The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria for malnutrition

The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria for malnutrition

Accepted Manuscript The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria fo...

584KB Sizes 1 Downloads 53 Views

Accepted Manuscript The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria for malnutrition Kalliopi-Anna Poulia, Stanislaw Klek, Ioannis Doundoulakis, Emmanouil Bouras, Dimitrios Karayiannis, Aristea Baschali, Marili Passakiotou, Michael Chourdakis, MD RD MPH PhD PII:

S0261-5614(16)30180-7

DOI:

10.1016/j.clnu.2016.07.014

Reference:

YCLNU 2881

To appear in:

Clinical Nutrition

Received Date: 18 January 2016 Revised Date:

14 July 2016

Accepted Date: 25 July 2016

Please cite this article as: Poulia K-A, Klek S, Doundoulakis I, Bouras E, Karayiannis D, Baschali A, Passakiotou M, Chourdakis M, The two most popular malnutrition screening tools in the light of the new ESPEN consensus definition of the diagnostic criteria for malnutrition, Clinical Nutrition (2016), doi: 10.1016/j.clnu.2016.07.014. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

ACCEPTED MANUSCRIPT 1

1

Title: The two most popular malnutrition screening tools in the light of the new ESPEN

2

consensus definition of the diagnostic criteria for malnutrition

3

Authors: Kalliopi-Anna Poulia1, Stanislaw Klek2, Ioannis Doundoulakis3, Emmanouil Bouras3,

5

Dimitrios Karayiannis4, Aristea Baschali4, Marili Passakiotou5, Michael Chourdakis3 a

6

RI PT

4

1

Department of Nutrition and Dietetics, Laiko General Hospital, Athens, Greece

8

2

Stanley Dudrick's Memorial Hospital, Skawina, Poland

9

3

School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece

10

4

Department of Nutrition and Dietetics, Evangelismos Hospital, Athens, Greece

11

5

ICU, Ippokratio General Hospital, Thessaloniki, Greece

M AN U

SC

7

12 13

Names for Pubmed indexing: Poulia, Klek, Doundoulakis, Bouras, Karayiannis, Baschali,

14

Passakiotou, Chourdakis

15

Part of the data previously presented at the 36th ESPEN Congress (2015)

TE D

16 17 18

a

19

Michael Chourdakis, MD RD MPH PhD

20

Aristotle University of Thessaloniki, Greece

21

Department of Medicine

22

University Campus, 54124

23

Phone: +30 2310 999035, Fax: +30 2312 205270

24

Email: [email protected]

EP

AC C

25

Correspondence:

26

Abbreviations:

27

ASPEN: American Society for Enteral and Parenteral Nutrition; AUC: area under the (ROC)

28

curve;, BMI: body mass index; BAPEN: British Society of Enteral and Parenteral Nutrition;

29

DRM: disease related malnutrition; ESPEN: European Society for Clinical Nutrition and

ACCEPTED MANUSCRIPT 2

Metabolism; IQR: interquartile ranges; K: Cohen’s Kappa value; LOS: length of hospital stay;

31

LR(+): positive likelihood ratio; LR(-): negative likelihood ratio; MUST: Malnutrition

32

Universal Screening Tool; NPV: negative predicting value; NRS2002: Nutritional Risk

33

Screening 2002; PPV: positive predictive value; ROC: receiver operating characteristic; SD:

34

standard deviation;

RI PT

30

AC C

EP

TE D

M AN U

SC

35

ACCEPTED MANUSCRIPT 3

Abstract

37

Background: The new definition of malnutrition in adults proposed recently by The European

38

Society for Clinical Nutrition and Metabolism (ESPEN) changed the view on the issue and raised

39

the question of the reliability of available diagnostic tools. Therefore, the aim of this study was to

40

verify the accuracy of the two most commonly used screening tools by comparing their findings

41

with the new ESPEN criteria.

42

Methods: Nutritional screening was performed in 1146 (median age 60 years, interquartile

43

range: 44–73 years, 617 males, 529 females) patients on admission to hospitals with two

44

nutritional screening tools: Nutritional Risk Screening 2002 (NRS2002) and Malnutrition

45

Universal Screening Tool (MUST). The screening results were then compared to the ESPEN

46

new diagnostic criteria for malnutrition.

47

Results: According to the NRS2002 13.5% and 27.9% of the outpatients and hospitalized

48

patients respectively were found to be at moderate/high risk of malnutrition. With the use of

49

MUST 9.1% and 14.9% of the outpatients and hospitalized patients respectively were found to

50

be at moderate/high risk of malnutrition. According to the ESPEN diagnostic criteria 6.4% and

51

11.3% of outpatients and hospitalized patients respectively were classified as malnourished.

