Dry Cold Application on pain and Ecchymosis among patients receiving Low Molecular Weight Heparin

 

I. Simeon1, Dr. Thenmozhi. P2

1M.Sc(N) II Year, Medical Surgical Nursing Department, Saveetha College of Nursing,

Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, India.

2Associate Professor, Medical Surgical Nursing Department, Saveetha College of Nursing,

Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, India.

*Corresponding Author E-mail: thenmozhi.sethu@gmail.com

 

ABSTRACT:

Objective: Anticoagulation has proved to be an important treatment modality in preventing thrombus formation. Local side effects of heparin injection include pain, erythema and ecchymosis. Role of nurse is. Strategic measures to be designed to minimize the local side effects during the administration of heparin. Hence the study was conducted with objective to determine the effectiveness of dry cold application on pain and ecchymosis. Methods: Post-test only research design was adopted to conduct the study with 60 samples who met the inclusion criteria and samples were randomly allocated into experimental group (n=30) and control group (n=30). The demographic variables were collected at the beginning of the study. Experimental group received dry cold application for 3 minutes on the heparin injection site before the administration of heparin injection whereas control group received the routine care. Level of pain was assessed immediately after withdrawing the needle, 4 hours and 8 hours by using numerical pain rating scale and ecchymosis was assessed 48 hours and 72 hours after the administration of injection by using transparent ruler scale for both experimental and control group. Data were analyzed using SPSS statistical package. Results: There was a significant difference was observed in the level of pain in all post-tests at the level of p<0.001 between the experimental and control group after the intervention but there was no difference was found in the size of ecchymosis both within experimental group and between the experimental and control group statistically. Conclusion: The findings of the study concluded that dry cold application is effective in reducing the level of pain and size of ecchymosis among patients receiving heparin injection.

 

KEYWORDS: Pain, Ecchymosis, Dry cold application, Heparin injection, Injection site, Subcutaneous.

 

 


INTRODUCTION:

Problems of the vascular system are common and can be serious. Heparin is widely used for thromboprophylaxis or treatment in many clinical conditions, including cardiovascular, neurovascular, orthopaedic surgery, invasive procedures, acute coronary syndromes, venous thromboembolism, atrial fibrillation, peripheral occlusive disease, dialysis, during extracorporeal circulation and who must remain in bed for a long time1. The action of Heparin is to prevent blood clot formation and thinning the blood viscosity.

 

It can be administered either directly into the bloodstream or as an injection under the skin. Subcutaneous administration of heparin is frequently performed nursing intervention2. Subcutaneous injection is normally chosen when slow and continuous absorption of the drug is needed. The drug is injected into fat and connective tissue underlying the dermis, where there is less blood flow and as a result a slower absorption rate. Suitable sites for subcutaneous injections are often the umbilical region of the abdomen and the lateral sides of the arms and thighs3.

 

Administration and injection techniques that are used for subcutaneous heparin injection may cause adverse outcomes such as bruising, haematoma and pain at the injection site4,5. Heparin can cause not only local side effects such as local bruising, hematoma and pain at the injection site but also cause the systemic effects of bleeding and thrombocytopenia6-13. 18.57% patients with myocardial infarction receiving heparin suffered with local bleeding14. Heparin poses many side effects include pain, erythema and ecchymosis. Hemorrhagic side effects have occurred in 3% to 7% of patients. Rarely painful red indurations and necrotic ulcerations at the injection site have been reported. Ecchymosis is one of the common side effects associated with heparin. Ecchymosis is the injury to biological tissue and capillary damage occurs, allowing blood to seep into surrounding tissue15. Bruising occurred in 53% of subjects out of a total of 43 subjects who received subcutaneous heparin16. It was reported that up to 90% individuals develop a bruise from subcutaneous administration of heparin17. These local adverse effects such as bruises and hematomas not only constitute physical trauma, but also cause changes in skin integrity and make it difficult to choose a site for future injections. This is because use of the traumatized area for later injections both causes pain and has a negative effect on the absorption of drugs7,13,18.

