Effect of Dry
Cold Application on Pain Perception and Ecchymosis
among Patients Receiving Low Molecular Weight Heparin
Miss. Shijila. S1,
Mrs. Jean Tresa. J2*
1Quality Control Executive, NIMS, Trivandrum
2Associate Professor, Department of Medical Surgical Nursing, College of
Nursing, Sri Ramakrishna Institute of Paramedical Sciences, Coimbatore.
*Corresponding
Author Email: jeantresa@gmail.com
ABSTRACT:
The study to assess the effect of dry cold application
on pain perception and ecchymosis among patients
receiving low molecular weight heparin was conducted using true experimental
posttest only control group design. Using total enumerative sampling technique
25 samples were selected and randomly assigned to experimental group (n=13) and the control group (n=12). Dry cold application was given for 3 minutes
on the LMWH injection site for the experimental group. Pain perception
and ecchymosis was assessed using numerical pain
rating scale and transparent ruler scale respectively. Using unpaired ‘t’ test,
the effect of dry cold application on pain perception was analyzed immediately
after withdrawing the needle, after 4 hours and 8 hours(t = 2.205, 2.827 and 2.912 respectively, df =
23, p < 0.05) and ecchymosis was analyzed
after 48 hours and 72 hours (t = 2.129
and 2.118 respectively, df = 23, p < 0.05).
Hence it is concluded that application of dry cold is effective in reducing the
level of pain perception and ecchymosis among
patients receiving low molecular weight heparin.
KEYWORDS: Dry cold application, pain perception, ecchymosis.
INTRODUCTION:
Health is the functional efficiency of a living
organism(Webster, 1913). Health systems need to be strengthened to deliver
better care for peoples. Primary care is the only access to medical treatment
and use of low-technology interventions(United National Report, 2007).
Subcutaneous low molecular weight heparin (LMWH) is frequently prescribed for
stroke, deep vein thrombosis and other cardiovascular disorders. Low molecular
weight heparin (LMWH) is a class of medication used as an anticoagulant. They
are administered subcutaneously in fixed doses once or twice daily (Melba and Priyalatha, 2009).
NEED FOR THE STUDY:
Approximately 318 patients receive Injection LMWH per
year in a selected hospital, Coimbatore. Subcutaneous administration of heparin
is a frequently performed nursing intervention(Batra,
2014). Pain and Ecchymosis are the common side
effects associated with LMWH. Dry cold application is a simple and inexpensive
therapy which has been accepted for an effective non pharmacologic intervention
for pain management and progression of ecchymosis (Melba and Priyalatha,
2009).
STATEMENT OF THE PROBLEM:
Effect of Dry
Cold Application on Pain Perception and Ecchymosis
among Patients Receiving Low Molecular Weight Heparin at Selected Hospital,
Coimbatore.
OBJECTIVES:
· To assess the pain perception and ecchymosis among patients receiving low molecular weight
heparin.
· To evaluate the effect of dry cold
application on pain perception and ecchymosis among
patients receiving low molecular weight heparin.
Hypothesis:
H1 : There will be a significant difference in the level
of pain perception between the experimental group and control group after dry
cold application among patients receiving low molecular weight heparin.
H2 : There will be a significant difference in
the size of ecchymosis between the experimental group
and control group after dry cold application among patients receiving low
molecular weight heparin.
METHODOLOGY:
Quantitative research approach was adopted for the
study with true experimental posttest
only control group design. The study was conducted in the general and special
wards of Sri Ramakrishna Hospital, Coimbatore. Total Enumerative Sampling
technique was used to select the samples. All the 25 patients who met the
sampling criteria were randomly assigned to experimental group (n=13) and
control group (n=12) using lottery method. The independent variable of the
study was dry cold application. The dependent variables of the study were pain perception and ecchymosis
among patients receiving low molecular weight heparin. The demographic
profile, clinical profile, numerical rating scale and transparent ruler scale
were framed based on the expert opinion and the supportive literatures. Ethical
consent was obtained from the institutional ethical committee. Informed consent
was obtained from each study participant. Dry cold application was given for 3
minutes on LMWH injection site to the experimental group. Injection LMWH was
administered subcutaneously to the experimental and control group by the
researcher. Posttest was done to assess the pain perception immediately after
withdrawing needle, 4 hours, and 8 hours by using numerical pain rating scale
and ecchymosis was assessed 48 hours and 72 hours
after the day of injection by using transparent ruler scale.
