Postoperative hospital gown
By designing connecting sets and components for postoperative hospital gowns, the problem of existing compression garments being unable to restrict arm movement in breast cancer patients was solved, achieving the effect of postoperative activity restriction and recovery promotion.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-04-27
- Publication Date
- 2026-03-31
AI Technical Summary
Existing compression garments cannot effectively restrict arm movement in breast cancer patients, affecting postoperative recovery.
A postoperative hospital gown was designed, comprising a gown body, a connecting sleeve, and a connecting component. The connecting sleeve includes a receiving cavity for accommodating an arm, and is connected to the gown body via the connecting component to restrict arm movement.
It effectively restricts arm movement in breast cancer patients, promotes postoperative recovery, meets the needs of postoperative activity restriction, and improves patient comfort.
Smart Images

Figure CN224055404U_ABST
Abstract
Description
Technical Field
[0001] This application relates to the field of medical supplies, and in particular to postoperative patient gowns. Background Technology
[0002] Axillary lymph node dissection is a surgical procedure that removes and examines the lymph nodes in the armpit. It is often performed in conjunction with a mastectomy and is used to prevent the further spread of breast cancer.
[0003] Compression gowns are typically worn after mastectomy to reduce postoperative bleeding and effusion. However, current compression gowns do not restrict arm movement in breast cancer patients. In contrast, after combined axillary lymph node dissection and mastectomy, arm movement needs to be restricted for 24 hours, and current compression gowns do not offer this restriction. Utility Model Content
[0004] This application primarily addresses the technical problem that existing compression garments do not restrict arm movement in breast cancer patients. It provides a postoperative hospital gown that can restrict arm movement in breast cancer patients.
[0005] To address the aforementioned technical problems, this application provides a postoperative hospital gown, characterized in that the postoperative hospital gown is used by breast cancer patients after axillary lymph node dissection, and the postoperative hospital gown comprises...
[0006] The patient gown body has side seams on both sides along the first direction;
[0007] The patient gown body has connecting sleeves on both sides along the first direction. The connecting sleeves include at least one connecting sleeve. The connecting sleeve has a first receiving cavity through it along the first direction. The first receiving cavity is used to receive the arm of a breast cancer patient.
[0008] A connecting component is provided, wherein the connecting sleeve is connected to the patient gown body via the connecting component to drive a first receiving cavity within the connecting sleeve to be positioned close to the side seam on the patient gown body and to restrict the movement of the breast cancer patient's arm.
[0009] In one embodiment, the connecting sleeve assembly includes two connecting sleeves, namely a first connecting sleeve and a second connecting sleeve, wherein a first receiving cavity in the first connecting sleeve is used to receive the upper arm of a breast cancer patient, and a first receiving cavity in the second connecting sleeve is used to receive the lower arm of a breast cancer patient.
[0010] In one embodiment, the connecting sleeve assembly includes one connecting sleeve, and the connecting sleeve is a first connecting sleeve, wherein a first receiving cavity within the first connecting sleeve is used to receive the upper arm of a breast cancer patient.
[0011] In one possible implementation, the connection component includes,
[0012] A connecting rope, which is connected to the connecting sleeve;
[0013] The first connector includes a first connecting structure and a second connecting structure. The first connecting structure is disposed on the connecting rope, and the second connecting structure is disposed on the patient gown body. The first connecting structure and the second connecting structure are detachably connected, and multiple adjustment positions are formed between the first connecting structure and the second connecting structure to adjust the relative position between the connecting sleeve and the side seam of the patient gown body.
[0014] In one embodiment, a plurality of connecting straps are spaced apart on the outer circumference of the connecting sleeve, and a connecting space is formed between the connecting straps and the connecting sleeve. The connecting rope passes through the connecting space in sequence to fit the connecting rope over the connecting sleeve and to connect the connecting rope to the connecting sleeve.
[0015] In one possible implementation, the connection component further includes,
[0016] A connecting rod, made of a rigid material, is arranged along the first direction. The two ends of the connecting rod along the first direction are respectively connected to the first connecting sleeve and the second connecting sleeve. The connecting rod fits against the arm of the breast cancer patient to keep the arm in an upright position.