52

MUST was found to be better correlated to the latter for both outpatients (K=0.777, p<0.001)

53

and hospitalized patients (K=0.843, p<0.001) as compared to NRS2002 (k=0.256, p<0.001 and

54

k=0.228, p<0.001). ROC plots Area Under the Curve (AUC) was found to be higher for MUST

55

compared to NRS2002 (0.964 vs. 0.695 for outpatients and 0.980 vs 0.686 for hospitalized

56

patients respectively).

57

Conclusion: To our knowledge, this study is the first to analyze the clinical value of a

58

malnutrition screening tool in the light of the new ESPEN definition for malnutrition. According

AC C

EP

TE D

M AN U

SC

RI PT

36

ACCEPTED MANUSCRIPT 4 59

to our results, MUST was better correlated with ESPEN criteria for the definition of

60

malnutrition, leading us to the conclusion that it can more efficiently identify the malnourished

61

patients, during the screening process.

RI PT

62

Keywords

64

Disease related malnutrition, nutritional screening, screening tools, diagnostic criteria, ESPEN

65

malnutrition definition

AC C

EP

TE D

M AN U

SC

63

ACCEPTED MANUSCRIPT 5

66

Introduction Malnutrition, also called disease-related malnutrition (DRM), can be the result of poor

68

nutritional intake, impaired utilization or loss of macro- and/ or micronutrients, or may stem

69

from acute or chronic inflammation [1-3]. It is clear that nutritional status may deteriorate during

70

hospital stay, leading to malnutrition, which occurs in 20-60% of hospitalized patients, but also

71

affects outpatients in lower percentages (7-16%)[1-10]. This very often passes unnoticed,

72

ignored or untreated despite the fact that it has been recognized as a major public health concern

73

leading to a significant economic burden. As a consequence, increased morbidity, mortality,

74

hospital readmissions and length of hospital stay have been observed [3-5, 7].

M AN U

SC

RI PT

67

The first step to successfully treat malnutrition is the appropriate diagnosis. There are two

76

major difficulties linked to that issue: the first one is the definition of malnutrition and the second

77

is choosing an appropriate screening tool to assess the risk. Quite recently the European Society

78

for Clinical Nutrition and Metabolism (ESPEN) published consensus-based new criteria for

79

malnutrition, which were meant to be applied independently of clinical setting and aetiology [8,

80

11] when screening for malnutrition gives a positive result. Few years earlier, a similar task was

81

undertaken be the American Society for Enteral and Parenteral Nutrition (ASPEN) [3].

EP

TE D

75

As defining malnutrition according to the ESPEN criteria has as prerequisite a positive

83

screening result from a screening tool, we have to keep in mind that screening for malnutrition is

84

not a simple task either. Over the last decades several screening tools have been introduced and

85

evaluated. Most of them combine almost the same variables, such as percentage of weight loss

86

during a defined period of time, body mass index (BMI), reduction of food intake, and the

87

presence of disease and its severity [8]. The Nutritional Risk Screening 2002 (NRS-2002) is the

88

tool proposed by the ESPEN guidelines mainly for detection of indications for nutritional

AC C

82

ACCEPTED MANUSCRIPT 6 89

support [12]. Another popular screening tool is the Malnutrition Universal Screening Tool

90

(MUST), which was developed to detect the risk of malnutrition for all adult patients across all

91

health care settings [13, 14]. Despite the widespread use of these screening tools, the new ESPEN definition for

93

malnutrition changes the screening strategy as it gives a base upon which the results of the

94

screening process could be evaluated. At the same time, however, it raises a question of the

95

validity of the former screening modalities. As the two afore mentioned tools are designed to

96

screen malnutrition -anyhow examining it from another point of view- we decided to assess

97

whether “high risk for malnutrition” or “high nutritional risk” as identified by the two screening

98

tools actually corresponds to the prevalence of malnutrition according to the ESPEN criteria.

99

Therefore, the aim of current study was to assess the tools used in clinical practise to screen

SC

M AN U

100

RI PT

92

patient for malnutrition in the light of the new ESPEN consensus definition of malnutrition.

102

Materials and methods

103

Subjects

TE D

101

This multicenter study enrolled one thousand one hundred forty-six patients [median age

105

60 years (interquartile range-IQR: 44–73 years), 617 males, 529 females] on admission to 19

106

hospitals in 11 Greek cities, from November 2014 until April 2015. Adult patients (≥18 years

107

old) admitted to internal and surgery wards/outpatients units (50.9%, 583 internal medicine and

108

49.1%, 563 surgical patients) were eligible to participate. They were consecutively invited to

109

participate whenever data collection was possible within the first 24 hours after admission and/or

110

during their examination waiting time at the outpatient’s units or emergency unit. Demographic

111

and medical data along with the two questionnaires for nutritional risk were collected during a

AC C

EP

104

ACCEPTED MANUSCRIPT 7 112

structured interview. Patients unable to communicate with the study’s personnel were excluded.

