The impact of intra-operative cell salvage during open nephrectomy

Ned Kinner ＊,Lin Hu Bridget Heijkoop Derek Hennessey ,Dniel Spernt

a Department of Urology,The Queen Elizabeth Hospital,Adelaide,Australiab Department of Urology,Craigavon Area Hospital,Portadown,UK

Abstract Objective:To assess the impact of intra-operative cell salvage on outcomes in open nephrectomy.Methods:A retrospective cohort study was performed of all patients undergoing open nephrectomy for suspected malignancy from 1 October 2013 to 1 October 2017.Patients were grouped and compared based on whether they received intra-operative cell salvage(ICS).Primary outcomes were allogeneic transfusion rates(ATRs),and if histology confirmed cancer,disease recurrence.Secondary outcomes were complications and transfusion-related cost.Results:Forty patients underwent open nephrectomy for suspected malignancy during the enrolment period.Sixteen patients received ICS while 24 did not(standard group).Compared with the standard group,ICS patients had similar median age(63.5 vs.61.0 years;p=0.83)but fewer females(19%vs.58%;p=0.013).The groups were similar in pre-operative and discharge haemoglobin,Charlson Comorbidity Index,length of hospital stay and proportion with thoracoabdominal surgical approach.The ICS group had a smaller proportion undergoing partial nephrectomy(19%vs.54%;p=0.025)and shorter median follow-up(278 vs.827 days;p=0.0005).Histology was malignant for 14 ICS and 15 standard patients.The ICS group had more frequent ≥T2 disease(79%vs.27%;p=0.005).There were no positive margins.Both groups had similar ATRs(6%vs.4%;p=0.96),complication rates(19%vs.29%;p=0.46)and recurrence rates(18%vs.7%;p=0.40).Transfusion costs were higher amongst ICS patients(AUD$878.18 vs.$49.65 per patient).Conclusion:ICS appears safe,with low rates of recurrence and complication.Both groups had low ATRs,and therefore cost benefit for ICS was not seen.

KEYWORDS Nephrectomy;Cell salvage;Autologous;Transfusion;Blood;Cost

1.Introduction

Renal cancer is the second most prevalent urological malignancy,with 338 000 new diagnoses worldwide in 2012[1]and worsening cancer-specific mortality[2].Nephrectomy is the most common treatment,and intra-operative haemorrhage remains a challenge.Even in high volume tertiary centres, allogeneic transfusion rates (ATRs) of 5%—30%[3—6]and 18%—45%[3,5,7]are reported for open partial and radical nephrectomy,respectively.

The development of well run blood banks have made allogeneic transfusion frequent in Western nations,with 14 million and 1.8 million units of red blood cells (RBCs)transfused annually in the USA and UK,respectively[8,9].However,allogeneic transfusion has key issues of morbidity,cost,supply and poorer oncological outcomes.Transfusionrelated acute lung injury, transfusion reactions, fluid overload and clerical error are familiar complications,contributing to an overall adverse event risk of 77 per 100 000 transfusions and death in 1 per 100 000[8].While rare at less than 1 per 1 million transfused RBC units,documented transfusion-transmitted infections (TTIs),bacterial and viral,still occur annually[8—10].Blood is a perishable resource dependent on constant donations,and supply shortages are well known[11].Transfusion is also expensive,with the administration of a single RBC unit costing approximately US Dollars(USD)$1000 in Australia and the USA and USD$600 in Western Europe[12,13].Furthermore,a meta-analysis of patients undergoing nephrectomy has associated allogeneic transfusion with higher cancer specific mortality [14]. The mechanisms involved are unclear,but may involve transfusion mediated immunomodulation[15].

These concerns have encouraged methods to decrease ATRs.Fortunately,the modern urologist has a range of blood conservation techniques at their disposal.These include pre-operative supplementation with iron or erythropoietin,pre-operative autologous donation(PAD),acute normovolaemic haemodilution (ANH), restrictive transfusion thresholds and intra-operative cell salvage(ICS)[16,17].However,each method holds challenges.Pre-operative supplementation is only applicable for patients with iron deficiency or anaemia,requires multiple healthcare episodes for testing,administration and retesting,and may not be cost effective[16].PAD became popular before effective screening existed for TTIs,particularly human immunodeficiency virus.However,PAD is expensive,discards approximately 50%of donated units and is now rarely used [16,18]. ANH involves intraoperative venesection,replacement with crystalloid or colloid,allowing the haemorrhage of dilute blood,then reinfusion of the patient's blood post-operatively.Despite being cost-effective,ANH may make patients hypocoagulable and is also not suitable for patients with pre-existing low haematocrit or cardiorespiratory comorbidities[16,19,20].Restrictive transfusion practices are widely used and have clear benefit[21],but are not appropriate for patients with significant or symptomatic bleeding.

