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Quality Improvement on Pediatric Peritoneal Dialysis (PPD)
Appropriate organization Appropriate organization of PN Centerof PN Center
Quality reassurance in Quality reassurance in PPD (guidelines)PPD (guidelines)
Evaluation of Evaluation of the clinical outcomethe clinical outcomeModify strategiesModify strategies
Constantinos J. Stefanidis
Advantages of PD in children
The quality of life of children and their family is better during PD
than HD.
The residual renal function is better preserved during PD than HD.
There are logistical advantages of PD.
It requires: a lower staff : patient ratio than HD
a lower dose of rHUEPO
PD is the dialysis of choice :
For children with weight < 15 kg
For children expected to have a prolonged
period of dialysis
For children living too far from a pediatric
hemodialysis unit
Appropriate organization Appropriate organization of PN Centerof PN Center
Quality reassurance in Quality reassurance in PPD (guidelines)PPD (guidelines)
Evaluation of Evaluation of the clinical outcomethe clinical outcomeModify strategiesModify strategies
Quality Improvement on PPD
Paediatric Nephrology Centers
CRICRI TxTx
HDHD
PDPD
PaediatriciansPaediatricians(early referral)(early referral)
Paediatric surgeonsPaediatric surgeons (dialyis access)(dialyis access)
Tx surgeonsTx surgeons
Paediatric Nephrology Centers per million of child population
0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
``
Loirat et al. Nephr Dial Transplant 1993Loirat et al. Nephr Dial Transplant 1993
Paediatric Nephrology Centers
HD PD Tx65%
HD PD22%
HD8%Tx
5%
130 centers in 130 centers in 22 European countries22 European countries
Loirat et al. Nephr Dial Transplant 1993Loirat et al. Nephr Dial Transplant 1993
End Stage Renal Disease in Children
5 - 105 - 10 children/year per million of child population (pmcp) children/year per million of child population (pmcp)
Pediatric ESRD is accounting for only 1.8% of all ESRDPediatric ESRD is accounting for only 1.8% of all ESRD United States Renal Data System (USRDS)United States Renal Data System (USRDS)
11 PN center pmcp (per 4-6 m total population)PN center pmcp (per 4-6 m total population) (cp = 25-40% of total population)(cp = 25-40% of total population)
5 - 105 - 10 new children with ESRD / yearnew children with ESRD / year
220 - 440220 - 440 children/yr start dialysis in countries of SEPNWG children/yr start dialysis in countries of SEPNWG
If 50 - 60% of them receive a transplant / year If 50 - 60% of them receive a transplant / year
The number of ESRD children will increase by 100-200/yrThe number of ESRD children will increase by 100-200/yr
Child population per paediatric nephrologist
131131
146146
381381132132 212212
225225
233233 140140
220220
191191
155155623623
353353
547547
317317243243
Child population (x1000) per paediatric nephrologist
467467Child population (millions) 9595 4242 Paediatric nephrologists 500500 120120 Members of ESPN 320320 5050
Multi-disciplinary team
• Structure Structure Doctors, nurses, dietitians, social workers, Doctors, nurses, dietitians, social workers, psychologists, play therapists, teachers. psychologists, play therapists, teachers.
• Goal Goal To deliver to children the care required for To deliver to children the care required for their long-term well being and for their their long-term well being and for their optimal quality of life. optimal quality of life.
• Team meetings Team meetings give the entire team opportunity forgive the entire team opportunity for interaction and collaborative decision interaction and collaborative decision
making. making.
Team working improves patient care and Team working improves patient care and enhances the quality of the working life.enhances the quality of the working life.
• CContinuous education of all health professionals.ontinuous education of all health professionals.
• Each member of the team should have inovative Each member of the team should have inovative approach and the goal to achieve the eapproach and the goal to achieve the excellence.xcellence.
• A set of standards of clinical practice and detailed A set of standards of clinical practice and detailed protocols should be available.protocols should be available.
• A detailed registry of patients should be updated.A detailed registry of patients should be updated.