 

The role of nurses is to minimize local side effects such as pain, ecchymosis, bruising, hematoma formation and alleviate the discomfort during the administration of heparin wherever and whenever possible. Several studies have revealed the effects of the temperature, syringe size, needle gauge, injection volume and air bubble in the syringe, etc on the incidence of bruising, haematoma and pain at the injection site4,5. Other studies have explored the effect of the duration of the injection on the incidence of bruising and pain19. Strategies are preventing the hematoma, bruising, ecchymosis formation and decrease the level of pain during clinical practice. Administration techniques included syringe size, change of needles after drawing medication into the syringe, use of an air bubble, and type of sponge (dry or alcohol) applied to the site after injection also play a vital role in preventing bruising. The method 15 seconds injection duration and waiting for 5 seconds before withdrawing the needle is recommended to be used for subcutaneous heparin injection by clinical nurses. As to the results, the severity of pain in abdomen was lower than in thighs20. In another study proved that application of ice decrease the incidence or size of hematoma; however, the subject's perception of pain was significantly less21.

 

Ice is a therapeutic agent used in medicine as an integral part of injury treatment and rehabilitation. The use of ice pack is widespread because of their effectiveness, convenience, low cost, and ease of transportation. Ice packs can be made with any form of ice; however, 2 commonly used forms are cubed ice and crushed ice as well dry cold or moist cold. Ice is believed to control pain by inducing local anesthesia around the treatment area. Application of ice reduces the perception of pain during intramuscular injection, episiotomy pain, arteriovenous fistula puncture related pain, arthritis related joint pain and pain during chest tube removal among postoperative patients22-28. Investigators have also shown that it decreases oedema, nerve conduction velocities, cellular metabolism, and local blood flow29. A dry cold application can be made by filling an ice bag with crushed ice and wrapping it in a towel or washed cloth which will be colder than moist applications. Dry cold also prevents moisture from coming in direct contact with the skin30. The physiological effects of cold application are peripheral vasoconstriction, decreased capillary permeability, oxygen consumption, local metabolism, muscle tone, blood flow, lymph flow, motility of leucocytes and increased blood viscosity 31. Considering these potential benefits of cold application the investigators aimed to conduct the study on effectiveness of dry cold application on pain and ecchymosis.

 

MATERIALS AND METHODS:

A true experimental post-test only design was adopted to conduct the study after obtaining formal permission form the Hospital. A total of 60 samples who met the inclusion criteria were selected by using simple random sampling by lottery method and they were randomly assigned into experimental group (n=30) and control group (n=30). Patients who were receiving low molecular weight heparin (LMWH) injection subcutaneously and were oriented and able to perceive the pain intensity were included in the study. The exclusion criteria were patients with heparin injection with any other anticoagulant treatment, had previous history of coagulopathy and with skin problem such as eczema, psoriasis, vitiligo etc., Participants were explained about the purpose of the study and informed consent was obtained after assuring confidence. Each participant was assessed on the bed side. The demographic variables were collected by using structured interview questionnaire by interview method. Dry cold application was given for 3 minutes on the heparin injection site for the experimental group. Injection heparin administered subcutaneously to the experimental group before administration of heparin injection subcutaneously. Control group was received the routine care of hospital. Level of pain was assessed immediately after withdrawing the needle, 4 hours and 8 hours by using numerical pain rating scale for both experimental and control group. Ecchymosis was assessed 48 hours and 72 hours after the administration of injection by using transparent ruler scale for both experimental and control group. Confidentiality was maintained throughout the procedure. The data were tabulated and analyzed by descriptive and inferential statistics using SPSS statistical package.


 

RESULTS:

Table 1: Frequency and percentage distribution of demographic variables of patients receiving heparin injection. n = 60 (30+30)

Demographic Variables

Experimental Group

Control Group

Chi-Square for

homogeneity

No.

%

No.

