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91.Wong SS, Kwaan HC, Ing TS.  Venous air embolism related to the use of central catheters revisited:
with emphasis on dialysis catheters. Clin Kidney J.
2017;10(6):797–803.
92.Stegmayr B.  Air contamination during hemodialysis should be minimized. Hemodial Int.
2017;21(2):168–72.
93.Stegmayr B, Forsberg U, Jonsson P, Stegmayr
C. The sensor in the venous chamber does not prevent passage of air bubbles during hemodialysis.
Artif Organs. 2007;31(2):162–6.
94. Ward M, Shadforth M, Hill A, Kerr D. Air embolism
during haemodialysis. Br Med J. 1971;3(5766):74–8.
95. Baskin S, Wozniak R. Hyperbaric oxygenation in the
treatment of hemodialysis-associated air embolism.
N Engl J Med. 1975;293(4):184–5.
96. Dunbar E, Fox R, Watson B, Akrill P. Successful late
treatment of venous air embolism with hyperbaric
oxygen. Postgrad Med J. 1990;66(776):469–70.
97.Lau L, London K.  Cortical blindness and altered
mental status following routine hemodialysis, a
case of iatrogenic cerebral air embolism. Case Rep
Emerg Med. 2018;2018:9496818.
98.Jonsson P, Lindmark L, Axelsson J, Karlsson L,
Lundberg L, Stegmayr B. Formation of blood foam
in the air trap during hemodialysis due to insufficient automatic priming of dialyzers. Artif Organs.
2018;42(5):533–9.
99.Jonsson P, Karlsson L, Forsberg U, Gref M,
Stegmayr C, Stegmayr B. Air bubbles pass the security system of the dialysis device without alarming.
Artif Organs. 2007;31(2):132–9.

100.Keshavarzi G, Barber TJ, Yeoh G, Simmons A,
Reizes JA.  Two-dimensional computational analysis of microbubbles in hemodialysis. Artif Organs.


2013;37(8):E139–44.

101.
Keshavarzi G, Simmons A, Yeoh G, Barber
T.  Effectiveness of microbubble removal in an
airtrap with a free surface interface. J Biomech.
2015;48(7):1237–40.
102.Barak M, Nakhoul F, Katz Y. Pathophysiology and
clinical implications of microbubbles during hemodialysis. Semin Dial. 2008;21(3):232–8.

103.Polaschegg H.  Hemodialysis machine air detectors need not detect microbubbles. Artif Organs.
2007;31(12):911–2.
104. Wagner S, Rode C, Wojke R, Canaud B. Observation
of microbubbles during standard dialysis treatments.
Clin Kidney J. 2015;8(4):400–4.

105.Forsberg U, Jonsson P, Stegmayr C, Jonsson F,
Nilsson B, Nilsson Ekdahl K, et  al. A high blood
level in the venous chamber and a wet-stored dialyzer help to reduce exposure for microemboli during hemodialysis. Hemodial Int. 2013;17(4):612–7.

106.Stegmayr BG.  Sources of mortality on dialysis
with an emphasis on microemboli. Semin Dial.
2016;29(6):442–6.
107.Kosmadakis G, Aguilera D, Carceles O, Da Costa
Correia E, Boletis I.  Pulmonary hypertension in
dialysis patients. Ren Fail. 2013;35(4):514–20.

D. Borzych-Duz.ałka and E. Harvey
108.Stegmayr B, Brannstrom T, Forsberg U, Jonson P,
Stegmayr C, Hultdin J.  Microbubbles of air may

occur in the organs of hemodialysis patients. ASAIO
J. 2012;58(2):177–9.
109.Madero M, Sarnak MJ. Does hemodialysis hurt the
brain? Semin Dial. 2011;24(3):266–8.