• Networking with other PN centers, multicenter Networking with other PN centers, multicenter studies and global cooperation should be a prioritystudies and global cooperation should be a priority
Quality improvement on the organization of PN centers
Quality Improvement on PPD
Appropriate organization Appropriate organization of PN Centerof PN Center
Quality reassurance in Quality reassurance in PPD (guidelines)PPD (guidelines)
Evaluation of Evaluation of the clinical outcomethe clinical outcomeModify strategiesModify strategies
Steps for quality reassurance in PPD
• All children on PD should be managed in a All children on PD should be managed in a pediatric nehrology center.pediatric nehrology center.
• Peritoneal catheters should implanted surgically Peritoneal catheters should implanted surgically under general anesthesia. under general anesthesia. A lateral technique through the rectus muscle and two A lateral technique through the rectus muscle and two purse-string sutures around the peritoneum might reduce purse-string sutures around the peritoneum might reduce the risk for leakagethe risk for leakage..
• The training for the parents at the initiating PD The training for the parents at the initiating PD treatment should be detailed and last > 2 weeks.treatment should be detailed and last > 2 weeks.
• A '’closed twin-bag PD system with Y-line'' or A '’closed twin-bag PD system with Y-line'' or automated PD should be preferred. automated PD should be preferred.
Targets for adequacy of peritoneal dialysis
Adequate dose of PD is the amount of PD below Adequate dose of PD is the amount of PD below which there is an increase in morbidity and mortality which there is an increase in morbidity and mortality
Optimal dose of PD is the amount of PD yielding Optimal dose of PD is the amount of PD yielding clinical results which cannot further improveclinical results which cannot further improve
CJ Stefanidis 2001
Adequate doseAdequate dose
Optimal doseOptimal dose
NKF-DOQINKF-DOQI began in March 1995 began in March 1995 Work Groups of 70 professionals reviewed > 11,000 articles.Work Groups of 70 professionals reviewed > 11,000 articles.Only 206 articles were included at the final publication.Only 206 articles were included at the final publication.
In 1997 114 evidence-based clinical practice guidelines were In 1997 114 evidence-based clinical practice guidelines were developeddeveloped. . Am J Kidney Dis 1997 Sep;30 (3 Suppl 2) : S67-136Am J Kidney Dis 1997 Sep;30 (3 Suppl 2) : S67-136
Continuous quality improvement: DOQI becomes K/DOQI and is updated. National Kidney Foundation's Dialysis Outcomes Quality Initiative. Am J Kidney Dis 2001 Jan;37(1):179-194Am J Kidney Dis 2001 Jan;37(1):179-194
Νational Κidney Νational Κidney FoundationFoundation
D O Q ID O Q IDialysis Outcomes Quality InitiativeDialysis Outcomes Quality Initiative
BUN BUN (= Purea / 2)(= Purea / 2)
PNA = 6.25 x UNA (g/kg) + 0.5= 6.25 x UNA (g/kg) + 0.5
Protein intake
ΤΤBWBW
Muscle mass catabolismMuscle mass catabolism
S. creatinineS. creatinine
Creatinine of urine and PDCreatinine of urine and PD
Creatinine clearanceCreatinine clearance
0.660.66 x 12 L x 7 x 1.73 x 12 L x 7 x 1.73mm22
1.6m1.6m22
= = 60 L/1.73m60 L/1.73m22/week/week
== 0.85 0.85 x 12 L x 7 days x 12 L x 7 days
60kg x 0.6 (L/kg) 60kg x 0.6 (L/kg)
= = 22
==
D/PD/Pcreatcreat x V x VPDPD
SS==
D/PD/Pureaurea x V x VPDPD
ΤΤBWBW==
KKtt/Vurea/Vurea
Creatinine and urea adequacy parameters
44 5.75.7 7.17.1
Weight: 70 kg S=1.7m2 ΤΒW =42 L
Weight : 35 kg S=1.2m2 ΤΒW= 21 L
Weight : 14 kg S=0.6m2 ΤΒW: 8.5 L
Creat. clear.Creat. clear. D/P creat x VD/P creat x VPD XPD X 1.73 /S 1.73 /S
D/PD/Pureaurea x V x VPDPD / Τ / ΤBWBWKt/VureaKt/Vurea== ==
D/P creat.D/P creat.