%

Age

χ2=4.167

d.f=3

p = 0.244 N.S

21 - 30 years

0

0.00

2

6.67

31 - 40 years

5

16.67

5

16.67

41 - 50 years

10

33.33

14

46.67

Above 51 years

15

50.00

9

30.00

Gender

χ 2=0.617

d.f=1

p = 0.432 N.S

Male

19

63.33

16

53.33

Female

11

36.67

14

46.67

Educational status

χ 2=4.953

d.f=3

p = 0.175 N.S

 

 

χ 2=2.308

d.f=1

p = 0.129 N.S

Illiterate

14

46.67

13

43.33

Secondary school

12

40.00

7

23.33

Higher secondary

2

6.67

2

6.67

Graduate

2

6.67

8

26.67

Marital status

 

 

 

 

Single

2

6.67

6

20.00

Married

28

93.33

24

80.00

Widow

0

0.00

0

0.00

Occupation

 

χ 2=1.938

d.f=3

p = 0.585 N.S

Unemployed

5

16.67

4

13.33

Coolie

11

36.67

14

46.67

Government job

2

6.67

4

13.33

Private job

12

40.00

8

26.67

Diagnosis

 

χ 2=1.961

d.f=2

p = 0.375 N.S

Cardiovascular problems

3

10.00

6

20.00

Neurovascular problems

21

70.00

16

53.33

Others

6

20.00

8

26.67

N.S – Not Significant

 

The table 1 shows that in the experimental group, maximum 15(50%) were aged above 51 years, 19(63.33%) were male, 14(46.67%) were illiterate, 28(93.33%) were married, 12(40%) were employed in private, and 21(70%) were diagnosed to have neurovascular problems. Whereas in the control group, maximum 14(46.67%) were in the age group of 41 - 50 years, 16(53.33%) were male, 13(43.33%) were illiterate, 24(80%) were married, 14(46.67%) were coolie, and 16(53.33%) were diagnosed to have neurovascular problems. The chi-square was computed to check the homogeneity of the demographic variables and proves that homogeneity was maintained.


 

Table 2: Frequency and percentage distribution of post-tests level of pain among patients receiving heparin injection in the experimental group. n=30

Test

No Pain (0)

Mild Pain (1 – 3)

Moderate Pain (4 – 6)

Severe Pain (6 – 9)

Worst Pain (10)

No

%

No.

%

No.

%

No.

%

No.

%

Post Test 1

(After withdrawal)

7

23.33

14

46.67

9

30.0

0

0

0

0

Post Test 2

(After 4 hours)

11

36.67

15

50.0

4

13.33

0

0

0

0

Post Test 3

(After 8 hours)

19

63.34

10

33.33

1

3.33

0

0

0

0

 


The table 2 depicts that after the administration of dry cold application in post-test 1 (after withdrawal) 14(46.67%) had mild pain, 9(30%) had moderate pain and 7(23.33%) had no pain. In post-test 2 (after 4 hours), 15(50%) had mild pain, 11(36.67%) had no pain and 4(13.33%) had moderate pain. In post-test 3 (after 8 hours), 19(63.34%) had no pain, 10(33.33%) had mild pain and only one (3.33%) had moderate pain among patients receiving heparin injection in the experimental group.


 

Table 3: Frequency and percentage distribution of post-tests level of pain among patients receiving heparin injection in the control group.               n = 30

Test

No Pain (0)

Mild Pain (1 – 3)

Moderate Pain

(4 – 6)

Severe Pain (6 – 9)

Worst Pain (10)

No.

%

No.

%

No.

%

No.

%

No.

%

Post Test 1 (After withdrawal)

 

0

 

0

 

6

 

20.0

 

21

 

70.0

 

3

 

10.0

 

0

 

0

Post Test 2 (After 4 hours)

0

0

10

33.33

16

53.34

4

13.33

0

0

Post Test 3 (After 8 hours)

0

0

11

36.67

14

46.66

5

16.67

0

0


The table 3 depicts that in post-test 1 (after withdrawal) 21(70%) had moderate pain, 6(20%) had mild pain and 3(10%) had severe pain. In post-test 2 (after 4 hours), 16(53.34%) had moderate pain, 10(33.33%) had mild pain and 4(13.33%) had severe pain. In post-test 3 (after 8 hours), 14(46.66%) had moderate pain, 11(36.67%) had mild pain and 5(16.67%) had severe pain. among patients receiving heparin injection in the control group.

