Four and a half years experience with a vertical flow sterile enclosure

Summary During the use of a vertical flow enclosure of our own design for almost five years, bacteriological studies and the infection rates in different groups of patients have taught us the following:1. In a clean room operating theatre, the use of a respired air exhaust system improves the sterility compared with the use of ordinary masks. In a vertical flow enclosure, the chest, the arms, and the hands of the team are contaminated from respired airborne bacteria if helmets, etc., are not worn.2. In our vertical flow enclosure with almost continuous absolute sterility of the air, the infection rate in primary total hip replacement is very low and less than 1%, including early and late infections. Antibiotics have not been used.In secondary surgery, i.e., total hip replacement in hip joints previously operated upon, the infection rate is markedly higher, probably because of a flare-up of latent infection.Clean room surgery therefore, can only prevent air borne contamination, and no more; but this is very valuable.3. Vertical flow enclosures of the Charnley-Howorth (1975) and Weber et al. (1971) type provide considerable improvement in sterility of the air compared with adaptations of more conventional theatres. We recommend that these facilities be made available for implant surgery. It is also necessary to have a stringent operational policy with cooperation and discipline on the part of all members of the theatre team.

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Résumé Durant l'utilisation, depuis plus de 5 ans, de la serre stérile à flux laminaire vertical que nous avons construite, nous avons pratiqué des études bactériologiques et pu comparer les taux d'infection suivant les groupes de patients.1. Dans une salle d'opération propre, la stérilité est considérablement améliorée par le port de casques possédant un système d'aspiration de l'air expiré, ceci par rapport au port de masques ordinaires. De plus, si l'on ne porte pas le casque dans une serre à flux laminaire vertical, le tronc, les mains et les membres supérieurs de l'équipe chirurgicale sont contaminés par les microbes en suspension dans l'air expiré.2. Dans notre serre où l'air est pratiquement stérile, le taux d'infections précoces et tardives est inférieur à 1% dans les arthroplasties de la hanche, et cela sans utilisation d'antibiotiques.Lors d'interventions dites secondaires, c'est-à-dire dans les cas déjà opérés au préalable, par exemple par ostéotomie, ostéosynthèse, etc., le taux d'infection est plus élevé. On doit probablement en rechercher la cause dans une contamination de la plaie lors de la première intervention, l'infection alors à l'état latent pouvant se réveiller à la faveur d'une nouvelle opération.En opérant dans une serre stérile, on peut donc prévenir la contamination par l'air ambiant, mais pas plus. Cela est cependant déjà très appréciable.3. Comparées aux salles d'opération conventionnelles modernes, les serres stériles à flux laminaire vertical, comme celle de Charnley-Howorth (1975) et Weber-Meierhans (1971), améliorent considérablement la stérilité de l'air. Surtout pour la chirurgie prothétique de la hanche, dont les risques d'infection sont élevés, nous recommandons l'emploi de ce genre d'installation. Mais il est nécessaire que tous les membres de l'équipe chirurgicale adoptent des règles très strictes de discipline.

     

RELATIONSHIP BETWEEN CORNEAL DELLEN AND TEARFILM BREAKUP TIME

The BUT of 51 strabismus patients were measured before and after operation. The average pre-op BUT was 28.75 seconds(10.96"-91.80"). The post-op BUT in all operated eyes were reduced significantly, no matter what procedures had been performed and whether dellen appeared or not(P<0.01). The BUT in the group complicated dellen reduced from 23.22"(pre-op) to 8.61"(post-op). The incidence of dellen was 22.54% in this study. The incidence of dellen after rectus resection procedure(47.75%) was much higher than that after rectus recession(5.13%)(P<0.01). This study showed that dellen was closelyre related to the BUT and occurred more often in the eyes on which resection procedure was performed. It is considered that excessive lacrimation and elevation of the bulbar conjunctiva near the limbus may disturb the stability of the precornea tearfilm and cause the tearfilm break up earlier. Local corneal dehydration and dellen formation may be caused by reduced BUT. The incidence of dellen after operation may be higher if the cornea was carefully observed.     

Quality control of surgical technique in a multicenter, prospective, randomized, controlled study on the surgical treatment of gastric cancer.

To evaluate the effect of lymph node dissection on gastric cancer patients operated upon with curative intent, we are carrying out a multicenter, prospective, randomized, controlled study in the Netherlands. The trial compares conventional gastrectomy to gastrectomy with extended lymph node dissection. In the first four months, a Japanese supervisor attended all the extended surgery and instructed many Dutch surgeons, including the eight consulting surgeons; since then, all extended gastrectomies have been attended by one of the consulting surgeons. The study coordinator attended all conventional cases. This assured that the quality of the extended surgery was as good as the Japanese standard, of which excellent results have been reported. To achieve this quality control, randomization before surgery was obligatory for practical reasons. Curability assessment at laparotomy, however, is done quite objectively with histological proof, except for the judgement of irresectability. Although this has resulted in many non-curative cases being randomized but subsequently not given the allocated surgery, the sample size should be sufficient to allow analysis according to randomization or the initial "intention to treat." This is the first protocol for a multicenter trial in surgical oncology to have such excellent surgical quality control and to assure a quality as high as that in the original report with uniformity in the level of technique. In studies comparing surgical techniques, it is vital that attention should be given to surgical quality control, otherwise survival rates may show little improvement and fail to make any impact on surgical practice.     

Pediatric surgery in the Renaissance period

The emergence of surgery during the Renaissance marked the birth of surgery as a discipline based on clinical observation and improvement of technical skill. Some of the most experienced surgeons dealing with pediatric problems were Paré, Phaer, Würtz and, especially, Hildanus, who described more than 150 cases in children. Some minor malformations were curable, and some major anomalies were described for the first time. Renaissance surgeons had no explanations for the etiology of diseases and malformations. In many instances, the imaginatio was considered to be responsible.     

