To investigate any intra-operative alteration in management in those patients who had a pre-operative echocardiogram, a retrospective study for one year (March 2004 to February 2005) was carried out at West Middlesex University Hospital. Total number of 176 hip fractures, echocardiogram was done pre-operatively in 22 patients (12.5%). The request for echo was given by the anaesthetic team in 18/22 patients, the commonest reason for request being a cardiac murmur detected clinically in 20/22 patients. There was a delay in surgery more than 24 hours in 17/22 patients who had an echocardiogram (77%) compared to a 38% delay in patients who did not. The echocardiogram findings showed significant aortic stenosis in 4/22 (18%). There was no cancellation of surgery due to echocardiogram findings Five had general anaesthetic. There was alteration in intra-operative management in two out of the 22 patients (8%) Invasive arterial monitoring was used in those two patients. None had intra-operative complications or ITU/HDU care post-operatively. Post-operatively 6/22 developed complications. 15/22 patients had a delay in discharge (68%) of more than 21 days compared to the 41% delay in patients who did not have an echocardiogram. We had a mortality rate of 22.7% (5/22) in these patients at 1 month compared to a mortality rate of 12% in patients without echocardiogram.Aim
Results
Percutaneous A1 pulley release is being increasingly used as an alternative to open surgical release and injection of local steroids for the treatment of the trigger digit. We treated 43 patients, average age 57 years (range12-78). All trigger digits were grade III-IV (Quinnell classification). A mean duration of pre-operative symptoms was 7.3 months (range 2-13 months). A percutaneous release was performed with a 19-gauge hypodermic needle under local anaesthesia in the outpatient setting. All patients were evaluated with respect to clinical resolution of symptoms and general satisfaction. We report a 97% successful release and only one case of incomplete release. A result in terms of abolishing triggering was immediate and patient acceptance was excellent. By two weeks, all the patients had no pain at the operative site. After a mean follow-up of 30.2 months (range12-50), there had been no recurrences. There were no digital nerve injuries, flexor tendon injuries, and infections. The percutaneous release is a safe and effective technique, which provides significant cost savings. The time from onset of symptoms and grading prognostically is significant and affects the treatment outcome. We recommend the percutaneous technique for typical cases of trigger finger with a palpable nodule and reproducible mechanical triggering. This technique can be the treatment of choice for the established trigger finger (grade III and IV) with symptoms of more than few months' duration. The open technique is reserved for complicated cases such as florid tenosynovitis, locked digit, failed percutaneous release or those involving the thumb.
Ostoearthritis of the trapeziometacarpal (TMC) joint, the key joint in thumb opposition, is one of the most common diseases involving the hand, especially among middle-aged and elderly women, and can seriously impair overall hand function.
A Jamar dynamometer was used to assess the grip and pinch strengths which showed a 63% of recovering of the grip strength. Overall survival after a mean follow up of 36 months was 93%. At final follow up mean Quick DASH score was 27.4 Radiological review of the surviving joints showed subsidence of trapezial component in 4 joints and further lucencies in 3 joints. However, these patients had good hand function and grip strength. No sign of osteolysis was seen in any of the cases. We found that the radiological findings did not correlate with clinical findings. Satisfaction rate was 26 good to excellent, with 5 fair and 3 poor.
Plasma D-dimer levels were measured as a prerequisite test in all patients before undergoing VQ scan to confirm the absence of PE. All patients had either mechanical, such as foot pumps, or chemical DVT prophylaxis.
The classical triad of dyspnoea, pleuritic chest pain and haemoptysis occurred in only 2 patients. Signs of DVT were present in 3 patients. The electrocardiographs were normal in only 4 patients, though changes particularly suggestive of PE (S1Q3T3, Right bundle branch block or right heart strains) were absent in all of the patients. Chest X-ray changes were of limited value. None showed any of the supposedly characteristic changes. All of the patients had a VQ scan were started on chemical treatment for PE and non of them had definite PE, 12 the patients had probable PE Those patient with probable scan were not subsequently given anticoagulants owing to their medical conditions
Elevated plasma levels of D-dimer have been found to be a useful screening tool in the diagnosis of deep venous thrombosis (DVT) in the general population. In the post operative setting however their role is less clear. The majority of NHS trusts use D-dimer as a prerequisite test prior to radiological imaging to diagnose DVT.
Plasma D-dimer levels were measured pre operatively and on post operative days 1, 3, 5, and 7 in 78 patients undergoing primary total hip or knee arthroplasty. On day 7 patients underwent bilateral duplex ultrasound scanning in order to confirm the absence of DVT. All patients wore pneumatic foot pumps for DVT prophylaxis. Chemical thromboprophylaxis was not used.
Comparing D-dimer levels between hip and knee arthroplasty we found that both groups displayed the same trend in post operative D-dimer levels; however levels were significantly higher following knee replacement. We compared D-dimer levels of these patients with a second group of 43 patients who had a confirmed DVT following hip or knee arthroplasty. The mean D-dimer level in this group was 2.20 (sd=0.98 or range 0.80 – 4.46). This group was subdivided into two groups, those with D-dimer samples before day 8 and those after. We found a significant difference between the groups (p=0.01). Mean <
day 8 = 2.70. Mean ³ day 7 = 1.97. The group of patients with Confirmed DVT before day 8 were compared with those free of clot. There was no significant difference found between the D-dimer levels of the two groups. (p=0.37).
Soft tissue tumours on the sole of the foot are rare and difficult to diagnose, we report a series of five patients who presented with a late diagnosis of a soft tissue tumour on the soles of their feet. We reviewed the notes of five patients who presented with lesions on the soles of their feet. There were 3 males and two females with an age range from 35yrs to 78 yrs. Our results showed that there was at least a one year delay in their diagnosis from their initial symptoms. They all sought medical treatment late, and were all originally diagnosed with benign lesions at their first presentation. All but one, were found to have malignant lesions on biopsy which required surgical excision. As a consequence of the delay in their presentation and diagnosis, there was also a delay in their treatment. Our conclusions are that tumours on the soles of the feet are difficult to diagnose and almost invariably present late.