[0017] In one possible implementation, the connection component further includes,
[0018] A connecting piece assembly, the connecting piece assembly being made of a rigid material, the connecting piece assembly including a first connecting piece and a second connecting piece, the first connecting piece being disposed on a first connecting sleeve, the second connecting piece being disposed on a second connecting sleeve, the connecting rod being connected to the first connecting sleeve via the first connecting piece, and the connecting rod being connected to the second connecting sleeve via the second connecting piece.
[0019] In one embodiment, a first rotating column is provided on the first connecting piece, and a second rotating column is provided on the second connecting piece, and the connecting rod is rotatably connected to the first rotating column and the second rotating column.
[0020] In one embodiment, the first connecting piece and the second connecting piece are provided with rotating grooves, the first rotating column and the second rotating column are both located in the rotating grooves, and the connecting rod portion is located in the rotating grooves.
[0021] In one possible implementation, the postoperative patient gown further includes,
[0022] A connecting pocket is attached to the patient gown body.
[0023] Compared to existing technologies, in practical use, the breast cancer arm is placed in the receiving cavity of the connecting sleeve, and the connecting sleeve is connected to the main body of the hospital gown through the connecting component. At the same time, the breast cancer arm is set close to the side seam of the main body of the hospital gown. After the postoperative hospital gown is put on the breast cancer patient, the movement of the breast cancer patient's arm can be restricted. Attached Figure Description
[0024] Appendix Figure 1 This is a schematic diagram of the structure of a postoperative patient gown for this application;
[0025] Appendix Figure 2 This is another structural diagram of the postoperative hospital gown in this application;
[0026] Appendix Figure 3 This is a schematic diagram of a structure between the connecting rod and the connecting sleeve in this application;
[0027] Appendix Figure 4 This is a schematic diagram of one structure of the first connecting sleeve of this application.
[0028] Explanation of the labels in the diagram:
[0029] X, first direction; Y, second direction;
[0030] 10. Postoperative hospital gown;
[0031] 100. The main body of the patient gown; 110. Side seams;
[0032] 200. Connecting sleeve assembly; 210. First connecting sleeve; 220. Second connecting sleeve; 230. First receiving cavity; 240. Second connecting piece;
[0033] 300. Connecting assembly; 310. Connecting rope; 320. First connector; 321. First connecting structure; 322. Second connecting structure; 330. Connecting belt; 340. Connecting rod; 350. Connecting piece assembly; 351. First connecting piece; 352. Second connecting piece; 353. First rotating column; 354. Second rotating column; 355. Rotating groove;
[0034] 400. Connecting pocket. Detailed Implementation
[0035] To make the objectives, features, and advantages of this application more apparent and understandable, the technical solutions in the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this application, and not all embodiments. Based on the embodiments of this application, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this application.
[0036] The existing compression garments do not have the technical problem of restricting arm movement in breast cancer patients.
[0037] Therefore, this application provides a postoperative hospital gown, wherein the postoperative hospital gown is used by breast cancer patients after axillary lymph node dissection, and the postoperative hospital gown includes,
[0038] The patient gown body has side seams on both sides along the first direction;
[0039] The patient gown body has connecting sleeves on both sides along the first direction. The connecting sleeves include at least one connecting sleeve. The connecting sleeve has a first receiving cavity through it along the first direction. The first receiving cavity is used to receive the arm of a breast cancer patient.
[0040] A connecting component is provided, wherein the connecting sleeve is connected to the patient gown body via the connecting component to drive a first receiving cavity within the connecting sleeve to be positioned close to the side seam on the patient gown body and to restrict the movement of the breast cancer patient's arm.
[0041] Example 1:
[0042] In current technology, breast cancer is one of the most common malignant tumors in women, characterized by its invasiveness and metastasis. The axilla is one of the most common sites of metastasis for breast cancer. Mastectomy is often performed in conjunction with axillary lymph node dissection, a procedure that removes and examines the axillary lymph nodes to prevent further spread of breast cancer. After mastectomy, compression garments are typically worn to reduce postoperative bleeding and effusion, and to promote recovery and healing. However, after combined axillary lymph node dissection and mastectomy, the entire arm of the breast cancer patient needs to be restricted for 24 hours. Further recovery is required within one to three days post-surgery through exercises such as clenching the fist, extending the fingers, flexing the wrist, and flexing the elbow. Elbow flexion is performed by swinging the forearm; therefore, only upper arm movement needs to be restricted within the first one to three days post-surgery. Current compression garments do not restrict arm movement in breast cancer patients.
