PURPOSE: To test the hypothesis that needlescopic cholecystectomies (NC) offer superior outcomes in comparison to common laparoscopic cholecystectomies (LC). METHODS: Sixty consecutive patients with gallbladder disease undergoing either LC or NC were evaluated with respect to differences in operative time, frequency of per-operative incidents, post-operative pain, late postoperative symptoms, length of scars and level of postoperative satisfaction. RESULTS: Mean operative time was similar in both groups. Most of the patients, irrespective of the technique, informed mild postoperative pain. NC patients had lower levels of pain on the 7th postoperative day (PO7) (p<0.01) and decreased need for additional analgesia. Less frequency of epigastric wound pain was observed in NC patients until PO4 (p<0.01). Aesthetic result was far superior after NC (total length of scars less than half after LC). No differences regarding postoperative satisfaction with the operation were observed between the studied groups. CONCLUSIONS: Both techniques were safe and effective, presenting similar operative times and low levels of postoperative pain. Downsizing the ports to 2-3 mm was associated with significantly less frequency of postoperative pain only in the epigastric wound until PO4. Aesthetic outcome of NC was significantly superior to LC, although this advantage did not influence patient level of satisfaction.
Cholecystectomy, Laparoscopic; Pain Postoperative
OBJETIVO: Testar a hipótese de que colecistectomias agulhascópicas oferecem resultados superiores aos da colecistectomia laparoscópica usual (CL). MÉTODOS: Sessenta pacientes consecutivos com colecistopatia submetidos à CA ou CV foram avaliados quanto ao tempo operatório, freqüência de acidentes peroperatórios, dor pós-operatória, sintomas pós-operatórios tardios, comprimento das cicatrizes e grau de satisfação. RESULTADOS: O tempo operatório médio foi semelhante em ambos os grupos. A maioria dos pacientes, independentemente da técnica, relataram dor pós-operatória leve. Aqueles operados por CA tiveram menores níveis de dor no 7º dia de pós-operatório (PO7) (p<0.01) e menor necessidade de analgesia adicional. Menor freqüência de dor epigástrica foi observada no grupo CA até o PO4 (p<0.01). O resultado estético foi amplamente superior após CA (comprimento total das cicatrizes menor que a metade após CL). Não houve diferença quanto ao grau de satisfação entre os grupos. CONCLUSÕES: As duas técnicas foram seguras e eficazes, apresentando tempos operatórios semelhantes e baixos níveis de dor pós-operatória. A redução dos portais para 2-3 mm associou-se a menor freqüência de dor pós-operatória apenas na incisão epigástrica até o PO4. O resultado estético da agulhascopia foi significantemente superior ao da laparoscopia, apesar desta vantagem não ter influenciado o grau de satisfação dos doentes.
Colecistectomia Laparoscópica; Dor Pós-Operatória
12 - TECHNICAL SKILL
Needlescopic versus laparoscopic cholecystectomy. A prospective study of 60 patients1 1 Research performed at Federal University of Amazonas (UFAM) and Hospital of Royal and Benevolent Portuguese Society of Amazonas, Manaus, Brazil.
Colecistectomia agulhascópica versus colecistectomia laparoscópica. Um estudo prospectivo de 60 pacientes
Pedro Henrique Oliveira CabralI; Ivan Tramujas da Costa e SilvaII; Janaína Vieira MeloIII; Felicidad Santos GimenezIV; Celso Rômulo Barbosa CabralV; Ana Paula Calheiros de LimaVI
IMD, Resident in General Surgery, Santa Casa de São Paulo, Medical Sciences Faculty (FCMSCSP), Brazil
IIAssistant Professor, Department of Surgery, Medical College, UFAM, Manaus, Brazil
IIIMD, Anesthesiologist, Hospital of Royal and Benevolent Portuguese Society of Amazonas, Manaus, Brazil
IVMD, Surgeon at University Hospital, UFAM, Manaus, Brazil
VPhD, Department of Statistics, UFAM, Manaus, Brazil
VIMD, Resident in Internal Medicine, University of Campinas (UNICAMP), Sao Paulo, Brazil
PURPOSE: To test the hypothesis that needlescopic cholecystectomies (NC) offer superior outcomes in comparison to common laparoscopic cholecystectomies (LC).