110.Forsberg U, Jonsson P, Stegmayr C, Stegmayr
B.  Microemboli, developed during haemodialysis, pass the lung barrier and may cause ischaemic
lesions in organs such as the brain. Nephrol Dial
Transplant. 2010;25(8):2691–5.
111.George S, Holt S, Hildick-Smith D. Patent foramen
ovale, dialysis and microembolization. Nephrology.
2012;17(6):569–74.

112.Forsberg U, Jonsson P, Stegmayr C, Stegmayr
B.  A high blood level in the air trap reduces
microemboli during hemodialysis. Artif Organs.
2012;36(6):525–9.
113.Palanchon P, Birmele B, Tranquart F.  Acoustical
bubble trapper applied to hemodialysis. Ultrasound
Med Biol. 2008;34(4):681–4.

114.Lindley E, Finney D, Jones P, Lewington A,
O'Reagan A, Webb G. Unexpected triggering of the
dialysate blood leak detector by haemolysis. Acta
Clin Belg. 2015;70(3):226–9.
115.Avila J, Prasad D, Weisberg L, Kasama R. Pseudo-­
blood leak? A hemodialysis mystery. J Clin Nephrol.
2013;79(4):323–5.
116.Lim K, Heher E, Steele D, Fenves A, Tucker J,
Thadhani R, et al. Hemodialysis failure secondary to

hydroxyocobalamin exposure. Proc (Bayl Univ Med
Cent). 2017;30(2):167–8.
117.Gizaw A, Kidd JM.  All that leaks is not blood.
Kidney Int. 2015;88(3):645.
118.Tharmaraj D, Kerr PG. Haemolysis in haemodialysis. Nephrology. 2017;22(11):838–47.

119.Kirsch AH, Pollheimer MJ, Troppan K, Horina
JH, Rosenkranz AR, Eller K. The case | acute kidney injury and hemolysis in a 58-year-old woman.
Kidney Int. 2017;91(4):993–4.

120.Malinauskas R.  Decreased hemodialysis circuit
pressures indicating postpump tubing kinks: a retrospective investigation of hemolysis in five patients.
Hemodial Int. 2008;12(3):383–93.
121.Paluszkiewicz A, Kellner J, Elshehabi M, Schneditz
D. Effect of hemolysis and free hemoglobin on optical hematocrit measurements in the extracorporeal
circulation. ASAIO J. 2008;54(2):181–4.

122.(CDC) CfDCaP.  Multistate outbreak of hemolysis in hemodialysis patients  - Nebraska and
Maryland. MMWR Morb Mortal Wkly Rep.
1998;47(23):483–4.
123.Duffy R, Tomashek K, Spangenberg M, Spry

L, Dwyer D, Safranek TJ, et  al. Multistate outbreak of hemolysis in hemodialysis patients
traced to faulty blood tubing sets. Kidney Int.
2000;57(4):1668–74.
124.Abtahi M, Uzan M, Souid M.  Hemolysis-induced
acute pancreatitis secondary to kinked hemodialysis
blood lines. Hemodial Int. 2007;11(1):38–41.



25  Non-infectious Complications of Hemodialysis in Children

125.
Gault M, Duffett S, Purchase L, Murphy
J. Hemodialysis intravascular hemolysis and kinked
blood lines. Nephron. 1992;62(3):267–71.

126.Sweet S, McCarthy S, Steingart R, Callahan
T.  Hemolytic reactions mechanically induced
by kinked hemodialysis lines. Am J Kidney Dis.
1996;27(2):262–6.
127.Shibata E, Nagai K, Takeuchi R, Noda Y, Makino
T, Chikata Y, et  al. Re-evaluation of pre-pump
arterial pressure to avoid inadequate dialysis and
hemolysis: importance of prepump arterial pressure
monitoring in hemodialysis patients. Artif Organs.
2015;39(7):627–34.
128.Yoon J, Thapa S, Chow R, Jaar B. Hemolysis as a
rare but potentially life-threatening complication
of hemodialysis: a case report. BMC Res Notes.
2014;7:475.
129.Polaschegg HD. Red blood cell damage from extracorporeal circulation in hemodialysis. Semin Dial.
2009;22(5):524–31.
130.Techert F, Techert S, Woo L, Beck W, Lebsanft H,
Wizemann V.  High blood flow rates with adjustment of needle diameter do not increase hemolysis during hemodialysis treatment. J Vasc Access.
2007;8(4):252–7.
131.Mehta HK, Deabreu D, McDougall JG, Goldstein
MB. Correction of discrepancy between prescribed
and actual blood flow rates in chronic hemodialysis patients with use of larger gauge needles. Am J
Kidney Dis. 2002;39(6):1231–5.