ICS involves the reinfusion of spilled blood.A dual-lumen sucker aspirates blood lost on the surgical field,adds heparinized saline or citrate via the second lumen to prevent coagulation,and stores this in a reservoir.When required,this fluid is washed and centrifuged to obtain a concentrate with haematocrit approximately 60%, passed through a leucocyte depletion filter to remove nucleated cells including bacteria and tumour cells,and reinfused[22].The practice of ICS avoids many of the concerns of allogeneic transfusion.It virtually eliminates TTIs,more cost effective and supply is proportional to demand[8,16].It is safe,with large audits of 18 000—64 000 units of reinfused ICS blood reporting complication rates of ＜0.027%[23—25].Safety and efficacy have been proven in other specialties,with a Cochrane Review of 75 randomised controlled trials in cardiac, vascular or orthopaedic surgery finding ICS reduced ATRs by 38%[17].However,urology has been slow to embrace ICS,due to concerns of equivocal benefit and reinfusion of malignant cells[26,27].These fears have not been born out,with reassuring findings in a slew of urooncological studies including a meta-analysis[28—38].

To date,the only comparative study of ICS use in nephrectomy is Lyon et al.'s analysis[38]of patients undergoing open partial nephrectomy. This study aims to compare the outcomes of patients who did and did not receive ICS while undergoing open nephrectomy at our institution.

2.Materials and methods

A retrospective cohort study was performed,enrolling all patients undergoing open nephrectomy for suspected renal malignancy at our institution from 1 October 2013 to 1 October 2017 inclusive.Data were collected from hospital electronic and hard copy records.Patients were included regardless of whether partial or radical nephrectomy was performed,or whether laparotomy or thoracoabdominal surgical approach was utilised.Thoracoabdominal approach was defined as any supra-costal access. Patients were excluded if nephrectomy was performed for suspected urothelial malignancy,or for benign conditions,such as trauma or xanthogranulomatous pyelonephritis.All patients underwent surveillance for tumour recurrence,according to the Canadian Urological Association post-Nephrectomy Guidelines[39].This represented at minimum assessment with history,examination,serum testing and chest X-ray examination annually,and computed tomography of the abdomen and pelvis at 2- and 5-year post-operatively.Disease recurrence included any local recurrence or distant metastasis.

Patients who did(ICS group)and did not(standard group)receive ICS were compared.Primary outcomes were ATRs,and disease recurrence among those with histologically confirmed cancer.Secondary outcomes were complications and transfusion-related cost. Complications were categorised based on the Clavien-Dindo grading system[40].Ethics approval was granted by the Central Adelaide Local Health Network Human Research Ethics Committee,reference HREC/17/TQEH/255.

2.1.ICS practice

Our institution commenced using ICS for open nephrectomy in August 2015.Usage was intermittent,reserved for cases deemed high bleeding risk,until in December 2016 it was decided to employ ICS routinely, allowing for surgeon preference,due to departmental review of evidence.We use the Fresenius Kabi CATSmart Continuous Autotransfusion System?,with a Haemonectics?RS1VAE leucocyte depletion filter(LDF).As recommended by several authors[41,42],we use ICS in a financially tiered system.For all cases utilizing ICS, anticoagulated salvaged blood is collected in a reservoir(basic setup).When desired,this blood is then processed and reinfused(reinfusion setup).Thus,the ICS processor set and other single-use items are not wasted during cases where blood is not returned to the patient.

The transfusion trigger is decided by the anaesthetist,based on patient pre-operative haemoglobin,cardiorespiratory comorbidities,volume of blood collected,ongoing haemorrhage, intra-operative heart rate and blood pressure.