[0043] Please refer to the attached document. Figure 1 To be continued Figure 4As shown, the first direction X of this application refers to the height direction of the postoperative gown 10, that is, the direction of the postoperative gown 10 from top to bottom or from bottom to top. In this application, the first connecting sleeve 210 is positioned higher than the second connecting sleeve 220, and the second connecting sleeve 220 is positioned lower than the first connecting sleeve 210. The second direction Y of this application refers to the width direction of the postoperative gown, that is, the direction of the postoperative gown 10 from left to right or from right to left.
[0044] Appendix Figure 1 This is a structural diagram of one possible postoperative patient gown (model 10) for this application. Please refer to the attached diagram. Figure 1 As shown, the postoperative patient gown 10 of this application is used for use after axillary lymph node dissection in breast cancer patients, and the postoperative patient gown 10 of this application is used in conjunction with a compression garment. In specific use, the postoperative patient gown 10 is worn over the compression garment.
[0045] Please refer to the attached document. Figure 1 As shown, the postoperative hospital gown 10 of this application includes a gown body 100, which is worn on the upper body of a breast cancer patient. The gown body 100 has side seams 110 on both sides along the first direction X. When the postoperative hospital gown 10 is used, the side seams 110 correspond to the arms of the breast cancer patient. The arms of the breast cancer patient include the upper arm and the lower arm. The gown body 100 of this application can be a sleeved structure or a sleeveless structure.
[0046] Please refer to the attached document. Figure 1 As shown, the patient gown body 100 of this application also includes a connecting sleeve assembly 200, which is disposed on both sides of the patient gown body 100 along the first direction X. In this application, the connecting sleeve assembly 200 includes two connecting sleeves, namely a first connecting sleeve 210 and a second connecting sleeve 220. The first connecting sleeve 210 and the second connecting sleeve 220 are arranged alternately along the first direction X. A first receiving cavity 230 is provided through the first connecting sleeve 210 and the second connecting sleeve 220 along the first direction X. The first receiving cavity 230 is used to receive the arm of a breast cancer patient. Further, the first receiving cavity 230 of the first connecting sleeve 210 is used to receive the upper arm of the breast cancer patient, and the first receiving cavity 230 of the second connecting sleeve 220 is used to receive the lower arm of the breast cancer patient. In this application, restricting the movement of the breast cancer patient's arm refers to binding the breast cancer patient's arm to the upper body through the postoperative patient gown 10 to prevent relative movement of the arm.
[0047] In one embodiment, both the first connecting sleeve 210 and the second connecting sleeve 220 are made of flexible material, and further, both the first connecting sleeve 210 and the second connecting sleeve 220 are made of cotton cloth.
[0048] In one embodiment, the first receiving cavity 230 has a circular cross-section.
[0049] Please refer to the attached document. Figure 1 As shown, the patient gown body 100 of this application also includes a connecting component 300. The first connecting sleeve 210 and the second connecting sleeve 220 are connected to the patient gown body 100 through the connecting component 300, so as to drive the first receiving cavity 230 in the first connecting sleeve 210 and the second connecting sleeve 220 to be positioned close to the side seam 110 on the patient gown body 100. The upper arm located in the first connecting sleeve 210 and the lower arm located in the second connecting sleeve 220 are simultaneously positioned close to the side seam 110 on the patient gown body 100. At this time, the upper arm and lower arm of the breast cancer patient are simultaneously bound to the upper body of the breast cancer patient, which can further restrict the movement of the breast cancer patient's arm and accelerate the postoperative recovery speed of the breast cancer patient.
[0050] The connecting component 300 includes a connecting rope 310, which is a long strip structure and made of a flexible material. The connecting component 300 also includes a first connector 320, through which the connecting rope 310 is detachably connected to the patient gown body 100. The first connector 320 includes a first connecting structure 321 and a second connecting structure 322. The first connecting structure 321 is disposed on the connecting rope 310, and the second connecting structure 322 is disposed on the patient gown body 100. The first connecting structure 321 and the second connecting structure 322 are detachably connected, and multiple adjustment positions are formed between the first connecting structure 321 and the second connecting structure 322 to adjust the relative position between the connecting sleeve and the side seam 110 of the patient gown body 100.