113

The population of the study group was homogenous, Caucasians, Greek or originated for Balkan

114

and other European countries. Participants were informed about the aim of the study and written consent was obtained

116

by all participants. The study was approved by the Medical Research Ethics Committee of the

117

Medical School of the Aristotle University of Thessaloniki.

119

SC

118

RI PT

115

Anthropometric measurements

Anthropometric measurements were performed with the subjects wearing light clothing,

121

without shoes. Body weight and height were measured at the time of recruitment, i.e. on

122

admission, using a calibrated weighting scale and a wall-mounted stadiometer to the nearest 0.5

123

kg and 0.5 cm, respectively. If height measurement was not feasible (e.g. in the case of an unable

124

to stand patient), self-reported height and weight were used (if reliable and realistic), from the

125

patient or the patient’s caregiver. BMI was computed as weight (in kilograms) divided by the

126

square of height (in meters squared). Percentage of unintentional weight loss over the last three

127

months was calculated from patients’ reports.

130

TE D

EP

129

Assessment of the nutritional risk

AC C

128

M AN U

120

For each patient, the steps of each tool were completed by the same investigator in the

131

same order. The total score for each screening tool was computed during the analysis of the data.

132

The assessors were encouraged not to add the scores for each tool during data collection in order

133

to avoid bias by the knowledge of the categorization in a screening tool.

ACCEPTED MANUSCRIPT 8

MUST uses current BMI, unintentional weight loss and the presence of any acute disease

135

effect that could compromise nutritional intake for >5 days [13]. It includes three parameters

136

rating them as 0, 1 or 2 as follows: BMI>20 kg/m2=0; 18.5–20.0 kg/m2=1; <18.5 kg/m2=2;

137

unintentional weight loss in the past 3-6 months <5%=0; 5–10%=1; >10%=2; acute disease:

138

absent=0; present=2. Overall risk of malnutrition is established after addition of all points

139

allocated, as follows: 0=low risk; 1=medium risk; 2=high risk [14]. It was primarily designed for

140

the use in the community but it has been validated in all settings, including hospital.

SC

RI PT

134

NRS2002, the nutritional screening tool proposed by the ESPEN guidelines for the

142

nutritional screening of patients [12, 15] includes an initial screening including four questions

143

about the following parameters: BMI (if it is <20.5), presence of weight loss in the past three

144

months, presence of low dietary intake in the past week and the severity of disease. In the case of

145

any positive response a final screening is required [12]. The final screening evaluates impaired

146

nutritional status (Score=0 for normal nutritional status, Score=1 for weight loss >5% in the last

147

3 months or food intake below 50-75% of the normal requirements, Score=2 for weight loss >5%

148

in the last two months or BMI 18.5-20.5 + impaired general condition or food intake 25-60% of

149

normal requirements and Score=3 for weight loss >5% in the last month or BMI <18.5+impaired

150

general condition or Food intake 0-25% of normal requirement) and the “severity of disease

151

score” of 0-3 plus an additional point if the patient is older than 70 years. Nutritional risk is

152

established after addition of all points allocated, as follows: <3 at no or low risk, ≥3= at high

153

risk.

TE D

EP

AC C

154

M AN U

141

We retrospectively used the new European Society for Clinical Nutrition and Metabolism

155

(ESPEN) criteria for the definition of malnutrition [11], namely BMI≤18.5 kg/m2, or weight loss

156

>10% (indefinite of time) or 5% (in 3 months) and BMI <20 kg/m2 for patients <70 years or <22

ACCEPTED MANUSCRIPT 9

kg/m2 for patients ≥70 years, but not Fat Free Mass Index-FFMI (below <15 and <17 kg/m²) to

158

identify malnourished patients in our study’s population and evaluate the correlation of these

159

criteria with the prognostic value of the two screening tools. As the analysis was performed

160

retrospectively, no data regarding FFMI in our population were available; therefore, the

161

categorization of malnutrition according to the ESPEN criteria, was based only in the BMI and

162

weight loss. As both options are given in the consensus it can be assumed that by choosing one

163

versus the other, the results of our evaluation would not be biased. The aforementioned analysis

164

was performed by an investigator from our group who was neither involved in the initial

165

screening tools analysis nor aware of its results, for blinding purposes.

M AN U

SC

RI PT

157

The total score and classification of malnutrition risk (low, medium or high) was

167

determined for each study participant and screening tool. The scores obtained by the two

168

screening tools were then related to the ESPEN newly established consensus definition of

169

malnutrition.

TE D

166

For the cross-tabulation of risk classification between the tools we decided to group the

171

classification of malnutrition risk into two categories (i.e. “high/moderate” vs. “low/no risk”) as

172

patients allocated in the high group category are the ones that need to be further referred for

173

assessment to the dietetic and medical team.