METHODS: Sixty consecutive patients with gallbladder disease undergoing either LC or NC were evaluated with respect to differences in operative time, frequency of per-operative incidents, post-operative pain, late postoperative symptoms, length of scars and level of postoperative satisfaction.
RESULTS: Mean operative time was similar in both groups. Most of the patients, irrespective of the technique, informed mild postoperative pain. NC patients had lower levels of pain on the 7th postoperative day (PO7) (p<0.01) and decreased need for additional analgesia. Less frequency of epigastric wound pain was observed in NC patients until PO4 (p<0.01). Aesthetic result was far superior after NC (total length of scars less than half after LC). No differences regarding postoperative satisfaction with the operation were observed between the studied groups.
CONCLUSIONS: Both techniques were safe and effective, presenting similar operative times and low levels of postoperative pain. Downsizing the ports to 2-3 mm was associated with significantly less frequency of postoperative pain only in the epigastric wound until PO4. Aesthetic outcome of NC was significantly superior to LC, although this advantage did not influence patient level of satisfaction
Key words: Cholecystectomy, Laparoscopic. Pain Postoperative.
OBJETIVO: Testar a hipótese de que colecistectomias agulhascópicas oferecem resultados superiores aos da colecistectomia laparoscópica usual (CL).
MÉTODOS: Sessenta pacientes consecutivos com colecistopatia submetidos à CA ou CV foram avaliados quanto ao tempo operatório, freqüência de acidentes peroperatórios, dor pós-operatória, sintomas pós-operatórios tardios, comprimento das cicatrizes e grau de satisfação.
RESULTADOS: O tempo operatório médio foi semelhante em ambos os grupos. A maioria dos pacientes, independentemente da técnica, relataram dor pós-operatória leve. Aqueles operados por CA tiveram menores níveis de dor no 7º dia de pós-operatório (PO7) (p<0.01) e menor necessidade de analgesia adicional. Menor freqüência de dor epigástrica foi observada no grupo CA até o PO4 (p<0.01). O resultado estético foi amplamente superior após CA (comprimento total das cicatrizes menor que a metade após CL). Não houve diferença quanto ao grau de satisfação entre os grupos.
CONCLUSÕES: As duas técnicas foram seguras e eficazes, apresentando tempos operatórios semelhantes e baixos níveis de dor pós-operatória. A redução dos portais para 2-3 mm associou-se a menor freqüência de dor pós-operatória apenas na incisão epigástrica até o PO4. O resultado estético da agulhascopia foi significantemente superior ao da laparoscopia, apesar desta vantagem não ter influenciado o grau de satisfação dos doentes.
Descritores: Colecistectomia Laparoscópica. Dor Pós-Operatória.
Laparoscopic cholecystectomy (LC) was firstly considered the gold-standard operation for gallstone disease in 19921, mainly because of the advantages brought about by the minimally invasive techniques it began to employ1. Since then, several technological developments have been achieved, some of them comprising an increasing interest towards attempting to reduce even further the surgical trauma by diminishing the caliber of the instruments. As a result of these initiatives, Gagner and Garcia-Ruiz2 introduced the term "needlescopic" for operations performed with laparoscopic instruments up to 3 mm in diameter, a definition which has been adopted by other authors2,3,4.