132.Berkes S, Kahn S, Chazan J, Garella S.  Prolonged
hemolysis from overheated dialysate. Ann Intern
Med. 1975;83(3):363.

133.Pendergrast JM, Hladunewich MA, Richardson
RM.  Hemolysis due to inadvertent hemodialysis
against distilled water: perils of bedside dialysate
preparation. Crit Care Med. 2006;34(10):2666–73.

134.Matter B, Pederson J, Psimenos G, Lindeman
R. Lethal copper intoxication in hemodialysis. Trans
Am Soc Artif Intern Organs. 1969;15:309–15.

135.Orringer E, Mattern W.  Formaldehyde-induced
hemolysis during chronic hemodialysis. N Engl J
Med. 1976;294(26):1416–20.
136. Punn K, Yeung C, Chen T. Acute intravascular hemolysis due to accidental formalin intoxication during
hemodialysis. Clin Nephrol. 1984;21(3):188–90.
137.de Oliveira RM, de los Santos CA, Antonello I,
d'Avila D. Warning: an anemia outbreak due to chloramine exposure in a clean hemodialysis unit--an
issue to be revisited. Ren Fail. 2009;31(1):81–3.
138.Pengo MF, Ioratti D, Bisogni V, Ravarotto V,

Rossi B, Bonfante L, et al. In patients with chronic
kidney disease short term blood pressure variability is associated with the presence and severity of sleep disorders. Kidney Blood Press Res.
2017;42(5):804–15.
139.Scherer JS, Combs SA, Brennan F. Sleep disorders,
restless legs syndrome, and uremic pruritus: diagnosis and treatment of common symptoms in dialysis
patients. Am J Kidney Dis. 2017;69(1):117–28.


459

140.Gerogianni G, Kouzoupis A, Grapsa E.  A holistic approach to factors affecting depression
in haemodialysis patients. Int Urol Nephrol.
2018;50(8):1467–76.
141. Davis ID, Baron J, O'Riordan MA, Rosen CL. Sleep
disturbances in pediatric dialysis patients. Pediatr
Nephrol. 2005;20(1):69–75.
142.Davis ID, Greenbaum LA, Gipson D, Wu LL, Sinha
R, Matsuda-Abedini M, et al. Prevalence of sleep disturbances in children and adolescents with chronic
kidney disease. Pediatr Nephrol. 2012;27(3):451–9.
143. El-Refaey A, Elsayed R, Sarhan A, Bakr A, Hammad
A, Elmougy A, et al. Sleep quality assessment using
polysomnography in children on regular hemodialysis. Saudi J Kidney Dis Transpl. 2013;24(4):714–8.
144.Amin R, Sharma N, Al-Mokali K, Sayal P, Al-Saleh
S, Narang I, et al. Sleep-disordered breathing in children with chronic kidney disease. Pediatr Nephrol.
2015;30(12):2135–43.
145.Gomes C, Oliveira L, Ferreira R, Simao C.  Sleep
disturbance in pediatric patients on automated peritoneal dialysis. Sleep Med. 2017;32:87–91.
146. Allen RP, Picchietti DL, Garcia-Borreguero D, Ondo
WG, Walters AS, Winkelman JW, et al. Restless legs
syndrome/Willis-Ekbom disease diagnostic criteria: updated International Restless Legs Syndrome
Study Group (IRLSSG) consensus criteria--history,
rationale, description, and significance. Sleep Med.
2014;15(8):860–73.