[0051] In one embodiment, the first connector 320 is a Velcro structure, the first connecting structure 321 is one of a fleece layer and a serrated layer, and the second connecting structure 322 is the other of a fleece layer and a side layer. Both the first connecting structure 321 and the second connecting structure 322 have a certain length in the second direction Y. Therefore, by adjusting the different connection positions of the first connecting structure 321 and the second connecting structure 322 in the second direction Y, the closeness between the connecting sleeve and the side seam 110 of the patient gown body 100 can be adjusted to further ensure the closeness between the breast cancer patient's arm and upper body.
[0052] In one embodiment, the first connector 320 is a snap fastener structure, the first connecting structure 321 is one of a male and female snap fastener, and the second connecting structure 322 is the other of a male and female snap fastener.
[0053] Please refer to the attached document. Figure 1As shown, the connecting component 300 of this application also includes connecting straps 330. A plurality of connecting straps 330 are spaced apart circumferentially on the outer side of the connecting sleeve. The connecting component 300 has two or more connecting straps 330. There is a certain gap between the connecting straps 330 and the connecting sleeve. The gap between the connecting straps 330 and the connecting sleeve constitutes a connecting space. Connecting ropes 310 pass through the connecting space sequentially to be fitted over the connecting sleeve, thus connecting the connecting ropes 310 to the connecting sleeve. After the connecting ropes 310 are fitted over the connecting sleeve, both ends of the connecting ropes 310 are connected to the patient gown body 100 via a first connector 320.
[0054] Please refer to the attached document. Figure 1 As shown, the connecting component 300 of this application also includes a connecting rod 340. The connecting rod 340 is designed to keep the breast cancer patient's arm in an upright position, further restricting the movement of the breast cancer patient's arm. The connecting rod 340 is made of a rigid material, and more specifically, it is made of plastic to ensure that the connecting rod 340 will not bend. The connecting rod 340 is arranged along a first direction X, and the direction in which the connecting rod 340 is positioned is consistent with the direction in which the breast cancer patient's arm is in an upright position. After the two ends of the connecting rod 340 along the first direction X are connected to the first connecting sleeve 210 and the second connecting sleeve 220 respectively, the connecting rod 340 fits against the breast cancer patient's arm to ensure that the breast cancer patient's arm is in an upright position, thereby further restricting the movement of the breast cancer patient's arm.
[0055] Please refer to the attached document. Figure 1 As shown, the connecting component 300 of this application also includes a connecting pocket 400, which is connected to the patient gown body 100. The opening of the connecting pocket 400 is set upwards, and the connecting pocket 400 is used to place a negative pressure drainage ball.
[0056] Appendix Figure 2 This is another structural diagram of the postoperative patient gown 10 in this application. Please refer to the attached diagram. Figure 2 As shown, attached Figure 2 Postoperative patient medication 10 is relative to the attached Figure 1 The difference between the postoperative patient gown 10 and the 200-piece connecting sleeve set lies in the number of connecting sleeves in the connecting sleeve set. Figure 2 Postoperative patient medication 10 and supplementary Figure 1 The postoperative patient medication is the same as that in other cases, so I will not repeat the details.
[0057] Please refer to the attached document. Figure 2As shown, the patient gown body 100 of this application also includes a connecting sleeve assembly 200, which is disposed on both sides of the patient gown body 100 along the first direction X. In this application, the connecting sleeve assembly 200 includes a connecting sleeve, and the connecting sleeve is a first connecting sleeve 210. A first receiving cavity 230 is provided through the first connecting sleeve 210 along the first direction X. The first receiving cavity in the first connecting sleeve 210 is used to receive the upper arm of a breast cancer patient.
[0058] In one embodiment, the first connecting sleeve 210 is made of a flexible material, and further, the first connecting sleeve 210 is made of cotton cloth.
[0059] In one embodiment, the first receiving cavity 230 has a circular cross-section.
[0060] In this application, when the connecting sleeve assembly 200 is provided with only one connecting sleeve, the upper arm of the breast cancer patient can be restricted by the connecting sleeve, while the lower arm of the breast cancer patient can move, further meeting the need for recovery by practicing clenching fists, extending fingers, flexing wrists and flexing elbows within one to three days after surgery.