Intramedullary spinal cord ependymomas — a study of 45 cases with long-term follow-up

Summary Of the 62 patients with intramedullary spinal cord ependymoma treated surgically at our Neurosurgery Division between January 1951 and December 1990 45 had a follow-up of at least 3 years and the longest 30 years. The 28 conus-cauda equina-filum ependymomas operated during the same period are not considered in this study. An analysis of our cases and of the larger published series shows that favourable prognostic factors, apart of course from total tumour removal, which is now usually possible, are a site below the high cervical segments and a mild pre-operative symptom pattern. Patient age at diagnosis, tumour size and low dose (< 40 Gy) radiotherapy seem to have no influence on the prognosis. Aggressive surgical removal is the treatment of choice and also for long-term recurrence.     

Craniocervical junction malformation treated by transoral approach. A survey of 25 cases with emphasis on postoperative instability and outcome

Summary An experience with 25 consecutive cases of craniocervical junction (CCJ) malformations operated upon via the transoral route is reported. Twenty-two patients also underwent posterior occipitocervical stabilization with alloplastic material and in only one patient was transoral odontoidectomy and fusion with bone autograph performed.Indication for the transoral route consisted of an irreducible ventral compression of the cervicobulbar junction by the abnormal bone complex.Two patients died during the early postoperative period and the remaining 23 survivors were followed for an average of 3.5 years: 17 of these showed marked improvement and 5 a stabilization of the neurological disturbances. A further patient, who refused posterior stabilization, eventually died because of progressive cranial settling.Long-term results have shown this approach to be decisive in the surgical management of well-selected CCJ anomalies.     

Local anesthesia in reduction mastoplasty for out-patient surgery

To perform a breast reduction under local anesthesia we need a large amount of anesthetic with lasting effects. For this I use a solution of 25 cc of lidocaine, 25 cc of bupivacaine, and 1 cc of epinephrine in 350 cc of saline solution. The bupivacaine allows a 4–6-hour operation. Once the breast is infiltrated, a great amount of anesthetic is lost in the incision, in the dissection, and in the resected tissue. Thus, a low dose remains subcutaneously to be metabolized by the liver. The serum lidocaine levels are low during these operations, as demonstrated by fluorescence polarization immunoassay. Under analgesic sedation the submammary sulcus and the retroglandular space are infiltrated, blocking the perforants of the intercostal nerves, under the areola, beneath the skin where the incision is made and where the aerola is placed. This procedure has been applied to many techniques of breast reduction by modifying the infiltration under the incision lines. For hypertrophy up to 1000 g, 200–300 cc of anesthetic solution is used for both breasts at one stage, while for gigantomastia, about 400 cc of anesthetic is used, infiltrating and reducing one after the other. As the blood loss is minimal and the recovery very fast, with an appropriate adhesive bandage and a soutien, the patient could be discharged in the afternoon. Our experience includes 94 reduction mastoplasties with local anesthesia, and also 74 other mastoplasties with equally good results. There were no patient complaints and, in general, they felt very comfortable, awakening without pain or side effects.     

The Rationale and Results of Gastroplasty/Distal Gastric Bypass

A recent review of the results of gastroplasties done at the University of Alberta Hospital showed that there was a high incidence of late weight loss failure. Therefore a new operation, gastroplasty/distal gastric bypass, has been performed on 263 patients. This operation results in a profound (mean greatest percentage excess weight loss of 87% at approximately 2 years) and lasting weight loss (mean final percentage excess weight loss of 78%) at 4 years, range 2-7.5 years post-operatively. Only 0.9% of patients failed to maintain at least a 40% excess weight loss. The operation achieves its effect through a moderate restriction that permits patients to eat normal table food from the time of discharge and with a mild malabsorption that is not ordinarily associated with diarrhea or notable deficiencies. Certain patients required debanding of the stoma and others developed staple-line eventration. Neither of these events after long-term follow-up resulted in weight loss failure nor in other serious side-effects. It is concluded that moderate failure of the gastroplasty stoma and staple line does not necessarily result in weight loss failure, because the malabsorptive portion of the operation remains intact. Low hemoglobin occurred in 16% of cases and deficiency of serum iron in 34%; a much smaller number of patients had chronic or intermittent deficiencies of these entities. Correction was easily achieved with oral replacement. Deficiencies in albumin, calcium, phosphorus and folate were rarely seen and minimal elevation of serum AST values occurred in just over 1% of patients. Chronic deficiencies or elevations were not seen in these patients. Stomal ulcer occurred in 6% of patients and bleeding associated with stomal ulcer in 1%. Half the patients with ulcer were managed with H₂ blockers, the other half with vagotomy. Both forms of treatment when individualized effectively prevent re-ulceration.     

Revisional Surgery for Severe Obesity with Fascia Banded Stoma Roux-en-Y Gastric Bypass

The fascia banded stoma Roux-en-Y gastric bypass (RYGBP) has been effective both as a primary and revision operation for severe obesity or failure of another operation. Since May 1984, 361 primary and 100 revisional fascia banded RYGBP operations have been reported. Weight loss achieved a mean body mass index of 30 for primary and 31 for revision patients at most recent follow-up of 3-6 years (mean 4.3 years) postoperatively. Mean overweight was 28% for primary, and 34% for revision patients. Eighty percent of primary and 79% of revision patients were within 50% of ideal weight. Revision rates for these patients were 0 for primary and 1% for revision patients. Operative mortality was 0 for primary and 1% for revision patients. Since morbidity and mortality, although low, are higher for revision than primary surgery, it is important to use an effective primary operation.