D/PD/Pureaurea
ΤΤBWBWxx
SS
(x 100)(x 100)
ΤΤBWBW
S S (x 100)(x 100)
60602 x 1002 x 100
70703.1 x 1003.1 x 100
80804 x 1004 x 1003.33.3 4.44.4 5.05.0
Age Years Protein intake0-0.5 2.8-30.5-1 2.3-2.51-6 1.9-27-14 1.7-1.815-18 1.4-1.5
Recommended protein intake for children on PD
Initial prescription 0.6-0.8 L/m²/day, 0.8-1 L/m² overnight Adapted prescription 1-1.2 L/m²/day, up to1.4 L/m² overnight
Recommended volume of PD fluid (VPD )
K/DOQI Guidelines for K/DOQI Guidelines for PD AdequacyPD AdequacyAm J Kidn Dis S94-S99 2001Am J Kidn Dis S94-S99 2001
Guidelines of EPPWG on Adequacy and the dialysis prescriptionGuidelines of EPPWG on Adequacy and the dialysis prescription
Quality Improvement on PPD
Appropriate organization Appropriate organization of PN Centerof PN Center
Quality reassurance in Quality reassurance in PPD (guidelines)PPD (guidelines)
Evaluation of Evaluation of the clinical outcomethe clinical outcomeModify strategiesModify strategies
• Measurement of PD Patient SurvivalMeasurement of PD Patient Survival• Measurement of PDTechnical SurvivalMeasurement of PDTechnical Survival• Measurement of HospitalizationMeasurement of Hospitalization
• Measurement of Hemoglobin /HematocritMeasurement of Hemoglobin /Hematocrit• Measurement of Albumin ConcentrationMeasurement of Albumin Concentration• Measurement of Normalized PNAMeasurement of Normalized PNA
• Measurement of Patient-Based Assessment of Measurement of Patient-Based Assessment of quality of lifequality of life
• Measurement of Growth, Developmental Progress Measurement of Growth, Developmental Progress and School Attendenceand School Attendence
Am J Kidn Dis S94-S99 2001Am J Kidn Dis S94-S99 2001
Clinical outcome goals of K/DOQI for PD patients
Clinical outcome goals of K/DOQI for PD patients
PD Patient Survival PD Patient Survival is dependent uponis dependent upon uncontrollable and uncontrollable and controllable (inadequste dialysis) variablescontrollable (inadequste dialysis) variables
PD Technical Survival PD Technical Survival is dependent uponis dependent upon::
• Complications (peritonitis)Complications (peritonitis)
inadequste dialysis malnutrition peritonitisinadequste dialysis malnutrition peritonitis
` 75% 2-year technique survival rate` 75% 2-year technique survival rate
• Inability to perform PD Inability to perform PD (lack of access, medical contraindications)(lack of access, medical contraindications)
• Patient request/lifestyle issues (burnout) Patient request/lifestyle issues (burnout)
•Measurement of HospitalizationsMeasurement of Hospitalizations1.8 times/year (CANUSA)1.8 times/year (CANUSA)
•Measurement of HemoglobinMeasurement of Hemoglobin Should be 11-13 g/dl in 75% of patients.Should be 11-13 g/dl in 75% of patients.
•Measurement of Albumin Measurement of Albumin ConcentrationConcentration
•Measurement of Normalized PNAMeasurement of Normalized PNAAm J Kidn Dis S94-S99 2001Am J Kidn Dis S94-S99 2001
Clinical outcome goals of K/DOQI for PD patients
w h a t S E P N W G s h o u l d d o ? Quality Improvement on PPD
Register the PN centers of the area of SEPNWG.
Enhance the appropriate organization of the PN. centers and
disseminate the use of clinical guidelines.
The clinical outcome of patients should be continuously evaluated.
The problems of children on PD should be discussed and
appropriate solutions should be advised.