2.2.Transfusion-related cost calculations

All costs were calculated as of 30 June 2017.Transfusionrelated costs were calculated as allogeneic transfusion cost+ICS setup cost+ICS reinfusion cost.Costs related to length of hospital stay and complications were not included.

Allogeneic transfusion costs include both the product cost of each RBC unit and the process costs.The product cost of AUD$412.66 per unit was determined by the current listings of the National Blood Authority,Australia[43],after confirming these were the prices currently paid by our institution. Process costs of transfusion, including inhospital logistics,blood tests,staffing and overhead expenses,are known to be three to five times higher than the product cost of the unit of blood itself[12,13].These have previously been used in Australia to calculate more comprehensive estimates of the cost of transfusion[44,45].The first estimate of process costs in Australia by Wood et al.[44]in 2006 of AUD$370 per unit of RBC infused were updated by Leahy and Mukhtar[45]in 2010 to AUD$536 using the Australian Bureau of Statistics consumer price index for hospital and medical services.Utilising the same method translated to a subsequent 45.3%increase from end-of-financial-year 2010 to 2017,giving a current process cost of AUD$779[46],and a total cost per unit of RBC infused of AUD$1191.66.

To calculate ICS costs,every equipment item used during ICS was systematically listed and its current replacement price obtained from the theatre logistics department.ICS staffing costs were included,and represent the majority of the ICS setup cost.The machine is run by one of several dedicated ICS-trained in-house year ≥9 anaesthetic nurse.When ICS is electively requested, the practice of our institution is to roster an additional anaesthetic nurse to liberate one who is ICS trained.Due to a limited in-house staffing pool,it is often necessary to hire an agency nurse for this purpose.Current pricing in our institution for an inhouse year ≥9 anaesthetic nurse is AUD$42.28 per hour for a set 8 h shift,and for an equivalent agency nurse AUD$77 per hour for a flexible duration shift.Of the ICS cases,seven utilised in-house nurse cover totalling 56 h,while for nine an agency nurse was employed for 70.75 h in all.This represented a total ICS staffing cost of$7815.43,or$488.46 per ICS case.Incorporating this,ICS setup cost was AUD$609.85 per case,with reinfusion costing an additional AUD$382.00 per case(Table 1).2.3.Statistical analysis Continuous data were summarized as medians with interquartile range(IQR),and significance assessed using the Wilcoxon(Mann—Whitney)test.Categorical measures were summarized as proportions and assessed with Pearson's chisquare test.All tests were two-tailed and significance was assessed at the 5%alpha level.Data were analysed using SAS v9.3(SAS Institute Inc.,Cary,NC,USA).

3.Results

3.1.Demographics and surgical approach

Forty patients underwent open nephrectomy for suspected malignancy during the enrolment period.Sixteen patients received ICS(ICS group)while 24 did not(standard group)(Table 2).The ICS group had similar median age(63.5 vs.61.0 years,p=0.83)but a lower proportion of females(19%vs.58%,p=0.013).Median pre-operative(144 vs.139 g/L,p=0.99),post-operative haemoglobin(120 vs.112 g/L,p=0.86)and median Charlson Comorbidity Index(4 vs.3,p=0.35)were comparable.

The groups had similar proportions with left-sided tumours (44% vs. 42%, p = 0.90) and thoracoabdominal approach(88%vs.79%,p=0.50).Other approaches for the ICS and standard group were midline laparotomy(one and three cases respectively)and subcostal chevron incision(one and two cases respectively).The ICS group had a higher proportion of radical rather than partial nephrectomy(81%vs.46%,p=0.025)and shorter median followup(278 vs.827 days,p=0.0005).

Table 1 The cost of ICS set-up and reinfusion in Australian dollars,as of 30 June 2017.