175 176

AC C

174

EP

170

Statistical analysis

Normally distributed continuous variables were presented as mean values and standard

177

deviations (SD), skewed variables were presented as medians and IQR, whereas categorical

178

variables as absolute and relative (%) frequencies. The Kolmogorov-Smirnov test was applied to

179

evaluate normality of the distributions. All reported P-values are based on two-sided tests and

ACCEPTED MANUSCRIPT 10

compared to a significance level of 5%. Cohen’s kappa (Κ) statistic was calculated to determine

181

diagnostic concordance between the assessment tools (i.e. MUST, NRS2002) and ESPEN’s

182

diagnostic criteria for malnutrition. K coefficient is a statistical measure of inter–annotator

183

agreement for qualitative variables. In case of complete agreement between the variables K=1,

184

whereas if there is no agreement among the variables measured (other than what would be

185

expected by chance) then K≤0. Positive and negative likelihood ratios (LR+ and LR-

186

respectively) were calculated for both tools. For diagnostic procedures similar to nutritional

187

screening with the tools that were used in the study, it is desired LR+ to be >10 and LR-<0.1.

SC

RI PT

180

Sensitivity, specificity, predictive values for the two nutrition screening tools were

189

calculated with the use of diagnostic criteria as the way to identify the malnourished patients, as

190

can be seen in Supplementary Table 1.

M AN U

188

Receiver operating characteristic (ROC) curves were also used to evaluate the ability of

192

NRS2002 and MUST to correctly distinguish between the malnourished and the non-

193

malnourished patients (according to the ESPEN consensus definition of malnutrition). Area

194

under the ROC curve equal to 0.5 indicates that a tool cannot distinguish between the two

195

groups, whereas area under the ROC curve equal to 1 indicates perfect separation of the values

196

of the two groups.

198 199

EP

Statistical analysis was performed using SPSS for Windows, version 16.0 (SPSS Inc,

AC C

197

TE D

191

Chicago, IL).

ACCEPTED MANUSCRIPT 11

200

Results The baseline characteristics of the sample are presented in Table 1. Median BMI was

202

26.5 kg/m2 (IQR: 24.1–29.4 kg/m2) and median hospital stay among the hospitalized patients

203

was 3 days (IQR: 2–7 days).

RI PT

201

204 205

Table 1: Characteristics of the sample of patients

(n=784)

185 (51.1%)

617 (53.8%)

177 (48.9%)

529 (46.2%)

Age§ (years)

57 (36–70)

62 (46–75)

60 (44–73)

BMI§ (kg/m2)

26.4 (24.9–29.8)

26.8 (23.9–30.5)

26.5 ( 24.1–29.4)

BMI (<18,5 kg/m2)*

12 (1.5%)

10 (2.8%)

22 (1.9%)

Recent weight loss (>5% in 3 months)*

71 (9.1%)

54 (14.9%)

125 (10.9%)



3 (2–7)



M AN U

352 (44.9%)

TE D

207

§

Values expressed as medians and interquartile range (IQR)

EP

208

The classification of the risk of malnutrition of the patients by the two screening tools showed a variation among the two tools and the ESPEN criteria as can be seen in Table 2.

AC C

212

(n=1146)

Female*

*Values expressed as frequencies and percentages

211

(n=362)

432 (55.1%)

206

210

Overall

Male*

Length of stay in hospital§ (days)

209

Hospitalized

SC

Outpatients

Table 2: Classification of the risk of malnutrition by the two screening tools and the ESPEN criteria

Risk of malnutrition Moderate/high Low

Outpatients (n=784)

MUST

NRS2002

9.1% (71/784) 90.9%

13.5% (106/784) 86.5%

Hospitalized (n=362) ESPEN Criteria* 6.4% (50/784) 93.6%

MUST

NRS2002

14.9% (54/362) 85.1%

27.9% (101/362) 72.1%

ESPEN Criteria* 11.3% (41/362) 88.7%

ACCEPTED MANUSCRIPT 12 (713/784) 213

(678/784)

(734/784)

(308/362) (261/362)

(321/362)

* Classification of malnutrition according to the ESPEN consensus definition of malnutrition Cross tabulation of the results of screening of nutritional risk with MUST and NRS2002

215

and the classification of malnutrition according to the ESPEN diagnostic criteria can be found in

216

Table 3.

