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Assurance de qualité pour le cancer rectal – phase 2 ...

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122 PROCARE <strong>–</strong> <strong>phase</strong> 2 KCE reports 81PROPORTION OF CSTAGE II-III PATIENTS THAT RECEIVED ALONG COURSE OF NEOADJUVANT PELVIC RT(the same algorithm is used as the previous QI)Measurement in prospective PROCARE database (Figure 33)As for the previous QI, stage II and III RC patients are se<strong>le</strong>cted using the variab<strong>le</strong>s‘SPR_V147’ and ‘PT_V106’ for the cStage. In this group of patients, those receivingsurgery are se<strong>le</strong>cted using variab<strong>le</strong> ‘AD_V111’. Within this group of patients, patientsreceiving preoperative radiotherapy are again se<strong>le</strong>cted using variab<strong>le</strong> ‘RD_V101’.Patients receiving a long course of radiotherapy (i.e. at <strong>le</strong>ast 25 fractions of 1.8 Gy) arese<strong>le</strong>cted using variab<strong>le</strong>s ‘RD_V106’ (number of fractions) and ‘RD_V109’ (total dose).Measurement in coup<strong>le</strong>d administrative databaseAgain, in the nomenclature, co<strong>de</strong>s are availab<strong>le</strong> for radiotherapy (Tab<strong>le</strong> 70). However, itis not possib<strong>le</strong> to i<strong>de</strong>ntify the exact number of fractions and radiation dose with theseco<strong>de</strong>s. Therefore, the i<strong>de</strong>ntification of a long course of RT is impossib<strong>le</strong>. The sameapplies to the ICD-9-CM co<strong>de</strong>s (Tab<strong>le</strong> 71).PROPORTION OF STAGE II-III PATIENTS THAT RECEIVEDNEOADJUVANT CHEMORADIATION WITH A REGIMENCONTAINING 5-FUMeasurement in prospective PROCARE database (Figure 34)cStage II and III RC patients receiving surgery are se<strong>le</strong>cted in the same way as the twoprevious QI. When neoadjuvant CRT is provi<strong>de</strong>d (patients receiving neoadjuvantradiotherapy or chemotherapy as monotherapy are exclu<strong>de</strong>d), the variab<strong>le</strong> ‘CH_V101’is checked in the chemotherapy section of the data entry form. When the neoadjuvantchemotherapy regimen contained 5-FU, this is registered in variab<strong>le</strong>s ‘CH_V109’ and‘CH_V110’ or in variab<strong>le</strong>s ‘CH_V119’ and ‘CH_V120’.Measurement in coup<strong>le</strong>d administrative database (Figure 35)Patients with <strong>rectal</strong> <strong>cancer</strong> cStage II-III are se<strong>le</strong>cted from the BCR database. Thosepatients receiving surgery are se<strong>le</strong>cted using the nomenclature co<strong>de</strong>s forabdominoperineal resection, Hartmann’s procedure and sphincter-sparing surgery(Tab<strong>le</strong> 64). The i<strong>de</strong>ntified ICD-9-CM co<strong>de</strong>s were not used for this se<strong>le</strong>ction (Tab<strong>le</strong> 66).Within the group of cStage II-III patients un<strong>de</strong>rgoing surgery, those receivingneoadjuvant chemoradiotherapy are se<strong>le</strong>cted using the nomenclature co<strong>de</strong>s forradiotherapy (Tab<strong>le</strong> 70) and the ATC co<strong>de</strong>s for chemotherapy (Tab<strong>le</strong> 72), but only ifthe date of chemoradiotherapy falls within the interval between the inci<strong>de</strong>nce date andsurgery date. The ATC co<strong>de</strong>s for 5-fluorouracil are used to calculate the <strong>de</strong>nominator(Tab<strong>le</strong> 72).

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