In recent years, an increasing number of papers have advocated this technique as feasible for a variety of abdominal procedures, including appendectomies, adrenalectomies, splenectomies, gastric fundoplications, urologic procedures and cholecystectomies4-7. There is some controversy, though, regarding the benefits of needlescopic cholecystectomy (NC), for some surgeons consider it a natural evolution of LC8, while others contend that tissue trauma in needlescopic cholecystectomy (NC) is not significantly reduced, for the 5 mm ports of LC are already minimal and no benefit can be achieved from further reduction. It is also argued that NC is more troublesome and time consuming, and that visceral pain resulting from removal of the gallbladder is similar for both procedures3,9,10.
Prospective trials comparing LC and NC have shown conflicting results, especially concerning postoperative pain. Look et al.11 randomized 64 patients and evaluated pain using a five-grade scale, concluding that there were no differences between the techniques in terms of postoperative pain, safety, operative time and functional recovery11. Other authors had similar findings12. Conversely, Cheah et al.13 assessed postoperative pain among 75 patients using a 10-grade visual pain scale and found NC was less painful, in agreement with other trials14-16.
In Brazil, Carvalho et al.17 reported the results of 719 NC and found no differences in morbidity or mortality compared to LC. However, this was a retrospective uncontrolled series and other relevant aspects, such as postoperative pain and satisfaction, were not compared.
Due to these inconsistent results in the literature and because of the small number of regional trials on needlescopic surgery, the authors undertook this prospective controlled trial of 60 patients to evaluate if NC offers superior outcomes in comparison to LC.
Inclusion and exclusion criteria.
In a non-randomized, prospective, controlled trial, 60 patients from the private clinic of one of the authors (ITCS) were consecutively operated on from January 2005 to March 2006. Patients with symptomatic cholelithiasis or gallbladder polyps were included, in the absence of the following): 1) clinical, ultrasonographic or intraoperative signs of acute cholecystitis; 2) prior surgical procedures in the upper abdomen; 3) need to enlarge one of the incisions during the laparoscopic procedure; 4) Body Mass Index (BMI) > 35 kg/m2; 5) contraindication to the anaesthetic protocol adopted; 6) Previous episodes of pancreatitis.
Patients were assigned either to NC or LC groups according to their intention to undergo elective needlescopic or laparoscopic cholecystectomy, after a careful explanation of the technical aspects of each one of the procedures. The above mentioned strict admittance criteria were used as an attempt to equalize baseline characteristics and make the groups comparable, for randomization was not possible due to the characteristics of the studied population (from a private surgical practice), for many patients were referred for consultation willing to be operated by the needlescopic technique.
Surgery and anaesthesia
All the operations were performed by the same surgical team according to a standardized technique described elsewhere18. Four ports were used in both groups (umbilicus, epigastrium, right hypochondrium and right flank), with the following dimensions: 12 mm, 10 mm, 5 mm and 5 mm, respectively, for the LC group; and 12 mm, 2 mm, 2 mm and 3 mm, respectively, for the NC group. For the needlescopic procedure, a second camera was employed with a 2 mm needlescope in the epigastric port for controlling the sealing of the cystic artery and cystic duct with titanium clips through the umbilical port with a 10 mm clip applier. The division of the ligated structures was subsequently done with single use 2 mm scissors in the epigastric port after reintroducing the 10 mm laparoscope in the umbilical port. The 10 and 12 mm aponeurotic wounds were closed with simple inverted "figure-of-8" stitches using nonabsorbable polypropylene monofilament sutures, while needlescopic incisions were simply coapted with sterile surgical adhesive tape.
General anesthesia was also standardized: induction with usual doses of fentanyl and a hypnotic drug (either etomidate or propofol) and maintenance with isoflurane or halothane. On anaesthetic induction, cefazolin (2 g) was infused for antimicrobial prophylaxis. All incisions were infiltrated with bupivacaine 0.25% and an antiemetic drug was administered (ondansetron, 4 mg) on completion of the procedure. The same dressings were applied throughout the study.