[0061] Appendix Figure 3 This is a schematic diagram of a structure between the connecting rod 340 and the connecting sleeve 200 of this application. Please attach... Figure 3 As shown, the connecting assembly 300 of this application further includes a connecting piece group 350, which is made of a rigid material and, more specifically, of plastic. The connecting piece group 350 includes a first connecting piece 351 and a second connecting piece 352. The first connecting piece 351 is disposed on the first connecting sleeve 210 and is fixedly connected to the first connecting sleeve 210. The second connecting piece 352 is disposed on the second connecting sleeve 220 and is fixedly connected to the second connecting sleeve 220. The connecting rod 340 is connected to both the first connecting piece 351 and the second connecting piece 352 to achieve connection with the first connecting sleeve 210 and the second connecting sleeve 220. In this application, the connecting piece group 350 is provided to enhance the stability of the connecting rod 340 during connection and prevent relative displacement between the connecting rod 340 and the first connecting sleeve 210 and the second connecting sleeve 220. Since the first connecting sleeve 210 and the second connecting sleeve 220 are made of flexible material, if the connecting rod 340 is directly connected to the first connecting sleeve 210 and the second connecting sleeve 220, the possibility of relative displacement between the connecting rod 340 and the first connecting sleeve 210 and the second connecting sleeve 220 will be increased.
[0062] Please refer to the attached document. Figure 3As shown, the first connecting piece 351 of this application is provided with a first rotating post 353, the second connecting piece 352 is provided with a second rotating post 354, and the connecting rod 340 is provided with a rotating hole that forms a rotating connection with the first rotating post 353 and the second rotating post 354, so as to realize the rotating connection between the connecting rod 340 and the first rotating post 353 and the second rotating post 354. In the specific use of the postoperative hospital gown 10 of this application, a corresponding positional deviation will form between the first connecting sleeve 210 and the second connecting sleeve 220. That is, the second connecting sleeve 220 will be set closer to the side seam 110 of the gown body 100 relative to the first connecting sleeve 210. Therefore, the line connecting the first connecting sleeve 210 and the second connecting sleeve 220 in the first direction X will also be tilted. At this time, when the connecting rod 340 is set to be rotatably connected with the first connecting piece 351 and the second connecting piece 352, the tilt of the connecting rod 340 can be formed simultaneously to eliminate the situation where the connecting rod 340 drags the first connecting sleeve 210 and the second connecting sleeve 220 when the first connecting piece 351 and the second connecting piece 352 are rigidly connected, and to enhance the comfort of the postoperative hospital gown 10 when wearing it.
[0063] Furthermore, the first connecting piece 351 and the second connecting piece 352 are provided with rotating grooves 355, the first rotating column 353 and the second rotating column 354 are both located in the rotating grooves 355, and the connecting rod 340 is partially located in the rotating grooves 355, thereby limiting the rotation angle of the connecting rod 340 to further limit the movement of the breast cancer patient's arm.
[0064] Appendix Figure 4 This is a schematic diagram of one structure of the first connecting sleeve 210 of this application. Please refer to the attached diagram. Figure 4 As shown, the specific structure of the first connecting sleeve 210 is illustrated. In this application, the specific structure of the second connecting sleeve 220 is identical to that of the first connecting sleeve 210, and will not be described again in this application. A first receiving cavity 230 is provided through the first connecting sleeve 210 along the first direction X. The receiving cavity of the first connecting sleeve 210 is used to accommodate the upper arm of a breast cancer patient. A first connecting piece 351 is disposed on the outside of the first connecting sleeve 210 and is fixedly connected to the first connecting sleeve 210. Furthermore, the first connecting sleeve 210 is detachable, and the detached portion of the first connecting sleeve 210 is detachably connected via a second connecting member 240. The size of the first receiving cavity 230 can be adjusted via the second connecting member 240. Specifically, the larger the overlapping portion of the detached portion of the first connecting sleeve 210, the smaller the size of the first receiving cavity 230, thereby maximizing the fit between the first connecting sleeve 210 and the arm of the breast cancer patient.
[0065] In one embodiment, the second connector 240 is a Velcro structure or a snap fastener structure.
[0066] In the description of this specification, the references to terms such as "one embodiment," "some embodiments," "example," "specific example," or "some examples," etc., indicate that a specific feature, structure, material, or characteristic described in connection with that embodiment or example is included in at least one embodiment or example of this application. Furthermore, the specific features, structures, materials, or characteristics described may be combined in any suitable manner in one or more embodiments or examples. Moreover, without contradiction, those skilled in the art can combine and integrate the different embodiments or examples described in this specification, as well as the features of those different embodiments or examples.