147.Applebee GA, Guillot AP, Schuman CC, Teddy
S, Attarian HP.  Restless legs syndrome in pediatric patients with chronic kidney disease. Pediatr
Nephrol. 2009;24(3):545–8.


148.Riar SK, Leu RM, Turner-Green TC, Rye DB,
Kendrick-Allwood SR, McCracken C, et al. Restless
legs syndrome in children with chronic kidney disease. Pediatr Nephrol. 2013;28(5):773–95.
149. Kennedy C, Ryan SA, Kane T, Costello RW, Conlon
PJ.  The impact of change of renal replacement
therapy modality on sleep quality in patients with
end-stage renal disease: a systematic review and
meta-analysis. J Nephrol. 2018;31(1):61–70.
150.Li L, Tang X, Kim S, Zhang Y, Li Y, Fu P.  Effect
of nocturnal hemodialysis on sleep parameters
in patients with end-stage renal disease: a systematic review and meta-analysis. PLoS One.
2018;13(9):e0203710.
151.Brekke FB, Waldum-Grevbo B, von der Lippe N,
Os I.  The effect of renal transplantation on quality of sleep in former dialysis patients. Transpl Int.
2017;30(1):49–56.

152.
Ball E, Kara T, McNamara D, Edwards
EA.  Resolution of sleep-disordered breathing in a
dialysis-dependent child post-renal transplantation.
Pediatr Nephrol. 2010;25(1):173–7.

153.Sharma N, Harvey E, Amin R.  Sleep-disordered
breathing in 2 pediatric patients on peritoneal dialysis. Perit Dial Int. 2016;36(1):109–12.

154.Stabouli S, Papadimitriou E, Printza N, Dotis
J, Papachristou F.  Sleep disorders in pediatric


460

chronic kidney disease patients. Pediatr Nephrol.
2016;31(8):1221–9.

155.Fenves A, Emmett M, White M, Greenway G,
Michaels D. Carpal tunnel syndrome with cystic bone
lesions secondary to amyloidosis in chronic hemodialysis patients. Am J Kidney Dis. 1986;7(2):130–4.
156.Dulgheru EC, Balos LL, Baer AN. Gastrointestinal
complications of beta2-microglobulin amyloidosis:
a case report and review of the literature. Arthritis
Rheum. 2005;53(1):142–5.
157. Jadoul M, Garbar C, Noël H, Sennesael J, Vanholder
R, Bernaert P, et  al. Histological prevalence of
β2-microglobulin amyloidosis in hemodialysis: a prospective post-mortem study. Kidney Int.
1997;51(6):1928–32.
158.van Ypersele de Strihou C, Jadoul M, Malghem J,
Maldague B, Jamart J. Effect of dialysis membrane
and patient's age on signs of dialysis-related amyloidosis. The Working Party on Dialysis Amyloidosis.
Kidney Int. 1991;39(5):1012–9.
159.McCarthy J, Williams A, Johnson W.  Serum beta
2-microglobulin concentration in dialysis patients:
importance of intrinsic renal function. J Lab Clin
Med. 1994;123(4):495–505.

160.Dember L, Jaber B.  Dialysis-related amyloidosis: late finding or hidden epidemic? Semin Dial.
2006;19(2):105–9.
161.Robindranath K, Strippoli G, Daly C, Roderick P,
Wallace S, MacLeod A. Haemodiafiltration, haemofiltration and haemodialysis for end-stage kidney
disease (Review). Cochrane Database Syst Rev.
2006;4:1–93.