Postoperatively, all the patients were allowed to resume oral intake soon after full recovery from anesthesia, as long as no intraoperative incidents had occurred. Intravenous (IV) dipyrone (1 g q.i.d.) and tenoxicam (20 mg b.i.d.) were systematically prescribed for postoperative analgesia and meperidine was also administered according to the request of each patient. After discharge from hospital, the patients were prescribed oral tenoxicam 20 mg b.i.d. and were allowed to take dipyrone ad libitum (up to 500 mg q.i.d.).
Assessment of variables
Data was collected by two observers (PHOP, ACPL) throughout the study. Operative time, from the first umbilical incision up to the last skin suture needed for wound closure, and intraoperative incidents were recorded for each surgery. On the first postoperative day (PO1), the following outcomes were collected: 1) overall pain intensity and presence or absence of pain in the port sites; 2) nature of postoperative symptoms; 3) surgical wounds condition, including presence of secretion and inflammation; and 4) number of doses of meperidine required for additional analgesia.
All patients were discharged from hospital within 24 hours after surgery and were given a protocol form to be completed daily with scores of intensity of wound pain and with the number of dipyrone tablets needed for pain relief.
Each patient was interviewed daily by telephone contact until PO7, being asked about the presence or absence of pain in each individual port site. On PO8, each patient came back for consultation with the surgeon, returning the completed Protocol Form. Complete clinical evaluation was again performed.
The overall postoperative pain intensity from PO1 to PO7 was assessed through a 6-level visual pain scale (Wong-Baker scale)19, in which level zero means no pain and score 5 means the worst possible pain (arithmetic means for each group were calculated for comparison). The pain intensity was also categorized as mild, moderate and severe for additional analysis.
Three months after surgery, each patient was visited at home and the length of their visible scars (epigastrium, right hypochondrium and flank, excluding the umbilicus) was measured with a pachymeter. The level of satisfaction (from 0 to 10) was also evaluated for comparison.
Statistical analysis and ethics
Collected data were included in an electronic spreadsheet (Microsoft Excel®). For categorized variables, Fisher's exact and Chi-squared tests were used. The continuous variables were compared after calculation of the arithmetic means using Student's t test, considering that data had a normal distribution. Results were considered statistically significant when p < 0.05. This trial was submitted and approved by the Ethics Committee of the Federal University of Amazonas.
Eighty-eight patients were operated on along 14 months, of which 28 were excluded and 60 were included for analysis. Acute cholecystitis (nine patients) and non-adherence to some aspect of the protocol such as hypersensitivity to a standardized drug (10 patients) were the chief reasons for exclusion. Only eight cases were excluded by the need of conversions: seven from needlescopic to common laparoscopic surgery and one requiring open surgery because of an intra-hepatic scleroatrophic gallbladder. Another patient was excluded because of previous upper abdominal operation.
Baseline characteristics were similar in both groups (Table 1). Most patients were middle-aged women.
There was no significant difference in the mean operative time between the groups: 43.6 min for LC and 44.9 min for NC (p=0.90). Intraoperative incidents occurred in 25% of the patients, presenting equal distribution in the two groups (Table 2). They were not serious and all the patients received oral feeding after recovery from anesthesia and were discharged from hospital in the first postoperative day.
Most patients classified their overall postoperative pain as mild and no difference was found between NC and LC until PO5 (Table 3). However, NC patients presented a tendency of faster recovery from pain and statistical significance was observed on PO5 and PO7. In the latter, for example, more than 90% of NC patients referred no pain. When the mean pain scores (instead of categorized pain) were compared, this pattern could again be observed (Figure 1).
Fewer patients informed pain in the epigastric port (p < 0.01) in the NC group (Figure 2). The frequency of pain at the other port sites tended to be lower for the needlescopic technique, but no statistical difference was found (Table 4).
There was no difference concerning requirement of additional on-demand doses of meperidine in the immediate PO period, but NC patients consumed less dipyrone tablets after discharge from hospital (p=0.05) (Table 5).
Regarding the esthetic result 3 months after surgery, NC was superior to LC as the total length of needlescopic scars was 165% shorter than LC (Table 6).