RI PT

214

217

Table 3: Cross tabulation of the results of screening of nutritional risk with MUST (≥1) and NRS2002

219

(≥3) and the classification of malnutrition according to the ESPEN consensus definition of malnutrition

SC

218

M AN U

Outpatients (n=784)

Hospitalized (n=362)

Not at moderate/high nutritional risk

Malnourished

Not malnourished

Malnourished

Not malnourished

(N=50)

(N=734)

(N=41)

(N=321)

48

23

41

13

2

711

0

308

TE D

220

At moderate/high nutritional risk

ESPEN Criteria

At moderate/high nutritional risk

25

81

25

76

Not at moderate/high nutritional risk

25

653

16

245

EP

NRS2002

MUST

ESPEN Criteria

The analysis of the agreement between the diagnostic criteria of malnutrition and the

222

results of nutritional screening was found to be different, according to the tool used for the

223

screening. More specifically, better agreement with the diagnostic criteria of malnutrition was

224

found in MUST for hospitalized [96.4% (349/362) of the cases (K=0.843, p<0.001)] and

225

outpatients [96.8% (759/784) of the cases (K=0.777, p<0.001)]. NRS2002 was found to be in

226

lower agreement in both outpatients [86.5% (678/784) of the cases (K=0.256, p<0.001)] and

227

hospitalized patients [74.6% (270/362) of the cases (K=0.228, p<0.001)]. MUST was also found

228

to have a very high sensitivity and specificity for both inpatients and outpatients (MUST

AC C

221

ACCEPTED MANUSCRIPT 13

Sensitivity=96.0% for outpatients and 100% for hospitalized respectively and MUST

230

Specificity=96.0% for both subgroups vs NRS-2002 Sensitivity = 50.0% in the outpatients and

231

61.0% in the hospitalized respectively.), showing that the likelihood that a patient screened

232

positive for malnutrition risk with MUST to be actually malnourished according to the ESPEN

233

diagnostic criteria was higher, compared to NRS 2002, with which according to our results, 50%

234

and 39% respectively of malnourished patients according to ESPEN criteria were not identified

235

as at risk of malnutrition.

SC

RI PT

229

On the other hand, NRS2002 was found to have a lower sensitivity (50% for outpatients

237

and 61% for hospitalized) and specificity (89.0% for outpatients vs. 76.3% for hospitalized), and

238

in combination with the low positive predictive value (23.6% for outpatients and 24.8% for

239

inpatients) it was found that the likelihood of a false positive malnutrition screening result was

240

higher for patients screened with NRS2002.

M AN U

236

Furthermore, MUST was found to have higher LR+ and lower LR- compared to

242

NRS2002 for both groups confirming the better performance of MUST regarding the agreement

243

with the diagnostic criteria of ESPEN for malnutrition. More specifically, NRS2002 did not

244

perform well with only a fair agreement with the ESPEN criteria and low positive likelihood

245

ratio (LR+).

EP

Finally, the area under the curve as it was calculated by the ROC curves was also higher

AC C

246

TE D

241

247

in MUST compared to NRS2002 (0.964 vs. 0.695 for outpatients and 0.980 vs 0.686 for

248

hospitalized patients respectively), confirming the better ability of MUST to distinguish a

249

malnourished patient compared to NRS2002. Results are presented in details in Table 4.

250

ACCEPTED MANUSCRIPT 14 251

Table 4: Statistical evaluation of the nutritional screening tools compared to the diagnostic criteria of

252

malnutrition (MUST (≥1) and NRS2002 (≥3). Outpatients

Hospitalized

(n=784)

(n=362) MUST

NRS2002

50.0

96.0

Specificity (%)

89.0

96.9

Positive predictive value (%)

23.6

67.6

Negative predictive value (%)

96.3

99.7

Positive Likelihood ratio (LR+)

4.53

30.64

2.58

24.69

Negative likelihood ratio (LR-)

0.56

0.04

0.51

-

0.695

AUC

100.0

76.3

96.0

24.8

75.9

93.9

100.0

0.777 (<0.001) 0.228 (<0.001) 0.843 (<0.001)

M AN U

0.256 (<0.001)

61.0

SC

Sensitivity (%)

Κ value (p)

0.964

0.686

253

Κ value derived from Cohen kappa statistics.

254

MUST: Malnutrition Universal Screening Tool. NRS2002: Nutritional Risk Screening 2002,

255

AUC=Area under the curve from ROC plots

0.980

TE D

256 257

MUST

RI PT

NRS2002

Discussion

The purpose of using a screening tools is to identify patients at risk of malnutrition and to

259

select those individuals, who are in need for further evaluation and potential intervention.

260

According to the NRS2002 13.5% and 27.9% of the outpatients and hospitalized patients

261

respectively were found to be at moderate/high risk of malnutrition. With the use of MUST 9.1%

262

and 14.9% of the outpatients and hospitalized patients respectively were found to be at

263

moderate/high risk of malnutrition. Other studies evaluating the risk of malnutrition, showed

264

results ranging from 20-60% or even higher, reaching 80% when the population of patients is

265

elderly [2, 8, 9, 16-18].