[0067] Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include at least one of that feature. In the description of this application, "a plurality of" means two or more, unless otherwise explicitly specified.
[0068] The above description is merely a specific embodiment of this application, but the scope of protection of this application is not limited thereto. Any variations or substitutions that can be easily conceived by those skilled in the art within the scope of the technology disclosed in this application should be included within the scope of protection of this application. Therefore, the scope of protection of this application should be determined by the scope of the claims.
Claims
1. A post-operative hospital gown, characterized in that, The postoperative hospital gown is used for breast cancer patients after axillary lymph node dissection, and the postoperative hospital gown comprises, A hospital gown body has side seams on both sides in a first direction; A connecting sleeve set is provided on both sides of the hospital gown body in the first direction, and the connecting sleeve set comprises at least one connecting sleeve, and a first accommodating cavity is provided through the connecting sleeve in the first direction, and the first accommodating cavity is used for accommodating the arm of the breast cancer patient. A connecting assembly is used to connect the connecting sleeve to the hospital gown body, so that the first accommodating cavity in the connecting sleeve is arranged close to the side seam on the hospital gown body, and the movement of the arm of the breast cancer patient is limited.
2. The post-operative hospital gown of claim 1, wherein, The connecting sleeve set comprises two connecting sleeves, which are a first connecting sleeve and a second connecting sleeve, respectively, the first accommodating cavity in the first connecting sleeve is used for accommodating the upper arm of the breast cancer patient, and the first accommodating cavity in the second connecting sleeve is used for accommodating the lower arm of the breast cancer patient.
3. The post-operative hospital gown of claim 1, wherein, The connecting sleeve set comprises one connecting sleeve, which is a first connecting sleeve, and the first accommodating cavity in the first connecting sleeve is used for accommodating the upper arm of the breast cancer patient.
4. The post-operative hospital gown of claim 2 or claim 3, wherein, The connecting assembly comprises, A connecting rope is connected to the connecting sleeve; A first connecting piece comprises a first connecting structure and a second connecting structure, the first connecting structure is arranged on the connecting rope, the second connecting structure is arranged on the hospital gown body, the first connecting structure and the second connecting structure are detachably connected, and a plurality of adjustment positions are formed between the first connecting structure and the second connecting structure to adjust the relative position between the connecting sleeve and the side seam of the hospital gown body.
5. The post-operative hospital gown of claim 4, wherein, A plurality of connecting bands are arranged on the outer periphery of the connecting sleeve at intervals, a connecting space is formed between the connecting band and the connecting sleeve, the connecting rope passes through the connecting space in sequence, the connecting rope is sleeved outside the connecting sleeve, and the connection between the connecting rope and the connecting sleeve is realized.
6. The post-operative hospital gown of claim 2, wherein, The connecting assembly further comprises, A connecting rod is made of hard material, the connecting rod is arranged in the first direction, the connecting rod is connected to the first connecting sleeve and the second connecting sleeve at both ends in the first direction, and the connecting rod is attached to the arm of the breast cancer patient to keep the arm of the breast cancer patient in an upright state.
7. The post-operative hospital gown of claim 6, wherein, The connecting assembly further comprises, A connecting piece set is made of hard material, the connecting piece set comprises a first connecting piece and a second connecting piece, the first connecting piece is arranged on the first connecting sleeve, the second connecting piece is arranged on the second connecting sleeve, the connecting rod is connected to the first connecting sleeve through the first connecting piece, and the connecting rod is connected to the second connecting sleeve through the second connecting piece.
8. The post-operative hospital gown of claim 7, wherein, A first rotating column is arranged on the first connecting piece, a second rotating column is arranged on the second connecting piece, and the connecting rod is rotatably connected to the first rotating column and the second rotating column.
9. The post-operative hospital gown of claim 8, wherein, The first connecting piece and the second connecting piece are provided with rotating grooves, the first rotating column and the second rotating column are located in the rotating grooves, and the connecting rod is partially located in the rotating grooves.
10. The post-operative hospital gown of claim 1, wherein, The postoperative patient garment further comprises, A connecting pocket connected with the patient garment body.