During the initial three months of postoperative follow-up, late symptoms developed in 12 (20%) patients. The most common was some degree of fatty foods intolerance (eight patients). Three patients complained of mild upper right abdominal quadrant discomfort and one patient presented exacerbation of the gastrocolic reflex. There was no instance of postcholecystectomy syndrome (Table 7).
One late postoperative complication did occur in a patient with umbilical port wound infection and abscess formation, on PO30. This patient presented leukopenia and was subsequently diagnosed as having a myelodysplastic syndrome.
Overall, most of the patients were satisfied with the operation and no significant difference was found between the groups (Table 8).
No randomization was undertaken in this series due to the characteristics of the studied population (derived from the private practice of one of the authors - ITCS). In order to partly compensate this drawback so as to decrease its influence on the power of evidence of the compiled data, a well-known valuable tool (restriction) was used to make the groups comparable and the results as trustworthy as they could be20,21. The results were analyzed per protocol, after exclusion of 7 converted cases (NC to LC), rather than on an intention to treat basis. This design was deemed favorable because the purpose was to compare the outcome of successful NCs to successful usual LCs.
Operative time length is an important factor to be considered when comparing surgical procedures. A shorter time is theoretically beneficial for it reduces the anesthetic time, is prone to less bleeding, less third space fluid shift and, specifically in videolaparoscopic surgery, less exposure to carbon dioxide11,13.
Huang et al.12 conducted a comparative trial between NC and LC and stated that needlescopic procedures were about 30 minutes longer. However, that represented the initial experience of the surgeon who conducted the study. On the other hand, other authors have reported no differences in operative times regarding NC in comparison to LC11 demonstrating the importance of an experienced surgical team on the individual technique employed. Cheah et al.13, for example, studied 150 patients and stated that their conversion rate was lower for the last 50 patients they had operated, reflecting the experience acquired with the operations of their first 100 patients. The surgical team which undertook the present study had already performed more than 280 needlescopic procedures prior to evaluating this series of patients, and this stage of the team's learning curve certainly favored the outcomes.
Needlescopic instruments do impose some difficulties for manipulation and visualization of the surgical field, as well as for grasping fibrotic and edematous tissues2. The instruments are sharp-pointed and the 2 mm optic, important for visualization of cystic duct and vessels clipping during NC, has less resolution and illumination capacity3,11,14,15. These are aspects reported by some authors as responsible for intraoperative complications during needlescopic procedures (especially gallbladder wall and liver parenchyma perforation) as opposed to LC. However, in the present study, in analogy to others in the literature, intraoperative incidents were not more frequent during needlescopic procedures9. In this series, intraoperative incidents were all minor and could be corrected by the operative technique that was being used, contributing only to an increase in the operative time. There was no instance of severe complications such as biliary tract or hepatic artery injuries, associated with any of the techniques employed and there were no deaths up to three months of follow-up. Lai et al.13, in the greatest series of the literature, performed 1,011 NC with a major complication rate of 1%.
All of the patients studied herein were discharged from hospital after an overnight-stay, a practice that was proven to be safe and cost-effective22. No re-hospitalizations were needed up to 3 months of follow-up. These results emphasize that NC and LC are equally safe for patients who undergo cholecystectomy, assuming that characteristics that can render the procedures more difficult, such as cholecystitis or previous upper abdominal surgery, are absent.
These favorable results are due to the natural improvement of the technique. The visualization handicap of the 2 mm camera, for example, has been overcome by the use of the 10 mm optics up to the critical step of exposure of Calot's triangle for the appropriate dissection of the cystic duct and artery. The needlescopic optics is then employed only to monitor clip occlusion of the isolated structures13.