AC C

EP

258

ACCEPTED MANUSCRIPT 15

Finally, 6.4% and 11.3% of outpatients and hospitalized patients among our study

267

population were classified as malnourished according to the ESPEN diagnostic criteria. This is

268

the first study to show the prevalence of malnutrition in a Greek outpatients and hospitalized

269

patients in a multicenter study, from several areas in Greece, and at the same time it is also

270

interesting to see the difference of the prevalence of malnutrition in outpatients and hospitalized

271

patients, putting emphasis on the need of more actions needed for the early identification of

272

malnutrition during hospital stay.

SC

RI PT

266

The wide range of the assessed prevalence of malnutrition or the risk of malnutrition can

274

be attributed to the differences in the nutritional screening tools and/or differences in the

275

population included. The outpatients’ group included free living subjects, either outpatients or

276

those visiting an emergency unit. Our study showed that MUST was found to have a greater K

277

value than NSR2002, which shows that patients found at high risk with MUST were in greater

278

proportion identified as malnourished, according to the diagnostic criteria of ESPEN, when

279

compared to NRS2002. An alternative reading of this is that those are malnourished according to

280

the ESPEN criteria are better detected with the use of MUST. Moreover, MUST was also found

281

to have greater sensitivity and specificity compared to NRS2002. MUST has been proven to be a

282

valid tool for the identification of nutritional risk in specific patients’ population. According to a

283

systematic review for the identification of malnourishment in colorectal cancer patients, MUST

284

was found to have a high sensitivity and specificity and excellent diagnostic accuracy [19].

TE D

EP

AC C

285

M AN U

273

Available published data regarding the performance of the two aforementioned screening

286

tools show that NRS2002 was found to be better in predicting clinical outcome in hospitalized

287

patients compared to MUST [20] and the performance of the tools was increased when it was

288

combined with Subjective Global Assessment (SGA), a more complex tool that includes data

ACCEPTED MANUSCRIPT 16

from nutritional assessment.[21]. In another study by Velasco et al, a comparison of four tools,

290

namely NRS2002, SGA, MUST and Mini Nutritional Assessment (MNA), was performed using

291

SGA as the gold standard, in an era that diagnostic criteria for malnutrition did not exist. [22]. In

292

that study, NRS2002 and MUST were found to perform equally well, suggesting the use of those

293

tools for the screening of patients on admission to the hospital. The only study that did not use a

294

screening tool as the gold standard -since a gold standard for nutritional screening does not

295

actually exist- was a study by Poulia et al [23] in an elderly hospitalized population, confirming

296

our results for the better performance of MUST in comparison to NRS2002. In the

297

aforementioned study, the criterion of a patient being recognized as malnourished was to fulfil

298

the criteria of malnutrition in 4 out of 6 screening tools used, a method used in other studies as

299

well. Moreover, the statistical analysis and comparison of the tools was based on the extended

300

methods of triads, a method used for the analysis of measurements for which no gold standard is

301

set.

TE D

M AN U

SC

RI PT

289

The varying results of this comparison can be attributed to differences in the original

303

design of the two screening tools. In particular, NRS2002 was originally designed to screen

304

patients who would benefit from receiving nutritional support [12] and therefore its use might be

305

linked with an increased number of patients classified to be at moderate/high risk of

306

malnutrition, as a larger number of patients could indeed benefit from receiving nutritional

307

support. On the other hand, MUST is the only tool that was specifically developed for screening

308

of malnutrition [13, 14]. Therefore, its higher level of agreement may imply that those identified

309

at high risk of malnutrition are actually those who are more possibly indeed malnourished

310

according to the ESPEN criteria.

AC C

EP

302

ACCEPTED MANUSCRIPT 17

As nutritional screening tools are the first step to identify patients either as malnourished

312

or as at greater risk to become malnourished [24] and therefore to identify this problem before

313

the healthcare team schedules a treating plan, the importance of using a reliable and easy to

314

perform screening tool should be emphasized. Given the fact that there is no gold standard for

315

nutritional screening, a more specific definition of malnutrition could better serve to test whether

316

the identification at moderate/high risk of malnutrition is somehow correlated with the actual

317

nutritional status (i.e. if the patients screened as “high risk” are actually among those who fulfill

318

the newly established criteria of malnutrition by ESPEN) [11].

SC

RI PT

311

Due to the fact the both tools were found to have a very high negative predictive value in

320

both groups (96.3% for NRS2002 and 99.7% for MUST for outpatients and 93.9% for NRS2002

321

and 100% for MUST for hospitalized patients) one could safely assume that the probability for a

322

patient who was found not at risk in both tools to be malnourished is practically minimal.