 

Table 4: Frequency and percentage distribution of post-tests level of ecchymosis among patients receiving heparin injection in experimental group.                                 n = 30

 

Test

Small Size (0.1 – 1 cm2)

Moderate Size (1.1 – 2 cm2)

Big Size (2.1 – 3cm2)

No.

%

No.

%

No.

%

Post Test 1 (After withdrawal)

30

100

0

0

0

0

Post Test 2 (After 48 hours)

30

100

0

0

0

0

Post Test 3 (After 72 hours)

30

100

0

0

0

0

 

The table 4 shows that after the administration of dry cold application in post-test 1 (after withdrawal), post-test 2 (after 48 hours) and post-test 3 (after 72 hours) almost all 30(100%) had small size (01.-1cm2) of ecchymosis.

 

Table 5: Frequency and percentage distribution of post-tests level of ecchymosis among patients receiving heparin injection in the control group.    n = 30

 

Test

Small Size (0.1 – 1 cm2)

Moderate Size (1.1 – 2 cm2)

Big Size (2.1 – 3 cm2)

No.

%

No.

%

No.

%

Post Test 1 (After withdrawal)

27

90.0

3

10.0

0

0

Post Test 2 (After 48 hours)

28

93.3

2

6.67

0

0

Post Test 3 (After 72 hours)

29

96.7

1

3.33

0

0

 


The table 5 portrays that in post-test 1 (after withdrawal) 27(90%) had small size of ecchymosis and 3(10%) had moderate size of ecchymosis. In post- test 2 (after 48 hours), 28(93.33%) had small size of ecchymosis and 2(6.67%) had moderate size of ecchymosis. In post-test 3 (after 72 hours), 29(96.67%) had small size of ecchymosis and only one (3.33%) had moderate size of ecchymosis.

 

Table 6: Comparison of post-tests level of pain among patients receiving heparin injection within the experimental group. n = 30

Test

Pain

Paired ‘t’ Test

Value

Mean

S.D

Post test1 (After withdrawal)

2.17

1.89

t = 3.247

P=0.003, S**

Post Test 2 (After 4 hours)

1.50

1.43

Post Test 2 (After 4 hours)

1.50

1.43

t = 4.205

P=0.0001, S***

Post Test 3 (After 8 hours)

0.67

1.06

Post test1 (After withdrawal)

2.17

1.89

t = 4.677

P=0.0001, S***

Post Test 3 (After 8 hours)

0.67

1.06

***p<0.001, **p<0.01, S – Significant, N.S – Not Significant

 

The table 6 portrays that, the mean score of pain in post-test 1(after withdrawal) was 2.17±1.89, the mean score of pain in post-test 2 (after 4 hours) was 150±1.43 and the mean score of pain in post-test 3 (after 8 hours) was 0.67±1.06. The calculated paired ‘t’ value of t = 3.247 between post-test 1 and post-test 2 was found to be statistically moderately significant at p<0.01 level. The table further revealed that the calculated ‘t’ value of t = 4.205 between post-test 2 and post-test 3 and t = 4.677 between post-test 1 and post-test 3 was found to be statistically highly significant at p<0.001 level. This clearly indicates that the administration of dry cold application before heparin injection among patients was found to be effective in reducing the level of pain in the experimental group

 

Table 7: Comparison of post-tests level of ecchymosis among patients receiving heparin injection within the experimental group.             n = 30

Test

Ecchymosis

Paired ‘t’ Test

Value

Mean

S.D

Post test1 (After withdrawal)

0.03

0.10

t = 1.975

P=0.058, N.S

Post Test 2 (After 48 hours)

0.01

0.04

Post Test 2 (After 48 hours)

0.01

0.04

t = 1.000

P=0.326, N.S

Post Test 3 (After 72 hours)

0.00

0.00

Post test1 (After withdrawal)

0.33

0.10

t = 1.775

P=0.086, N.S

Post Test 3 (After 72 hours)

0.00

0.00

N.S – Not Significant

 

The table 7 portrays that, the mean score of ecchymosis in post-test 1(after withdrawal) was 0.03±0.10, the mean score of ecchymosis in post-test 2 (after 48 hours) was 0.01±0.04 and the mean score of ecchymosis in post-test 3 (after 72 hours) was 0.00±0.00.