The multimodal analgesic therapy employed, including local anesthetic infiltration of the wounds, probably contributed to the observed low levels of postoperative pain, which are similar to other published series12,15,23. Look and colleagues found that approximately 60% of the patients they studied had mild pain or were painless, concluding that pain referral was similar after needlescopic or laparoscopic procedures11. However, they assessed pain levels only until PO3. Our study observed a significant difference in pain statement only after PO5. Although there has been at least one report showing less overall PO pain after NC11, the pattern of a more rapid pain recovery among NC patients is a clear finding of this study.
Pain after abdominal surgical interventions is inherently complex and multifactorial, involving visceral, wound and psychological components13. The data herein compiled show that interference in only one of these determinants (the size of the incision) did not affect substantially the overall pain intensity in most of the postoperative period.
Nonetheless, when incisional pain was analyzed separately in each port site, the epigastric port was found to have elicited less pain among NC patients. Theoretically, smaller incisions cause less tissue damage and, consequently, less pain. Therefore, the lower pain scores in the epigastric port of NC patients can be explained by the fact that this is the port where greater incision reduction was obtained (from 10 mm to 2 mm). Accordingly, the umbilical port wound was reported as the most painful, probably because of its larger dimensions and also for being more manipulated during the procedures. When comparing 5 mm to 2-3 mm incisions at the other port sites, the frequency of pain did not differ significantly. In this aspect our results are comparable to those of Huang et al.12.
Of the 60 patients studied, only one (from the NC group) required additional doses of opioid (meperidine) during hospitalization. This is inconsistent with other series in which up to 50% of patients received additional on-demand analgesia12-14,24. Cheah et al.13 showed a mean of seven and 12 doses of meperidine for patients operated on by needlescopic and laparoscopic cholecystectomy, respectively, concluding that the needlescopic group required fewer intramuscular meperidine injections (p=0.05). Nevertheless, in our series, two drugs (instead of one as in the cited trials) were systematically administered as pain relievers, according to the previous experience of this group and this is a reasonable explanation for the observed differences.
Concerning the esthetic outcome, NC was shown to be superior to LC, a reality that has already been demonstrated by others11,13,16,25. In all these studies, the length of the wound was measured early in the postoperative period. Our study was designed to evaluate the influence of the healing process on the size of the scars, so the measurements were done 90 days after surgery. NC was far superior to LC regarding length of residual scars three months after the operation. Notwithstanding this remarkable advantage, LC patients were as satisfied with the result of the operation as the patients pertaining to the NC group, implying that esthetic satisfaction may be but one of the expectations to be fulfilled by patients submitted to cholecystectomies.
For patients with uncomplicated gallstone disease, in this series, NC and LC procedures had similar operative times and were equally safe and effective. Overall postoperative pain intensity was similar for both techniques, although NC proved to be superior to LC in the need for home consumption of on-demand analgesics and in evoking less pain in the epigastric port wound. Nonetheless, despite these advantages and the better cosmetic results observed for NC patients at PO90, no difference in the degree of satisfaction with the procedure was detected between NC and LC groups.
Received: May 14, 2008
Review: July 15, 2008
Accepted: August 18, 2008
Conflict of interest: none
Financial source: none
How to cite this article
Cabral PHO, Silva ITC, Melo JV, Gimenez FS, Cabral CRB, Lima APC. Needlescopic versus laparoscopic cholecystectomy. A prospective study of 60 patients. Acta Cir Bras. [serial on the Internet] 2008 Nov-Dec;23(6). Available from URL: http://www.scielo.br/acb
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Correspondence:Ivan Tramujas da Costa e SilvaDepartment of SurgeryMedical College of the Federal University of AmazonasR. Afonso Pena, 58969020-160 Manaus - AM BrazilPhone: (55 92)3233-9730Fax: (55 92)3232-3411
Research performed at Federal University of Amazonas (UFAM) and Hospital of Royal and Benevolent Portuguese Society of Amazonas, Manaus, Brazil.
Publication in this collection
12 Nov 2008
Date of issue
18 Aug 2008
15 July 2008
14 May 2008