M AN U

319

The strengths of our study are its multicentre setting and the large number of participants. To

324

our best knowledge, this is the first study that assesses different screening tools in a large

325

population in the light of the newly established ESPEN consensus. We acknowledge that our

326

study may have suffered from a sample selection bias as some patients who were severely sick

327

may have not joined the study as was also the case for a substantial number of patients that were

328

on nutritional support at study entry. A further potential limitation of this study is the fact that we

329

did not perform full nutritional assessment as a reference for the comparison of the screening

330

scores. Furthermore, our study evaluated the screening tools in the specific study population

331

enrolled, and extrapolation of results to other populations may be done cautiously. Finally, the

332

lack of FFMI is a limitation affecting the results of the study. According to Rojer et al [25], the

333

combination of FFMI and WL compared to BMI and WL, but yet it remains unclear if the

AC C

EP

TE D

323

ACCEPTED MANUSCRIPT 18 334

selection of the one criterion versus the other could affect the results of the classification of the

335

prevalence of malnutrition. Nutritional indices, due to their objectivity, could also be rather helpful in estimating

337

malnutrition risk on admission to the hospital [26]. MUST is an easy-to-use tool with more

338

straight forward, objective questions [14]. NRS2002, although containing similar questions with

339

MUST, relies on the decision of the medical professional regarding the severity of disease. Also,

340

it may impose a subjective bias or an added difficulty, especially for conditions not included in

341

the list of the referred clinical states and especially when the person performing the screening is

342

not a medical doctor. Therefore, MUST seems to be an extremely useful tool in settings where

343

time is limited and personnel dedicated in the nutritional screening is also rather compromised.

M AN U

SC

RI PT

336

344 345

Conclusion

To our knowledge, this study is the first to analyze the clinical value of a malnutrition

347

screening tool in the light of the new ESPEN definition for malnutrition. According to our

348

results, MUST was better correlated with ESPEN criteria for the definition of malnutrition,

349

leading us to the conclusion that it can more efficiently identify the malnourished patients,

350

during the screening process. More studies, however, are needed to fully assess all diagnostic

351

modalities.

353 354

EP

AC C

352

TE D

346

Acknowledgments

We would like to thank those who helped on site and all members of the participating wards.

355

356

Statement of authorship

ACCEPTED MANUSCRIPT 19

KAP conceived the study, wrote the manuscript, and helped with the statistical analyses.

358

SK contributed writing the manuscript and coordinated intragroup discussions. ID and EB

359

contributed to the sample collection and statistical data interpretation and helped with the

360

statistical analysis. DK and AB participated in the initial part of study design and contributed in

361

the sample collection and the data acquisition. MP participated in study’s design and contributed

362

in writing the manuscript. MC coordinated the study, the intragroup reviews and communication,

363

participated in its design, wrote the study protocol, and drafted the manuscript. KAP, SK, ID, EB

364

and MC commented on the first and subsequent drafts. All authors read and approved the final

365

manuscript.

366

367

CONFLICT OF INTEREST

M AN U

SC

RI PT

357

The authors hereby declare that the article is original, is not under consideration for

369

publication anywhere else and has not been previously published. Authors declare no potential or

370

actual personal, political or financial interest in the material, information or techniques described

371

in the paper.

AC C

EP

TE D

368

REFERENCES 1. 2. 3.

Bistrian, B., et al., Protein status of general surgical patients. J Am Med Assoc, 1974. 230: p. 85860. Hill, G., et al., Malnutrition in surgical patients. An unrecognised problem. Lancet, 1977. 1(8013): p. 689-92. White, J., et al., Academy Malnutrition Work Group; A.S.P.E.N. Malnutrition Task Force; A.S.P.E.N. Board of Directors. Consensus statement: Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition). JPEN J Parenter Enteral Nutr, 2012. 36(3): p. 275-83.

ACCEPTED MANUSCRIPT 20

10. 11. 12. 13.

14.

15. 16. 17. 18. 19.

20. 21.

22. 23. 24.

RI PT

9.

SC

8.

M AN U

7.

TE D

6.

EP

5.

