolgte der Einsatz von Gelenkköpfen ≤ 36 mm. In dieser Gruppe betrug die Luxationsrate 15,1% (n=42). Bei 10 Patienten wurden 40-mm- oder 44-mm-Gelenkköpfe eingesetzt. In diesen Fällen wurde das Luxationsrisiko entsprechend der vorgeschlagenen Klassifikation mit 3A (hoch) bis 4B (sehr hoch) bewertet. Bei einem mittleren Follow up von 22,8 Monaten wurde bei diesen Patienten keine Luxation festgestellt. Die mit 40-mm- sowie 44-mm-Köpfen erzielten Ergebnisse und die aktuelle Literatur sprechen für eine wesentlich höhere Gelenkstabilität und eine deutlich verminderte Luxationsneigung größerer Köpfe. Deren Einsatz ist daher gegenwärtig bei Risiko-patienten gerechtfertigt, sofern dieser in Abhängigkeit vom Pfannenaußendurch-messer konstruktiv möglich ist. In der weiteren Entwicklung der Hüftendoprothetik sollte die Verwendung größerer Köpfe angestrebt werden.

Introdução: Os hidroxietilamidos (HES) são considerados expansores plasmáticos efetivos em pacientes submetidos a procedimentos cirúrgicos de grande porte. Entretanto, seu uso clínico é limitado principalmente por sua interferência na hemostasia, representada por alterações da função plaquetária e na coagulação. A extensão dessas alterações está relacionada ao seu ipeso molecular ou à sua substituição molar. Este estudo clínico, foi realizado durante cirurgia de artroplastia de quadril em pacientes adultos para comparar os efeitos do HES (130/0,4) e a solução de Ringer lactato em relação ao sangramento intra-operatório, parâmetros hemodinâmicos, alterações na coagulação, necessidade de transfusões e resultados clínicos. Métodos: Quarenta e oito pacientes candidatos à cirurgia de artroplastia total de quadril sob anestesia subaracnoidea foram distribuídos aleatoriamente em dois grupos 24 pacientes foram selecionados para receber HES (30 ml/kg após anestesia) e 24 pacientes para receber solução de Ringer lactato (30ml/kg). O período de observação teve início após a indução da anestesia e terminou 5 horas após o termino do procedimento cirúrgico. Durante esse período o critério para a infusão de doses adicionais de fluido (10ml/kg de Solução de Ringer lactato para ambos os grupos) foi pressão arterial sistólica inferior a 90 mmHg e/ou um decréscimo de 20% da pressão arterial inicial, frequência cardíaca acima de 100 bpm, e/ou débito urinário menor de 0,4ml/kg/h. Vasopressor foi utilizado nos casos em que a hipotensão persistiu, após a reposição de volume. Transfusão de concentrado de hemácias foi administrada nos pacientes que se mantiveram instáveis hemodinamicamente após bolus adicionais de Ringer lactato ou vasopressor, Parâmetros hemodinâmicos foram mensurados em três períodos da cirurgia; dados bioquímicos foram coletados e testes da coagulação realizados e comparados. Os pacientes foram acompanhados durante sua internação hospitalar. Resultados: Os grupos foram uniformes em relação aos dados demográficos, tipo e duração da cirurgia, assim como a doenças pré-existentes. Não foram observadas diferenças significativas em relação aos parâmetros hemodinâmicos ou temperatura corporal durante o estudo. Os testes de coagulação, função plaquetária, análise de gases sanguíneos e dados bioquímicos mostraramse semelhantes entre os grupos. Perdas sanguíneas foram significativamente maiores no grupo HES (1296x890,p=0,04), necessitou de menos unidades de concentrado de hemácias durante o período observacional (17%versus46%, p=0,029) apresentou menores taxas de infecção (0 versus 4 ,p<0,03), comparado ao grupo Ringer lactato. Conclusões: Em cirurgia de artroplastia total de quadrill, a hemodiluição com hidroxietilamido resultou em maiores taxas de sangramento, menos transfusões sanguíneas e menos infecção pós-operatória. / Introduction: Hydroxyethyl starches (HES) are considered effective plasma expanders in patients undergoing major surgeries. However, the clinical use of HES is limited mainly by their affection of hemostasis, detectable by impaired platelet function and altered coagulation. The extent of such alteration has classically been related to the molecular weight or molar substitution of the used HES solution. This prospective, randomized study was performed during hip arthroplasty in adult patients under spinal anesthesia to compare the effects of HES 130/0.4 with lactateds Ringer solution regarding intraoperative bleeding, hemodynamic parameters, coagulation profile, transfusion requirements and clinical outcomes. Methods: Forty eight patients scheduled to hip arthroplasty after spinal anesthesia were randomized in two groups 24 patients were allocated to receive HES 130/0.4 (30 ml/Kg just after anesthesia) and 24 patients were signaled to receive lactateds Ringer solution (30 ml/Kg). The observational period started after the induction of anesthesia and finished 5 hours after the end of the surgery. During this period, the triggers for infusion of additional boluses of fluids (10 ml/Kg of lactateds Ringer for both groups) were a systolic blood pressure lower than 90 mmHg and/or a decrease of 20% from baseline, a heart rate higher than 100 bpm, and/or a urine output lower than 0.4 ml.Kg-1.h-1. Vasopressors were used if there was persistent hypotension despite of fluid reposition. Red blood cell transfusion was administered if patient remained unstable despite of additional boluses of Ringer or vasopressors, according to the preestablished triggers. Hemodynamic measurements were done in three periods of the surgery, biochemical parameters were analyzed and coagulation tests were performed and compared between groups. After surgery, patients were followed during the hospital stay. Results: The groups were well matched regarding demographic data, type of surgery, and duration of surgery, as well as preexisting diseases. No significant differences in hemodynamic or body temperature were seen during the study. Coagulation variables, platelet function, gases analysis and biochemical parameters were not different between groups. Blood losses were significantly higher in HES 130/0.4 group comparing to Ringers group (1296 x 890 ml, p= 0.046). Despite of that, HES group required less units of blood in the observational period comparing to Ringer group (17% versus 46%, p=0.029). HES group presented lower infection rate compared to Ringer group (0 versus 4 cases, p=0.03). Conclusions: During hip arthroplasty, hemodilution with hydroxyethyl starch 130/0.4 resulted in higher rates of bleeding. However, patients treated with hydroxyethyl starch required less transfusion and presented lower rate of infection.