RESULTS:
Table I: Effect of Dry Cold
Application on Pain Perception among Patients receiving Low Molecular Weight
Heparin in the Experimental Group and Control Group
|
S. No |
Pain Perception |
Group |
Mean |
SD |
Mean difference |
't' value |
|
1. |
Immediately after withdrawing needle |
Experimental
Group |
0.439 |
0.555 |
1.422 |
2.205* |
|
Control Group |
1.861 |
2.155 |
||||
|
2. |
After 4 Hours |
Experimental
Group |
0 |
0 |
0.294 |
2.827* |
|
Control Group |
0.294 |
0.359 |
||||
|
3. |
After 8 Hours |
Experimental
Group |
0 |
0 |
0.099 |
2.912* |
|
Control Group |
0.099 |
0.119 |
*Significant at 0.05 level
Table 2: Effect of Dry Cold
Application on Ecchymosis among Patients Receiving
Low Molecular Weight Heparin in the Experimental Group and Control Group
|
S. No |
Ecchymosis |
Group |
Mean (cm2) |
SD |
Mean difference |
't' value |
|
1. |
48 hours |
Experimental
Group |
0.003 |
0 |
0.066 |
2.129* |
|
Control Group |
0.069 |
0.108 |
||||
|
2. |
72 hours |
Experimental
Group |
0.001 |
0 |
0.108 |
2.118* |
|
Control Group |
0.109 |
0.175 |
*Significant at 0.05 level
Unpaired 't' test was used to analyze the effect of
dry cold application on pain perception among patients receiving LMWH in
experimental and control groups. Level of pain perception was assessed
immediately after withdrawing needle, it was identified that, the mean score
and standard deviation of experimental group was 0.439 and 0.555 respectively
and control group was 1.861 and 2.155 respectively with the mean difference of
1.422. Calculated ‘t’ value was 2.205, which was greater than the table value (tv= 2.07, df=23) at
0.05 level of significance. Pain perception was assessed after 4 hours, it was
identified that, the mean score and standard deviation of experimental group
was 0 and control group 0.294 and 0.359 respectively with the mean difference
of 0.294. Calculated ‘t’ value was 2.827, which was greater than the table
value (tv= 2.07, df=23)
at 0.05 level of significance. Pain perception assessed after 8 hours, it was
identified that, the mean score and standard deviation of experimental group
was 0 and the control group was 0.099 and 0.119 respectively with the mean
difference of 0.099. Calculated ‘t’ value was 2.912, which was greater than the
table value (tv= 2.07, df=23)
at 0.05 level of significance. Hence it shows there is a significant difference
in the level of pain perception among patients receiving LMWH immediately after
withdrawing needle, after 4 hours and after 8 hours in the experimental and
control group. Unpaired 't' test was
used to analyze effect of dry cold application on ecchymosis
among patients receiving LMWH in experimental and control groups. Size of ecchymosis was assessed 48 hours after the day of
injection, it was identified that, the mean score and the standard deviation of
experimental group was 0.003 and 0 respectively and control group was 0.069 and
0.108 respectively with the mean difference of 0.066. Calculated ‘t’ value was
2.129, which was greater than the table value (tv=
2.07, df=23) at 0.05 level of significance. Ecchymosis was assessed 72 hours after the day of injection,
it was identified that, the mean score and the standard deviation of
experimental group was 0.001 and 0 and control group was 0.109 and 0.175
respectively with the mean difference of0.108. Calculated ‘t’ value was 2.118,
which was greater than the table value (tv=
2.07, df=23) at 0.05 level of significance. Hence it
shows there is a significant difference in the size of ecchymosis
among patients receiving LMWH in 48 hours and 72 hours after the day of
injection.
MAJOR FINDINGS:
From the present study, it was found that the dry cold
application was effective in reducing the level of pain perception and ecchymosis among patients receiving low molecular weight
heparin.
CONCLUSION:
The patients receiving LMWH experience pain and
develop ecchymosis. The study was conducted to
identify the effect of dry cold application on pain perception and ecchymosis among patients receiving low molecular weight
heparin. This study proves that the dry cold application is effective in
reducing pain perception and ecchymosis among
patients receiving low molecular weight heparin. Therefore the dry cold
application can be used as a measure in reducing injection LMWH induced pain
perception and ecchymosis.
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Received on 26.06.2016 Modified on 10.07.2016
Accepted on 17.07.2016 ©
A&V Publications all right reserved
Asian J. Nur. Edu. and Research.2016; 6(4): 503-505.
DOI: 10.5958/2349-2996.2016.00094.X