,i #aagth ,,congress #ast ,session ,h4 ,r4 #ecca ,,in ,,the ,,house ,,of ,,representatives ,september #bb1 #bjba,mr4 ,danny ,k4 ,davis of ,illinois 7for himself1 ,mr4 ,rush1 ,mr4 ,wenstrup1 and ,mr4 ,hollingsworth7 introduced the following bill2 which was referred to the ,committee on ,energy and ,commerce1 and in addition to the ,committee on ,ways and ,means1 for a period to be subsequently determined by the ,speaker1 in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned ,a ,,bill ,to amend title ,,xviii of the ,social ,security ,act to improve access to innovative new medical devices furnished to individuals with end stage renal disease under part ,b of the ,medicare program by establishing a new device add-on payment adjustment under such part4 #a4 ,short title ,this ,act may be cited as the ,patient ,access to ,,esrd ,new ,innovative ,devices ,act4 #b4 ,findings ,congress finds the following3 7#a7 ,there are approximately #djj1jjj ,medicare beneficiaries with end-stage renal disease1 making up #a percent of the ,medicare population but accounting for approximately #g percent of all ,medicare spending4 7#b7 ,expected remaining lifetime for dialysis patients under #hj years old is one-third as long as their counterparts without ,,esrd1 and for dialysis patients over #hj years old1 it is one-half as long as that of their counterparts without ,,esrd4 7#c7 ,on average1 hemodialysis patients are hospitalized nearly twice per year and about #cj percent have an unplanned rehospitalization within the #cj days following discharge1 contributing to high costs for treating ,,esrd ,medicare beneficiaries4 7#d7 ,there is a lack of innovative new devices for ,,esrd ,medicare beneficiaries1 in part because of the lack of reimbursement incentives for novel devices4 #c4 ,temporary add-on payment for new medical devices to diagnose1 treat1 or manage end stage renal disease ,the ,secretary of ,health and ,human ,services shall provide-- 7#a7 a three-year temporary add-on payment adjustment 7as described in section #dac4bcf7;d7 of title #db1 ,code of ,federal ,regulations7 for a new medical device approved by the ,food and ,drug ,administration under section #eac7;f77#b7 of the ,federal ,food1 ,drug1 and ,cosmetic ,act 7#ba ,u4,s4,c4 #cfj;c7 on or after ,january #a1 #bjbj1 and furnished to an individual entitled to benefits under part ,b of title ,,xviii of the ,social ,security ,act for the diagnosis1 treatment1 or management of end stage renal disease2 and 7#b7 for the adjustment under paragraph 7#a7 to be implemented in a nonbudget neutral manner under subparagraph 7,d77iv7 of section #ahha7;b77#ad7 of the ,social ,security ,act 7#db ,u4,s4,c4 #acierr7b77#ad77;,d77iv774