D. Borzych-Duz.ałka and E. Harvey
162.Raj D, Ouwendyk M, Francoeur R, Pierratos A.
b2-microglobulin kinetics in nocturnal haemodialysis. Nephrol Dial Transplant. 2000;15:58–64.
163.Schiffl H, D'Agostini B, Held E.  Removal of beta
2-microglobulin by hemodialysis and hemofiltration: a four year follow up. Biomater Artif Cell
Immobil Biotechnol. 1992;20(5):1223–32.
164.Lornoy W, Becaus I, Billiouw J, Sierens L, van
Malderen P, D'Haenens P.  On-line haemodiafiltration. Remarkable removel of b2-microglobulin.
Long-term clinical observations. Nephrol Dial
Transplant. 2000;15(1):49–54.
165.van Ypersele de Strihou C. b2-Microglobulin amyloidosis: effect of ESRF treatment modality and
dialysis membrane type. Nephrol Dial Transplant.
1996;11(2):147–9.

166.Ward RA, Greene T, Hartmann B, Samtleben
W.  Resistance to intercompartmental mass transfer
limits beta2-microglobulin removal by post-dilution
hemodiafiltration. Kidney Int. 2006;69(8):1431–7.
167. van Ypersele de Strihou C, Floege J, Jadoul M, Koch
K.  Amyloidosis and its relationship to different
dialysers. Nephrol Dial Transplant. 1994;9(Suppl
2):156–61.
168. Drueke TB, Massy ZA. Beta2-microglobulin. Semin
Dial. 2009;22(4):378–80.
169.Flythe JE, Hilliard T, Castillo G, Ikeler K, Orazi
J, Abdel-Rahman E, et  al. Symptom prioritization
among adults receiving in-center hemodialysis:
a mixed methods study. Clin J Am Soc Nephrol.
2018;13(5):735–45.



Part V
Management of Secondary Complications
of Chronic Dialysis


Nutritional Assessment
and Prescription for Children
Receiving Maintenance Dialysis

26

Christina L. Nelms, Nonnie Polderman,
and Rosanne J. Woloschuk

Introduction and Overview
Among the many priorities for the child receiving
maintenance dialysis, attaining an optimal nutritional status is paramount and forms the foundation
for a number of positive patient outcomes ranging
from clinical status and biochemical control to
quality of life and psychological well-being.
Adequate nutritional intake, especially in the
early years of life, optimizes long-term growth
[1]. Neurocognitive development and final adult
height outcomes, which are established in the
early years of life, are negatively impacted by
poor nutritional intake in a child nearing or reaching end-stage kidney disease (ESKD) [2].
Historically, the focus of nutrition intervention
has been to improve upon inadequate nutrition;
however, the rising incidence of obesity is refocusing nutrition goals toward providing adequate,

but not excessive, nutrition in order to reduce
long-term obesity-related health concerns [3, 4].

C. L. Nelms (*)
PedsFeeds, University of Nebraska, Kearney, NE,
USA
e-mail:
N. Polderman
Division of Nephrology, British Columbia Children’s
Hospital, Vancouver, BC, Canada
e-mail:
R. J. Woloschuk
Jim Pattison Children’s Hospital, Royal University
Hospital, Saskatoon, SK, Canada

Nutritional management, in concert with other
medical management such as pharmacology, fluid
balance, and dialysis prescription plays a key role
in the achievement of electrolyte and biochemical
control [5]. Each child on dialysis is unique, and
each nutrition care plan must be individualized
accordingly. Management of unique formula prescriptions and determination of best delivery route
increase management complexity [6]. The multidisciplinary team caring for infants, children, and
adolescents on dialysis must include a skilled
clinical nutrition expert, such as a pediatric renal
dietitian, who specializes in both pediatric and
dialysis-specific nutrition management [7].

Nutrition Overview
for Hemodialysis

A classic “sodium-, potassium-, and phosphorus-­
controlled diet” is the usual nutrition prescription
for the pediatric hemodialysis (HD) patient. The
typical thrice-weekly HD regimen does not provide adequate reduction of solutes to allow for
complete diet liberalization. Post-dialysis treatment side effects impair appetite. While children
with greater urine output enjoy more liberal fluid
allowances, most children require some degree of
fluid restriction. The use of HD in infants is rare,
but in these patients, strict fluid management is
imperative given the small size of the young child
and concern for blood volume shifts during treatment [5, 8, 9].