 

The calculated paired ‘t’ value of t = 1.975 between post-test 1 and post-test 2, t = 1.000 between post-test 2 and post-test 3 and t = 1.775 between post-test 1 and post-test 3 was not found to be statistically significant. This clearly indicates that most of the patients had no ecchymosis after the administration of dry cold application in the experimental group

 

Figure 1: Comparison of post-tests level of pain among patients receiving heparin injection between the experimental and control group.

 

The figure: 1 depicts that the calculated unpaired ‘t’ value t = 5.902, t = 6.963 and t = 8.826 was found to be statistically highly significant at p<0.001 level. This clearly indicates that there was significant difference in the level of pain scores between the experimental and control group at the level of post-test 1 (after withdrawal), post-test 2 (after 4 hours) and post-test 3 (after 8 hours). This clearly indicates that dry cold application administered to the patients receiving heparin injection was found to be effective in reducing the level of pain in the experimental group than the patients in the control group.

 

Table 8: Comparison of post-tests level of ecchymosis among patients receiving heparin injection between the experimental and control group.        n = 60(30+30)

Test

Experimental Group

Control Group

Unpaired ‘t’

Value

Mean

S.D

Mean

S.D

Post test1 (After withdrawal)

0.03

0.10

0.28

0.46

t = 2.833

p=0.008, S**

Post Test 2 (After 48 hours)

0.01

0.04

0.23

0.39

t = 3.040

p=0.005, S**

Post Test 3 (After 72 hours)

0.00

0.00

0.19

0.37

t = 2.814

p=0.009, S**

**p<0.01, S - Significant

 

The table 8 shows that the calculated unpaired ‘t’ value t = 2.833, t = 3.040 and t = 2.814 was not found to be statistically significant. This clearly indicates that there was no significant difference in the level of ecchymosis scores between the experimental and control group at the level of post-test 1 (after withdrawal), post-test 2 (after 48 hours) and post-test 3 (after 72 hours).


 

Table 9: Association of post test 3 (after 8 hours) level of pain among patients receiving heparin injection with selected demographic

variables in the experimental group.                                                                                                                                              n=30

Demographic Variables

No Pain (0)

Mild Pain (1 – 3)

Moderate Pain (4 – 6)

Chi-Square Value

No.

%

No.

%

No.

%

 

Diagnosis

2=12.816

d.f=4

p = 0.012

S*

Cardiovascular problems

0

0

2

6.7

1

3.3

Neurovascular problems

14

46.7

7

23.3

0

0

Peripheral vascular problems

5

16.7

1

3.3

0

0

*p<0.05, S – Significant, N.S – Not Significant

 


The table 9 shows that the demographic variable diagnosis had shown statistically significant association with post- test 3 (After 8 hours) level of pain score at p<0.05 level.

 

DISCUSSION:

Anticoagulation has proved to be an important treatment modality in preventing thrombus formation for the treatment of vascular problems of heart, lung conditions, during cardiothoracic, cardiovascular and orthopedic surgery and kidney dialysis, the most commonly used route of administration is subcutaneous which can causes the local side effects of pain, bruising, ecchymosis, hematoma formation. The current study intensively analyze the side effects of pain and ecchymosis and to prove the hypothesis of significant reduction in the level of pain and size of ecchymosis after administration of dry cold application in experimental group than control group. Regarding demographic variables majority of the participants were male with the age group of above 50 year and on the treatment of LMWH for neurovascular problems. Many other studies have conducted with the participants who had cardiovascular problem. The present study findings observed that the participants were experienced pain and ecchymosis due to the administration of heparin injection subcutaneously. The level of pain was assessed immediately after withdrawing from the needle, after 4 hours and after 8 hours of administration of both experimental and control group. They perceived the level of pain from no pain to moderate pain and none of them have perceived severe to worst pain in the experimental group. The highest percentage was observed 9(307%) had moderate pain after withdrawal of the needle but only one (3.333%) had moderate pain after 8 hours of injection. Whereas in control group 21(70%), 16(53.34%) and 14(46.66%) had moderate pain immediately after withdrawal, after 4 hours and after 8 hours of injection respectively and 3- 5(10-16%) had severe pain too. Paired t test also reveals that there is a significant reduction in the level of pain between post-test 1&2, 2&3 and 1&3 at the level of p<0.001. Un-paired‘t’ value t = 5.902, t = 6.963 and t = 8.826 was found to be statistically highly significant at p<0.001 level. This clearly indicates that there was significant difference in the level of pain scores between the experimental and control group at the level of post-test 1 (after withdrawal), post-test 2 (after 4 hours) and post-test 3 (after 8 hours). This finding of the present study was supported by the study conducted by Emine Korkmaz Kilic at al who found that two-minute cold application before and after subcutaneous heparin injections reduced pain score and the size of bruises 48 and 72 hours after heparin. However in the current study dry cold application was given 5 minutes prior to the injection32. Similarly another study by Batra G who proven the same evidence that 3 minutes of ice application significantly reduce the level of pain and ecchymosis33. The present study also observed the size of ecchymosis was within 0.1-1 cm2 in experimental group when it was assessed immediately after withdrawal, after 48 hours and after 72 hours of heparin injection administration. Whereas in control group, very few three (10%) had moderate size and none of them had big size of ecchymosis. Within the experimental group paired t test reveals no significant difference between post-test 1 and 2, 2 and 3 and 1 and 3. Mean score of experimental and control group was compared by unpaired t test and found to be no significant difference in the size of ecchymosis between the experimental and control group. This finding is closely in line with the result finding of the study by Shijila S et al and concluded that application of dry cold is effective in reducing the level of pain perception and ecchymosis among patients receiving low molecular weight heparin34. Similarly, Lt Col Rajeena et al and, who found that ice cold application was effective in reducing pain and ecchymosis and enhancing the comfort of patient35. In another study by Supreet Rupam et al who demonstrated that cold application is effective in reducing the pain and size of bruising among hospitalized receiving subcutaneous heparin36. Amaniyan S et al stated that cold application as a fundamental nursing intervention can be an effective intervention to prevent adverse drug reactions at the injection site in terms of the occurrence and size of bruising in patients receiving subcutaneous heparin37. But current study is limited to assess the bruising. The study conducted by Varghese et al with the objective of prevention and reduction of pain, bruise and hematoma by 'Moist Ice Pack' application on the site of subcutaneous heparin injection administered to the patients and the results showed that statistically significant in favour of the use of moist ice pack while comparing the pain and bruise at subcutaneous injection site between experimental and control group at 12, 48 and 72 hours38. The present study limits to assess the hematoma hence further study can be conducted to assess hematoma, bruising with the comparison of moist and dry cold application. Many studies have explored that both moist and dry application shows the significant effect however comparative study between dry and moist cold application will give better evidence to utilize for the cold application reducing the local effects thereby relive the psychological distress, better absorption of heparin and improve the comfort of the patients. Hence the stated hypothesis of reduction level of pain was accepted and rejected the reducing the size of ecchymosis from the study findings.

 

CONCLUSION:

The findings of the present study concluded that the application of the dry cold prior to the administration of heparin injection subcutaneously can significantly reduce the level of pain and the size of ecchymosis not reduced statistically. In order to comply with treatment modality, pain reduction and thereby physical and psychological comfort to the patients is considered the most important factor. It is incumbent upon health care professionals to be knowledgeable and sensitive towards adverse outcomes result from heparin therapy and promote safety and relieve physical discomfort of the patient.

 

ACKNOWLEDGEMENT:

The authors would like to thank all the participants for participating in this research study and also thank the health care team members for their support to complete the study successfully.

 

CONFLICT OF INTEREST:

Authors declare no conflict of Interest

 

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Received on 14.04.2020            Modified on 21.09.2020

Accepted on 01.02.2021            © RJPT All right reserved

Research J. Pharm. and Tech 2021; 14(11):5790-5796.

DOI: 10.52711/0974-360X.2021.01007