Strong, J.P., The natural history of atherosclerosis in childhood. Ann N Y Acad Sci, 1991. 623: p. 915. Jensen, G., et al., Malnutrition syndromes: a conundrum vs continuum. . JPEN J Parenter Enteral Nutr, 2009. 33: p. 710-716. Jensen, G.L., et al., Adult starvation and disease-related malnutrition: A proposal for etiologybased diagnosis in the clinical practice setting from the International Consensus Guideline Committee. Clin Nutr, 2010. 29: p. 151-153. McWhirter, J.P. and C.R. Pennington, Incidence and recognition of malnutrition in hospital. BMJ, 1994. 308(6934): p. 945-8. Kondrup, J., et al., Incidence of nutritional risk and causes of inadequate nutritional care in hospitals. Clin Nutr, 2002. 21(6): p. 461-8. Leistra, E., et al., Prevalence of undernutrition in Dutch hospital outpatients. Eur J Intern Med, 2009. 20(5): p. 509-13. Neelemaat, F., et al., Screening malnutrition in hospital outpatients. Can the SNAQ malnutrition screening tool also be applied to this population? . Clin Nutr, 2008. 27(3): p. 439-446. Cederholm, T., et al., Diagnostic criteria for malnutrition - An ESPEN Consensus Statement. Clin Nutr, 2015. 34(3): p. 335-40. Kondrup, J., et al., ESPEN guidelines for nutrition screening 2002. Clin Nutr, 2003. 22(4): p. 41521. Stratton, R.J., et al., Malnutrition in hospital outpatients and inpatients: prevalence, concurrent validity and ease of use of the "malnutrition universal screening tool" ("MUST") for adults. British Journal of Nutrition, 2004. 92(05): p. 799-808. Elia, M., Screening for Malnutrition: A Multidisciplinary Responsibility. Development and Use of the ‘Malnutrition Universal Screening Tool’ (‘MUST’) for Adults. Malnutrition Advisory Group (MAG), a Standing Committee of BAPEN. Redditch, . Worcs.: BAPEN, 2003. Kondrup, J., et al., Nutritional risk screening (NRS 2002): a new method based on an analysis of controlled clinical trials. Clin Nutr, 2003. 22(3): p. 321-36. Guigoz, Y., S. Lauque, and B.J. Vellas, Identifying the elderly at risk for malnutrition. The Mini Nutritional Assessment. Clin Geriatr Med, 2002. 18(4): p. 737 - 757. Omran, M.L. and J.E. Morley, Assessment of protein energy malnutrition in older persons, part I: History, examination, body composition, and screening tools. Nutrition, 2000. 16(1): p. 50-63. Christensson, L., M. Unosson, and A.C. Ek, Evaluation of nutritional assessment techniques in elderly people newly admitted to municipal care. Eur J Clin Nutr, 2002. 56(9): p. 810-8. Håkonsen, S., et al., Diagnostic test accuracy of nutritional tools used to identify undernutrition in patients with colorectal cancer: a systematic review. JBI Database System Rev Implement Rep, 2015. 13(4): p. 141-87. Raslan, M., et al., Comparison of nutritional risk screening tools for predicting clinical outcomes in hospitalized patients. Nutrition, 2010. 26(7-8): p. 721-6. Raslan, M., et al., Complementarity of Subjective Global Assessment (SGA) and Nutritional Risk Screening 2002 (NRS 2002) for predicting poor clinical outcomes in hospitalized patients. Clin Nutr, 2011. 30(1): p. 49-53. Velasco, C., et al., Comparison of four nutritional screening tools to detect nutritional risk in hospitalized patients: a multicentre study. Eur J Clin Nutr, 2011. 65(2): p. 269-74. Poulia, K., et al., Evaluation of the efficacy of six nutritional screening tools to predict malnutrition in the elderly. Clin Nutr, 2012 31(3): p. 378-85. Blackburn, G. and P. Thornton, Nutritional assessment of the hospitalized patient. Med. Clin. North Am, 1979. 63: p. 1103-1115.

AC C

4.

ACCEPTED MANUSCRIPT 21

RI PT SC M AN U TE D EP

26.

Rojer, A.G., et al., The prevalence of malnutrition according to the new ESPEN definition in four diverse populations. Clin Nutr, 2016. 35(3): p. 758-62. Schneider, S. and X. Hebuterne, Use of nutritional scores to predict clinical outcomes in chronic diseases. . Nutrition reviews 2000. 58: p. 31-38.

AC C

25.

ACCEPTED MANUSCRIPT 22

Supplemental Files

RI PT

Supplementary Table 1: Calculation model for sensitivity, specificity and predictive values

Malnourished (ESPEN Criteria)

Not malnourished (ESPEN Criteria)

A

B

SC

Moderate/ High nutritional risk

C

D

M AN U

Not at moderate/ high nutritional risk

Sensitivity, specificity, predictive values for the two nutrition screening tools were calculated by the use of diagnostic criteria as the way to identify the malnourished patients, as follows: Sensitivity= A/A+C; Specificity= D/B+D; Positive predictive value= A/A+B; Negative predictive value = D/C+D,

AC C

EP

TE D

Where, A: high risk of malnutrition as resulted from the nutritional tool and malnourished according to the diagnostic criteria, B: high risk of malnutrition as resulted from the nutritional screening tool but not malnourished according to the diagnostic criteria, C: malnourished only from the diagnostic criteria but not screened at high risk of malnutrition from the nutritional screening tool and D: not malnourished according to the diagnostic criteria and not screened at high risk of malnutrition Positive likelihood ratio was calculated from sensitivity and specificity as follows: Positive Likelihood ratio (LR+) = Sensitivity/1-specificity and Negative Likelihood ratio (LR-) as follows: Negative Likelihood ratio (LR -) = 1-sensitivity/specificity