Table 2 Patient demographics and surgical approach.Index ICS Standard p-Value Demographics Patients(n) 16 24 A Fe ge ma(y le e,a rn),(%m)e dian(IQR) 6 3 3(.159(%5)6 —7 0) 6 1 14((55 18—%)7 1) 0 0..80 3 13 Ap PPCLFpeo rohr enl s o al-tgaoro-ltcw os phh o p e- nu eo r p arfCa ts(iott v d imav e a ey oy h r)(ha,bdaeiam ed mymie)to,dyog imglIa onln oe bdbd ie(niiIxnaQ,(nR g(mg)/(/I LeQL)d,R)i,)am mnee(dIdiQaiRann) (I(QI Q RR) ) 11472 427((40825——(((19157 153))4—0——1 125 575)2 4 )) 11378 312((92726——(((11559 304))319—— — 111 423 951))9 ) 00000.....98340 9652 005 Thoracoabdominal,n(%) 14(88%) 19(79%) 0.50 Left-sided tumour,n(%) 7(44%) 10(42%) 0.90 Radical,n(%) 13(81%) 11(46%) 0.025 ICS,intra-operative cell salvage;IQR,interquartile range.

3.2.Histology

Fourteen ICS patients and 15 standard patients had histologically confirmed renal cancer(Table 3).The tumour type was clear cell renal cell carcinoma(RCC)for 12 and 11 patients in the ICS and standard groups respectively.Other histological types in the ICS group were one case each of chromophobe and papillary RCC,while in the standard group there were three cases of papillary RCC and one of large cell undifferentiated urothelial carcinoma. The number of patients with pathological tumour stage T1,T2 and T3 was three,four and seven in the ICS group and ten,one and three in the standard group respectively.Significantly more ICS patients had stage ≥T2 disease(79%vs.27%;p=0.005).Both groups had one patient with nodal stage N1,while three ICS patients and one standard patient had metastasis detected pre-operatively. These represented six separate patients.

3.3.Intra-operative cell salvage use

Of the 16 patients in the ICS group for whom lost blood was collected,five(31%)had salvaged blood reinfused.The median volume returned was 276 mL(IQR:223—536 mL).

3.4.Primary outcomes

One patient each in the ICS and standard groups received allogeneic transfusion(6%vs.4%).These patients had preoperative haemoglobin of 101 g/L and 117 g/L,and had two and one units given respectively.Amongst patients with histologically confirmed malignancy without evidence of metastasis pre-operatively,tumour recurrence rates were similar(18%vs.7%,p=0.40).Two patients recurred in the ICS group.The first had a T2aN0 100 mm RCC while the second had a T3aN1 115 mm RCC.The sole standard group patient with recurrence had an 85 mm T3aN1 large cell undifferentiated urothelial carcinoma.All three cases had negative surgical margins,and were resected radically.The two patients with N1 disease were the study's only instances of nodal positivity.

3.5.Secondary outcomes

Complication rates were comparable(19%vs.29%;p=0.46)(Tables 3 and 4).There were no deaths during the index admission,and no TTIs.Regarding price estimation,machine set-up costs applied to all ICS patients,of whom five used further resources through reinfusion. Calculating total transfusion-related costs as allogeneic transfusion cost+ICS setupcost+ICSreinfusioncost,theICSgroup'scostswereAUD$14 050.92($2383.32+$9757.60+$1910.00)compared with AUD$1191.66 for the standard group($1191.66+$0+$0).Correspondingly,per capita transfusion-related costs were markedly higher in the ICS group(AUD$878.18 vs.$49.65 per patient)(Table 3).

Analyses were re-run with patients segregated by partial or radical surgical approach,comparing those with and without ICS use.Results were unchanged,with no statistical difference for ATRs,recurrence and complications(data not shown).

4.Discussion .

The literature to date regarding ICS use in urology is restricted to a collection of case reports and case series,and 14 comparative cohort studies[19,26,29—38,41,47],with no grade I or II evidence.Our study represents the first comparative study of ICS to include radical nephrectomy and the first in any urological procedure outside the UK and the USA.It is also only the fourth comparative study of ICS in any specialty in Australia[48—50].

ATRs were low at 4%—6%,regardless of ICS use,representing only one patient in each group.This was an unexpected finding,and below published norms for open partial(5%—30%)[3—6]and radical nephrectomy(18%—45%)[3,5,7].It is also below the 8%—21%ATRs reported in Lyon et al.'s analysis[38]of ICS in partial nephrectomy.Causes for this low transfusion rate are likely to be multi-factorial,including the favourable Charlson Comorbidity Index and preoperative haemoglobin,and the high degree of renal hilar control afforded by the thoracoabdominal approach.Both patients requiring transfusion had low starting haemoglobin concentration,highlighting the importance of pre-operative optimisation including correction of anaemia.