© Springer Nature Switzerland AG 2021
B. A. Warady et al. (eds.), Pediatric Dialysis, />
463


C. L. Nelms et al.

464

Less than 2% of all North American dialysis
patients receive home hemodialysis [10] with the
numbers of pediatric recipients unknown. One
advantage of home HD is flexibility in providing
intensified dialysis regimens in the form of
shorter sessions of daily dialysis or nocturnal
dialysis [11]. Patients undergoing nocturnal dialysis typically achieve excellent solute removal;
supplementation of phosphorus, calcium, and
vitamin D may be required. Although fluid and

diet restrictions may be discontinued, electrolytes must be closely monitored to avoid suboptimal levels [12–14]. Patients receiving frequent
daily dialysis do not enjoy the same dietary freedoms as those on nocturnal hemodialysis, but do
report improved mental affect and quality of life,
liberalized fluid allowances, and improved appetites [11, 15].

 utrition Overview for Peritoneal
N
Dialysis
Peritoneal dialysis (PD) is the most common
modality of dialysis in pediatric patients worldwide [7]. The use of PD therapy requires in-depth
assessment of factors related to PD to individualize the nutrition prescription. The National
Kidney Foundation (NKF) Kidney Disease
Outcomes Quality Initiative (KDOQI) pediatric
nutrition care guidelines [5] identify higher protein needs for PD patients compared to HD
patients because of protein losses associated with
PD (Tables 26.1 and 26.2). Ad lib eaters including children on PD typically consume adequate
protein, but children receiving formula may
require additional protein [16, 17].
The transport capacity of the peritoneum
also impacts dietary needs (Table  26.1). High
transporters have higher protein needs and
greater peritoneal losses of other nutrients and
will occasionally need potassium supplementation [18, 19]. Children who are low transporters have fewer nutrient losses, but
potentially suffer from greater uremic affects
resulting from relatively low solute removal,
which can have a negative impact on appetite
and gastrointestinal symptoms. Glucose

absorption from the dextrose-­containing dialysate is greater in high transporters and may
alter the recommended nutrition prescription

and biochemical status [5, 7]. For the young
child with an underlying renal tubular disorder
who is managed on PD, increased sodium supplementation and tighter potassium control
may be required to offset an increased loss of
sodium in the dialysis effluent and urine and
associated potassium retention [5].

Growth
Suboptimal growth is a complication of CKD
unique to children. Growth failure or “short stature” occurs at all stages of reduced kidney function, worsening with the progressive decline in
kidney function [20, 21]. For each standard deviation score (SDS) decline in growth velocity,
there is a reported 12–14% increase in mortality.
Short stature is also associated with increased
hospitalizations and infections, suggesting that
linear growth is not just a cosmetic issue [21, 22].
Patients who receive a kidney transplant and who
have very short stature have, on average, reduced
allograft survival [20]. Lastly, final adult height
impacts the education level and employment outcomes and thus overall quality of life [22, 23].
Early reports on growth from the North
American Pediatric Renal Trials and
Collaborative Studies (NAPTRCS) found that in
the years leading up to 2004, 37% of pre-dialysis
children fell below a height standard deviation
score (HtSDS) of −1.88. While improvements to
linear growth are being realized, recent reports
from the Chronic Kidney Disease in Children
(CKiD) study (2014) suggest that growth retardation remains prevalent with 12% of children
with moderate CKD exhibiting a HtSDS of ≤
−1.88. Data suggests that for each drop in estimated glomerular filtration rate (eGFR) of

10  ml/min/1.73  m2, height is expected to drop
by 0.14 SDS [24]. A child at or below the
3rd%ile, which is equivalent to a HtSDS of
−1.88, or with a height velocity of −2 SDS, warrants further evaluation of factors which may be
contributing to the poor growth and may ulti-



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