Both groups had similar low rates of tumour recurrence,being present in two ICS patients and one standard patient.This is consistent with the results of Lyon et al.[38],as well as comparative studies of prostatectomy and cystectomy,all of which found recurrence in ICS patients was equivalent to[29—33,35,36]or less than controls[34,37].This finding was the more reassuring given the less favourable oncological characteristics amongst our ICS group,with larger,higher stage tumours.The groups also had comparable complication rates,in line with many other studies supporting the safety of ICS in uro-oncology[19,33,38,41,47].

Three studies to date have reported cost analyses for ICS in urology.All were retrospective cohort studies.In 1995,Gilbert et al.'s USA-based study[26]reported 172 patients undergoing radical retrograde prostatectomy.Half utilised PAD and ICS,with the remainder receiving PAD only.They found transfusion-related costs were greater in the ICS group,at USD$1409 vs.$976 per patient.Two more recent UK studies published in 2010 and 2011 comparing ICS to no blood conservation technique found the reverse.An analysis of 30 patients undergoing radical cystectomy noted lower costs in the ICS group,at UK Pounds(UKP)￡320 vs.￡675[19].Similar savings were reported in another study of 50 men receiving radical retrograde prostatectomy(UKP￡163 vs.￡372)[35].

ICS was not cost effective for open nephrectomy in our institution.The two main contributors to this finding were the surprisingly low ATRs and the high staffing cost of ICS.

Table 3 Histopathology and outcomes.

Table 4 Complications.

Published indications for ICS use are elective or emergency surgery where the estimated blood loss is ＞20%of total blood volume,induces anaemia or requires transfusion in ＞10%of patients[42,51].The ATRs observed in this study were below this level,limiting the potential benefits of ICS.The use of casual agency staff to liberate in-house ICS-trained anaesthetic nurses was also more expensive than anticipated.Additionally,in most ICS cases reinfusion did not occur,with the dedicated ICS anaesthetic nurse largely unoccupied after machine setup.Driven by these results,our department is taking steps to reduce these costs.These include creation of a larger pool of in-house anaesthetic nurses,and negotiations withamorecompetitivelypricednursingagency.Additionally,we are exploring modifying ICS operational practice,with the machine potentially becoming a responsibility of the preexisting anaesthetic nurse,who is present for all cases alongside an anaesthetist,regardless of ICS use.This may remove ICS-specific staffing costs altogether.

We believe that in sites with similar allogeneic transfusion and ICS costs and no separate ICS staffing,ICS will reduce transfusion-related costs only for procedures with expected transfusion rates ＞50%.Future advances in ICS technology may improve its cost effectiveness,by reducing setup costs,and returning a higher proportion of shed blood.

This study is limited by its retrospective nature,small size,non-randomised nature and short follow-up.Differences between groups, the principal feature of nonrandomised studies, were significant for important characteristics such as tumour stage,and this selection bias may have impacted our findings.

5.Conclusion

ICS use in open nephrectomy appears safe,with similar tumour recurrence and complications compared to the standard group.ATRs were unexpectedly low in both groups.Therefore,ICS was not cost effective for open nephrectomy in our institution.ICS use may offer greater cost benefit when used in urological centres or procedures with higher ATRs.Larger and prospective studies are required to confirm these findings.

Author contributions

Study design:Ned Kinnear

Data acquisition:Ned Kinnear,Lina Hua,Bridget Heijkoop

Data analysis:Ned Kinnear,Lina Hua,Bridget Heijkoop

Drafting of manuscript:Ned Kinnear

Critical revision of the manuscript:Ned Kinnear,Lina Hua,

Bridget Heijkoop,Derek Hennessey,Daniel Spernat

Conflicts of interest

The authors declare no conflict of interest.

Acknowledgements

The authors recognize the efforts of The Queen Elizabeth Hospital anaesthetist Dr.Jellsingh Jeyadoss in campaigning for routine use of intra-operative cell salvage in our institution's open uro-oncological cases.We would like to thank theatre administrators Rosemary Obst,Karen Taylor and Caroline Saniotis for their help obtaining data,and also haematologists Dr.Simon McRae,Dr.Ben Saxon and Dr.Kathryn Robinson for their guidance in transfusionrelated costing.